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PLOS Medicine logoLink to PLOS Medicine
. 2021 Oct 21;18(10):e1003807. doi: 10.1371/journal.pmed.1003807

Changes in the associations of race and rurality with SARS-CoV-2 infection, mortality, and case fatality in the United States from February 2020 to March 2021: A population-based cohort study

George N Ioannou 1,2,*, Jacqueline M Ferguson 3, Ann M O’Hare 4, Amy S B Bohnert 5, Lisa I Backus 6, Edward J Boyko 7, Thomas F Osborne 8, Matthew L Maciejewski 9,10,11,12, C Barrett Bowling 13, Denise M Hynes 14,15, Theodore J Iwashyna 16,17, Melody Saysana 2, Pamela Green 2, Kristin Berry 2
Editor: Jon Zelner18
PMCID: PMC8530298  PMID: 34673772

Abstract

Background

We examined whether key sociodemographic and clinical risk factors for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and mortality changed over time in a population-based cohort study.

Methods and findings

In a cohort of 9,127,673 persons enrolled in the United States Veterans Affairs (VA) healthcare system, we evaluated the independent associations of sociodemographic and clinical characteristics with SARS-CoV-2 infection (n = 216,046), SARS-CoV-2–related mortality (n = 10,230), and case fatality at monthly intervals between February 1, 2020 and March 31, 2021. VA enrollees had a mean age of 61 years (SD 17.7) and were predominantly male (90.9%) and White (64.5%), with 14.6% of Black race and 6.3% of Hispanic ethnicity. Black (versus White) race was strongly associated with SARS-CoV-2 infection (adjusted odds ratio [AOR] 5.10, [95% CI 4.65 to 5.59], p-value <0.001), mortality (AOR 3.85 [95% CI 3.30 to 4.50], p-value < 0.001), and case fatality (AOR 2.56, 95% CI 2.23 to 2.93, p-value < 0.001) in February to March 2020, but these associations were attenuated and not statistically significant by November 2020 for infection (AOR 1.03 [95% CI 1.00 to 1.07] p-value = 0.05) and mortality (AOR 1.08 [95% CI 0.96 to 1.20], p-value = 0.21) and were reversed for case fatality (AOR 0.86, 95% CI 0.78 to 0.95, p-value = 0.005). American Indian/Alaska Native (AI/AN versus White) race was associated with higher risk of SARS-CoV-2 infection in April and May 2020; this association declined over time and reversed by March 2021 (AOR 0.66 [95% CI 0.51 to 0.85] p-value = 0.004). Hispanic (versus non-Hispanic) ethnicity was associated with higher risk of SARS-CoV-2 infection and mortality during almost every time period, with no evidence of attenuation over time. Urban (versus rural) residence was associated with higher risk of infection (AOR 2.02, [95% CI 1.83 to 2.22], p-value < 0.001), mortality (AOR 2.48 [95% CI 2.08 to 2.96], p-value < 0.001), and case fatality (AOR 2.24, 95% CI 1.93 to 2.60, p-value < 0.001) in February to April 2020, but these associations attenuated over time and reversed by September 2020 (AOR 0.85, 95% CI 0.81 to 0.89, p-value < 0.001 for infection, AOR 0.72, 95% CI 0.62 to 0.83, p-value < 0.001 for mortality and AOR 0.81, 95% CI 0.71 to 0.93, p-value = 0.006 for case fatality). Throughout the observation period, high comorbidity burden, younger age, and obesity were consistently associated with infection, while high comorbidity burden, older age, and male sex were consistently associated with mortality. Limitations of the study include that changes over time in the associations of some risk factors may be affected by changes in the likelihood of testing for SARS-CoV-2 according to those risk factors; also, study results apply directly to VA enrollees who are predominantly male and have comprehensive healthcare and need to be confirmed in other populations.

Conclusions

In this study, we found that strongly positive associations of Black and AI/AN (versus White) race and urban (versus rural) residence with SARS-CoV-2 infection, mortality, and case fatality observed early in the pandemic were ameliorated or reversed by March 2021.


George Ioannou and co-workers study the distribution of SARS-CoV-2 infections and outcomes among the United States population.

Author summary

Why was this study done?

  • As the Coronavirus Disease 2019 (COVID-19) pandemic continues to evolve, some risk factors for infection with COVID-19 and death due to COVID-19 that were described early in the pandemic may be changing.

  • Recognizing such changes is important in informing population-based approaches to prevent infection and reduce mortality.

What did the researchers do and find?

  • We investigated how the associations of key sociodemographic and clinical factors with COVID-19 infection, mortality, or case fatality changed between February 2020 and March 2021 among a cohort of approximately 9.1 million persons enrolled in the national US Veterans Affairs (VA) healthcare system, including 216,046 who tested positive and 10,230 who died of COVID-19 during the study period.

  • Black (versus White) race was strongly associated with a 5-fold higher risk of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection, a 4-fold higher risk of mortality, and a 2.5-fold higher risk of case fatality in February to March 2020, but these associations attenuated over time and were no longer statistically significant by November 2020 for infection and mortality and were reversed for case fatality.

  • American Indian/Alaska Native (AI/AN versus White) race was associated with SARS-CoV-2 infection early in the pandemic, but this association declined over time and reversed by March 2021.

  • Urban (versus rural) residence was associated with 2-fold higher risk of infection, a 2.5-fold higher risk of mortality, and 2.2-fold higher risk of case fatality in February to April 2020, but these associations attenuated over time and reversed by September 2020.

  • Throughout the observation period, high comorbidity burden, younger age, Hispanic ethnicity, and obesity were consistently associated with infection, while high comorbidity burden, older age, Hispanic ethnicity, and male sex were consistently associated with mortality.

What do these findings mean?

  • Early in the pandemic, there were strongly positive associations of Black and AI/AN (versus White) race and urban (versus rural) residence with SARS-CoV-2 infection, mortality, and case fatality, but these were ameliorated or even reversed by March 2021.

  • Our results apply directly to VA enrollees who are predominantly male and have access to universal healthcare; they need to be confirmed in other populations.

Introduction

Sociodemographic factors and comorbidity burden have emerged as major risk factors for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection and mortality [113]. Black, American Indian/Alaska Native (AI/AN), and Hispanic persons have been reported to have higher risk of SARS-CoV-2 infection and mortality than White and non-Hispanic persons [711,14]. Obese persons [12,15] and those with higher comorbidity burden [9] have also been reported to have higher risk of SARS-CoV-2 infection and mortality, while older age is one of the strongest risk factors for SARS-CoV-2–related mortality [2,9]. Over the course of the pandemic, residing in a geographical region with high incidence of SARS-CoV-2 infection at a given time has proven to be a strong risk factor for SARS-CoV-2 infection and mortality [2,5,16].

Three “waves” of the SARS-CoV-2 pandemic have been described in the US, with peaks in cases in April 2020 (first wave), July 2020 (second wave), and December 2020 to January 2021 (third wave). Risk factors for SARS-CoV-2–related infection and mortality may be changing over time since the pandemic began, especially in relation to these waves. Although it is clear that geographical regions with high infection, hospitalization, and mortality rates changed over time as the pandemic surged in different parts of the country, prior studies have not examined whether risk factors such as age, comorbidity burden, race, and ethnicity also varied. Over the course of the pandemic, there have been marked changes in use of prophylactic measures and access to care as well as viral characteristics (e.g., emergence of new variants) and availability of treatments (e.g., use of different pharmacotherapies). These changes may have affected the associations of sociodemographic and other risk factors with SARS-CoV-2 infection or mortality. Understanding changing patterns of risk factors could be important in informing population-based approaches to prevent infection and reduce mortality by targeting those at highest risk at any given time during the time course of an evolving pandemic. Also, changing patterns over time in sociodemographic risk factors for SARS-CoV-2 may provide insights that are more broadly applicable to disparities research in general.

We identified a cohort of approximately 9.1 million persons who were enrolled in the national US Department of Veterans Affairs (VA) healthcare system at the beginning of the pandemic in February 2020 and followed this cohort over the ensuing 14-month period to determine whether the magnitude and direction of the associations of established risk factors with SARS-CoV-2 infection, mortality, and case fatality changed over time.

Methods

Study population and data source

The VA supports the largest integrated national healthcare system in the US, providing care at 168 medical centers and 1,112 outpatient clinics throughout the country. We identified a cohort of all persons aged ≥18 years who were alive and enrolled in the VA healthcare system on February 1, 2020 (n = 9,127,673). We followed this cohort for the development of SARS-CoV-2 infection and SARS-CoV-2–related mortality until March 31, 2021.

The VA employs a comprehensive, nationwide electronic health record (EHR) system. EHR data from all VA facilities are transferred to the VA’s centralized relational database, the Corporate Data Warehouse (CDW), on a nightly basis to support research and clinical operations [17]. The CDW includes the “COVID-19 Shared Data Resource,” a set of analytic variables and datasets related to Coronavirus Disease 2019 (COVID-19) developed and maintained by the VA Informatics and Computing Infrastructure (VINCI) specifically to facilitate COVID-19 research and operations, which we used in combination with other CDW data.

The study was approved by the VA Puget Sound Institutional Review Board (IRB# 01885), which waived the requirement to obtain informed consent because this was a retrospective study of data from an existing database.

Definition of SARS-CoV-2 infection and SARS-CoV-2–related death

Cohort members who tested positive for SARS-CoV-2 within the VA system based on polymerase chain reaction (PCR) tests were defined as having infection. The earliest date of a documented positive test was taken as each patient’s date of infection. Patients who died of any cause within 30 days of infection were defined as having a SARS-CoV-2–related death consistent with prior studies [2,3]. Deaths occurring both within and outside the VA are comprehensively captured in CDW from a variety of VA and non-VA sources including VA inpatient files, VA Beneficiary Identification and Records Locator System (BIRLS), Social Security Administration (SSA) death files, and the Department of Defense [18]. Deaths occurring from February 1, 2020 to February 28, 2021 were ascertained from files that were updated on June 25, 2021 to allow time for deaths to be electronically recorded in CDW.

Study outcomes: Monthly SARS-CoV-2 infection rates, mortality rates, and case fatality rates

SARS-CoV-2 infection and mortality rates were calculated monthly as a proportion of all cohort members who were still alive and at risk on the first day of each month. For the monthly analysis of SARS-CoV-2 infection rates, we excluded persons who died of any cause or were infected with SARS-CoV-2 before the beginning of each monthly period. For the analysis of SARS-CoV-2 mortality rates, we excluded persons who died of any cause before the beginning of each monthly period or were infected with SARS-CoV-2 more than 30 days before the beginning of the month (since SARS-CoV-2–related mortality was defined as death within 30 days of infection). The aim of removing from our cohort persons who were no longer at risk at the beginning of each observation period was to avoid a spurious attenuation of risk factors over time due to “depletion” of at-risk persons.

Monthly case fatality rates were calculated as the proportion of the patients who tested positive each month who died of any cause within 30 days of the earliest positive test.

Sociodemographic factors and comorbidity burden

We ascertained the following 8 characteristics for all cohort members on the first day of each monthly observation period: age (categorized as shown in Table 1 or modeled as restricted cubic splines with 5 knots at ages 30, 49, 64, 73, and 88 years corresponding to 5, 27.5, 50, 72.5, and 95 percentiles as recommended [19]), sex, self-reported race (White, Black, Asian, AI/AN, Pacific Islander/Native Hawaiian [PI/NH], and Other) and ethnicity (Hispanic and non-Hispanic), urban versus rural residence (based on zip codes, using data from the VA Office of Rural Health [20], which uses the Secondary Rural–Urban Commuting Area [RUCA] for defining rurality), geographic location (divided into 10 standard US Federal Regions [21]), body mass index (BMI, categorized using the World Health Organization groups [22] as shown in Table 1 or modeled as restricted cubic splines with 5 knots at BMIs of 21.3, 26.0, 29.0, 32.5, and 39.9 kg/m2 corresponding to 5, 27.5, 50, 72.5, and 95 percentiles), and Charlson comorbidity index (CCI) [23] calculated using the Deyo modification [24], which takes into account 19 comorbid conditions reported in the 2 years prior to each observation period. We focused on these sociodemographic factors, obesity, and the CCI because they are some of the most important risk factors for SARS-CoV-2 infection or mortality reported in the literature [113] and because trends in the associations over time could be plausibly hypothesized.

Table 1. Cohort characteristics and incidence of SARS-CoV-2 infection presented by month in a cohort of 9.1 million VA enrollees followed from February 2020 to March 2021.

Cohort characteristics
N (%)
Number of SARS-CoV-2–positive persons (and incidence per 10,000 persons per month)
Time period and number of VA enrollees at risk* Entire period: February 2020 to March 2021
N = 9,127,673
February to March 2020
N = 9,127,673
April 2020
N = 9,090,196
May 2020
N = 9,053,082
June 2020
N = 9,022,051
July 2020
N = 8,990,833
August 2020
N = 8,948,674
September 2020
N = 8,913,864
October 2020
N = 8,881,573
November 2020
N = 8,844,680
December 2020
N = 8,804,424
January 2021
N = 8,744,388
February 2021
N = 8,671,916
March 2021
N = 8,630,283
All persons infected 216,046
(100%)
2,470
(2.7)
7,346
(8.1)
4,957
(5.5)
7,634
(8.5)
16,105
(17.9)
9,189
(10.3)
7,526
(8.4)
13,523
(15.2)
33,553
(37.9)
47,357
(53.8)
39,431
(45.1)
17,698
(20.4)
9,257
(10.7)
Sex
Female 829,355
(9.1)
218
(2.6)
695
(8.4)
453
(5.5)
853
(10.3)
1,946
(23.6)
968
(11.8)
716
(8.7)
1,243
(15.2)
3,315
(40.6)
4,859
(59.7)
3,942
(48.7)
1,825
(22.7)
1,003
(12.5)
Male 8,298,318
(90.9)
2,252
(2.7)
6,651
(8.1)
4,504
(5.5)
6,781
(8.3)
14,159
(17.3)
8,221
(10.1)
6,810
(8.4)
12,280
(15.2)
30,238
(37.7)
42,498
(53.2)
35,489
(44.7)
15,873
(20.2)
8,254
(10.5)
Age (years)
18 to 24 81,085
(0.9)
8
(1.0)
26
(3.2)
16
(2.0)
88
(10.9)
153
(18.9)
66
(8.2)
42
(5.2)
69
(8.6)
207
(25.7)
303
(37.7)
229
(28.6)
86
(10.8)
59
(7.4)
25 to 34 828,607
(9.1)
144
(1.7)
388
(4.7)
273
(3.3)
919
(11.1)
1,681
(20.3)
737
(8.9)
538
(6.5)
993
(12.1)
2,648
(32.2)
3,633
(44.3)
2,745
(33.6)
1,220
(15.0)
767
(9.4)
35 to 44 1,069,496
(11.7)
279
(2.6)
614
(5.7)
405
(3.8)
1,005
(9.4)
2,168
(20.3)
1,018
(9.6)
794
(7.5)
1,488
(14.0)
3,898
(36.7)
5,409
(51.2)
4,382
(41.7)
1,879
(17.9)
1,205
(11.5)
45 to 54 1,175,283
(12.9)
369
(3.1)
860
(7.3)
546
(4.7)
1,174
(10.0)
2,708
(23.1)
1,364
(11.7)
1,103
(9.5)
1,952
(16.8)
4,938
(42.5)
6,790
(58.7)
5,524
(48.1)
2,455
(21.5)
1,496
(13.1)
55 to 64 1,517,143
(16.6)
562
(3.7)
1,514
(10.0)
1,061
(7.0)
1,420
(9.4)
3,086
(20.5)
1,810
(12.1)
1,385
(9.3)
2,506
(16.8)
6,093
(40.9)
8,846
(59.7)
7,579
(51.5)
3,478
(23.8)
1,927
(13.2)
65 to 74 2,434,839
(26.7)
688
(2.8)
2,111
(8.7)
1,399
(5.8)
1,808
(7.5)
3,989
(16.6)
2,554
(10.7)
2,215
(9.3)
3,938
(16.6)
9,484
(40.1)
13,197
(56.1)
11,319
(48.5)
5,167
(22.3)
2,355
(10.2)
75 to 84 1,257,097
(13.8)
279
(2.2)
1,022
(8.2)
693
(5.6)
795
(6.5)
1,564
(12.8)
1,123
(9.2)
999
(8.3)
1,797
(15.0)
4,389
(36.8)
6,368
(53.7)
5,380
(45.7)
2,384
(20.5)
1,050
(9.1)
≥85 764,123
(8.4)
141
(1.8)
811
(10.8)
564
(7.7)
425
(5.9)
756
(10.6)
517
(7.3)
450
(6.5)
780
(11.4)
1,896
(28.0)
2,811
(41.9)
2,273
(34.2)
1,029
(15.9)
398
(6.2)
Race
White 5,886,250
(64.5)
956
(1.6)
3,774
(6.4)
2,739
(4.7)
4,414
(7.6)
9,315
(16.1)
5,690
(9.9)
5,141
(9.0)
9,898
(17.3)
24,753
(43.5)
33,126
(58.5)
26,626
(47.4)
11,932
(21.4)
6,425
(11.6)
Black 1,337,163
(14.6)
1,293
(9.7)
2,919
(21.9)
1,729
(13.0)
2,319
(17.6)
4,922
(37.4)
2,544
(19.4)
1,602
(12.3)
2,267
(17.4)
5,337
(41.2)
8,959
(69.5)
8,488
(66.4)
3,909
(30.8)
1,914
(15.2)
Asian 114,794
(1.3)
27
(2.4)
55
(4.8)
37
(3.2)
75
(6.6)
168
(14.7)
81
(7.1)
70
(6.2)
95
(8.4)
278
(24.6)
550
(48.8)
442
(39.4)
191
(17.1)
82
(7.4)
AI/AN 79,738
(0.9)
14
(1.8)
54
(6.8)
48
(6.1)
92
(11.6)
155
(19.7)
79
(10.1)
76
(9.7)
147
(18.9)
340
(43.9)
439
(56.9)
349
(45.6)
162
(21.3)
60
(7.9)
PI/NH 75,186
(0.8)
13
(1.7)
57
(7.6)
44
(5.9)
77
(10.3)
157
(21.1)
101
(13.7)
73
(9.9)
115
(15.7)
301
(41.1)
440
(60.4)
393
(54.3)
177
(24.7)
68
(9.5)
Missing/unknown/refused 1,634,542
(17.9)
167
(1.0)
487
(3.0)
360
(2.2)
657
(4.1)
1,388
(8.6)
694
(4.3)
564
(3.5)
1,001
(6.3)
2,544
(16.0)
3,843
(24.2)
3,133
(19.8)
1,327
(8.4)
708
(4.5)
Ethnicity
Non-Hispanic 7,201,109
(78.9)
2,119
(2.9)
6,441
(9.0)
4,365
(6.1)
6,101
(8.6)
12,936
(18.3)
7,825
(11.1)
6,615
(9.4)
11,868
(17.0)
29,477
(42.3)
40,749
(58.8)
33,980
(49.4)
15,482
(22.7)
8,014
(11.8)
Hispanic 571,236
(6.3)
272
(4.8)
649
(11.4)
426
(7.5)
1,235
(21.8)
2,583
(45.7)
1,037
(18.5)
645
(11.5)
1,159
(20.8)
2,819
(50.7)
4,648
(84.1)
3,791
(69.2)
1,487
(27.4)
861
(15.9)
Missing/unknown/refused 1,355,328
(14.8)
79
(0.6)
256
(1.9)
166
(1.2)
298
(2.2)
586
(4.4)
327
(2.4)
266
(2.0)
496
(3.7)
1,257
(9.5)
1,960
(14.8)
1,660
(12.6)
729
(5.6)
382
(2.9)
US Federal Region
1 400,339
(4.4)
95
(2.4)
852
(21.4)
398
(10.1)
196
(5.0)
143
(3.6)
102
(2.6)
99
(2.5)
219
(5.6)
946
(24.5)
1,674
(43.4)
1,520
(39.7)
760
(20.0)
419
(11.1)
2 665,463
(7.3)
615
(9.2)
1,717
(26.0)
590
(9.0)
267
(4.1)
340
(5.2)
217
(3.4)
209
(3.2)
380
(5.9)
1,248
(19.5)
2,183
(34.2)
2,114
(33.3)
1,079
(17.1)
759
(12.1)
3 958,643
(10.5)
185
(1.9)
838
(8.8)
657
(6.9)
459
(4.8)
773
(8.2)
581
(6.2)
474
(5.1)
830
(8.9)
2,528
(27.1)
4,474
(48.2)
3,725
(40.4)
1,815
(19.8)
1,048
(11.5)
4 2,290,207
(25.1)
363
(1.6)
1,085
(4.8)
1,006
(4.4)
2,474
(10.9)
5,993
(26.5)
3,416
(15.2)
2,328
(10.4)
3,045
(13.7)
5,555
(25.0)
11,123
(50.3)
11,489
(52.3)
5,354
(24.6)
2,470
(11.4)
5 1,325,949
(14.5)
413
(3.1)
1,230
(9.3)
955
(7.3)
605
(4.6)
1,217
(9.3)
1,007
(7.8)
1,095
(8.5)
3,058
(23.7)
8,438
(65.8)
7,528
(59.2)
4,576
(36.3)
2,187
(17.5)
1,436
(11.5)
6 1,194,444
(13.1)
459
(3.8)
658
(5.5)
486
(4.1)
1,744
(14.7)
4,019
(34.1)
1,687
(14.4)
1,206
(10.3)
2,161
(18.6)
4,403
(38.0)
6,419
(55.7)
6,182
(54.0)
2,338
(20.6)
1,104
(9.8)
7 458,363
(5.0)
58
(1.3)
238
(5.2)
250
(5.5)
221
(4.9)
600
(13.3)
681
(15.2)
853
(19.1)
1,432
(32.2)
3,652
(82.6)
3,057
(69.8)
2,007
(46.2)
935
(21.7)
465
(10.9)
8 374,484
(4.1)
74
(2.0)
208
(5.6)
179
(4.8)
147
(4.0)
277
(7.5)
241
(6.5)
414
(11.3)
1,100
(30.1)
2,568
(70.6)
1,908
(52.8)
992
(27.7)
515
(14.4)
369
(10.4)
9 1,041,079
(11.4)
164
(1.6)
387
(3.7)
344
(3.3)
1,376
(13.3)
2,356
(22.9)
967
(9.5)
627
(6.2)
860
(8.5)
3,112
(30.7)
7,725
(76.6)
6,059
(60.6)
2,253
(22.8)
875
(8.9)
10 418,702
(4.6)
44
(1.1)
133
(3.2)
92
(2.2)
145
(3.5)
387
(9.3)
290
(7.0)
221
(5.4)
438
(10.7)
1,103
(27.0)
1,266
(31.1)
767
(18.9)
462
(11.4)
312
(7.8)
Urban versus rural
Rural 4,469,258
(49.0)
579
(1.3)
1,870
(4.2)
1,623
(3.7)
2,955
(6.7)
6,872
(15.6)
4,680
(10.7)
4,147
(9.5)
7,468
(17.2)
17,506
(40.4)
23,772
(55.1)
19,440
(45.4)
8,734
(20.6)
4,513
(10.7)
Urban 4,658,415
(51.0)
1,891
(4.1)
5,476
(11.8)
3,334
(7.2)
4,679
(10.2)
9,233
(20.1)
4,509
(9.9)
3,379
(7.4)
6,055
(13.4)
16,047
(35.6)
23,585
(52.5)
19,991
(44.8)
8,964
(20.3)
4,744
(10.8)
BMI (kg/m2)
<18.5 (underweight) 64,634
(0.7)
38
(5.9)
148
(23.5)
101
(16.4)
95
(15.7)
115
(19.3)
98
(16.7)
74
(12.8)
105
(18.4)
223
(39.6)
374
(66.9)
367
(66.4)
159
(29.4)
89
(16.6)
18.5 to <25 (normal weight) 1,841,422
(20.2)
413
(2.2)
1,448
(7.9)
1,030
(5.7)
1,218
(6.7)
2,414
(13.4)
1,362
(7.6)
1,171
(6.6)
1,864
(10.5)
4,658
(26.5)
6,929
(39.5)
5,908
(33.9)
2,703
(15.7)
1,345
(7.8)
25 to <30 (overweight) 3,314,997
(36.3)
794
(2.4)
2,348
(7.1)
1,602
(4.9)
2,509
(7.7)
5,183
(15.9)
2,920
(9.0)
2,460
(7.6)
4,410
(13.6)
10,898
(33.9)
15,526
(48.4)
12,829
(40.3)
5,759
(18.2)
2,928
(9.3)
30 to <35 (obese I) 2,433,428
(26.7)
677
(2.8)
1,901
(7.8)
1,260
(5.2)
2,181
(9.0)
4,684
(19.5)
2,679
(11.2)
2,163
(9.1)
3,969
(16.7)
9,903
(41.7)
13,689
(57.9)
11,498
(49.0)
5,096
(21.9)
2,744
(11.8)
35 to <40 (obese II) 1,026,570
(11.2)
355
(3.5)
946
(9.2)
633
(6.2)
1,039
(10.2)
2,358
(23.2)
1,398
(13.8)
1,031
(10.2)
2,007
(20.0)
4,995
(49.9)
6,941
(69.7)
5,696
(57.6)
2,540
(25.9)
1,371
(14.1)
≥40 (obese III) 446,622
(4.9)
193
(4.3)
555
(12.5)
331
(7.5)
592
(13.4)
1,351
(30.6)
732
(16.7)
627
(14.3)
1,168
(26.8)
2,876
(66.3)
3,898
(90.6)
3,133
(73.5)
1,441
(34.2)
780
(18.6)
CCI
0 to 1 6,063,266
(66.4)
955
(1.6)
2,620
(4.3)
1,805
(3.0)
3,799
(6.3)
7,918
(13.2)
4,197
(7.0)
3,313
(5.5)
6,130
(10.3)
15,701
(26.4)
21,571
(36.3)
17,532
(29.7)
8,062
(13.7)
4,708
(8.0)
2 to 3 1,520,767
(16.7)
552
(3.6)
1,649
(10.9)
1,154
(7.7)
1,575
(10.5)
3,703
(24.8)
2,093
(14.1)
1,813
(12.3)
3,253
(22.2)
7,929
(54.3)
11,334
(78.1)
9,722
(67.7)
4,332
(30.5)
2,198
(15.6)
4 to 5 768,966
(8.4)
346
(4.5)
1,153
(15.1)
807
(10.7)
985
(13.1)
1,990
(26.6)
1,301
(17.5)
1,073
(14.6)
1,815
(24.8)
4,613
(63.4)
6,557
(90.9)
5,671
(79.5)
2,427
(34.6)
1,110
(15.9)
≥6 774,674
(8.5)
617
(8.0)
1,924
(25.2)
1,191
(15.8)
1,275
(17.1)
2,494
(33.8)
1,598
(21.9)
1,327
(18.4)
2,325
(32.7)
5,310
(75.5)
7,895
(113.4)
6,506
(94.9)
2,877
(42.9)
1,241
(18.7)

* VA enrollees at risk are those who are still alive and not yet infected at the beginning of each time period.

Categorized according to the 10 US Federal Regions drawn up by the Office of Management and Budget: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, PR, and Virgin Island), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Missing values for BMI (20.9%) were multiply imputed using values of the other covariates included in multivariable analyses. “Missing” values for race (18.7%) or ethnicity (15.6%) included persons who refused to declare their race/ethnicity or reported unknown or mixed race/ethnicity and did not self-identify as belonging to one of the prespecified racial or ethnic group. For these persons, we did not perform imputation of race/ethnicity, but rather included them in a “missing/unknown/refused” category.

Statistical analysis

We calculated the number of new SARS-CoV-2 infections and deaths each month and the monthly incidence as a proportion of all persons in our cohort who were still alive and at risk on the first day of the month. Monthly case fatality was calculated as the proportion of patients who tested positive each month who died within 30 days. For each monthly observation period (for infections) or bimonthly observation period (for mortality and case fatality), we used a separate multivariable logistic regression model to simultaneously adjust for the 8 characteristics listed above to determine the associations between each risk factor and SARS-CoV-2 infection, mortality, or case fatality reported as an adjusted odds ratio (AOR). We used bimonthly periods for trends in mortality and case fatality because there were too few deaths in some subgroups to generate reasonably precise monthly analyses of time trends.

We used a Wald test with cluster-robust standard errors to formally evaluate whether the associations between risk factors and each outcome (infection, mortality, or case fatality) changed over time by creating another model that combined all time periods and included an interaction term separately for each risk factor (risk factor * time period) where time period was an ordinal variable (see S1 and S2 Tables).

Almost all analyses were proposed a priori as shown in the S1 Analytic Plan. Notable exceptions were the analyses of case fatality as an outcome and additionally modeling age and BMI as restricted cubic splines that were performed in response to reviewers’ comments.

We followed the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guidelines as summarized in S1 STROBE Checklist.

Results

Baseline characteristics of VA enrollees

The baseline characteristics of the cohort of VA enrollees (n = 9,127,673) in February 2020 are shown in Table 1. Mean and median age were 61.0 and 64 years, respectively, with a substantial proportion in categories 65 to 74 (26.7%), 75 to 84 (13.8%), and ≥85 (8.4%) years of age. Most cohort members were male (90.9%) and White (64.5%), with 14.6% of Black race and 6.3% of Hispanic ethnicity. Cohort members were distributed almost evenly between urban versus rural locations, and the cohort included Veterans residing in all US Federal Regions and states, with the greatest contribution from region 4 (Southeast US, states of AL, FL, GA, KY, MS, NC, SC, and TN). Overweight (36.3%) and obesity (42.8%) were common among cohort members and 33.6% had a CCI ≥2.

Trends over time in the associations of risk factors with SARS-CoV-2 infection

During the entire follow-up period (February 1, 2020 to March 31, 2021), 216,046 out of 9,127,673 VA enrollees (2.4%) in our cohort tested positive for SARS-CoV-2 (Table 1). Infection rates peaked in accordance with the 3 well-described national waves of the pandemic in April 2020 (first wave), July 2020 (second wave), and December 2020 (third wave) as shown in Fig 1 (for infection rates), Fig 2 (for mortality rates), and Fig 3 (for case fatality rates). Characteristics independently associated with testing positive over the entire period included Black (versus White) race (AOR 1.39, 95% CI 1.37 to 1.41, p-value = <0.001), Hispanic ethnicity (AOR 1.64, 95% CI 1.62 to 1.67, p-value = <0.001), higher BMI (e.g., BMI 40 versus BMI 25 kg/m2, AOR 1.51, 95% CI 1.49 to 1.53, p-value < 0.001), and higher CCI (e.g., CCI ≥ 6 versus CCI = 0 to 1, AOR 3.16, 95% CI 3.12 to 3.21, p-value < 0.001) (Table 2). The highest risk of infection was observed at age 45 with progressively lower risk at both older ages (e.g., 85 versus 45 years old, AOR 0.50, 95% CI 0.43 to 0.58, p-value < 0.001) and younger ages (e.g., 25 versus 45 years old, AOR 0.77, 95% CI 0.76 to 0.79, p-value < 0.001). Men had significantly lower risk of infection than women (AOR 0.88, 95% CI 0.87 to 0.90, p-value = <0.001). Compared to Federal Region 4 (Southeast US), which served as the reference category, some regions were associated with significantly higher risk of positive SARS-CoV-2 test (e.g., Federal Regions 5 to 9), while others were associated with significantly lower risk (Federal Regions 1 to 3 and 10).

Fig 1. Monthly results in the VA healthcare system from February 2020 to March 2021 of SARS-CoV-2 infection rates among a cohort of VA enrollees.

Fig 1

SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Fig 2. Monthly results in the VA healthcare system from February 2020 to March 2021 of SARS-CoV-2 mortality rates among a cohort of VA enrollees.

Fig 2

SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Fig 3. Monthly results in the VA healthcare system from February 2020 to March 2021 of SARS-CoV-2 case fatality rates among VA enrollees testing positive for SARS-CoV-2.

Fig 3

SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Table 2. Trends over time in the associations (AORs*) of sociodemographic characteristics and comorbidity burden with risk of SARS-CoV-2 infection in a cohort of 9.1 million VA enrollees from February 2020 to March 2021.

AORs* for SARS-CoV-2 infection (95% CI)
Entire period: February 2020 to March 2021
N = 9,127,673
February to March 2020
N = 9,127,673
April 2020
N = 9,090,196
May 2020
N = 9,053,082
June 2020
N = 9,022,051
July 2020
N = 8,990,833
August 2020
N = 8,948,674
September 2020
N = 8,913,864
October 2020
N = 8,881,573
November 2020
N = 8,844,680
December 2020
N = 8,804,424
January 2021
N = 8,744,388
February 2021
N = 8,671,916
March 2021
N = 8,630,283
Sex
Female 1 1 1 1 1 1 1 1 1 1 1 1 1 1
Male 0.88
(0.87 to 0.90)
1.20
(1.04 to 1.39)
0.91
(0.84 to 0.98)
0.94
(0.85 to 1.04)
0.97
(0.90 to 1.05)
0.89
(0.85 to 0.94)
0.92
(0.86 to 0.98)
0.94
(0.87 to 1.02)
0.94
(0.88 to 0.99)
0.87
(0.83 to 0.90)
0.85
(0.83 to 0.88)
0.89
(0.86 to 0.92)
0.86
(0.81 to 0.90)
0.90
(0.84 to 0.96)
Age (years)
25 0.77
(0.76 to 0.79)
0.62
(0.49 to 0.79)
0.81
(0.70 to 0.94)
0.94
(0.79 to 1.12)
1.25
(1.12 to 1.39)
0.96
(0.89 to 1.03)
0.87
(0.78 to 0.97)
0.76
(0.67 to 0.87)
0.69
(0.62 to 0.76)
0.72
(0.68 to 0.77)
0.75
(0.71 to 0.79)
0.72
(0.68 to 0.76)
0.69
(0.63 to 0.76)
0.71
(0.64 to 0.79)
35 0.92
(0.91 to 0.92)
0.84
(0.76 to 0.93)
0.92
(0.86 to 0.97)
0.96
(0.89 to 1.03)
1.13
(1.08 to 1.18)
1.01
(0.98 to 1.04)
0.95
(0.91 to 1.00)
0.91
(0.86 to 0.96)
0.87
(0.84 to 0.91)
0.89
(0.87 to 0.91)
0.91
(0.89 to 0.93)
0.89
(0.87 to 0.91)
0.87
(0.84 to 0.90)
0.88
(0.84 to 0.92)
45 (reference) 1 1 1 1 1 1 1 1 1 1 1 1 1 1
55 0.89
(0.88 to 0.89)
0.86
(0.80 to 0.93)
0.99
(0.94 to 1.04)
1.09
(1.03 to 1.16)
0.83
(0.80 to 0.87)
0.85
(0.82 to 0.88)
0.93
(0.89 to 0.97)
0.89
(0.85 to 0.93)
0.88
(0.85 to 0.91)
0.86
(0.85 to 0.88)
0.87
(0.86 to 0.89)
0.90
(0.88 to 0.92)
0.94
(0.91 to 0.97)
0.90
(0.86 to 0.93)
65 0.71
(0.70 to 0.73)
0.65
(0.57 to 0.75)
0.86
(0.79 to 0.94)
1.01
(0.91 to 1.13)
0.65
(0.60 to 0.71)
0.66
(0.62 to 0.69)
0.79
(0.73 to 0.85)
0.73
(0.68 to 0.80)
0.71
(0.67 to 0.75)
0.68
(0.65 to 0.71)
0.70
(0.68 to 0.72)
0.75
(0.72 to 0.77)
0.80
(0.76 to 0.85)
0.68
(0.64 to 0.73)
75 0.64
(0.63 to 0.65)
0.57
(0.51 to 0.65)
0.75
(0.70 to 0.82)
0.80
(0.73 to 0.88)
0.54
(0.50 to 0.58)
0.54
(0.52 to 0.57)
0.70
(0.65 to 0.74)
0.68
(0.64 to 0.73)
0.66
(0.62 to 0.69)
0.62
(0.60 to 0.64)
0.65
(0.63 to 0.67)
0.71
(0.69 to 0.73)
0.76
(0.73 to 0.80)
0.54
(0.51 to 0.58)
85 0.58
(0.57 to 0.59)
0.50
(0.43 to 0.58)
0.91
(0.84 to 0.99)
1.03
(0.93 to 1.13)
0.56
(0.52 to 0.61)
0.52
(0.49 to 0.55)
0.67
(0.62 to 0.73)
0.66
(0.61 to 0.72)
0.60
(0.57 to 0.64)
0.57
(0.55 to 0.60)
0.62
(0.60 to 0.65)
0.66
(0.64 to 0.69)
0.71
(0.67 to 0.75)
0.47
(0.43 to 0.51)
Race
White 1 1 1 1 1 1 1 1 1 1 1 1 1 1
Black 1.39
(1.37 to 1.41)
5.10
(4.65 to 5.59)
3.13
(2.97 to 3.31)
2.55
(2.39 to 2.73)
1.96
(1.85 to 2.07)
1.91
(1.84 to 1.98)
1.75
(1.66 to 1.84)
1.33
(1.25 to 1.41)
1.06
(1.01 to 1.11)
1.03
(1.00 to 1.07)
1.15
(1.12 to 1.18)
1.26
(1.23 to 1.29)
1.30
(1.25 to 1.35)
1.16
(1.10 to 1.23)
Asian 0.84
(0.80 to 0.87)
1.78
(1.21 to 2.63)
1.07
(0.81 to 1.39)
0.96
(0.69 to 1.34)
0.70
(0.56 to 0.88)
0.87
(0.75 to 1.02)
0.90
(0.72 to 1.13)
0.99
(0.78 to 1.26)
0.78
(0.64 to 0.96)
0.75
(0.67 to 0.85)
0.82
(0.75 to 0.89)
0.84
(0.76 to 0.93)
0.89
(0.77 to 1.03)
0.74
(0.59 to 0.92)
AI/AN 0.93
(0.89 to 0.98)
1.13
(0.67 to 1.92)
1.40
(1.07 to 1.83)
1.54
(1.16 to 2.05)
1.21
(0.98 to 1.48)
0.94
(0.80 to 1.11)
0.89
(0.71 to 1.11)
1.00
(0.79 to 1.25)
0.99
(0.84 to 1.17)
0.93
(0.84 to 1.04)
0.88
(0.80 to 0.97)
0.89
(0.80 to 0.99)
0.97
(0.83 to 1.13)
0.66
(0.51 to 0.85)
PI/NH 0.98
(0.93 to 1.02)
0.99
(0.57 to 1.70)
1.31
(1.01 to 1.71)
1.34
(1.00 to 1.81)
0.95
(0.75 to 1.19)
0.95
(0.81 to 1.11)
1.22
(1.00 to 1.49)
1.12
(0.89 to 1.41)
0.97
(0.81 to 1.17)
0.97
(0.87 to 1.09)
0.88
(0.80 to 0.97)
0.98
(0.89 to 1.08)
1.06
(0.91 to 1.23)
0.78
(0.62 to 1.00)
Missing/unknown/refused 0.82
(0.81 to 0.84)
1.27
(1.05 to 1.55)
1.05
(0.93 to 1.17)
1.10
(0.96 to 1.25)
0.84
(0.77 to 0.93)
0.89
(0.83 to 0.95)
0.85
(0.77 to 0.93)
0.87
(0.78 to 0.96)
0.79
(0.73 to 0.86)
0.81
(0.77 to 0.85)
0.81
(0.77 to 0.84)
0.80
(0.76 to 0.84)
0.78
(0.73 to 0.84)
0.77
(0.70 to 0.85)
Ethnicity
Non-Hispanic 1 1 1 1 1 1 1 1 1 1 1 1 1 1
Hispanic 1.64
(1.62 to 1.67)
1.57
(1.37 to 1.81)
1.27
(1.16 to 1.38)
1.55
(1.40 to 1.73)
2.39
(2.24 to 2.56)
2.55
(2.43 to 2.67)
2.10
(1.96 to 2.25)
1.57
(1.44 to 1.71)
1.57
(1.47 to 1.67)
1.46
(1.40 to 1.52)
1.53
(1.48 to 1.58)
1.49
(1.43 to 1.54)
1.38
(1.30 to 1.46)
1.48
(1.37 to 1.60)
Missing/unknown/refused 0.40
(0.39 to 0.41)
0.38
(0.29 to 0.50)
0.37
(0.32 to 0.43)
0.32
(0.27 to 0.39)
0.44
(0.38 to 0.50)
0.41
(0.37 to 0.45)
0.39
(0.34 to 0.45)
0.36
(0.31 to 0.41)
0.38
(0.34 to 0.42)
0.37
(0.34 to 0.39)
0.41
(0.39 to 0.43)
0.43
(0.40 to 0.46)
0.42
(0.38 to 0.46)
0.40
(0.35 to 0.46)
US Federal Region
1 0.89
(0.86 to 0.91)
2.48
(1.97 to 3.12)
6.04
(5.50 to 6.62)
2.89
(2.56 to 3.25)
0.57
(0.49 to 0.66)
0.17
(0.15 to 0.21)
0.21
(0.18 to 0.26)
0.28
(0.23 to 0.35)
0.46
(0.40 to 0.52)
1.07
(1.00 to 1.15)
0.97
(0.92 to 1.02)
0.86
(0.81 to 0.91)
0.92
(0.86 to 1.00)
1.12
(1.00 to 1.24)
2 0.72
(0.71 to 0.74)
5.81
(5.08 to 6.65)
5.14
(4.75 to 5.56)
1.85
(1.66 to 2.05)
0.33
(0.29 to 0.38)
0.18
(0.16 to 0.20)
0.22
(0.19 to 0.25)
0.32
(0.28 to 0.37)
0.44
(0.39 to 0.49)
0.79
(0.74 to 0.84)
0.69
(0.65 to 0.72)
0.64
(0.61 to 0.68)
0.72
(0.67 to 0.77)
1.10
(1.01 to 1.20)
3 0.83
(0.81 to 0.84)
1.22
(1.03 to 1.46)
1.84
(1.68 to 2.01)
1.59
(1.44 to 1.76)
0.47
(0.42 to 0.51)
0.33
(0.30 to 0.35)
0.44
(0.40 to 0.48)
0.52
(0.47 to 0.57)
0.69
(0.64 to 0.74)
1.14
(1.09 to 1.19)
1.01
(0.97 to 1.05)
0.81
(0.78 to 0.84)
0.85
(0.80 to 0.90)
1.06
(0.99 to 1.14)
4 (reference) 1 1 1 1 1 1 1 1 1 1 1 1 1 1
5 1.13
(1.11 to 1.15)
2.50
(2.17 to 2.88)
2.25
(2.07 to 2.45)
1.86
(1.70 to 2.03)
0.48
(0.44 to 0.53)
0.40
(0.38 to 0.43)
0.57
(0.53 to 0.62)
0.87
(0.81 to 0.93)
1.79
(1.70 to 1.89)
2.72
(2.63 to 2.82)
1.23
(1.20 to 1.27)
0.73
(0.71 to 0.76)
0.75
(0.71 to 0.79)
1.07
(1.01 to 1.15)
6 1.13
(1.12 to 1.15)
2.76
(2.41 to 3.17)
1.30
(1.18 to 1.43)
1.00
(0.89 to 1.11)
1.30
(1.22 to 1.38)
1.23
(1.18 to 1.28)
0.93
(0.88 to 0.99)
0.99
(0.92 to 1.06)
1.33
(1.26 to 1.41)
1.50
(1.44 to 1.56)
1.10
(1.07 to 1.13)
1.04
(1.01 to 1.07)
0.86
(0.81 to 0.90)
0.85
(0.79 to 0.92)
7 1.42
(1.39 to 1.44)
1.22
(0.93 to 1.62)
1.46
(1.26 to 1.68)
1.56
(1.35 to 1.79)
0.54
(0.47 to 0.62)
0.60
(0.55 to 0.66)
1.12
(1.03 to 1.22)
1.92
(1.77 to 2.08)
2.38
(2.23 to 2.53)
3.37
(3.23 to 3.52)
1.44
(1.38 to 1.50)
0.93
(0.88 to 0.97)
0.93
(0.87 to 1.00)
1.00
(0.91 to 1.11)
8 1.17
(1.14 to 1.19)
2.65
(2.06 to 3.42)
2.04
(1.76 to 2.37)
1.67
(1.43 to 1.97)
0.48
(0.40 to 0.56)
0.36
(0.32 to 0.41)
0.53
(0.46 to 0.60)
1.23
(1.11 to 1.37)
2.39
(2.22 to 2.56)
3.10
(2.95 to 3.25)
1.18
(1.12 to 1.24)
0.61
(0.57 to 0.65)
0.68
(0.62 to 0.74)
1.03
(0.92 to 1.15)
9 1.23
(1.21 to 1.24)
1.36
(1.12 to 1.64)
0.99
(0.88 to 1.12)
0.90
(0.79 to 1.02)
1.31
(1.22 to 1.40)
0.93
(0.88 to 0.98)
0.71
(0.66 to 0.77)
0.68
(0.62 to 0.74)
0.69
(0.64 to 0.75)
1.37
(1.31 to 1.43)
1.73
(1.68 to 1.78)
1.34
(1.30 to 1.38)
1.08
(1.03 to 1.14)
0.89
(0.82 to 0.96)
10 0.68
(0.66 to 0.70)
1.38
(1.00 to 1.89)
1.16
(0.97 to 1.40)
0.79
(0.64 to 0.98)
0.44
(0.37 to 0.52)
0.48
(0.43 to 0.53)
0.60
(0.53 to 0.68)
0.62
(0.54 to 0.71)
0.89
(0.81 to 0.99)
1.23
(1.15 to 1.31)
0.73
(0.68 to 0.77)
0.43
(0.40 to 0.47)
0.56
(0.51 to 0.62)
0.80
(0.71 to 0.90)
Urban versus rural
Rural 1 1 1 1 1 1 1 1 1 1 1 1 1 1
Urban 1.01
(1.00 to 1.02)
2.02
(1.83 to 2.22)
1.95
(1.85 to 2.06)
1.60
(1.50 to 1.70)
1.39
(1.32 to 1.45)
1.23
(1.20 to 1.28)
0.93
(0.89 to 0.97)
0.85
(0.81 to 0.89)
0.88
(0.85 to 0.91)
0.96
(0.94 to 0.98)
0.94
(0.92 to 0.96)
0.96
(0.94 to 0.98)
0.96
(0.93 to 0.99)
0.98
(0.94 to 1.02)
BMI (kg/m2)
15
20 0.99
(0.97 to 1.00)
1.12
(0.96 to 1.31)
1.40
(1.29 to 1.52)
1.49
(1.35 to 1.63)
1.18
(1.08 to 1.30)
0.97
(0.90 to 1.04)
0.99
(0.90 to 1.08)
1.03
(0.93 to 1.14)
0.94
(0.87 to 1.02)
0.88
(0.83 to 0.92)
0.98
(0.94 to 1.02)
1.01
(0.97 to 1.06)
1.04
(0.97 to 1.11)
1.15
(1.05 to 1.26)
25 (reference) 1 1 1 1 1 1 1 1 1 1 1 1 1 1
30 1.23
(1.21 to 1.25)
1.21
(1.06 to 1.37)
1.14
(1.06 to 1.23)
1.10
(1.01 to 1.20)
1.24
(1.15 to 1.34)
1.19
(1.13 to 1.25)
1.14
(1.06 to 1.22)
1.17
(1.09 to 1.26)
1.28
(1.21 to 1.36)
1.22
(1.17 to 1.26)
1.24
(1.20 to 1.28)
1.24
(1.20 to 1.28)
1.22
(1.16 to 1.28)
1.27
(1.19 to 1.36)
35 1.38
(1.36 to 1.39)
1.36
(1.21 to 1.52)
1.26
(1.18 to 1.34)
1.14
(1.05 to 1.24)
1.28
(1.20 to 1.37)
1.32
(1.26 to 1.38)
1.36
(1.28 to 1.44)
1.28
(1.20 to 1.36)
1.41
(1.34 to 1.48)
1.39
(1.35 to 1.44)
1.39
(1.35 to 1.43)
1.37
(1.33 to 1.41)
1.36
(1.30 to 1.42)
1.43
(1.35 to 1.52)
40 1.51
(1.49 to 1.53)
1.41
(1.26 to 1.58)
1.39
(1.30 to 1.48)
1.22
(1.12 to 1.32)
1.39
(1.30 to 1.49)
1.46
(1.40 to 1.53)
1.45
(1.37 to 1.54)
1.38
(1.29 to 1.47)
1.54
(1.47 to 1.62)
1.52
(1.47 to 1.57)
1.52
(1.48 to 1.57)
1.50
(1.46 to 1.55)
1.50
(1.44 to 1.57)
1.59
(1.50 to 1.69)
CCI
0 to 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1
2 to 3 2.16
(2.14 to 2.19)
2.25
(2.01 to 2.52)
2.24
(2.10 to 2.40)
2.28
(2.10 to 2.47)
1.98
(1.85 to 2.11)
2.14
(2.05 to 2.23)
2.01
(1.90 to 2.13)
2.18
(2.05 to 2.32)
2.12
(2.02 to 2.22)
2.09
(2.03 to 2.15)
2.20
(2.14 to 2.25)
2.25
(2.19 to 2.31)
2.10
(2.02 to 2.18)
2.00
(1.89 to 2.11)
4 to 5 2.56
(2.52 to 2.60)
2.80
(2.45 to 3.20)
3.04
(2.82 to 3.28)
3.10
(2.83 to 3.40)
2.61
(2.41 to 2.82)
2.42
(2.29 to 2.55)
2.53
(2.37 to 2.71)
2.61
(2.42 to 2.82)
2.40
(2.27 to 2.54)
2.49
(2.40 to 2.58)
2.62
(2.54 to 2.70)
2.67
(2.59 to 2.76)
2.38
(2.27 to 2.50)
2.11
(1.97 to 2.26)
≥6 3.16
(3.12 to 3.21)
4.53
(4.03 to 5.10)
4.68
(4.37 to 5.01)
4.34
(3.99 to 4.72)
3.37
(3.13 to 3.62)
3.08
(2.93 to 3.25)
3.16
(2.96 to 3.38)
3.33
(3.10 to 3.58)
3.22
(3.06 to 3.40)
3.02
(2.92 to 3.13)
3.31
(3.21 to 3.41)
3.20
(3.10 to 3.30)
2.95
(2.81 to 3.09)
2.51
(2.35 to 2.69)

* Adjusted for sex, age (modeled as restricted cubic splines with 5 knots at ages 30, 49, 64, 73, and 88 years), race, ethnicity, geographical region, urban/rural location, BMI (modeled as restricted cubic splines with 5 knots at BMIs of 21.3, 26.0, 29.0, 32.5, 39.9 kg/m2), and CCI.

Categorized according to the 10 Federal Regions drawn up by the Federal Emergency Management Agency: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, and PR), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; AOR, adjusted odds ratio; BMI, body mass index; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

The magnitude of the association between Black (versus White) race and SARS-CoV-2 infection declined steadily from February/March 2020 (AOR 5.10, 95% CI 4.65 to 5.59, p-value < 0.001) to November 2020 (AOR 1.03, 95% CI 1.00 to 1.07, p-value = 0.05) when it was no longer significant (p-value < 0.001 for interaction term of [black race * time period] testing trends over time, see S1 and S2 Tables). However, during the last 4 months of the observation period from December 2020 to March 2021 (corresponding to the third wave of the pandemic), Black race was again significantly associated with infection with AORs ranging from 1.15 to 1.30, although the magnitude of this association was still much lower than in the early months of the pandemic (Table 2, Fig 4). When we categorized our cohort by age (<65 and ≥65 years), the associations and their trends over time between Black (versus White) race and SARS-CoV-2 infection were very similar for persons aged <65 and ≥65 years (S3 Table).

Fig 4.

Fig 4

Trends over time in the associations of the following factors with risk of SARS-CoV-2 infection and mortality: (A and B) Black versus White race. (C and D) Urban versus rural location. (E and F) CCI categories. (G and H) Age. CCI, Charlson comorbidity index; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2.

The magnitude of the association between AI/AN (versus White) race and SARS-CoV-2 infection declined steadily over time (p-value for trends over time <0.001; see S1 and S2 Tables) and shifted from a positive association during the period from February to June (AORs ranging from 1.13 to 1.54) to a negative association in March 2021 (AOR 0.66, 95% CI 0.51 to 0.85, p-value = 0.004).

The magnitude of the association between urban versus rural location also declined steadily over time (p-value for trends over time <0.001; see S1 and S2 Tables) and shifted from a positive association in February/March 2020 (AOR 2.02, 95% CI 1.83 to 2.22, p-value = <0.001) to a negative association in September to October 2020 and a nonsignificant association in March 2021 (AOR 0.98, 95% CI 0.94 to 1.02, p-value = 0.32) (Table 2, Fig 4).

The magnitude of the associations between CCI and SARS-CoV-2 infection attenuated early in the pandemic until July 2020 (p-value < 0.001) and then appeared to plateau between July 2020 and January 2021, before declining again from January to March 2021, after the introduction of vaccination. However, CCI was still strongly associated with infection even in March 2021. Geographical regions at higher risk of infection fluctuated over time reflecting surges in different parts of the country. For example, region 2 (NY, NJ, and PR), which represented the earliest epicenter of the pandemic in the US, had the highest risk of infection in February to March 2020, but one of the lowest risks of infection in July to August 2020 and approximately average risk by March 2021.

The magnitude of the association of the following characteristics with SARS-CoV-2 infection did not vary appreciably over the observation period: age, sex, PI/NH race, Hispanic ethnicity, and BMI.

Trends over time in the associations of risk factors with SARS-CoV-2–related mortality

From February 2020 to March 2021, 10,230 SARS-CoV-2–related deaths were identified among our cohort of 9,127,673 VA enrollees (Table 3). Monthly mortality rates are shown in Table 3 and Fig 2. Significant, independent risk factors for mortality over the entire observation period included male sex (AOR 1.59, 95% CI 1.38 to 1.82, p-value < 0.001), older age (e.g., AOR 20.37, 95% CI 17.48 to 23.74, p-value < 0.001, comparing ages 85 year versus 45 year (the reference age)), Black (AOR 1.55, 95% CI 1.47 to 1.64, p-value = <0.001), and AI/AN (AOR 1.66, 95% CI 1.39 to 1.98, p-value = <0.001) race relative to White race, Hispanic ethnicity (AOR 1.57, 95% CI 1.45 to 1.70, p-value = <0.001), higher BMI (e.g., AOR 1.48, 95% CI 1.40 to 1.57, p-value < 0.001, comparing BMI 40 kg/m2 to BMI 25 kg/m2), and higher CCI (AOR 9.46, 95% CI 8.89 to 10.07, p-value = <0.001 for CCI ≥6 relative to CCI 0 to 1) (Table 4).

Table 3. SARS-CoV-2–related mortality presented by month in a cohort of 9.1 million VA enrollees followed from February 2020 to February 2021.

Number of SARS-CoV-2–related deaths per month (and mortality per 100,000 persons per month)
Time period and number of VA enrollees at risk* Entire period: February 2020 to February 2021
N = 9,127,673
February to March 2020
N = 9,127,673
April 2020
N = 9,090,196
May 2020
N = 9,053,082
June 2020
N = 9,022,051
July 2020
N = 8,990,833
August 2020
N = 8,948,674
September 2020
N = 8,913,864
October 2020
N = 8,881,573
November 2020
N = 8,844,680
December 2020
N = 8,804,424
January 2021
N = 8,744,388
February 2021
N = 8,671,916
All persons 10,230
(9.3)
83
(0.9)
775
(8.5)
631
(7.0)
295
(3.3)
627
(7.0)
604
(6.7)
375
(4.2)
500
(5.6)
1,165
(13.2)
2,019
(22.8)
2,172
(24.7)
984
(11.3)
Sex
Female 208
(2.1)
1
(0.1)
14
(1.7)
18
(2.2)
7
(0.8)
14
(1.7)
15
(1.8)
3
(0.4)
11
(1.3)
21
(2.6)
42
(5.1)
38
(4.7)
24
(3.0)
Male 10,022
(10.1)
82
(1.0)
761
(9.2)
613
(7.4)
288
(3.5)
613
(7.5)
589
(7.2)
372
(4.6)
489
(6.1)
1,144
(14.2)
1,977
(24.7)
2,134
(26.8)
960
(12.1)
Age (years)
18 to 24 0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
25 to 34 10
(0.1)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
2
(0.2)
3
(0.4)
5
(0.6)
35 to 44 40
(0.3)
0
(0.0)
1
(0.1)
3
(0.3)
0
(0.0)
5
(0.5)
0
(0.0)
1
(0.1)
1
(0.1)
1
(0.1)
7
(0.7)
13
(1.2)
8
(0.8)
45 to 54 153
(1.1)
4
(0.3)
16
(1.4)
8
(0.7)
4
(0.3)
10
(0.9)
12
(1.0)
7
(0.6)
10
(0.9)
9
(0.8)
34
(2.9)
28
(2.4)
11
(1.0)
55 to 64 743
(4.1)
11
(0.7)
71
(4.7)
36
(2.4)
26
(1.7)
59
(3.9)
54
(3.6)
21
(1.4)
30
(2.0)
68
(4.6)
134
(9.0)
160
(10.8)
73
(5.0)
65 to 74 3,354
(11.5)
28
(1.1)
272
(11.2)
181
(7.5)
86
(3.6)
213
(8.9)
206
(8.6)
125
(5.2)
165
(6.9)
363
(15.3)
662
(28.0)
733
(31.2)
320
(13.8)
75 to 84 2,993
(19.8)
20
(1.6)
180
(14.4)
157
(12.7)
77
(6.2)
171
(14.0)
162
(13.3)
113
(9.3)
148
(12.3)
366
(30.7)
629
(52.8)
656
(55.5)
314
(26.9)
≥85 2,937
(32.0)
20
(2.6)
235
(31.3)
246
(33.4)
102
(14.0)
169
(23.6)
170
(24.1)
108
(15.5)
146
(21.3)
358
(52.9)
551
(81.9)
579
(86.9)
253
(38.9)
Race
White 7,273
(10.3)
34
(0.6)
411
(7.0)
406
(7.0)
194
(3.3)
409
(7.1)
396
(6.9)
271
(4.7)
398
(7.0)
913
(16.0)
1,541
(27.1)
1,561
(27.6)
739
(13.2)
Black 1,935
(12.1)
44
(3.3)
309
(23.2)
174
(13.1)
74
(5.6)
150
(11.4)
138
(10.5)
62
(4.7)
59
(4.5)
112
(8.6)
277
(21.4)
374
(29.0)
162
(12.7)
Asian 65
(4.7)
0
(0.0)
3
(2.6)
6
(5.2)
2
(1.8)
3
(2.6)
8
(7.0)
5
(4.4)
1
(0.9)
2
(1.8)
15
(13.3)
15
(13.3)
5
(4.5)
AI/AN 125
(13.1)
0
(0.0)
6
(7.5)
5
(6.3)
4
(5.1)
9
(11.4)
8
(10.2)
7
(9.0)
9
(11.6)
14
(18.0)
27
(34.9)
28
(36.4)
8
(10.5)
PI/NH 87
(9.6)
1
(1.3)
4
(5.3)
3
(4.0)
3
(4.0)
6
(8.1)
4
(5.4)
2
(2.7)
3
(4.1)
12
(16.4)
20
(27.3)
21
(28.9)
8
(11.1)
Missing/unknown/refused 745
(3.8)
4
(0.2)
42
(2.6)
37
(2.3)
18
(1.1)
50
(3.1)
50
(3.1)
28
(1.7)
30
(1.9)
112
(7.0)
139
(8.7)
173
(10.9)
62
(3.9)
Ethnicity
Non-Hispanic 9,097
(10.5)
75
(1.0)
711
(9.9)
577
(8.1)
257
(3.6)
516
(7.3)
529
(7.5)
341
(4.8)
458
(6.5)
1,053
(15.1)
1,813
(26.1)
1,904
(27.5)
863
(12.6)
Hispanic 745
(10.9)
8
(1.4)
45
(7.9)
32
(5.6)
28
(4.9)
89
(15.7)
51
(9.0)
21
(3.7)
23
(4.1)
75
(13.5)
133
(23.9)
158
(28.6)
82
(15.0)
Missing/unknown/refused 388
(2.4)
0
(0.0)
19
(1.4)
22
(1.6)
10
(0.7)
22
(1.6)
24
(1.8)
13
(1.0)
19
(1.4)
37
(2.8)
73
(5.5)
110
(8.3)
39
(3.0)
US Federal Region
1 418
(8.7)
2
(0.5)
99
(24.8)
86
(21.7)
13
(3.3)
6
(1.5)
6
(1.5)
3
(0.8)
3
(0.8)
24
(6.2)
70
(18.1)
65
(16.9)
41
(10.7)
2 704
(8.8)
24
(3.6)
237
(35.8)
115
(17.5)
16
(2.5)
13
(2.0)
4
(0.6)
5
(0.8)
9
(1.4)
25
(3.9)
82
(12.8)
114
(17.9)
60
(9.5)
3 905
(7.9)
3
(0.3)
86
(9.0)
72
(7.6)
36
(3.8)
29
(3.1)
31
(3.3)
19
(2.0)
46
(4.9)
80
(8.6)
190
(20.4)
213
(23.0)
100
(10.9)
4 2,385
(8.7)
7
(0.3)
77
(3.4)
106
(4.7)
85
(3.7)
209
(9.2)
237
(10.5)
145
(6.5)
116
(5.2)
181
(8.1)
362
(16.3)
590
(26.7)
270
(12.3)
5 1,567
(9.8)
17
(1.3)
134
(10.2)
113
(8.6)
41
(3.1)
34
(2.6)
56
(4.3)
35
(2.7)
78
(6.0)
316
(24.6)
387
(30.2)
236
(18.6)
120
(9.5)
6 1,567
(10.9)
20
(1.7)
74
(6.2)
48
(4.0)
33
(2.8)
179
(15.2)
133
(11.3)
53
(4.5)
91
(7.8)
212
(18.3)
273
(23.6)
306
(26.6)
145
(12.7)
7 710
(12.9)
2
(0.4)
16
(3.5)
28
(6.2)
9
(2.0)
12
(2.7)
35
(7.8)
53
(11.8)
67
(15.0)
143
(32.2)
170
(38.5)
125
(28.6)
50
(11.6)
8 387
(8.6)
2
(0.5)
11
(2.9)
24
(6.5)
11
(3.0)
8
(2.2)
7
(1.9)
19
(5.2)
48
(13.1)
83
(22.7)
104
(28.6)
51
(14.1)
19
(5.3)
9 1,340
(10.7)
3
(0.3)
33
(3.2)
26
(2.5)
46
(4.5)
123
(12.0)
76
(7.4)
30
(2.9)
28
(2.8)
68
(6.7)
325
(32.1)
425
(42.2)
157
(15.8)
10 247
(4.9)
3
(0.7)
8
(1.9)
13
(3.1)
5
(1.2)
14
(3.4)
19
(4.6)
13
(3.2)
14
(3.4)
33
(8.1)
56
(13.7)
47
(11.6)
22
(5.4)
Urban versus rural
Rural 5,002
(9.3)
20
(0.4)
151
(3.4)
171
(3.9)
116
(2.6)
263
(6.0)
319
(7.3)
226
(5.2)
320
(7.3)
707
(16.3)
1,124
(26.0)
1,104
(25.6)
481
(11.3)
Urban 5,228
(9.4)
63
(1.4)
624
(13.4)
460
(10.0)
179
(3.9)
364
(7.9)
285
(6.2)
149
(3.3)
180
(4.0)
458
(10.1)
895
(19.9)
1,068
(23.8)
503
(11.3)
BMI (kg/m2)
<18.5 (underweight) 304
(39.2)
3
(4.6)
28
(44.4)
28
(45.2)
16
(26.3)
19
(31.8)
15
(25.5)
10
(17.3)
12
(21.0)
32
(56.7)
46
(82.0)
66
(118.8)
29
(53.2)
18.5 to <25 (normal weight) 2,660
(12.0)
21
(1.1)
222
(12.1)
215
(11.8)
83
(4.6)
158
(8.8)
158
(8.8)
108
(6.1)
108
(6.1)
261
(14.8)
503
(28.6)
549
(31.4)
274
(15.8)
25 to <30 (overweight) 3,244
(8.2)
29
(0.9)
254
(7.7)
188
(5.7)
82
(2.5)
201
(6.1)
175
(5.4)
125
(3.9)
160
(4.9)
368
(11.4)
636
(19.8)
718
(22.4)
308
(9.7)
30 to <35 (obese I) 2,262
(7.7)
13
(0.5)
140
(5.8)
127
(5.2)
64
(2.7)
146
(6.1)
125
(5.2)
81
(3.4)
117
(4.9)
291
(12.2)
466
(19.6)
481
(20.4)
211
(9.0)
35 to <40 (obese II) 1,091
(8.9)
12
(1.2)
78
(7.6)
41
(4.0)
30
(2.9)
57
(5.6)
92
(9.1)
33
(3.3)
54
(5.4)
120
(12.0)
236
(23.6)
235
(23.6)
103
(10.5)
≥40 (obese III) 669
(12.5)
5
(1.1)
53
(11.9)
32
(7.2)
20
(4.5)
46
(10.4)
39
(8.9)
18
(4.1)
49
(11.2)
93
(21.4)
132
(30.5)
123
(28.6)
59
(13.9)
CCI
0 to 1 1,450
(2.0)
9
(0.1)
94
(1.6)
98
(1.6)
43
(0.7)
88
(1.5)
93
(1.5)
61
(1.0)
73
(1.2)
176
(3.0)
279
(4.7)
308
(5.2)
128
(2.2)
2 to 3 2,156
(11.8)
20
(1.3)
157
(10.4)
115
(7.6)
50
(3.3)
122
(8.2)
127
(8.5)
78
(5.3)
125
(8.5)
244
(16.7)
470
(32.2)
429
(29.6)
219
(15.3)
4 to 5 2,331
(25.3)
11
(1.4)
161
(21.1)
131
(17.3)
75
(10.0)
138
(18.4)
137
(18.4)
88
(11.9)
89
(12.1)
284
(39.0)
467
(64.3)
512
(71.2)
238
(33.6)
≥6 4,293
(46.2)
43
(5.6)
363
(47.5)
287
(38.0)
127
(17.0)
279
(37.7)
247
(33.8)
148
(20.5)
213
(29.9)
461
(65.3)
803
(114.5)
923
(133.3)
399
(58.9)

* VA enrollees at risk are those who are still alive at the beginning of each time period and had not been infected with SARS-CoV-2 more than 30 days before the beginning of the time period.

Categorized according to the 10 Federal Regions drawn up by the Federal Emergency Management Agency: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, and PR), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Table 4. Trends over time in the associations (AORs*) of sociodemographic characteristics and comorbidity burden with risk of SARS-CoV-2–related mortality in a cohort of 9.1 million VA enrollees from February 2020 to February 2021.

AORs* for SARS-CoV-2–related mortality (95% CI)
Entire period: February 2020 to February 2021
N = 9,127,673
February to April 2020
N = 9,127,673
May to June 2020
N = 9,059,880
July to August 2020
N = 8,998,307
September to October 2020
N = 8,922,764
November to December 2020
N = 8,857,881
January to February 2021
N = 8,790,422
Sex
Female 1 1 1 1 1 1 1
Male 1.59
(1.38 to 1.82)
2.14
(1.28 to 3.59)
1.21
(0.81 to 1.81)
1.52
(1.05 to 2.21)
1.96
(1.15 to 3.35)
1.50
(1.17 to 1.94)
1.68
(1.30 to 2.16)
Age (years)
25 0.09
(0.04 to 0.17)
0.02
(0.00 to 0.63)
0.04
(0.00 to 0.82)
0.01
(0.00 to 0.18)
0.01
(0.00 to 0.45)
0.03
(0.01 to 0.16)
0.32
(0.14 to 0.73)
35 0.31
(0.23 to 0.42)
0.15
(0.03 to 0.73)
0.22
(0.06 to 0.82)
0.14
(0.04 to 0.43)
0.10
(0.02 to 0.64)
0.20
(0.10 to 0.41)
0.56
(0.39 to 0.80)
45 (reference) 1 1 1 1 1 1 1
55 2.39
(2.14 to 2.67)
3.47
(1.97 to 6.10)
3.04
(1.88 to 4.92)
3.12
(2.09 to 4.67)
3.63
(1.86 to 7.08)
2.69
(2.09 to 3.46)
1.88
(1.61 to 2.19)
65 5.05
(4.27 to 5.98)
6.87
(3.55 to 13.30)
6.72
(3.53 to 12.80)
5.83
(3.57 to 9.52)
7.18
(3.42 to 15.08)
5.58
(3.98 to 7.82)
4.06
(3.05 to 5.41)
75 11.40
(9.77 to 13.30)
11.68
(6.23 to 21.91)
14.25
(7.81 to 25.99)
12.30
(7.77 to 19.48)
16.86
(8.29 to 34.28)
14.26
(10.41 to 19.52)
9.51
(7.36 to 12.30)
85 20.37
(17.48 to 23.74)
20.46
(10.92 to 38.34)
30.53
(16.82 to 55.41)
22.64
(14.30 to 35.85)
33.38
(16.43 to 67.82)
27.31
(19.97 to 37.34)
16.74
(12.97 to 21.61)
Race
White 1 1 1 1 1 1 1
Black 1.55
(1.47 to 1.64)
3.85
(3.30 to 4.50)
2.21
(1.89 to 2.60)
1.84
(1.59 to 2.13)
1.16
(0.95 to 1.43)
1.08
(0.96 to 1.20)
1.28
(1.16 to 1.42)
Asian 0.82
(0.64 to 1.05)
0.90
(0.29 to 2.83)
1.39
(0.68 to 2.82)
1.07
(0.59 to 1.96)
1.40
(0.62 to 3.17)
0.71
(0.44 to 1.16)
0.60
(0.38 to 0.93)
AI/AN 1.66
(1.39 to 1.98)
1.93
(0.86 to 4.32)
1.93
(1.00 to 3.73)
1.67
(1.03 to 2.71)
2.25
(1.37 to 3.71)
1.57
(1.15 to 2.13)
1.44
(1.04 to 2.01)
PI/NH 1.03
(0.83 to 1.28)
1.16
(0.48 to 2.80)
0.97
(0.43 to 2.17)
0.87
(0.46 to 1.62)
0.76
(0.32 to 1.84)
1.20
(0.85 to 1.71)
0.96
(0.67 to 1.39)
Missing/unknown/refused 0.85
(0.78 to 0.93)
1.17
(0.82 to 1.66)
0.77
(0.55 to 1.09)
0.91
(0.71 to 1.17)
0.73
(0.52 to 1.02)
0.95
(0.81 to 1.11)
0.71
(0.60 to 0.84)
Ethnicity
Non-Hispanic 1 1 1 1 1 1 1
Hispanic 1.57
(1.45 to 1.70)
0.74
(0.55 to 0.99)
1.20
(0.91 to 1.59)
2.65
(2.19 to 3.20)
1.42
(1.04 to 1.95)
1.57
(1.35 to 1.82)
1.60
(1.39 to 1.84)
Missing/unknown/refused 0.46
(0.40 to 0.52)
0.26
(0.15 to 0.44)
0.40
(0.26 to 0.63)
0.44
(0.31 to 0.63)
0.45
(0.29 to 0.71)
0.35
(0.28 to 0.44)
0.65
(0.52 to 0.80)
US Federal Region
1 0.90
(0.81 to 1.00)
7.21
(5.37 to 9.69)
2.61
(2.04 to 3.34)
0.15
(0.08 to 0.26)
0.12
(0.05 to 0.26)
0.86
(0.69 to 1.07)
0.62
(0.51 to 0.76)
2 0.74
(0.68 to 0.81)
7.93
(6.16 to 10.21)
1.54
(1.21 to 1.94)
0.08
(0.05 to 0.13)
0.15
(0.09 to 0.25)
0.51
(0.42 to 0.63)
0.51
(0.43 to 0.60)
3 0.89
(0.83 to 0.96)
2.26
(1.68 to 3.05)
1.24
(0.98 to 1.57)
0.32
(0.24 to 0.42)
0.59
(0.45 to 0.77)
1.18
(1.02 to 1.37)
0.86
(0.76 to 0.98)
4 (reference) 1 1 1 1 1 1 1
5 1.04
(0.98 to 1.11)
2.92
(2.23 to 3.82)
1.27
(1.03 to 1.57)
0.33
(0.26 to 0.41)
0.67
(0.54 to 0.84)
2.00
(1.78 to 2.23)
0.66
(0.58 to 0.75)
6 1.31
(1.23 to 1.40)
2.47
(1.84 to 3.31)
0.89
(0.68 to 1.15)
1.32
(1.14 to 1.53)
1.09
(0.89 to 1.34)
1.75
(1.54 to 1.98)
1.04
(0.93 to 1.17)
7 1.38
(1.27 to 1.51)
1.23
(0.74 to 2.05)
0.99
(0.69 to 1.41)
0.51
(0.38 to 0.69)
1.96
(1.58 to 2.44)
2.48
(2.16 to 2.86)
0.94
(0.80 to 1.11)
8 1.16
(1.04 to 1.29)
1.77
(0.98 to 3.18)
1.60
(1.11 to 2.30)
0.25
(0.15 to 0.41)
1.62
(1.23 to 2.12)
2.19
(1.85 to 2.59)
0.57
(0.44 to 0.72)
9 1.41
(1.32 to 1.51)
1.16
(0.78 to 1.72)
0.89
(0.68 to 1.18)
1.05
(0.88 to 1.24)
0.55
(0.41 to 0.74)
1.79
(1.57 to 2.05)
1.70
(1.52 to 1.89)
10 0.76
(0.67 to 0.87)
1.38
(0.73 to 2.60)
0.81
(0.50 to 1.32)
0.57
(0.40 to 0.82)
0.69
(0.46 to 1.03)
1.10
(0.88 to 1.37)
0.57
(0.45 to 0.73)
Urban versus rural
Rural 1 1 1 1 1 1 1
Urban 1.00
(0.96 to 1.04)
2.48
(2.08 to 2.96)
1.81
(1.57 to 2.10)
1.11
(0.99 to 1.24)
0.72
(0.62 to 0.83)
0.80
(0.74 to 0.86)
0.95
(0.88 to 1.02)
BMI (kg/m2)
20 1.62
(1.53 to 1.71)
1.53
(1.27 to 1.84)
1.98
(1.68 to 2.33)
1.68
(1.42 to 1.98)
1.58
(1.29 to 1.95)
1.77
(1.59 to 1.97)
1.75
(1.58 to 1.94)
25 (reference) 1 1 1 1 1 1 1
30 1.00
(0.94 to 1.06)
0.95
(0.78 to 1.17)
0.92
(0.76 to 1.13)
0.94
(0.79 to 1.13)
0.94
(0.76 to 1.15)
1.11
(0.99 to 1.23)
0.95
(0.85 to 1.06)
35 1.20
(1.13 to 1.27)
1.00
(0.82 to 1.22)
1.02
(0.84 to 1.24)
1.28
(1.09 to 1.50)
1.15
(0.95 to 1.39)
1.32
(1.20 to 1.46)
1.12
(1.02 to 1.24)
40 1.48
(1.40 to 1.57)
1.35
(1.11 to 1.64)
1.30
(1.07 to 1.59)
1.58
(1.34 to 1.86)
1.48
(1.22 to 1.80)
1.64
(1.48 to 1.81)
1.33
(1.20 to 1.47)
CCI
0 to 1 1 1 1 1 1 1 1
2 to 3 3.06
(2.86 to 3.27)
3.32
(2.60 to 4.26)
2.29
(1.82 to 2.88)
2.85
(2.35 to 3.47)
3.02
(2.42 to 3.77)
3.21
(2.85 to 3.61)
3.28
(2.90 to 3.72)
4 to 5 5.58
(5.22 to 5.97)
5.30
(4.12 to 6.81)
4.79
(3.85 to 5.97)
5.30
(4.36 to 6.42)
4.47
(3.55 to 5.63)
5.80
(5.15 to 6.54)
6.63
(5.87 to 7.50)
≥6 9.46
(8.89 to 10.07)
10.46
(8.34 to 13.12)
8.64
(7.07 to 10.56)
9.44
(7.91 to 11.27)
8.90
(7.24 to 10.94)
9.59
(8.58 to 10.72)
11.41
(10.18 to 12.79)

* Adjusted for sex, age (modeled as restricted cubic splines with 5 knots at ages 30, 49, 64, 73, and 88 years), race, ethnicity, geographical region, urban/rural location, BMI (modeled as restricted cubic splines with 5 knots at BMIs of 21.3, 26.0, 29.0, 32.5, and 39.9 kg/m2), and CCI.

Categorized according to the 10 Federal Regions drawn up by the Federal Emergency Management Agency: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, and PR), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; AOR, adjusted odds ratio; BMI, body mass index; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

The magnitude of the association between Black (versus White) race and SARS-CoV-2–related mortality declined steadily over time from February to April (AOR 3.85, 95% CI 3.30 to 4.50, p-value < 0.001) and became nonsignificant by September to October (AOR 1.16, 95% CI 0.95 to 1.43, p-value = 0.15) (Table 4, Fig 2); however, Black race was again positively associated with SARS-CoV-2–related mortality in January to February 2021 (AOR 1.28, 95% CI 1.16 to 1.42, p-value = <0.001), albeit at a much lower magnitude of association.

The magnitude of the association between urban versus rural location declined steadily over time (p-value for trends over time <0.001, see S1 and S2 Tables) and shifted from a positive association in February/April (AOR 2.48, 95% CI 2.08 to 2.96, p-value = <0.001) to a negative association in all the time periods after September 2020. Geographical regions with the highest risk of SARS-CoV-2–related mortality in February to April (Federal Regions 1 and 2) had the lowest risk of SARS-CoV-2–related mortality by September to October with some increase in risk thereafter.

Associations between sex, CCI, or age and SARS-CoV-2–related mortality appeared to be stable over time.

Trends over time in the associations of risk factors with SARS-CoV-2 case fatality

Among a total of 206,789 persons who tested positive for SARS-CoV-2 infection from February 1, 2020 to February 28, 2021, 10,429 (5.0%) SARS-CoV-2–related deaths occurred, i.e., deaths within 30 days of infection (Table 5). Case fatality declined progressively over time from 12.6% in persons who tested positive in February to March 2020 to 3.1% in persons who tested positive in February 2021 (Table 5, Fig 3). Significant, independent risk factors for case fatality over the entire observation period included male sex (AOR 1.73, 95% CI 1.50 to 2.00, p-value < 0.001), older age (e.g., AOR 50.09, 95% CI 42.87 to 58.52, p-value < 0.001, for age 85 versus age 45 years), Black (AOR 1.13, 95% CI 1.06 to 1.19, p-value < 0.001), and AI/AN (AOR 1.76, 95% CI 1.44 to 2.14, p-value < 0.001) race relative to White race, Hispanic versus non-Hispanic ethnicity (AOR 1.21, 95% CI 1.11 to 1.31, p-value < 0.001), obesity/high BMI (e.g., AOR 1.35, 95% CI 1.27 to 1.43, p-value < 0.001 comparing BMI 40 versus 25 kg/m2) or underweight/low BMI (e.g., AOR 1.44, 95% CI 1.35 to 1.53, p-value < 0.001 comparing BMI 20 versus 25 kg/m2), and progressively higher CCI (e.g., AOR 2.51, 95% CI 2.35 to 2.68, p-value = <0.001 for CCI ≥6 relative to CCI 0 to 1) (Table 6).

Table 5. SARS-CoV-2 case fatality presented for VA enrollees who tested positive for SARS-CoV-2 each monthly period from February 2020 to February 2021.

Number of SARS-CoV-2–related deaths among persons testing positive each month (and mortality per 100 persons)
Time period and number of VA enrollees with positive SARS-CoV-2 test Cohort characteristics
N = 206,789
Entire period: February 2020 to February 2021
N = 206,789
February to March 2020
N = 2,470
April 2020
N = 7,346
May 2020
N = 4,957
June 2020
N = 7,634
July 2020
N = 16,105
August 2020
N = 9,189
September 2020
N = 7,526
October 2020
N = 13,523
November 2020
N = 33,553
December 2020
N = 47,357
January 2021
N = 39,431
February 2021
N = 17,698
SARS-CoV-2–related deaths * , n (%) 10,429
(5.0%)
312
(12.6)
875
(11.9)
442
(8.9)
376
(4.9)
724
(4.5)
459
(5.0)
379
(5.0)
695
(5.1)
1,491
(4.4)
2,398
(5.1)
1,732
(4.4)
546
(3.1)
Sex
Female 21,033
(10.2)
211
(1.0)
7
(3.2)
16
(2.3)
14
(3.1)
8
(0.9)
18
(0.9)
9
(0.9)
4
(0.6)
16
(1.3)
22
(0.7)
48
(1.0)
35
(0.9)
14
(0.8)
Male 185,756
(89.8)
10,218
(5.5)
305
(13.5)
859
(12.9)
428
(9.5)
368
(5.4)
706
(5.0)
450
(5.5)
375
(5.5)
679
(5.5)
1,469
(4.9)
2,350
(5.5)
1,697
(4.8)
532
(3.4)
Age (years)
18 to 24 1,293
(0.6)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
25 to 34 15,919
(7.7)
11
(0.1)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
0
(0.0)
1
(0.0)
4
(0.1)
1
(0.0)
5
(0.4)
35 to 44 23,339
(11.3)
40
(0.2)
0
(0.0)
1
(0.2)
3
(0.7)
2
(0.2)
3
(0.1)
0
(0.0)
1
(0.1)
1
(0.1)
2
(0.1)
12
(0.2)
11
(0.3)
4
(0.2)
45 to 54 29,783
(14.4)
163
(0.5)
11
(3.0)
13
(1.5)
7
(1.3)
5
(0.4)
15
(0.6)
8
(0.6)
9
(0.8)
6
(0.3)
17
(0.3)
34
(0.5)
24
(0.4)
14
(0.6)
55 to 64 39,340
(19.0)
762
(1.9)
46
(8.2)
56
(3.7)
29
(2.7)
35
(2.5)
68
(2.2)
39
(2.2)
22
(1.6)
47
(1.9)
79
(1.3)
161
(1.8)
135
(1.8)
45
(1.3)
65 to 74 57,869
(28.0)
3,432
(5.9)
124
(18.0)
274
(13.0)
122
(8.7)
123
(6.8)
257
(6.4)
146
(5.7)
125
(5.6)
221
(5.6)
504
(5.3)
791
(6.0)
562
(5.0)
183
(3.5)
75 to 84 26,793
(13.0)
3,045
(11.4)
66
(23.7)
225
(22.0)
102
(14.7)
104
(13.1)
189
(12.1)
135
(12.0)
106
(10.6)
218
(12.1)
465
(10.6)
735
(11.5)
540
(10.0)
160
(6.7)
≥85 12,453
(6.0)
2,976
(23.9)
65
(46.1)
306
(37.7)
179
(31.7)
107
(25.2)
192
(25.4)
131
(25.3)
116
(25.8)
202
(25.9)
423
(22.3)
661
(23.5)
459
(20.2)
135
(13.1)
Race
White 138,364
(66.9)
7,416
(5.4)
120
(12.6)
522
(13.8)
296
(10.8)
244
(5.5)
480
(5.2)
307
(5.4)
290
(5.6)
547
(5.5)
1,156
(4.7)
1,778
(5.4)
1,282
(4.8)
394
(3.3)
Black 46,288
(22.4)
1,975
(4.3)
170
(13.1)
290
(9.9)
110
(6.4)
92
(4.0)
166
(3.4)
95
(3.7)
55
(3.4)
77
(3.4)
162
(3.0)
378
(4.2)
280
(3.3)
100
(2.6)
Asian 2,069
(1.0)
66
(3.2)
2
(7.4)
4
(7.3)
4
(10.8)
1
(1.3)
8
(4.8)
6
(7.4)
3
(4.3)
1
(1.1)
5
(1.8)
20
(3.6)
10
(2.3)
2
(1.0)
AI/AN 1,955
(0.9)
125
(6.4)
2
(14.3)
7
(13.0)
3
(6.3)
7
(7.6)
8
(5.2)
9
(11.4)
7
(9.2)
10
(6.8)
16
(4.7)
36
(8.2)
14
(4.0)
6
(3.7)
PI/NH 1,948
(0.9)
90
(4.6)
2
(15.4)
5
(8.8)
2
(4.5)
3
(3.9)
6
(3.8)
5
(5.0)
0
(0.0)
6
(5.2)
17
(5.6)
23
(5.2)
14
(3.6)
7
(4.0)
Missing/unknown/refused 16,165
(7.8)
757
(4.7)
16
(9.6)
47
(9.7)
27
(7.5)
29
(4.4)
56
(4.0)
37
(5.3)
24
(4.3)
54
(5.4)
135
(5.3)
163
(4.2)
132
(4.2)
37
(2.8)
Ethnicity
Non-Hispanic 177,958
(86.1)
9,274
(5.2)
284
(13.4)
806
(12.5)
401
(9.2)
310
(5.1)
607
(4.7)
411
(5.3)
349
(5.3)
628
(5.3)
1,351
(4.6)
2,124
(5.2)
1,513
(4.5)
490
(3.2)
Hispanic 20,751
(10.0)
759
(3.7)
24
(8.8)
43
(6.6)
26
(6.1)
51
(4.1)
91
(3.5)
30
(2.9)
18
(2.8)
45
(3.9)
91
(3.2)
174
(3.7)
131
(3.5)
35
(2.4)
Missing/unknown/refused 8,080
(3.9)
396
(4.9)
4
(5.1)
26
(10.2)
15
(9.0)
15
(5.0)
26
(4.4)
18
(5.5)
12
(4.5)
22
(4.4)
49
(3.9)
100
(5.1)
88
(5.3)
21
(2.9)
US Federal Region
1 7,004
(3.4)
427
(6.1)
10
(10.5)
150
(17.6)
34
(8.5)
8
(4.1)
9
(6.3)
2
(2.0)
4
(4.0)
5
(2.3)
41
(4.3)
77
(4.6)
68
(4.5)
19
(2.5)
2 10,959
(5.3)
718
(6.6)
112
(18.2)
217
(12.6)
55
(9.3)
14
(5.2)
7
(2.1)
6
(2.8)
6
(2.9)
16
(4.2)
39
(3.1)
119
(5.5)
91
(4.3)
36
(3.3)
3 17,339
(8.4)
931
(5.4)
25
(13.5)
96
(11.5)
55
(8.4)
34
(7.4)
32
(4.1)
21
(3.6)
30
(6.3)
49
(5.9)
123
(4.9)
243
(5.4)
168
(4.5)
55
(3.0)
4 53,231
(25.7)
2,447
(4.6)
26
(7.2)
110
(10.1)
100
(9.9)
94
(3.8)
270
(4.5)
191
(5.6)
123
(5.3)
146
(4.8)
213
(3.8)
537
(4.8)
485
(4.2)
152
(2.8)
5 32,309
(15.6)
1,592
(4.9)
60
(14.5)
146
(11.9)
83
(8.7)
26
(4.3)
52
(4.3)
49
(4.9)
40
(3.7)
149
(4.9)
389
(4.6)
336
(4.5)
188
(4.1)
74
(3.4)
6 31,762
(15.4)
1,594
(5.0)
50
(10.9)
65
(9.9)
39
(8.0)
82
(4.7)
192
(4.8)
89
(5.3)
50
(4.1)
135
(6.2)
234
(5.3)
324
(5.0)
254
(4.1)
80
(3.4)
7 13,984
(6.8)
718
(5.1)
7
(12.1)
23
(9.7)
22
(8.8)
10
(4.5)
20
(3.3)
32
(4.7)
66
(7.7)
80
(5.6)
159
(4.4)
176
(5.8)
96
(4.8)
27
(2.9)
8 8,623
(4.2)
394
(4.6)
4
(5.4)
18
(8.7)
26
(14.5)
2
(1.4)
10
(3.6)
14
(5.8)
23
(5.6)
57
(5.2)
109
(4.2)
79
(4.1)
40
(4.0)
12
(2.3)
9 26,230
(12.7)
1,358
(5.2)
13
(7.9)
35
(9.0)
23
(6.7)
99
(7.2)
110
(4.7)
43
(4.4)
24
(3.8)
37
(4.3)
141
(4.5)
446
(5.8)
308
(5.1)
79
(3.5)
10 5,348
(2.6)
250
(4.7)
5
(11.4)
15
(11.3)
5
(5.4)
7
(4.8)
22
(5.7)
12
(4.1)
13
(5.9)
21
(4.8)
43
(3.9)
61
(4.8)
34
(4.4)
12
(2.6)
Urban versus rural
Rural 99,646
(48.2)
5,106
(5.1)
57
(9.8)
196
(10.5)
137
(8.4)
156
(5.3)
335
(4.9)
261
(5.6)
233
(5.6)
425
(5.7)
870
(5.0)
1,289
(5.4)
867
(4.5)
280
(3.2)
Urban 107,143
(51.8)
5,323
(5.0)
255
(13.5)
679
(12.4)
305
(9.1)
220
(4.7)
389
(4.2)
198
(4.4)
146
(4.3)
270
(4.5)
621
(3.9)
1,109
(4.7)
865
(4.3)
266
(3.0)
BMI (kg/m2)
<18.5 (underweight) 1,897
(0.9)
312
(16.4)
13
(34.2)
31
(20.9)
23
(22.8)
20
(21.1)
12
(10.4)
13
(13.3)
13
(17.6)
15
(14.3)
39
(17.5)
57
(15.2)
57
(15.5)
19
(11.9)
18.5 to <25 (normal weight) 31,118
(15.0)
2,704
(8.7)
78
(18.9)
269
(18.6)
152
(14.8)
104
(8.5)
173
(7.2)
125
(9.2)
108
(9.2)
143
(7.7)
344
(7.4)
617
(8.9)
452
(7.7)
139
(5.1)
25 to <30 (overweight) 67,238
(32.5)
3,296
(4.9)
93
(11.7)
288
(12.3)
129
(8.1)
111
(4.4)
235
(4.5)
135
(4.6)
121
(4.9)
216
(4.9)
465
(4.3)
807
(5.2)
526
(4.1)
170
(3.0)
30 to <35 (obese I) 59,700
(28.9)
2,312
(3.9)
67
(9.9)
164
(8.6)
78
(6.2)
85
(3.9)
156
(3.3)
97
(3.6)
85
(3.9)
184
(4.6)
358
(3.6)
518
(3.8)
405
(3.5)
115
(2.3)
35 to <40 (obese II) 29,939
(14.5)
1,118
(3.7)
39
(11.0)
69
(7.3)
39
(6.2)
30
(2.9)
90
(3.8)
69
(4.9)
28
(2.7)
75
(3.7)
168
(3.4)
250
(3.6)
198
(3.5)
63
(2.5)
≥40 (obese III) 16,897
(8.2)
687
(4.1)
22
(11.4)
54
(9.7)
21
(6.3)
26
(4.4)
58
(4.3)
20
(2.7)
24
(3.8)
62
(5.3)
117
(4.1)
149
(3.8)
94
(3.0)
40
(2.8)
CCI
0 to 1 93,603
(45.3)
1,480
(1.6)
38
(4.0)
108
(4.1)
78
(4.3)
59
(1.6)
102
(1.3)
61
(1.5)
67
(2.0)
102
(1.7)
217
(1.4)
351
(1.6)
217
(1.2)
80
(1.0)
2 to 3 49,109
(23.7)
2,208
(4.5)
71
(12.9)
160
(9.7)
87
(7.5)
63
(4.0)
149
(4.0)
98
(4.7)
87
(4.8)
156
(4.8)
316
(4.0)
521
(4.6)
364
(3.7)
136
(3.1)
4 to 5 28,738
(13.9)
2,369
(8.2)
55
(15.9)
188
(16.3)
90
(11.2)
90
(9.1)
171
(8.6)
110
(8.5)
72
(6.7)
135
(7.4)
369
(8.0)
540
(8.2)
440
(7.8)
109
(4.5)
≥6 35,339
(17.1)
4,372
(12.4)
148
(24.0)
419
(21.8)
187
(15.7)
164
(12.9)
302
(12.1)
190
(11.9)
153
(11.5)
302
(13.0)
589
(11.1)
986
(12.5)
711
(10.9)
221
(7.7)

* The number of deaths each month are different than those shown in Table 3, because Table 5 shows the number of persons who tested positive each month (same as in Table 1) and among them those who died within 30 days—some of these deaths occurred in the following month, but patients are grouped based on the date of infection.

Categorized according to the 10 Federal Regions drawn up by the Federal Emergency Management Agency: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, and PR), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

Table 6. Trends over time in the associations (AORs*) of sociodemographic characteristics and comorbidity burden with risk of SARS-CoV-2 case fatality among 206,789 VA enrollees who tested positive for SARS-CoV-2 from February 1, 2020 to February 28, 2021, presented overall and divided into time periods.

AORs* for SARS-CoV-2–related death among persons testing positive (95% CI)
Entire period: February 2020 to February 2021
N = 206,789
February to April 2020
N = 9,816
May to June 2020
N = 12,591
July to August 2020
N = 25,294
September to October 2020
N = 21,049
November to December 2020
N = 80,910
January to February 2021
N = 57,129
Sex
Female 1 1 1 1 1 1 1
Male 1.73
(1.50 to 2.00)
1.90
(1.25 to 2.90)
1.36
(0.88 to 2.09)
1.62
(1.10 to 2.39)
1.67
(1.07 to 2.62)
1.72
(1.35 to 2.20)
1.63
(1.22 to 2.18)
Age (years)
25 0.15
(0.08 to 0.29)
0.02
(0.00 to 0.47)
0.05
(0.00 to 0.67)
0.02
(0.00 to 0.34)
0.01
(0.00 to 0.56)
0.21
(0.08 to 0.57)
0.36
(0.14 to 0.95)
35 0.38
(0.29 to 0.50)
0.15
(0.04 to 0.61)
0.22
(0.07 to 0.72)
0.16
(0.05 to 0.53)
0.10
(0.02 to 0.66)
0.44
(0.28 to 0.67)
0.57
(0.38 to 0.86)
45 (reference) 1 1 1 1 1 1 1
55 3.07
(2.76 to 3.42)
4.42
(2.65 to 7.38)
3.62
(2.35 to 5.58)
4.25
(2.74 to 6.61)
5.18
(2.64 to 10.15)
2.91
(2.44 to 3.46)
2.36
(1.97 to 2.82)
65 9.34
(7.87 to 11.09)
12.05
(6.59 to 22.04)
9.69
(5.29 to 17.77)
11.83
(6.93 to 20.19)
15.48
(7.41 to 32.35)
9.44
(7.05 to 12.64)
6.45
(4.65 to 8.95)
75 22.58
(19.33 to 26.38)
23.89
(13.42 to 42.53)
20.84
(11.91 to 36.44)
25.64
(15.46 to 42.52)
37.64
(18.47 to 76.71)
25.21
(19.33 to 32.88)
14.75
(10.99 to 19.79)
85 50.09
(42.87 to 58.52)
46.48
(26.11 to 82.73)
46.14
(26.45 to 80.47)
50.60
(30.48 to 84.01)
79.89
(39.17 to 162.93)
50.33
(38.62 to 65.60)
27.51
(20.51 to 36.91)
Race
White 1 1 1 1 1 1 1
Black 1.13
(1.06 to 1.19)
2.56
(2.23 to 2.93)
1.37
(1.15 to 1.64)
1.27
(1.09 to 1.47)
0.74
(0.61 to 0.90)
0.86
(0.78 to 0.95)
0.88
(0.78 to 0.99)
Asian 1.50
(1.14 to 1.98)
1.98
(0.86 to 4.56)
1.09
(0.44 to 2.68)
2.96
(1.70 to 5.15)
1.31
(0.48 to 3.56)
1.34
(0.88 to 2.03)
0.90
(0.50 to 1.62)
AI/AN 1.76
(1.44 to 2.14)
2.04
(1.04 to 3.99)
1.86
(0.99 to 3.52)
1.83
(1.12 to 2.99)
1.95
(1.20 to 3.19)
1.71
(1.28 to 2.27)
1.09
(0.70 to 1.71)
PI/NH 1.19
(0.95 to 1.49)
1.42
(0.67 to 3.03)
0.81
(0.33 to 1.98)
1.19
(0.65 to 2.17)
0.79
(0.35 to 1.77)
1.33
(0.96 to 1.83)
1.11
(0.71 to 1.72)
Missing/unknown/refused 1.16
(1.06 to 1.27)
1.35
(1.01 to 1.80)
1.05
(0.77 to 1.43)
1.22
(0.95 to 1.55)
1.19
(0.91 to 1.55)
1.17
(1.01 to 1.34)
0.99
(0.82 to 1.20)
Ethnicity
Non-Hispanic 1 1 1 1 1 1 1
Hispanic 1.21
(1.11 to 1.31)
0.74
(0.57 to 0.96)
1.48
(1.15 to 1.91)
1.73
(1.41 to 2.13)
1.15
(0.88 to 1.50)
1.13
(0.99 to 1.30)
1.11
(0.94 to 1.31)
Missing/unknown/refused 1.00
(0.88 to 1.13)
0.75
(0.50 to 1.11)
1.05
(0.70 to 1.59)
0.98
(0.70 to 1.38)
0.79
(0.53 to 1.16)
0.95
(0.78 to 1.15)
1.36
(1.08 to 1.71)
US Federal Region
1 0.99
(0.88 to 1.10)
7.14
(5.61 to 9.08)
1.09
(0.77 to 1.53)
0.13
(0.07 to 0.24)
0.19
(0.10 to 0.36)
0.90
(0.74 to 1.10)
0.76
(0.60 to 0.96)
2 1.01
(0.92 to 1.11)
7.69
(6.24 to 9.48)
0.97
(0.73 to 1.29)
0.09
(0.05 to 0.15)
0.29
(0.19 to 0.46)
0.76
(0.64 to 0.91)
0.70
(0.57 to 0.85)
3 1.00
(0.92 to 1.08)
2.11
(1.65 to 2.71)
1.14
(0.89 to 1.47)
0.30
(0.22 to 0.40)
0.78
(0.60 to 1.00)
1.32
(1.16 to 1.50)
0.92
(0.79 to 1.08)
4 (reference) 1 1 1 1 1 1 1
5 0.85
(0.79 to 0.91)
2.09
(1.67 to 2.60)
0.75
(0.59 to 0.95)
0.29
(0.23 to 0.36)
0.91
(0.75 to 1.09)
1.28
(1.15 to 1.43)
0.53
(0.46 to 0.62)
6 1.07
(1.00 to 1.15)
1.56
(1.21 to 2.00)
1.02
(0.81 to 1.28)
0.95
(0.82 to 1.11)
1.10
(0.90 to 1.33)
1.20
(1.07 to 1.35)
0.85
(0.74 to 0.97)
7 0.96
(0.88 to 1.05)
0.91
(0.61 to 1.35)
0.59
(0.40 to 0.86)
0.38
(0.28 to 0.50)
1.66
(1.35 to 2.04)
1.41
(1.24 to 1.62)
0.61
(0.50 to 0.75)
8 0.92
(0.82 to 1.04)
1.40
(0.89 to 2.22)
0.92
(0.62 to 1.38)
0.30
(0.20 to 0.46)
1.54
(1.20 to 1.99)
1.36
(1.15 to 1.60)
0.45
(0.34 to 0.60)
9 1.15
(1.07 to 1.24)
0.73
(0.52 to 1.02)
1.17
(0.92 to 1.48)
0.61
(0.51 to 0.74)
0.46
(0.35 to 0.62)
1.65
(1.47 to 1.85)
1.25
(1.09 to 1.43)
10 0.96
(0.83 to 1.10)
1.87
(1.16 to 3.01)
0.63
(0.35 to 1.13)
0.71
(0.50 to 1.01)
1.09
(0.76 to 1.57)
1.24
(1.00 to 1.53)
0.64
(0.47 to 0.87)
Urban versus rural
Rural 1 1 1 1 1 1 1
Urban 1.03
(0.98 to 1.07)
2.24
(1.93 to 2.60)
1.59
(1.37 to 1.86)
1.08
(0.96 to 1.22)
0.81
(0.71 to 0.93)
0.84
(0.78 to 0.90)
0.98
(0.90 to 1.07)
BMI (kg/m2)
20 1.44
(1.35 to 1.53)
1.30
(1.11 to 1.53)
1.58
(1.33 to 1.87)
1.20
(1.01 to 1.43)
1.35
(1.12 to 1.62)
1.29
(1.16 to 1.42)
1.42
(1.26 to 1.60)
25 (reference) 1 1 1 1 1 1 1
30 0.96
(0.90 to 1.02)
0.96
(0.80 to 1.15)
0.84
(0.68 to 1.03)
0.83
(0.69 to 0.99)
1.14
(0.94 to 1.37)
0.99
(0.90 to 1.09)
0.92
(0.80 to 1.04)
35 1.12
(1.06 to 1.19)
0.94
(0.79 to 1.11)
0.94
(0.76 to 1.16)
1.17
(0.99 to 1.38)
1.20
(1.01 to 1.44)
1.13
(1.03 to 1.24)
1.13
(1.00 to 1.27)
40 1.35
(1.27 to 1.43)
1.16
(0.98 to 1.39)
1.13
(0.92 to 1.40)
1.35
(1.14 to 1.60)
1.48
(1.24 to 1.77)
1.32
(1.20 to 1.45)
1.29
(1.14 to 1.46)
CCI
0 to 1 1 1 1 1 1 1 1
2 to 3 1.30
(1.21 to 1.39)
1.30
(1.05 to 1.61)
0.92
(0.73 to 1.17)
1.32
(1.08 to 1.62)
1.21
(0.99 to 1.48)
1.26
(1.13 to 1.41)
1.52
(1.31 to 1.76)
4 to 5 1.81
(1.69 to 1.94)
1.72
(1.39 to 2.12)
1.37
(1.09 to 1.73)
1.89
(1.55 to 2.31)
1.28
(1.04 to 1.58)
1.74
(1.56 to 1.94)
2.14
(1.85 to 2.48)
≥6 2.51
(2.35 to 2.68)
2.56
(2.11 to 3.11)
1.81
(1.47 to 2.24)
2.40
(1.99 to 2.89)
2.10
(1.75 to 2.53)
2.22
(2.01 to 2.46)
2.63
(2.29 to 3.02)

* Adjusted for sex, age (modeled as restricted cubic splines with 5 knots at ages 30, 49, 64, 73, and 88 years), race, ethnicity, geographical region, urban/rural location, BMI (modeled as restricted cubic splines with 5 knots at BMIs of 21.3, 26.0, 29.0, 32.5, and 39.9 kg/m2), and CCI.

Categorized according to the 10 Federal Regions drawn up by the Federal Emergency Management Agency: 1 (CT, MA, ME, NH, RI, and VT), 2 (NJ, NY, and PR), 3 (DC, DE, MD, PA, VA, and WV), 4 (AL, FL, GA, KY, MS, NC, SC, and TN), 5 (IL, IN, MI, MN, OH, and WI), 6 (AR, LA, NM, OK, and TX), 7 (IA, KS, MO, and NE), 8 (CO, MT, ND, SD, UT, and WY), and 9 (AZ, CA, GU, HI, and NV), and 10 (AK, ID, OR, and WA).

AI/AN, American Indian/Alaska Native; AOR, adjusted odds ratio; BMI, body mass index; CCI, Charlson comorbidity index; PI/NH, Pacific Islander/Native Hawaiian; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

The magnitude of the association between Black (versus White) race and case fatality declined over time and shifted from a positive association in February to April (AOR 2.56, 95% CI 2.23 to 2.93, p-value < 0.001) to a negative association in all time periods after September 2020 (Table 6). Also, the magnitude of the association between urban versus rural location and case fatality declined steadily over time and shifted from a positive association in February/April (AOR 2.24, 95% CI 1.93 to 2.60, p-value = <0.001) to a negative association in all the time periods after September 2020. Geographical regions with some of the highest case fatality rates in February to April (e.g., Federal Regions 1, 2, and 5) had some of the lowest case fatality rates by January/February 2021. Associations between sex, CCI, or age and case fatality appeared to be stable over time.

Discussion

Our study of a national cohort of 9.1 million VA enrollees followed from February 2020 to March 2021 demonstrates that the strongly positive associations between Black (versus White) race and SARS-CoV-2 infection, mortality, and case fatality that were observed in the early months of the pandemic attenuated over time and were no longer significant by November 2020. Positive associations between AI/AN (versus White) race and risk of infection noted early in the pandemic also attenuated over time and reversed by March 2021. Similarly, strongly positive associations between urban (versus rural) location and SARS-CoV-2 infection, mortality, and case fatality that were present early in the pandemic attenuated over time and were no longer significant by March 2021. Throughout the observation period, high comorbidity burden, younger age, Hispanic ethnicity, and obesity were consistently associated with infection, while high comorbidity burden, older age, Hispanic ethnicity, obesity, and male sex were consistently associated with mortality.

Multiple studies reported higher risk of SARS-CoV-2 infection and mortality in Black versus White persons [8,9,14]. In a nationally representative US study, Black persons accounted for 18.7% of SARS-CoV-2–related deaths from May to August 2020 despite representing just 12.5% of the US population. During this time period, the percentage of decedents who were Black decreased from 20.3% in May to 17.4% in August but was still higher than the percentage of Black persons in the US population [8]. Our study extends these prior findings in significant ways. First, we demonstrate that the association between Black race and SARS-CoV-2–related mortality continued to decline in the VA healthcare system even after August and became nonsignificant by November 2020. Second, we simultaneously adjusted for comorbidity burden, age, sex, ethnicity, BMI, geographic region, and rural/urban location to identify the associations of Black race and mortality that were not explained by differences in these factors. Third, we show that the associations of Black race with infection also declined over time and became nonsignificant by November 2020, while the positive associations with case fatality attenuated over time and actually reversed after September 2020. However, we also show that during the third wave of the pandemic, from December 2020 to March 2021, Black race was again associated with higher risk of SARS-CoV-2 infection and mortality, albeit at a much lower level than in the early period of the pandemic.

It is unclear why such a dramatic reduction in risk of infection in Black persons relative to White persons occurred in the space of 9 months between February and November 2020 [25,26]. Although the pandemic shifted from early urban epicenters with high percentages of Black persons to a broad, nationwide distribution in both urban and rural communities with lower percentages of Black persons, our results persisted even after adjustment for both urban/rural location and geographic region. Some factors that mediate racial inequities and contributed to increased risk in Black persons are unlikely to be reversed quickly, such as occupation (e.g., disproportionate representation in essential work settings with high exposure risk such as healthcare facilities, farms, factories, grocery stores, and public transportation), inability to work from home, housing (e.g., crowded housing, multigenerational households, and residence in densely populated neighborhoods with high infection rates), and reliance on public transportation. Factors that can change quickly include those related to prophylactic measures (masking, handwashing, physical distancing, and adhering to stay-at-home orders), disease awareness and behavior (e.g., limiting unnecessary exposure to crowds), and increased rates of testing (leading to early identification and reduction in transmission rates [27]).

Our comparisons of Black versus White VA enrollees need to be interpreted with caution when trying to extrapolate to differences by race in the US population as a whole. Black Veterans report higher median incomes (US$44,000 versus US$26,000), lower unemployment (3% versus 5%), and lower poverty levels (10% versus 21%) than non-Veteran Black adults[28]. However, Black VA enrollees have lower socioeconomic status than White VA enrollees including much higher unemployment (22.5% versus 6.8%) [29]. Levels of perceived discrimination in healthcare have been shown to be equally high among Black Veteran and non-Veteran groups in the US, despite access to comprehensive healthcare through the VA [30]. Furthermore, racial discrimination experienced during military service has been shown to be common among Black Veterans and associated with long-term impacts on self-reported physical health [31,32].

AI/AN persons had significant higher risk of infection than White persons early in the pandemic, but this association attenuated over time and actually reversed during the third wave of the pandemic between December 2020 and March 2021. However, SARS-CoV-2 mortality remained higher in AI/AN persons throughout the observation period.

Hispanic ethnicity was associated with increased risk of SARS-CoV-2 infection and mortality during almost every time period that we investigated. In contrast to Black race, the associations of Hispanic ethnicity with infection or mortality did not attenuate over time. This suggests that the factors listed above that mediate inequities in SARS-CoV-2 infection and mortality were not improved over time in Hispanic communities.

Big cities and metropolitan areas constituted the initial epicenters of SARS-CoV-2 infection in the US. However, the virus quickly spread throughout the US to both rural and urban areas, likely explaining the observed attenuation in the association between urban residence and SARS-CoV-2 infection and mortality over time. Unique challenges exist in both urban (dense population, housing distress, overcrowding, and public transport) and rural (geographic inaccessibility to SARS-CoV-2–related screening and care, higher disability, lack of social capital, and high-risk occupations such as meat and poultry processing [33]) that tend to raise risk of SARS-CoV-2 infection and mortality.

Comorbidity burden, estimated by the CCI, was one of the strongest risk factors for both SARS-CoV-2 infection and mortality. Furthermore, after May 2020, we did not observe any attenuation over time in the associations of high CCI with SARS-CoV-2–related mortality. It is possible that increased likelihood of testing persons with high comorbidity burden even if minimally symptomatic or asymptomatic may have contributed to the observed association with risk of infection. However, this does not explain the strong associations between high CCI and SARS-CoV-2–related mortality and case fatality that we observed. Most of the component comorbidities that make up the CCI have been individually associated with adverse COVID-19 outcomes, especially diabetes, congestive heart failure, chronic pulmonary disease, cerebrovascular disease, liver disease, kidney disease, and malignancy [1,3439]. The cumulative burden of these comorbidities appears to have a dramatic effect on SARS-CoV-2–related mortality. The associations between high CCI and risk of infection appear to decline steadily from January to March 2021. This may be related to initiation of vaccination that was restricted to high-risk groups in that time period.

Compared to age 45 years (the reference age in our analysis), both older and younger persons had significantly lower risk of testing positive in all time periods after adjusting for sex, race, ethnicity, geographical region, urban/rural location, BMI, and CCI. It is interesting that risk of testing positive in older persons declined even further in March 2021, which may be related to initiation of vaccination in older age groups during that time period. Similar associations between age ≥65 and lower risk of infection have been described with influenza virus [40] and are likely related to lower risk of exposure to SARS-CoV-2 in older persons. Despite the lower incidence of infection, older age was the strongest risk factor for SARS-CoV-2–related mortality (driven by much higher case fatality in older persons), an association that did not change in magnitude over time.

Our results should be interpreted in the context of some important limitations. It is impossible to identify all cases of SARS-CoV-2 infection in a population, since many are asymptomatic and even some symptomatic cases do not get confirmed by testing. We identified only the cases who were tested and identified as positive within the VA system (positive tests performed outside the VA were only captured if documented in the EHR). Therefore, changes in the associations of certain risk factors over time that we observed may also be caused by changes in likelihood of testing for SARS-CoV-2 and identifying positive cases. “Attenuation” over time in risk associated with a high-risk group may also occur if a sufficiently high proportion of that group has already acquired infection and has developed immunity. To avoid this problem, we removed from our cohort persons with known infection prior to the beginning of each monthly/bimonthly observation period. However, persons infected but not tested would still be retained in our cohort and might contribute to attenuation in high-risk groups. Although we adjusted for federal region and urban/rural location, it is possible that some residual confounding by geographic location persists [41]. We did not have data on educational attainment, poverty rates, or income. It is possible that race or ethnicity may be serving as a proxy for low socioeconomic status; the extent to which the associations of race or ethnicity are confounded by socioeconomic status should be examined in future research. Finally, our results apply to US VA enrollees who are predominantly male and have access to comprehensive healthcare. Therefore, they need to be confirmed in other populations. In particular, access to the VA’s comprehensive healthcare system has been shown to attenuate some racial and geographic disparities in adverse outcomes in other contexts [42].

In conclusion, strongly positive associations of Black race, AI/AN race, and urban residence with SARS-CoV-2 infection, mortality, and case fatality that were observed early in the pandemic attenuated over time in the VA system. On the other hand, other risk factors, such age, comorbidity burden, Hispanic ethnicity, and obesity, were strongly associated with infection and mortality throughout the observation period. Recognizing the potentially dynamic nature of associations between known risk factors for infection and mortality can help to inform ongoing population-based approaches to prevention and treatment of SARS-CoV-2 as well as providing insights for disparities research in other fields.

Disclaimers

The contents do not represent the views of the US Department of Veterans Affairs or the US Government.

Supporting information

S1 STROBE Checklist. STROBE Statement—Checklist of items that should be included in reports of cohort studies.

STROBE, Strengthening the Reporting of Observational Studies in Epidemiology.

(DOCX)

S1 Table. AOR* for interaction term of risk factor and monthly time period of SARS-CoV-2 infection treated as an ordinal variable (risk factor * time period) among 9.1 million VA enrollees from February 2020 to March 2021, performed as a test of trends over time.

AOR, adjusted odds ratio; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

(DOCX)

S2 Table. AOR* for interaction term of risk factor and monthly time period of SARS-CoV-2–related mortality treated as an ordinal variable (risk factor * time period) among 9.1 million VA enrollees from February 2020 to February 2021, performed as a test of trends over time.

AOR, adjusted odds ratio; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

(DOCX)

S3 Table. Trends over time in the associations (AORs*) of race with risk of SARS-CoV-2 infection presented separately for persons aged <65 versus ≥65 year among 9.1 million VA enrollees from February 2020 to March 2021.

AOR, adjusted odds ratio;SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

(DOCX)

S1 Analytic Plan. Changes in risk factors for SARS-CoV-2 infection and mortality over time in a national healthcare system.

SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2.

(DOCX)

Abbreviations

AI/AN

American Indian/Alaska Native

AOR

adjusted odds ratio

BIRLS

Beneficiary Identification and Records Locator System

BMI

body mass index

CCI

Charlson comorbidity index

CDW

Corporate Data Warehouse

COVID-19

Coronavirus Disease 2019

EHR

electronic health record

IRB

Institutional Review Board

PCR

polymerase chain reaction

PI/NH

Pacific Islander/Native Hawaiian

RUCA

Rural–Urban Commuting Area

SARS-CoV-2

Severe Acute Respiratory Syndrome Coronavirus 2

SSA

Social Security Administration

STROBE

Strengthening the Reporting of Observational Studies in Epidemiology

VA

Veterans Affairs

VINCI

VA Informatics and Computing Infrastructure

Data Availability

Data cannot be shared publicly because the Department of Veterans Affairs prevents public sharing of national VA EHR data. Data are available only to VA investigators who obtain the required IRB approvals to access the data. For access to data please look at the current contact information for the Seattle-Denver Veterans Affairs Health Services Research and Development (HSR&D) Center of Innovation (COIN) at: https://www.hsrd.research.va.gov/centers/seattle-denver.cfm.

Funding Statement

The study was supported by the U.S. Department of Veterans Affairs, CSR&D grant COVID19-8900-11 to GI. The study was supported by the U.S. Department of Veterans Affairs HSR&D grant C19 21-278 to GI, AB, EB and MM. The study was supported by the U.S. Department of Veterans Affairs HSR&D grant C19 21-279 to TI, DH, AO and CBB. MM was also supported by a Research Career Scientist award from the Department of Veterans Affairs (RCS 10-391) and by the Center of Innovation to Accelerate Discovery and Practice Transformation (CIN 13-410) at the Durham VA Health Care System. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Richard Turner

16 Jun 2021

Dear Dr Ioannou,

Thank you for submitting your manuscript entitled "Changes in the associations of race and rurality with SARS-CoV-2 infection and mortality from February 2020 to March 2021" for consideration by PLOS Medicine.

Your manuscript has now been evaluated by the PLOS Medicine editorial staff and I am writing to let you know that we would like to send your submission out for external assessment.

However, we need you to complete your submission by providing the metadata for full assessment. To this end, please login to Editorial Manager where you will find the paper in the 'Submissions Needing Revisions' folder on your homepage. Please click 'Revise Submission' from the Action Links and complete all additional questions in the submission questionnaire.

Please re-submit your manuscript within two working days, i.e. by Jun 18 2021 11:59PM.

Login to Editorial Manager here: https://www.editorialmanager.com/pmedicine

Once your full submission is complete, your paper will undergo a series of checks in preparation for assessment.

Feel free to email us at plosmedicine@plos.org if you have any queries relating to your submission.

Kind regards,

Richard Turner, PhD

Senior Editor, PLOS Medicine

rturner@plos.org

Decision Letter 1

Richard Turner

22 Jul 2021

Dear Dr. Ioannou,

Thank you very much for submitting your manuscript "Changes in the associations of race and rurality with SARS-CoV-2 infection and mortality from February 2020 to March 2021" (PMEDICINE-D-21-02587R1) for consideration at PLOS Medicine.

Your paper was discussed among the editors and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to invite you to submit a revised version that addresses the reviewers' and editors' comments fully. You will appreciate that we cannot make a decision about publication until we have seen the revised manuscript and your response, and we expect to seek re-review by one or more of the reviewers.

In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments, the changes you have made in the manuscript, and include either an excerpt of the revised text or the location (eg: page and line number) where each change can be found. Please submit a clean version of the paper as the main article file; a version with changes marked should be uploaded as a marked up manuscript.

In addition, we request that you upload any figures associated with your paper as individual TIF or EPS files with 300dpi resolution at resubmission; please read our figure guidelines for more information on our requirements: http://journals.plos.org/plosmedicine/s/figures. While revising your submission, please upload your figure files to the PACE digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at PLOSMedicine@plos.org.

We hope to receive your revised manuscript by Aug 11 2021 11:59PM. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

We ask every co-author listed on the manuscript to fill in a contributing author statement, making sure to declare all competing interests. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. If new competing interests are declared later in the revision process, this may also hold up the submission. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT. You can see our competing interests policy here: http://journals.plos.org/plosmedicine/s/competing-interests.

Please use the following link to submit the revised manuscript:

https://www.editorialmanager.com/pmedicine/

Your article can be found in the "Submissions Needing Revision" folder.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

Please let me know if you have any questions, and we look forward to receiving your revised manuscript.

Sincerely,

Richard Turner, PhD

Senior Editor, PLOS Medicine

rturner@plos.org

-----------------------------------------------------------

Requests from the editors:

To your data statement, please add non-author contact details for those wishing to inquire about access to study data.

Please add a study descriptor to the title following a colon, e.g., "...: a population-based cohort study".

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Please remove the information on funding and competing interests from the title page. In the event of publication, this information will appear in the article metadata, via entries in the submission form.

Please combine the "Methods" and "Findings" subsections of your abstract.

To the new combined subsection, please add a new final sentence, which should begin "Study limitations include ..." or similar and should quote 2-3 of the study's main limitations.

Please quote aggregate demographic characteristics of study participants in the abstract.

In the abstract and throughout the paper, please quote p values alongside 95% CI, where available.

We suggest beginning the "Conclusions" subsection of the abstract with "In this study, we found that ..." or similar.

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Please highlight analyses that were not prespecified.

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Throughout the text, please format reference call-outs as follows; "... persons [8,9,14]." (noting the absence of spaces within the square brackets).

In the reference list, please list no more than 6 author names, followed where appropriate by "et al.".

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In the checklist, please refer to individual items by section (e.g., "Methods") and paragraph number, not by line or page numbers as these will generally change in the event of publication.

Comments from the reviewers:

*** Reviewer #1:

I confine my remarks to statistical aspects of this paper. The general approach is fine, but I have one issue to resolve and some comments on the figures.

The authors categorized BMI and age. Categorizing continuous variables is nearly always a bad idea. It increases type I and type II error and imposes arbitrary cutoffs. Here, I see why the authors did it - for ease of presentation of the tables and figures. But I'd like to see models with splines of those variables. You could then make graphs at several ages, to show how things change. So, e..g, the graph on the bottom of p. 18 could show age 18, 30, 40, 50 and 60 (or other ages - the authors could choose).

For figure 1: First, this is a hidden dual axis graph and these are generally frowned upon. (It's dual axis because the scales are different, per the footnote). What are the authors trying to show? If they want to show each series, they could use two line plots, stacked vertically. If they want to show the ratio of incidence and mortality, they could graph that. Yet another possibility is to have a scatter plot with mortality on one axis, incidence on the other, a dot for each time point, and a line with arrows connecting the dots.

Peter Flom

*** Reviewer #2:

The analysis is presented in a manner that is clear, concise, and precise. The manuscript provides important findings about changing associations between race and odds of COVID-19 infection and mortality. These findings should be disseminated, after the authors address the following issues concerning their study. This should not require redoing the statistical analysis.

1. The Discussion section should provide greater depth and detail about how the VA population of minority groups are different from the general US population of these groups. Rates of chronic poverty (i.e., persisting over multiple years) and multigenerational poverty are elevated in the US African American population. Chronic, multigenerational poverty may result in health disparities for reasons outlined by Link & Phelan (1995) and their progeny. Is the VA population of African Americans as likely to have experienced this chronic disadvantage as African Americans in general? Are there other reasons that the VA population might consist of a relatively advantaged or privileged group of African Americans (versus the Black population in general), aside from the reason mentioned by the authors (i.e., greater access to healthcare)? The authors might look at whether Blacks in the VA population are more likely to have graduated high school, to currently own a home, or to currently not be in poverty than US Blacks in general.

2. The authors should also address, relatedly, whether racial inequality within the VA population is analogous or parallel to racial inequality in the general population. Though this is not within my expertise, it is my understanding that there is much greater racial diversity among enlisted service members than among officers and especially upper-level officers. To what extent does this inequality in military rank parallel socioeconomic inequality between racial groups in the general population, whereby non-Hispanic Whites are more likely to have greater education and higher status/income jobs? How might differences in racial stratification within the military versus the general population affect differences in susceptibility to COVID-19 morbidity and mortality?

3. The authors do not control for educational attainment or other markers of socioeconomic status (SES) in their analysis. In the general US population, there are major differences between Blacks and Whites in educational attainment, poverty rates, and average income and wealth. In the analysis, race may thus be serving as a proxy for SES, and it may be the case that lower-SES individuals (regardless of race) were more likely to experience COVID morbidity and mortality. The authors could conduct a sensitivity analysis to determine whether results are substantially affected by controlling for an SES indicator, or their lack of controls for SES could be noted prominently as a limitation of the study requiring further exploration in later research.

4. Finally, I found the paper's presentation of its research methods to be somewhat confusing. If I am understanding it correctly, the paper provides results (in the tables) for separate regressions models run for monthly or bimonthly periods. The authors also state that they conducted a regression analysis with data combined from all periods, containing interactions between each predictor variable and a time-period ordinal variable. (This regression with the interaction terms is used—appropriately I believe—to test for change over time in the coefficients of the predictors.) The methods section is not explicit and clear enough in explaining that this single regression model with the interaction terms is distinct from the separate models for the different time periods, or that it is results from these separate regressions that are presented in the graph and tables. Likewise, I was looking for results in the form of a table for the combined regression containing the interaction terms, and I did not find them. This should be added to the paper, in the main text or the appendix.

*** Reviewer #3:

This is a useful and important analysis drawing on a richly detailed data source. With that said, I think that the analysis 1. could take more advantage of the available data to give more insight into the drivers of disparity in infection and mortality and how these have changed over time, and 2. requires modification ot the underlying statistical modeling to be suitable for publication. I have two major concerns related to these points:

1. The authors' findings about the differential associations between sociodemographic variables and infections vs. mortality are difficult to interpret, as mortality from SARS-CoV-2 is necessarily contingent on infection. As a result, risk factors for mortality are necessarily correlated with those for infection. Since the authors are analyzing individual-level EHR data, rather than aggregated data, they are able to examine both risks of infection and case-fatality, i.e. the risk of eath on infection.

Doing this is important as it would allow the specific contributions of factors such as the CCI to mortality to be understood in terms of their specific effects on infection and case-fatality. This would let us see, for example, whether the trend in mortality associated with increasing CCI reflects a stable case-fatality rate across CCI levels, versus some combination of changing infection risks (as evidenced in the relationship between CCI and infection), and case-fatality rates. Analyzing mortality and infection as separate outcomes acts as an unnecessary limitation on the analysis and is one the authors should rectifybefore the manuscript is suitable for publication.

2. The models included in the analysis employ a single parameter for each age group rather than allowing age-specific effects to vary as a function of race/ethnicity. A number of analyses have shown differential age-specific rates of SARS-CoV-2 infection by race/ethnicity, with older African-Americans experiencing much higher rates of infection than same-aged Whites in the early months of the pandemic. Consequently, adjusting for race using a single fixed effect, while not accounting for age x race/ethnicity interactions may result in biased estimates of both the group-specific effects and the associations between age, incidence, and mortality. The authors should provide updated results which include this interaction or show why it is not necessary (e.g. by using posterior predictions from the model which show good coverage of data as a function of age and race/ethnicity)

***

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 2

Richard Turner

3 Sep 2021

Dear Dr. Ioannou,

Thank you very much for re-submitting your manuscript "Changes in the associations of race and rurality with SARS-CoV-2 infection, mortality and case fatality in the United States from February 2020 to March 2021 : a population-based cohort study" (PMEDICINE-D-21-02587R2) for consideration at PLOS Medicine.

I have discussed the paper with editorial colleagues and it was also seen again by two reviewers. I am pleased to tell you that, provided the remaining editorial and production issues are fully dealt with, we expect to be able to accept the paper for publication in the journal.

The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:

[LINK]

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.

Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. If you haven't already, we ask that you provide a short, non-technical Author Summary of your research to make findings accessible to a wide audience that includes both scientists and non-scientists. The Author Summary should immediately follow the Abstract in your revised manuscript. This text is subject to editorial change and should be distinct from the scientific abstract.

We hope to receive your revised manuscript within 1 week. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

We ask every co-author listed on the manuscript to fill in a contributing author statement. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript.

Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.

Please let me know if you have any questions, and we look forward to receiving the revised manuscript.   

Sincerely,

Richard Turner, PhD

Senior Editor, PLOS Medicine

rturner@plos.org

------------------------------------------------------------

Requests from Editors:

Noting "p<0.01" in your abstract, please quote exact p values or "p<0.001" throughout the paper.

At the end of the abstract, please remove "even" (from "even reversed ...").

The Author summary is quite "data heavy" whereas it is intended to provide an accessible summary of the paper's findings. Therefore, please remove the points quoting quantitative elements also present in the abstract, aiming for three subsections, each of about three points each.

Please also avoid repetition in abstract and author summary.

Please refer to the analysis plan and STROBE checklist by attachment name in your Methods section.

Please use the journal name abbreviation "PLoS ONE" in the reference list.

Please remove the competing interest information from reference 33, and any other relevant references.

Comments from Reviewers:

*** Reviewer #2:

I believe the authors have sufficiently and satisfactorily responded to my prior comments. I recommend that the manuscript is accepted for publication.

*** Reviewer #3:

Thanks to the authors for their responsiveness to the comments from myself and the other reviewers. I am satisfied with the changes made by the authors and am happy to see this valuable contribution in its current form.

***

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 3

Richard Turner

9 Sep 2021

Dear Dr Ioannou, 

On behalf of my colleagues and the Academic Editor, Dr Zelner, I am pleased to inform you that we have agreed to publish your manuscript "Changes in the associations of race and rurality with SARS-CoV-2 infection, mortality and case fatality in the United States from February 2020 to March 2021: a population-based cohort study" (PMEDICINE-D-21-02587R3) in PLOS Medicine.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. Please be aware that it may take several days for you to receive this email; during this time no action is required by you. Once you have received these formatting requests, please note that your manuscript will not be scheduled for publication until you have made the required changes.

Prior to final acceptance, we ask you to remove the author's name from the data statement so as to comply with PLOS' data policy (https://journals.plos.org/plosmedicine/s/data-availability).

In the meantime, please log into Editorial Manager at http://www.editorialmanager.com/pmedicine/, click the "Update My Information" link at the top of the page, and update your user information to ensure an efficient production process. 

PRESS

We frequently collaborate with press offices. If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximise its impact. If the press office is planning to promote your findings, we would be grateful if they could coordinate with medicinepress@plos.org. If you have not yet opted out of the early version process, we ask that you notify us immediately of any press plans so that we may do so on your behalf.

We also ask that you take this opportunity to read our Embargo Policy regarding the discussion, promotion and media coverage of work that is yet to be published by PLOS. As your manuscript is not yet published, it is bound by the conditions of our Embargo Policy. Please be aware that this policy is in place both to ensure that any press coverage of your article is fully substantiated and to provide a direct link between such coverage and the published work. For full details of our Embargo Policy, please visit http://www.plos.org/about/media-inquiries/embargo-policy/.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Thank you again for submitting to PLOS Medicine. We look forward to publishing your paper. 

Sincerely, 

Richard Turner, PhD 

Senior Editor, PLOS Medicine

rturner@plos.org

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 STROBE Checklist. STROBE Statement—Checklist of items that should be included in reports of cohort studies.

    STROBE, Strengthening the Reporting of Observational Studies in Epidemiology.

    (DOCX)

    S1 Table. AOR* for interaction term of risk factor and monthly time period of SARS-CoV-2 infection treated as an ordinal variable (risk factor * time period) among 9.1 million VA enrollees from February 2020 to March 2021, performed as a test of trends over time.

    AOR, adjusted odds ratio; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

    (DOCX)

    S2 Table. AOR* for interaction term of risk factor and monthly time period of SARS-CoV-2–related mortality treated as an ordinal variable (risk factor * time period) among 9.1 million VA enrollees from February 2020 to February 2021, performed as a test of trends over time.

    AOR, adjusted odds ratio; SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

    (DOCX)

    S3 Table. Trends over time in the associations (AORs*) of race with risk of SARS-CoV-2 infection presented separately for persons aged <65 versus ≥65 year among 9.1 million VA enrollees from February 2020 to March 2021.

    AOR, adjusted odds ratio;SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2; VA, Veterans Affairs.

    (DOCX)

    S1 Analytic Plan. Changes in risk factors for SARS-CoV-2 infection and mortality over time in a national healthcare system.

    SARS-CoV-2, Severe Acute Respiratory Syndrome Coronavirus 2.

    (DOCX)

    Attachment

    Submitted filename: REPLY TRENDS IN RISK FACTORS.docx

    Attachment

    Submitted filename: FINAL REPLY TRENDS.docx

    Data Availability Statement

    Data cannot be shared publicly because the Department of Veterans Affairs prevents public sharing of national VA EHR data. Data are available only to VA investigators who obtain the required IRB approvals to access the data. For access to data please look at the current contact information for the Seattle-Denver Veterans Affairs Health Services Research and Development (HSR&D) Center of Innovation (COIN) at: https://www.hsrd.research.va.gov/centers/seattle-denver.cfm.


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