Abstract
Data on alcohol use trends in women living with HIV (WLWH) are lacking. We examine data collected before and across the COVID-19 pandemic (2014–2022) in WLWH and socio-demographically similar women living without HIV (WLWOH)(n = 1564; 67% WLWH) who self-reported alcohol use to establish and compare trends. Women were categorized into baseline groups based on use pattern from 10/2014 to 09/2017: abstinence (no alcohol at any visit), non-heavy drinking (0 heavy drinking visits), some heavy drinking (1–4 visits), and persistent heavy drinking (5–6 visits) with heavy drinking defined as > 7 drinks/week or > 3 drinks/day. A linear mixed model (LMM) was used to assess for changes in average number of drinks/week (ADW) by time segment: pre-pandemic (10/2017-09/2019), early pandemic (08/2020-05/2021), and late pandemic (06/2021-09/2022). Time, baseline group, and HIV status were included as interactions. In the LMM, WLWH with persistent heavy drinking histories had lower ADW compared to WLWOH. There were no significant differences in ADW in the other groups by HIV status and no significant interactions between HIV status and the time segments. The largest change in ADW occurred among the persistent heavy drinking group, with decreases at pandemic onset followed by increases into 2021. Overall, WLWH reported less alcohol use than WLWOH, but changes in alcohol use trends from 10/2017 to 09/2022 were similar regardless of HIV status. This suggests that the pandemic did not uniquely impact alcohol use among WLWH, rather socio-economically disadvantaged women generally. These findings support the need for greater research in the role of socioeconomic disruption on alcohol use among women.
Supplementary Information
The online version contains supplementary material available at 10.1007/s10461-025-04875-9.
Keywords: COVID-19 pandemic, HIV, Alcohol use, Alcohol consumption, Women
Background
Unhealthy alcohol use is a leading cause of preventable death among adults in the United States (U.S) [1]. Although alcohol use is less common in women than men, alcohol use, alcohol-related healthcare costs, and alcohol-related deaths have been increasing among women in the past several decades [2–4]. Women living with HIV (WLWH) have higher rates of alcohol use than their seronegative peers, with 13–21% of WLWH reporting heavy alcohol use compared to 9% among women in the general U.S. population [5–7]. Among WLWH, alcohol use is associated with decreased adherence to HIV antiretroviral therapy and unsuppressed HIV [8–10] as well as increases in HIV transmission risk behaviors [11–13]. Therefore, prevention and treatment of unhealthy alcohol use in this population is an important strategy for preventing new HIV infections and optimizing care across the HIV care continuum [14]. Yet, little is known about the impact of the coronavirus disease 2019 (COVID-19) pandemic on alcohol use trends among U.S. WLWH and how these trends compare to women living without HIV (WLWOH).
In the U.S., shortly after many communities issued stay-at-home orders during the early phase of the COVID-19 pandemic, national alcohol sales increased by 34% [15]. Cross sectional studies and “before” and “after” survey data from national samples of adults showed increases in self-reported alcohol use that were greatest among women [16–18]. These data contrast with a study of men and women living with HIV that found a decrease in binge drinking episodes early in the COVID-19 pandemic [19].
A limitation of these studies is that changes in alcohol use were measured over a short period of time and were not contextualized using longer-term pre-pandemic alcohol trends. Therefore, it remains unclear if changes in alcohol use early in the pandemic were a pandemic effect or part of a longer-term trend. Additionally, prior studies are limited to early in the pandemic; use trends following the wide-spread availability of SARS-CoV-2 vaccines in the U.S. are lacking, especially for WLWH. Participants also were not stratified based on their alcohol consumption history, which is relevant because prior alcohol use is predictive of future alcohol use [20, 21]. As a result of aggregate analysis approaches that don’t account for baseline differences in alcohol use, there could be masking of different alcohol use patterns that exist among sub-populations.
This study addresses several of these gaps by utilizing longitudinal data from the multisite Women’s Interagency HIV Study (WIHS). Our primary aim was to describe trends in self-reported alcohol use from 2017 to 2022 among WLWH and demographically similar women living without HIV (WLWOH) while accounting for earlier alcohol use history. We also hypothesized that changes in alcohol consumption following the COVID-19 pandemic would vary based on alcohol use history and HIV status.
Methods
Data Source
WIHS is the largest and longest running HIV cohort study of women in the U.S. It is demographically representative of WLWH nationally. Socio-demographically similar WLWOH were also enrolled. Recruitment was in a 2 WLWH to 1 WLWOH fashion. In 2019, the WIHS and the Multicenter AIDS Cohort Study (MACS) of men living with and without HIV, merged to create the MACS/WIHS Combined Cohort Study (MWCCS). There are 13 MWCCS sites across the U.S., 9 of which were originally WIHS sites. Additional details about the WIHS, recruitment of participants, and study instruments and procedures are described elsewhere [22, 23]. Data collection forms are publicly available (https://statepi.jhsph.edu/mwccs/). Clinical assessments and self-report surveys were completed on a semi-annual basis prior to the merger and now are conducted on an annual basis. From April to September 2020, participants were contacted to complete questionnaires by phone due to the need for remote contact in response to the COVID-19 pandemic. In-person annual visits resumed October 2020. Visits, including the phone questionnaires, were conducted in English and Spanish and participants were compensated.
Compliance with Ethical Standards
The WIHS and now MWCCS is approved by an Institutional Review Board at each study site. Written consent is obtained from all participants.
Study Sample
This analysis includes data collected from October 2014 to September 2022. We defined the period October 2014–September 2017 as the baseline period and October 2017–September 2022 as the follow-up period. The baseline period began in October 2014, because new WIHS sites in the Southern U.S. were added in 2013 with enrollment of most participants by 2014. Only participants with available baseline period alcohol data were included in the study. Participants who had baseline data, but no follow-up data were excluded. Participants who persistently did not drink alcohol across both study periods were excluded from the analysis since we were most interested in changes in alcohol consumption over time. These time frames are illustrated in Fig. 1 and study timepoints are outlined in Supplemental Table 1.
Fig. 1.
Analysis time periods. There was a total of 1564 women included in the study
Measures
Alcohol Consumption
Our primary measure is the number of alcoholic drinks per week. The frequency and quantity of alcohol use was assessed at each study visit. Participants were asked to recall how often they had a drink containing alcohol since their last study visit. During the first survey after the start of the pandemic (i.e., March to September 2020) the question asked about alcohol use since the pandemic start. Responses were ordinal (e.g. “at least once a day”, “nearly every day”, “3–4 times a week”, “1–2 days a week”, “1–2 times a month”, “about once a month”, “6–11 times a year”, “1–5 times a year”, “never”). If participants reported any alcohol use, they were asked how many drinks they had containing alcohol on a typical day when drinking. Responses were numeric (e.g. “1”, “2”, “3”, “4”, “5”, “6”, “7–9” and “10 or more”). Responses were used to calculate the average number of drinks per week since the last visit or pandemic start. Due to the structure of the data collection the maximum number of drinks per week captured was 77.
Demographic and Clinical Measures
Demographic measures included age, study site, race and ethnicity, employment, annual household income, and marital status. Clinical variables included HIV status and number of chronic medical comorbidities. These measures were selected based on prior associations with alcohol use. Medical comorbidities were ascertained using definitions adopted from previously published WIHS data (Supplemental Table 2) [24]. Each participant was assessed for eight common comorbidities (not including HIV status) and the number of conditions present was totaled to represent the overall comorbidity burden. Given that demographic data is often stable over time and the medical comorbidities are chronic in nature, data were carried forward from a prior visit if they were missing.
Statistical Analysis
Baseline Alcohol Use
Using data collected over 6 semiannual study visits during the baseline period (October 2014–September 2017), we created groups based on historic alcohol use patterns. We used this approach because participants with different historical alcohol use patterns likely have different ongoing alcohol use trends. To establish baseline alcohol use groups, we calculated the number of semiannual visits at which a participant met criteria for heavy drinking utilizing the National Institute on Alcohol Abuse and Alcoholism definition of > 7 drinks per week or > 3 drinks per day for women [25]. Baseline groups included abstinence (no alcohol at any of the 6 visits), non-heavy drinking (no visits with > 7 drinks per week or > 3 drinks per day), some heavy drinking (1–4 visits with > 7 drinks per week or > 3 drinks per day), and persistent heavy drinking (5–6 visits with > 7 drinks per week or > 3 drinks per day) (Table 1.). Descriptive statistics, Kruskal-Wallis tests, and chi-squared tests were used to compare demographic and clinical differences between women living with and without HIV and across baseline alcohol use groups.
Table 1.
Baseline alcohol use group definitions
| Group | Criteria |
|---|---|
| Abstinence | No alcohol consumption across any baseline visits |
| Non-heavy drinking | Some visits with 7 or less drinks per week and 3 or less drinks on one occasion; no heavy drinking visits |
| Some heavy drinking | At least one visit with more than 7 drinks per week or more than 3 drinks on one occasion |
| Persistent heavy drinking | At least 5 visits (out of 6) with more than 7 drinks per week or more than 3 drinks on one occasion |
Alcohol Trends Before and During the COVID-19 Pandemic
Follow up period data (October 2017–September 2022) were examined using linear mixed models (LMM) to assess for changes in alcohol use (i.e. average number of drinks per week) immediately before (pre) and during the COVID-19 pandemic. LMM provide comparisons between trends pre- and during-pandemic while accounting for correlation within participants. They also provide unbiased estimates when data are missing at random. The fixed effect model included an interaction between baseline alcohol use groups and time. The correlation between repeated measures for participants over time was accounted for by including a random intercept and random slope for individuals in the random effect model. To assess for statistical differences in alcohol trends between WLWH and WLWOH, we examined one LMM that included an additional interaction for HIV status. We also stratified our analysis based on HIV serostatus and ran individual models for WLWH and WLWOH for ease of interpretation. In addition to examining trends, we developed a LMM adjusting for age, race and ethnicity, employment, annual household income, education, marital status, tobacco use, and the medical comorbidity burden. We calculated the within-study site and within-subject intraclass correlation coefficients (ICC) to measure the homogeneity within the sites and participants using linear mixed effects models. The intraclass correlation analysis based on the LMM showed that the within-site ICC was negligible (1.8%) and within-subject ICC was substantial (58.4%). Therefore, we decided not to include site in our models.
Three time segments were assessed through piecewise regression: pre-COVID-19 pandemic (October 2017–mid-March 2020), early pandemic (mid-March 2020–May 2021), and late pandemic (June 2021–September 2022). March 13th, 2020 (the start of the public health emergency in the U.S.) was used as the beginning of the early pandemic time segment. May 31st, 2021 was used as the end of the early pandemic segment because at this time vaccines were widely available and most states had completed all stages of reopening, both of which could influence social, economic, and drinking behaviors [26]. Knots were used to allow for flexibility between time segments. Trends were assessed for changes with potential clinical or public health significance. Statistical significance based on p-values was not emphasized.
Missing Data
During the baseline period (October 2014–September 2017), estimated values for missing alcohol use data were generated using multiple imputation by chained equations (MICE) from the available clinical and demographic and alcohol use data [27]. During the follow-up period (October 2017–September 2022), we assessed the correlation between percentage of missing alcohol use data and the mean average number of drinks per week for each participant. There was no correlation between a participant’s proportion of visits with missing alcohol data and their mean number of drinks per week (correlation coefficient − 0.01) so imputation was not performed for the follow-up period data because the missing at random assumption was met. SAS Version 9.4 and the MICE R package were used for the analysis.
Results
Of the 2485 participants in the sample, we excluded 231 with no follow-up period data and an additional 690 participants (30.6%) who reported no alcohol use at all visits during the follow-up period, resulting in 1564 participants and 9578 included observations (Supplemental Fig. 1). There were missing alcohol use data in 6% of the included observations.
Table 2 shows the demographic and clinical characteristics of included participants (i.e. those reporting any alcohol use over the study time period). The majority were living with HIV (66.9%) and self-identified as being of Black/African American race (64.0%), having a single marital status (69.9%), and being unemployed (57.0%). Nearly half reported an annual household income of <$12K/year (46.0%). During the baseline period participants were categorized into the following drinking groups: abstinence (9.3%), non-heavy drinking (63.1%), some heavy drinking (18.3%), and persistent heavy drinking (9.3%). In analyses by HIV status, WLWH were more likely to be in the abstinent group (11.2% vs. 5.4%) and less likely to be in the persistent heavy drinking group (7.8% vs. 12.4%) compared to WLWOH (p < 0.001). Analyses of participant characteristics by baseline alcohol use group are shown in Supplemental Table 3.
Table 2.
Demographics and clinical characteristics of women living with and without HIV in the Women’s Interagency HIV study
| Total | Women Living with HIV | Women Living without HIV | P-value | |
|---|---|---|---|---|
| Total number | 1564 | 1047 | 517 | |
| N (%) or mean ± sd | ||||
| Baseline Alcohol Use Groups | ||||
| Abstinence | 145 (9.3%) | 117 (11.2%) | 28 (5.4%) | < 0.001 |
| Non-heavy consumption | 987 (63.1%) | 681 (65.0%) | 306 (59.2%) | |
| Some heavy consumption | 286 (18.3%) | 167 (16.0%) | 119 (23.0%) | |
| Persistent heavy consumption | 146 (9.3%) | 82 (7.8%) | 64 (12.4%) | |
| Age, years | 49.4 ± 9.33 | 50 ± 9.19 | 48.3 ± 9.5 | < 0.001 |
| Study Site | ||||
| Bronx | 205 (13.1%) | 117 (11.2%) | 88 (17.0%) | < 0.001 |
| Brooklyn | 225 (14.4%) | 155 (14.8%) | 70 (13.5%) | |
| Washington DC | 190 (12.1%) | 120 (11.5%) | 70 (13.5%) | |
| San Francisco | 206 (13.2%) | 131 (12.5%) | 75 (14.5%) | |
| Chicago | 179 (11.4%) | 123 (11.7%) | 56 (10.8%) | |
| Chapel Hill | 129 (8.2%) | 91 (8.7%) | 38 (7.4%) | |
| Atlanta | 196 (12.5%) | 133 (12.7%) | 63 (12.2%) | |
| Miami | 75 (4.8%) | 53 (5.1%) | 22 (4.3%) | |
| Birmingham | 76 (4.9%) | 59 (5.6%) | 17 (3.3%) | |
| Jackson | 83 (5.3%) | 65 (6.2%) | 18 (3.5%) | |
| Marital Status | ||||
| Single | 1048 (69.9%) | 717 (71.5%) | 331 (66.6%) | 0.052 |
| Married/Partnered | 452 (30.1%) | 286 (28.5%) | 166 (33.4%) | |
| Missing | 64 | 44 | 20 | |
| Race | ||||
| Black/African American | 1001 (64.0%) | 680 (64.9%) | 321 (62.1%) | 0.085 |
| White | 163 (10.4%) | 116 (11.1%) | 47 (9.1%) | |
| Other | 400 (25.6%) | 251 (24.0%) | 149 (28.8%) | |
| Hispanic Ethnicity | 207 (13.2%) | 126 (12.0%) | 81 (15.7%) | 0.046 |
| Employed | 669 (43.0%) | 425 (40.7%) | 244 (47.7%) | < 0.001 |
| Missing | 7 | 2 | 5 | |
| Annual Household Income | ||||
| <$12,000 | 665 (46.0%) | 453 (46.6%) | 212 (44.9%) | 0.260 |
| $12,000–30,000 | 423 (29.3%) | 292 (30.0%) | 131 (27.8%) | |
| >$30,001 | 357 (24.7%) | 228 (23.4%) | 129 (27.3%) | |
| Missing | 119 | 74 | 45 | |
| Educational Attainment | ||||
| No high school diploma | 470 (31.6%) | 318 (31.5%) | 152 (31.7%) | 0.950 |
| High school diploma | 445 (29.9%) | 304 (30.1%) | 141 (29.4%) | |
| Some college or more | 574 (38.5%) | 387 (38.4%) | 187 (39.0%) | |
| Missing | 75 | 38 | 37 | |
| Medical comorbidity burden | 3.20 ± 1.96 | 3.37 ± 1.96 | 2.86 ± 1.91 | <0.0001 |
| Tobacco smoking | ||||
| Never | 471 (31.5%) | 341 (33.8%) | 130 (26.9%) | 0.019 |
| Former | 405 (27.1%) | 271 (26.8%) | 134 (27.7%) | |
| Current | 618 (41.4%) | 398 (39.4%) | 220 (45.5%) | |
| Visits completed during the follow-up/COVID-19 time period | 5.76 ± 1.52 | 5.82 ± 1.45 | 5.63 ± 1.66 | 0.120 |
The Kruskal-Wallis test was used to compare means across baseline alcohol use groups. Chi-squared tests were used to compare proportions across baseline alcohol use groups
In the LMM of all women included in this analysis with HIV as an interaction term, WLWH with a history of persistent heavy drinking consumed less alcohol on average compared to WLWOH from October 2017 to September 2022 (-8.75 average drinks per week, 95% CI -13.31, -4.20, p < 0.001) (Supplemental Table 4). Despite differences in the amount of alcohol use, changes in the average drinks per week over time did not statistically differ by HIV status.
LMM trends stratified by HIV status are shown in Fig. 2; Table 3. The model outputs used to generate the trends are in Table 4. For WLWH and WLWOH, the mean number of drinks per week during the pre-pandemic period were mostly stable across all baseline drinking groups. Among those with a history of abstinence, there were increases in the average number of drinks per week observed across the early pandemic period that persisted in the late pandemic period. Among those with a history of non-heavy drinking, average drinks per week remained mostly stable across all time periods. For women with a history of some heavy drinking, the average number of drinks per week were stable across the pre-pandemic and early pandemic time periods, but there was a slight increase in alcohol use across the late pandemic period. For women with a history of heavy drinking there was a decrease in the average number of drinks per week at the early pandemic onset compared to pre-pandemic levels of alcohol use. However, alcohol use increased throughout the early pandemic period resulting in an increase in the average number of drinks per week to at or above pre-pandemic levels. This change did not persist into the late pandemic period where the average alcohol use in both groups decreased below pre-pandemic levels.
Fig. 2.
Linear mixed model fitted values illustrating trends in number of drinks per week before and during the COVID-19 Pandemic (2017–2022) among women living with and without HIV, by baseline (2014–2017) alcohol use group
Table 3.
Linear mixed model estimates of the number of drinks per week before and during the COVID-19 pandemic (2017–2022) among women living with and without HIV
| Baseline Group | Pre-pandemic | Early Pandemic | Late pandemic | ||
|---|---|---|---|---|---|
| Abstinence | HIV+ | Average at period start, mean (SD)* | 0.18 (1.61) | 0.83 (2.10) | 0.96 (1.83) |
| Slope during the period (95% CI)** | 0.008 (−0.053, 0.069) | 0.031 (−0.194, 0.257) | 0.029 (−0.193, 0.251) | ||
| HIV− | Average, mean (SD) | 0.47 (2.21) | 0.00 (2.27) | 1.11 (3.15) | |
| Slope (95% CI) | −0.020 (−0.174, 0.134) | 0.187 (−0.416, 0.791) | −0.005 (−0.576, 0.566) | ||
| Slope Difference (95% CI)*** | 0.027 (−0.122, 0.177) | −0.156 (−0.735, 0.423) | 0.034 (−0.517, 0.585) | ||
| Non-heavy drinking | HIV+ | Average, mean (SD) | 1.07 (1.57) | 1.66 (1.83) | 1.97 (1.61) |
| Slope (95% CI) | 0.022 (−0.068, 0.112) | 0.013 (−0.322, 0.347) | −0.300 (−0.355, 0.295) | ||
| HIV− | Average, mean (SD) | 1.44 (2.03) | 1.97 (2.44) | 3.47 (2.14) | |
| Slope (95% CI) | 0.025 (−0.198, 0.249) | 0.050 (−0.823, 0.924) | −0.125 (−0.949, 0.699) | ||
| Slope Difference (95% CI) | −0.031 (−0.189, 0.127) | −0.135 (−0.684, 0.414) | 0.062 (−0.516, 0.639) | ||
| Some heavy drinking | HIV+ | Average, mean (SD) | 6.06 (1.81) | 7.09 (1.86) | 4.82 (1.83) |
| Slope (95% CI) | 0.020 (−0.08, 0.121) | −0.107 (−0.486, 0.273) | 0.117 (−0.242, 0.476) | ||
| HIV− | Average, mean (SD) | 6.82 (2.07) | 4.79 (2.77) | 6.19 (2.62) | |
| Slope (95% CI) | −0.030 (−0.263, 0.202) | 0.052 (−0.858, 0.961) | 0.064 (−0.796, 0.924) | ||
| Slope Difference (95% CI) | 0.023 (−0.152, 0.197) | −0.138 (−0.729, 0.453) | 0.021(−0.616, 0.659) | ||
| Persistent heavy drinking | HIV+ | Average, mean (SD) | 11.56 (1.84) | 7.31 (2.03) | 11.03 (2.16) |
| Slope (95% CI) | −0.043 (−0.157, 0.070) | 0.670 (0.255, 1.086) | −0.185 (−0.637, 0.267) | ||
| HIV− | Average, mean (SD) | 16.58 (2.12) | 12.43 (3.08) | 19.75 (2.63) | |
| Slope (95% CI) | 0.058 (−0.184, 0.300) | 0.387 (−0.58, 1.354) | −0.577 (−1.476, 0.322) | ||
| Slope Difference (95% CI) | −0.133 (−0.326, 0.060) | 0.198 (−0.458, 0.855) | 0.363 (−0.377, 1.103) |
The column on the left represents the alcohol use group from the baseline period
*The average represents the estimated mean number of drinks per week at the start of the indicated time period. Standard errors are shown in parentheses. **The slope is an estimate of the change in drinks per week across the indicated time period. Confidence intervals are shown in parentheses. *** The slope difference represents the difference in the slopes between WLWH and WLWOH. A positive value indicates a faster increase among WLWH compared to WLWOH. Knots were introduced in the model at the start of each time period to allow for flexibility
Table 4.
Linear mixed models examining demographic and clinical associations with alcohol consumption trends before and during the COVID-19 pandemic among women living with and without HIV
| Women living with HIV | Women living without HIV | |||||||
|---|---|---|---|---|---|---|---|---|
| Unadjusted | Adjusted | Unadjusted | Adjusted | |||||
| Coefficient (CI 95%) | p-value | Coefficient (CI 95%) | p-value | Coefficient (CI 95%) | p-value | Coefficient (CI 95%) | p-value | |
| Intercept | 0.424 (-0.985, 1.833) | 0.555 | 0.886 (-1.452, 3.224) | 0.458 | -0.142 (-3.919, 3.635) | 0.941 | 1.409 (-3.995, 6.813) | 0.609 |
| Baseline Group | ||||||||
| Abstinence | REF | REF | REF | REF | ||||
| Non-heavy consumption | 1.313 (-0.216, 2.842) | 0.092 | 1.204 (-0.346, 2.754) | 0.128 | 2.352 (-1.605, 6.309) | 0.244 | 2.687 (-1.262, 6.636) | 0.183 |
| Some heavy consumption | 6.265 (4.421, 8.109) | < 0.0001 | 5.892 (4.016, 7.768) | < 0.0001 | 6.030 (1.777, 10.283) | 0.006 | 6.244 (1.989, 10.499) | 0.004 |
| Persistent heavy consumption | 9.808 (7.597, 12.019) | < 0.0001 | 9.479 (7.249, 11.709) | < 0.0001 | 18.504 (13.959, 23.049) | < 0.0001 | 17.652 (13.119, 22.185) | < 0.0001 |
| Pre-COVID-19 Time Segment | 0.008 (-0.053, 0.069) | 0.797 | 0.014 (-0.049, 0.077) | 0.674 | -0.020 (-0.175, 0.135) | 0.801 | -0.015 (-0.168, 0.138) | 0.851 |
| Pre-COVID-19 Time Segment*Group | ||||||||
| Pre-COVID-19*Abstinence | REF | REF | REF | REF | ||||
| Pre-COVID-19*Non-heavy consumption | 0.014 (-0.053, 0.081) | 0.686 | 0.012 (-0.057, 0.081) | 0.739 | 0.045 (-0.118, 0.208) | 0.585 | 0.048 (-0.113, 0.209) | 0.559 |
| Pre-COVID-19*Some heavy consumption | 0.012 (-0.068, 0.092) | 0.761 | 0.026 (-0.056, 0.108) | 0.535 | -0.011 (-0.185, 0.163) | 0.906 | -0.005 (-0.177, 0.167) | 0.957 |
| Pre-COVID-19*Persistent heavy consumption | -0.051 (-0.147, 0.045) | 0.295 | -0.050 (-0.148, 0.048) | 0.321 | 0.078 (-0.108, 0.264) | 0.412 | 0.038 (-0.146, 0.222) | 0.682 |
| Pandemic Onset Knot | 0.317 (-2.072, 2.706) | 0.795 | 0.273 (-2.185, 2.731) | 0.828 | -1.083 (-7.341, 5.175) | 0.735 | -1.162 (-7.330, 5.006) | 0.712 |
| Pandemic Onset Knot*Group | ||||||||
| Pandemic Onset Knot*Abstinence | REF | REF | REF | REF | ||||
| Pandemic Onset Knot*Non-heavy consumption | -0.408 (-3.017, 2.201) | 0.759 | -0.392 (-3.071, 2.287) | 0.775 | 0.749 (-5.809, 7.307) | 0.823 | 0.722 (-5.748, 7.192) | 0.827 |
| Pandemic Onset Knot*Some heavy consumption | 0.260 (-2.933, 3.453) | 0.873 | 0.057 (-3.224, 3.338) | 0.973 | -0.154 (-7.226, 6.918) | 0.966 | -0.241 (-7.254, 6.772) | 0.946 |
| Pandemic Onset Knot*Persistent heavy consumption | -5.426 (-9.207, -1.645) | 0.005 | -5.192 (-9.043, -1.341) | 0.008 | -5.431 (-13.136, 2.274) | 0.167 | -4.391 (-12.015, 3.233) | 0.259 |
| Early COVID-19 Time Segment | 0.031 (-0.194, 0.256) | 0.785 | 0.036 (-0.197, 0.269) | 0.764 | 0.187 (-0.417, 0.791) | 0.543 | 0.190 (-0.404, 0.784) | 0.532 |
| Early COVID-19 Time Segment*Group | ||||||||
| Early COVID-19*Abstinence | REF | REF | REF | REF | ||||
| Early COVID-19*Non-heavy consumption | -0.019 (-0.266, 0.228) | 0.881 | -0.022 (-0.277, 0.233) | 0.867 | -0.137 (-0.768, 0.494) | 0.671 | -0.138 (-0.761, 0.485) | 0.664 |
| Early COVID-19*Some heavy consumption | -0.138 (-0.444, 0.168) | 0.375 | -0.138 (-0.452, 0.176) | 0.390 | -0.136 (-0.816, 0.544) | 0.696 | -0.129 (-0.805, 0.547) | 0.708 |
| Early COVID-19*Persistent heavy consumption | 0.639 (0.290, 0.988) | < 0.0001 | 0.607 (0.250, 0.964) | 0.001 | 0.199 (-0.556, 0.954) | 0.605 | 0.094 (-0.653, 0.841) | 0.806 |
| Mid-Pandemic Knot | -0.253 (-2.830, 2.324) | 0.847 | -0.275 (-2.896, 2.346) | 0.837 | -0.440 (-7.335, 6.455) | 0.901 | -0.612 (-7.403, 6.179) | 0.860 |
| Mid-Pandemic Knot*Group | ||||||||
| Mid-Pandemic Knot*Abstinence | REF | REF | REF | REF | ||||
| Mid-Pandemic Knot*Non-heavy consumption | 0.399 (-2.406, 3.204) | 0.781 | 0.342 (-2.514, 3.198) | 0.815 | 1.295 (-5.918, 8.508) | 0.725 | 1.641 (-5.474, 8.756) | 0.651 |
| Mid-Pandemic Knot*Some heavy consumption | -0.618 (-4.048, 2.812) | 0.724 | -0.595 (-4.086, 2.896) | 0.738 | 1.200 (-6.618, 9.018) | 0.764 | 1.155 (-6.579, 8.889) | 0.770 |
| Mid-Pandemic Knot*Persistent heavy consumption | -3.729 (-8.212, 0.754) | 0.103 | -3.635 (-8.172, 0.902) | 0.116 | 2.747 (-5.767, 11.261) | 0.527 | 4.237 (-4.160, 12.634) | 0.323 |
| Late COVID-19 Time Segment | 0.029 (-0.192, 0.250) | 0.797 | 0.027 (-0.198, 0.252) | 0.817 | -0.005 (-0.575, 0.565) | 0.987 | 0.012 (-0.551, 0.575) | 0.966 |
| Late COVID-19 Time Segment*Group | ||||||||
| Late COVID-19*Abstinence | REF | REF | REF | REF | ||||
| Late COVID-19*Non-heavy consumption | -0.059 (-0.298, 0.180) | 0.627 | -0.049 (-0.290, 0.192) | 0.691 | -0.120 (-0.714, 0.474) | 0.692 | -0.155 (-0.741, 0.431) | 0.604 |
| Late COVID-19*Some heavy consumption | 0.088 (-0.194, 0.370) | 0.543 | 0.086 (-0.200, 0.372) | 0.555 | 0.069 (-0.574, 0.712) | 0.834 | 0.079 (-0.556, 0.714) | 0.809 |
| Late COVID-19*Persistent heavy consumption | -0.214 (-0.608, 0.180) | 0.287 | -0.194 (-0.592, 0.204) | 0.340 | -0.572 (-1.266, 0.122) | 0.106 | -0.567 (-1.251, 0.117) | 0.104 |
| Age, per 10 years | -0.191 (-0.503, 0.121) | 0.230 | -0.388 (-1.052, 0.276) | 0.253 | ||||
| Marital Status | ||||||||
| Single/Divorced/Widowed | REF | REF | ||||||
| Married/Partnered | -0.139 (-0.611, 0.333) | 0.564 | -0.278 (-1.140, 0.584) | 0.528 | ||||
| Race | ||||||||
| White | REF | REF | ||||||
| Black/African American | 0.397 (-0.438, 1.232) | 0.351 | 0.101 (-1.947, 2.149) | 0.923 | ||||
| Other | 0.924 (-0.005, 1.853) | 0.052 | 0.015 (-2.139, 2.169) | 0.989 | ||||
| Hispanic Ethnicity | -0.841 (-1.699, 0.017) | 0.055 | -0.031 (-1.726, 1.664) | 0.972 | ||||
| Educational Attainment | ||||||||
| No high school diploma | REF | REF | ||||||
| High school diploma | 0.007 (-0.642, 0.656) | 0.983 | -1.077 (-2.506, 0.352) | 0.140 | ||||
| Some college or more | -0.453 (-1.094, 0.188) | 0.166 | -0.809 (-2.214, 0.596) | 0.260 | ||||
| Employed | 0.100 (-0.357, 0.557) | 0.668 | -0.342 (-1.206, 0.522) | 0.438 | ||||
| Annual Household Income | ||||||||
| <$12,000 | REF | REF | ||||||
| $12,000–30,000 | -0.054 (-0.442, 0.334) | 0.784 | 0.003 (-0.710, 0.716) | 0.994 | ||||
| >$30,001 | -0.221 (-0.731, 0.289) | 0.395 | 0.407 (-0.534, 1.348) | 0.397 | ||||
| Medical Comorbidity Burden (per 1 condition increase) | -0.026 (-0.171, 0.119) | 0.723 | 0.250 (-0.097, 0.597) | 0.157 | ||||
| Tobacco Smoking | ||||||||
| Never | REF | REF | ||||||
| Former | 0.691 (0.095, 1.287) | 0.023 | -1.018 (-2.466, 0.430) | 0.169 | ||||
| Current | 1.359 (0.761, 1.957) | < 0.0001 | 1.290 (-0.145, 2.725) | 0.079 | ||||
After adjusting for covariates, there was little change in the LMM (Table 4). In WLWH, current tobacco use was associated with overall increases in the average number of drinks per week during the study time period from 2017 to 2022 compared to women with no history of tobacco use (1.36 average drinks per week, 95% CI 0.761, 1.957). In WLWOH, there was no association with tobacco use and the average number of drinks per week (1.29 average drinks per week, 95% CI -0.145, 2.725) compared to women with no history of tobacco use.
Discussion
Alcohol consumption remains a growing public health concern, especially among women, yet data on recent trends for WLWH and WLWOH in the U.S. are lacking. This study fills this gap by examining trends in alcohol use that span the pre-, early and late COVID-19 pandemic periods among a multi-site prospective cohort study of WLWH and socio-demographically similar WLWOH. Using longitudinal data from the WIHS, we captured longer-term alcohol use patterns and alcohol use history to identify drinking patterns that would otherwise be underappreciated using shorter time frames and more aggregate analytic approaches. We found that the amount of alcohol consumption varied by HIV status and previous alcohol use history, which could reflect differing drivers of alcohol use. Despite these differences, trends in alcohol use changes were similar between WLWH and WLWOH. This suggests that the pandemic did not have a unique impact on alcohol use among WLWH, but rather socio-economically disadvantaged women more broadly given that the trends observed in this cohort differed from previously observed national trends.
Unlike prior studies, we did not find overall higher alcohol consumption among WLWH compared to WLWOH [5]. Possible reasons include that WLWOH were enrolled based upon having similar risk behaviors and sociodemographic characteristics as WLWH and therefore do not represent the general population of US women. Furthermore, WIHS participants living with a long-standing HIV diagnosis may have higher levels of primary care engagement and access to services such as alcohol use disorder treatment [28]. Due to these features, WLWH may have had more counseling and treatment resources for unhealthy alcohol use, and greater awareness about health consequences of alcohol consumption especially in the setting of HIV infection, leading to behavior modification. There are also high levels of resilience among people living with HIV, which in turn may protect against maladaptive behaviors, such as unhealthy alcohol consumption [29–31]. Further research should explore protective factors to reduce unhealthy alcohol consumption in WLWH and socially vulnerable WLWOH.
Despite more self-reported alcohol consumption among WLWOH compared to WLWH, trends in alcohol use over the analysis period between the groups were similar. The largest changes in alcohol use following the COVID-19 pandemic occurred among those with a history of persistent heavy alcohol use, with initial decreases in use at the onset of the pandemic that substantially increased into 2021. A prior MWCCS analysis also found a reduction in binge drinking among PLWH at the onset of the pandemic [19]. Interestingly, the drinking declined during the late pandemic period in WLWH and WLWOH, suggesting that the increase in the early pandemic period was situational. These dynamic changes differ from nationally representative studies of U.S. adults where there were increases in alcohol use among women after the pandemic start and stability in alcohol consumption levels among women across the first year of the pandemic [16–18, 32]. Reasons for differences between WIHS participants and the general population are likely multifactorial and may reflect disproportionally high levels of economic strain, social isolation, and health concerns among WIHS participants as possible explanatory factors for the initial early pandemic decrease in alcohol use. Secondary increases in stress and anxiety are possible drivers for the subsequent increase in alcohol use [33].
Literature on alcohol use following economic crises and natural disasters has proposed household budget constraints as a mechanism for reduced alcohol use during periods of crisis [34, 35]. About half of WIHS participants are living below the poverty line and are therefore more susceptible to economic hardship. Participants with heavy drinking have a higher burden of alcohol expenses, which could explain why there was a large decrease in alcohol use following the onset of the pandemic among those with heavy drinking only. In a cross-sectional survey of U.S. adults following the pandemic onset (May 2020), nearly 13% reported decreased alcohol use citing financial concerns as one reason [36].
Social isolation and decreased access to bars early in the pandemic may be another contributing factor given that nearly all participants reported COVID-19 prevention behaviors [33]. As a result, there may have been decreases in heavy drinking due to limited access to alcohol and decreased opportunities for social drinking. Furthermore, participants have a high medical comorbidity burden and WLWH with heavy alcohol use have lower self-reported health status compared to those with non-heavy alcohol use [6]. Their perception of their health status may have increased personal concern for severe COVID-19 illness and therefore led to modifications in alcohol consumption and social behaviors during the early stages of the pandemic especially when there was a lack of comprehensive knowledge about the virus and no vaccines. This is supported by a qualitative study of PLWH in New York that found participants perceived themselves to be at greater risk for COVID-19 illness and therefore had high adherence to infection precautions [37].
Alcohol use trends have important implications for the public health community. For example, the initial decrease in alcohol use among those with histories of heavy drinking raise concern for alcohol withdrawal syndromes. In some communities there was an increase in hospitalizations associated with alcohol withdrawal during 2020, but not with alcohol use complications [38, 39]. These findings are consistent with reductions in consumption among those who had a history of heavy alcohol use and point to the need for public messaging on how to access formal treatment services and options for safely reducing consumption during periods of social disruption.
As the COVID-19 pandemic progressed, social restrictions lifted, COVID-19 vaccines were rolled out, and the above-mentioned drivers of the initial decrease in alcohol consumption may have been mitigated. However, during this time there was also an ongoing increase in stress and anxiety due to sequelae of the pandemic which may have driven the subsequent increase in alcohol use into 2021 [30, 32, 40–42]. During the late pandemic period, alcohol use declined among those with heavy drinking to below pre-pandemic levels. Longer-term trends will be needed to understand post-pandemic drinking patterns and if these changes are a function of decreased stressors, awareness of the health benefits of decreasing alcohol use, or increasing availability of treatment support following the relaxation of social restrictions and expansion of telehealth [43].
Other trends of interest include pandemic changes among those with a history of some heavy alcohol use where there was an increase in the average drinks per week throughout the late pandemic period in WLWH and WLWOH. Women in this alcohol use group may be progressing to unhealthy levels of alcohol use and need more support identifying their use as unhealthy and cutting back.
There was also a small increase in alcohol use after the pandemic start among those who previously were abstinent from alcohol and this increase persisted into 2022. Similar findings were observed among Mayo Clinic health network patients [44]. While the mean amount of alcohol in this group is well below national drinking guidelines for unhealthy use, initiation of drinking may still be cause for concern especially among this medically complex group. A large portion of alcohol-related harms occur among people who consume alcohol quantities below national low-risk drinking guidelines raising concern that smaller increases in drinking could increase medical complications [45]. Proactive efforts to prevent women from starting to consume alcohol are needed in addition to treating people who already consume unhealthy amounts of alcohol.
Limitations
Alcohol use was self-reported and therefore subject to recall and social desirability bias, both of which could lead to an underestimation of alcohol use [46]. Non-response bias is also possible, but we did not find a correlation between the amount of missing alcohol data and number of drinks per week at other time points. There could be differences in reporting of alcohol use between the phone survey used in the pandemic and the in-person survey method used at the regular study visits, which could impact the trend observed at the pandemic onset. However, a prior study found no difference in self-reporting of alcohol use and related harms by phone versus in-person and previous estimates of WIHS alcohol consumption during the pandemic were found to be unbiased after adjusting for baseline demographic and clinical differences between those who did and did not respond to the survey early in the COVID-19 pandemic [47, 48]. There was a limited number of timepoints following the COVID-19 pandemic, which limits the generalizability of the study. Associations with stress, childcare responsibilities, anxiety and depression were not examined, which may provide further context on the trends observed.
Conclusions
WLWH in WIHS from 2017 to 2022 consumed less alcohol on average compared to socio-demographically similar peers living without HIV, but alcohol use trajectories after the COVID-19 pandemic onset were similar between the two groups. Self-perceptions of health vulnerability and resilience from the experience of living with HIV are possible explanatory factors, but further research is needed to understand drivers for differences in quantities of alcohol consumption among WLWH and WLWOH. We also observed that trends varied by alcohol use history, highlighting the importance of examining alcohol use trends in the context of alcohol use history to avoid masking changes that may not be appreciated with more aggregated data analysis. Unique trends based on alcohol use histories should be used to inform targeted screening and messaging about alcohol use behaviors during future periods of social disruption and crisis. Longer term research is needed to examine if the COVID-19 pandemic has a lasting impact on the alcohol use trajectories of WLWH.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
The authors gratefully acknowledge the contributions of the study participants and dedication of the staff at the MWCCS sites.
Author Contributions
HRT, PCT, JCP, JAH, YM, and FX contributed the original concept and design of the study. MCK, DLJ, LFC, MFM, AC, ALF, ABS, JD, AS, JCP, PCT were involved in data collection. YM performed the data analysis and all authors interpreted the data. HRT drafted the manuscript. PCT and JCP are responsible for project supervision. All authors have critically revised this article and approved the final version to be published.
Funding
The contents of this publication are solely the responsibility of the authors and do not represent the official views of the National Institutes of Health (NIH). MWCCS (Principal Investigators): Atlanta CRS (Ighovwerha Ofotokun, Anandi Sheth, and Gina Wingood), U01-HL146241; Baltimore CRS (Todd Brown and Joseph Margolick), U01-HL146201; Bronx CRS (Kathryn Anastos, David Hanna, and Anjali Sharma), U01-HL146204; Brooklyn CRS (Deborah Gustafson and Tracey Wilson), U01-HL146202; Data Analysis and Coordination Center (Gypsyamber D’Souza, Stephen Gange and Elizabeth Topper), U01-HL146193; Chicago-Cook County CRS (Mardge Cohen, Audrey French and Ryan Ross), U01-HL146245; Chicago-Northwestern CRS (Frank Palella, Valentina Stoser and Steven Wolinsky), U01-HL146240; Northern California CRS (Bradley Aouizerat, Jennifer Price, and Phyllis Tien), U01-HL146242; Los Angeles CRS (Roger Detels and Matthew Mimiaga), U01-HL146333; Metropolitan Washington CRS (Seble Kassaye and Daniel Merenstein), U01-HL146205; Miami CRS (Maria Alcaide, Margaret Fischl, and Deborah Jones), U01-HL146203; Pittsburgh CRS (Jeremy Martinson and Charles Rinaldo), U01-HL146208; UAB-MS CRS (Mirjam-Colette Kempf, Emily Levitan, James B. Brock, and Deborah Konkle-Parker), U01-HL146192; UNC CRS (Brad Drummond and Michelle Floris-Moore), U01-HL146194. The MWCCS is funded primarily by the National Heart, Lung, and Blood Institute (NHLBI), with additional co-funding from the Eunice Kennedy Shriver National Institute Of Child Health & Human Development (NICHD), National Institute On Aging (NIA), National Institute Of Dental & Craniofacial Research (NIDCR), National Institute Of Allergy And Infectious Diseases (NIAID), National Institute Of Neurological Disorders And Stroke (NINDS), National Institute Of Mental Health (NIMH), National Institute On Drug Abuse (NIDA), National Institute Of Nursing Research (NINR), National Cancer Institute (NCI), National Institute on Alcohol Abuse and Alcoholism (NIAAA), National Institute on Deafness and Other Communication Disorders (NIDCD), National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institute on Minority Health and Health Disparities (NIMHD), and in coordination and alignment with the research priorities of the National Institutes of Health, Office of AIDS Research (OAR). MWCCS data collection is also supported by UL1-TR000004 (UCSF CTSA), UL1-TR003098 (JHU ICTR), UL1-TR001881 (UCLA CTSI), P30-AI-050409 (Atlanta CFAR), P30-AI-073961 (Miami CFAR), P30-AI-050410 (UNC CFAR), P30-AI-027767 (UAB CFAR), and P30-MH-116867 (Miami CHARM). HRT’s time on this project was supported by the Infectious Disease Society of America Foundation/HIV Medicine Association Grant for Emerging Researchers/Clinicians Mentorship Program, which had no role in the study design, analysis, manuscript preparation or approval. Support was also provided to JAH (NIH K24 AA022586) and LFC (NIH K23 AG084415) in the preparation of this manuscript.
Data Availability
Access to individual-level data from the MWCCS may be obtained upon review and approval of a MWCCS concept sheet. Links and instructions for online concept sheet submission are on the study website (http://mwccs.org/).
Declarations
Competing Interests
RJD has received consulting fees from the Department of Defense, Morehouse School of Medicine, Benten Technologies, and Northwell Health. AS has received consulting fees from Gilead; Gilead has provided her institution with funding for her research. Gilead, Merck, and Abbvie have provided JCP’s institution with funding for her research. Merck and Gilead have provided PCT’s institution with funding for her research. JAH has received consulting fees from Pear Therapeutics. The other authors have no conflicts of interest.
Footnotes
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Esser MB, Sherk A, Liu Y, et al. Deaths and years of potential life lost from excessive alcohol Use — United states, 2011–2015. Morb Mortal Wkly Rep. 2020;69:1428–33. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.White AM, Castle IJP, Hingson RW, Powell PA. Using death certificates to explore changes in Alcohol-Related mortality in the united states, 1999 to 2017. Alcoholism: Clin Experimental Res. 2020;44(1):178–87. [DOI] [PubMed] [Google Scholar]
- 3.White AM, Slater ME, Ng G, Hingson R, Breslow R. Trends in Alcohol-Related emergency department visits in the united states: results from the nationwide emergency department sample, 2006 to 2014. Alcoholism: Clin Experimental Res. 2018;42(2):352–9. [DOI] [PubMed] [Google Scholar]
- 4.Grucza RA, Sher KJ, Kerr WC, et al. Trends in adult alcohol use and binge drinking in the early 21st-Century united states: A Meta-Analysis of 6 National survey series. Alcoholism: Clin Experimental Res. 2018;42(10):1939–50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Duko B, Ayalew M, Ayano G. The prevalence of alcohol use disorders among people living with HIV/AIDS: a systematic review and meta-analysis. Subst Abuse Treat Prev Policy 2019;14(1). [DOI] [PMC free article] [PubMed]
- 6.Pytell JD, Li X, Thompson C et al. The Temporal relationship of alcohol use and subsequent self-reported health status among people with HIV. Am J Med Open 2023;9. [DOI] [PMC free article] [PubMed]
- 7.Administration SAaMHS. Results from the 2020 National Survey on Drug Use and Health. Rockville, MD2021.
- 8.Kahler CW, Liu T, Cioe PA, et al. Direct and indirect effects of heavy alcohol use on clinical outcomes in a longitudinal study of HIV patients on ART. AIDS Behav. 2017;21(7):1825–35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Crawford TN, Harris LM, Peyrani P. Examining age as a moderating effect on the relationship between alcohol use and viral suppression among women living with HIV. Women Health. 2019;59(7):789–800. [DOI] [PubMed] [Google Scholar]
- 10.Lipira L, Rao D, Nevin PE, et al. Patterns of alcohol use and associated characteristics and HIV-related outcomes among a sample of African-American women living with HIV. Drug Alcohol Depend. 2020;206:107753. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Hutton HE, Lesko CR, Li X, et al. Alcohol use patterns and subsequent sexual behaviors among women, men who have sex with men and men who have sex with women engaged in routine HIV care in the united States. AIDS Behav. 2019;23(6):1634–46. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Shoptaw S, Montgomery B, Williams CT, et al. Not just the needle. JAIDS J Acquir Immune Defic Syndr. 2013;63(Supplement 2):S174–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Theall KP, Clark RA, Powell A, Smith H, Kissinger P. Alcohol consumption, ART usage and high-risk sex among women infected with HIV. AIDS Behav. 2007;11(2):205–15. [DOI] [PubMed] [Google Scholar]
- 14.Matson TE, McGinnis KA, Rubinsky AD, et al. Gender and alcohol use: influences on HIV care continuum in a National cohort of patients with HIV. AIDS. 2018;32(15):2247–53. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Lee BP, Dodge JL, Leventhal A, Terrault NA. Retail alcohol and tobacco sales during COVID-19. Ann Intern Med 2021. [DOI] [PMC free article] [PubMed]
- 16.Barbosa C, Cowell AJ, Dowd WN. Alcohol consumption in response to the COVID-19 pandemic in the united States. J Addict Med 2020. [DOI] [PMC free article] [PubMed]
- 17.Pollard MS, Tucker JS, Green HD. Jr. Changes in adult alcohol use and consequences during the COVID-19 pandemic in the US. JAMA Netw Open. 2020;3(9):e2022942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Rodriguez LM, Litt DM, Stewart SH. Drinking to Cope with the pandemic: the unique associations of COVID-19-related perceived threat and psychological distress to drinking behaviors in American men and women. Addict Behav. 2020;110:106532. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Meanley S, Choi SK, Thompson AB, et al. Short-term binge drinking, marijuana, and recreational drug use trajectories in a prospective cohort of people living with HIV at the start of COVID-19 mitigation efforts in the united States. Drug Alcohol Depend. 2021;231:109233. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Wallach JD, Gueorguieva R, Phan H, Witkiewitz K, Wu R, O’Malley SS. Predictors of abstinence, no heavy drinking days, and a 2-level reduction in world health organization drinking levels during treatment for alcohol use disorder in the COMBINE study. Alcohol Clin Exp Res. 2022;46(7):1331–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Witkiewitz K, Kirouac M, Baurley JW, McMahan CS. Patterns of drinking behavior around a treatment episode for alcohol use disorder: predictions from pre-treatment measures. Alcohol Clin Exp Res (Hoboken). 2023;47(11):2138–48. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Adimora AA, Ramirez C, Benning L, et al. Cohort profile: the women’s interagency HIV study (WIHS). Int J Epidemiol. 2018;47(2):393–i394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.D’Souza G, Bhondoekhan F, Benning L et al. Characteristics of the MACS/WIHS combined cohort study: opportunities for research on aging with HIV in the longest US observational study of HIV. Am J Epidemiol. 2021. [DOI] [PMC free article] [PubMed]
- 24.Collins LF, Sheth AN, Mehta CC, et al. The prevalence and burden of Non-AIDS comorbidities among women living with or at risk for human immunodeficiency virus infection in the united States. Clin Infect Dis. 2021;72(8):1301–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Alcoholism NIoAAa. Alcohol’s Effects on Health. Drinking Levels Defined Web site. https://www.niaaa.nih.gov/alcohol-health/overview-alcohol-consumption/moderate-binge-drinking. Published 2023. Accessed June 18, 2023.
- 26.Hamel L, Kirzinger A, Lopes L, May. KFF COVID-19 Vaccine Monitor. : 2021. Kaiser Family Foundation. https://www.kff.org/coronavirus-covid-19/poll-finding/kff-covid-19-vaccine-monitor-may-2021/. Published 2021. Accessed June 18, 2023.
- 27.van Buuren S, Groothuis-Oudshoorn K. Mice: multivariate imputation by chained equations in R. J Stat Softw. 2011;45(3):1–67. [Google Scholar]
- 28.Wilson TE, Kay ES, Turan B, et al. Healthcare empowerment and HIV viral control: mediating roles of adherence and retention in care. Am J Prev Med. 2018;54(6):756–64. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Dale SK, Cohen MH, Kelso GA, et al. Resilience among women with HIV: impact of Silencing the self and socioeconomic factors. Sex Roles. 2014;70(5–6):221–31. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Diaz-Martinez J, Tamargo JA, Delgado-Enciso I et al. Resilience, anxiety, stress, and substance use patterns during COVID-19 pandemic in the Miami adult studies on HIV (MASH) cohort. AIDS Behav. 2021. [DOI] [PMC free article] [PubMed]
- 31.Monroe AK, Kulie PE, Byrne ME, et al. Psychosocial impacts of the COVID-19 pandemic from a cross-sectional survey of people living with HIV in washington, DC. AIDS Res Ther. 2023;20(1):27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Tucker JS, Rodriguez A, Green HD Jr., Pollard MS. Trajectories of alcohol use and problems during the COVID-19 pandemic: the role of social stressors and drinking motives for men and women. Drug Alcohol Depend. 2022;232:109285. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Friedman MR, Kempf MC, Benning L, et al. Prevalence of COVID-19–Related social disruptions and effects on psychosocial health in a Mixed-Serostatus cohort of men and women. J Acquir Immune Defic Syndr. 2021;88(5):426–38. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.De Goeij MCM, Suhrcke M, Toffolutti V, Van De Mheen D, Schoenmakers TM, Kunst AE. How economic crises affect alcohol consumption and alcohol-related health problems: A realist systematic review. Soc Sci Med. 2015;131:131–46. [DOI] [PubMed] [Google Scholar]
- 35.Gonçalves PD, Moura HF, Do Amaral RA, Castaldelli-Maia JM, Malbergier A. Alcohol use and COVID-19: can we predict the impact of the pandemic on alcohol use based on the previous crises in the 21st century?? A brief review. Front Psychiatry 2020;11. [DOI] [PMC free article] [PubMed]
- 36.Grossman ER, Benjamin-Neelon SE, Sonnenschein S. Alcohol consumption during the COVID-19 pandemic: A Cross-Sectional survey of US adults. Int J Environ Res Public Health. 2020;17(24):9189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Gwadz M, Campos S, Freeman R et al. Black and Latino persons living with HIV evidence risk and resilience in the context of COVID-19: A Mixed-Methods study of the early phase of the pandemic. AIDS Behav. 2021. [DOI] [PMC free article] [PubMed]
- 38.Sharma RA, Subedi K, Gbadebo BM, Wilson B, Jurkovitz C, Horton T. Alcohol withdrawal rates in hospitalized patients during the COVID-19 pandemic. JAMA Netw Open. 2021;4(3):e210422–210422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Schimmel J, Vargas-Torres C, Genes N, Probst MA, Manini AF. Changes in alcohol-related hospital visits during COVID-19 in new York City. Addiction.; 2021. [DOI] [PMC free article] [PubMed]
- 40.Manchia M, Gathier AW, Yapici-Eser H, et al. The impact of the prolonged COVID-19 pandemic on stress resilience and mental health: A critical review across waves. Eur Neuropsychopharmacol. 2022;55:22–83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Kalichman SC, El-Krab R. Social and behavioral impacts of COVID-19 on people living with HIV: review of the first year of research. Curr HIV/AIDS Rep. 2022;19(1):54–75. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Hong C, Queiroz A, Hoskin J. The impact of the COVID-19 pandemic on mental health, associated factors and coping strategies in people living with HIV: a scoping review. J Int AIDS Soc. 2023;26(3):e26060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Palzes VA, Chi FW, Metz VE et al. Overall and telehealth addiction treatment utilization by age, race, ethnicity, and socioeconomic status in California after COVID-19 policy changes. JAMA Health Forum 2023;4(5). [DOI] [PMC free article] [PubMed]
- 44.Sharma P, Nguyen QA, Kurani S et al. Association of socio-demographic characteristics with alcohol use initiation among never users during the COVID-19 pandemic: a longitudinal study. J Public Health (Oxf). 2022. [DOI] [PMC free article] [PubMed]
- 45.Sherk A, Thomas G, Churchill S, Stockwell T. Does drinking within Low-Risk guidelines prevent harm?? Implications for High-Income countries using the international model of alcohol harm?s and policies. J Stud Alcohol Drug. 2020;81:352–61. [PubMed] [Google Scholar]
- 46.Jain JP, Ma Y, Dawson-Rose C, et al. The prevalence and correlates of biomarker positive unhealthy alcohol use among women living with and without HIV in San francisco, California. PLoS ONE. 2024;19(10):e0308867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Tierney HR, Ma Y, Bacchetti P et al. Pivoting from in-person to phone survey assessment of alcohol and substance use: effects on representativeness in a united States prospective cohort of women living with and without HIV. Am J Drug Alcohol Abus 2023:1–10. [DOI] [PMC free article] [PubMed]
- 48.Midanik LT, Greenfield TK. Telephone versus in-person interviews for alcohol use: results of the 2000 National alcohol survey. Drug Alcohol Depend. 2003;72(3):209–14. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Access to individual-level data from the MWCCS may be obtained upon review and approval of a MWCCS concept sheet. Links and instructions for online concept sheet submission are on the study website (http://mwccs.org/).


