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Chinese Medical Journal logoLink to Chinese Medical Journal
. 2025 Feb 26;138(21):2824–2831. doi: 10.1097/CM9.0000000000003461

Life’s Essential 8 metrics and prognosis in patients with renal insufficiency: Results from the National Health and Nutrition Examination Survey, 2007–2018

Weihua Chen 1,2, Guitao Xiao 2, Shan Ding 3, Shanshan Shi 4, Yuxiong Pan 2, Jiabin Tu 2, Yanbin Zhang 2, Ying Liao 2, Liling Chen 2, Kaihong Chen 2,, Rongchong Huang 1,
Editor: Yuanyuan Ji
PMCID: PMC12574513  PMID: 40008794

Abstract

Background:

The benefits of ideal cardiovascular-health metrics (ICVHMs) in patients with renal insufficiency remain unclear. This study aimed to investigate the associations between ICVHM and prognosis in a renal insufficiency population.

Methods:

The trial enrolled 29,682 participants from the US National Health and Nutrition Examination Survey (NHANES), 2007–2018, with mortality follow-up through December 31, 2019. Participants were divided into three groups based on estimated glomerular filtration rates. Cardiovascular health was assessed using new “Life’s Essential 8” metrics. Cox regression analyses based on NHANES data were used to determine the associations between ICVHMs and cardiovascular mortality in patients with renal insufficiency.

Results:

During a mean follow-up of 6.58 years, ideal cardiovascular health (hazard ratio [HR] = 0.42; 95% confidence interval [CI]; 0.25–0.70) and ideal health behavior (HR = 0.53; 95% CI; 0.39–0.73) reduced cardiovascular mortality in participants with renal insufficiency. For each one ICVHM increment, a 25% reduction in cardiovascular mortality was recorded (95% CI; 0.69–0.82). When compared with participants with normal renal function, for those with mild renal insufficiency, the HR for cardiovascular mortality gradually decreased from 1.47 (95% CI; 0.85–2.52) in those who had ≤1 ICVHMs to 0.30 (95% CI; 0.12–0.77) in participants who had >6 ICVHMs.

Conclusions:

From an ICVHM perspective, enhanced cardiovascular benefits were observed in individuals with renal insufficiency, coupled with a reduced risk of all-cause mortality. Furthermore, when compared with individuals with normal renal function, increased ICVHMs can mitigate adverse risks associated with renal impairment.

Keywords: Cardiovascular health, Cardiovascular mortality, NHANES, Prognosis, Renal insufficiency, Life’s Essential 8

Introduction

Incidences of renal insufficiency are increasing and mortality remains unacceptably high.[15] Notably, the risk of cardiovascular disease (CVD) is significantly increased in individuals with renal insufficiency and is increased by twofold to fourfold when combined with impaired kidney function.[6] Potential non-pharmacological interventions can help to reduce the cardiovascular burden in renal insufficiency cohorts.[79]

Cardiovascular health (CVH) was previously defined and has become an important factor in reducing the substantial CVD burden and other chronic health conditions in the past decade.[10,11] Recently, the American Heart Association (AHA) published an updated algorithm for quantifying CVH scores and redefining CVH—Life’s Essential 8.[11] Many studies have reported that individuals with a more ideal CVH have markedly lower risks for CVD events and end-stage renal disease (ESRD).[12,13] A recent study reported that participants with pre-diabetes or diabetes who achieved at least five ideal cardiovascular health metrics (ICVHMs) decreased their risk of cardiovascular events when compared with normal individuals.[14] It was also reported that the coronary risks conferred by chronic kidney disease (CKD) surpassed those conferred by diabetes.[15,16] However, as an important subpopulation with high CVD incidence and mortality, CVH status in renal insufficient populations is not ideal, and similarly, the benefits of updated CVH metrics in this population remain unclear.

Therefore, we investigated ICVHM benefits in populations with renal insufficiency. Additionally, we explored whether a higher number of ICVHMs, when compared with the general population, could mitigate cardiovascular damage caused by renal dysfunction.

Methods

Study design and participants

The National Health and Nutrition Examination Survey (NHANES) is a continuously monitored health system based on a typical sampling of the American civilian non-medical population. Available data, materials, and guidelines on methods are publicly accessible from the National Center for Health Statistics of the Centers for Disease Control and Prevention (https://www.cdc.gov/nchs/nhanes/index.htm).

Our study was limited to adult participants from the 2007–2018 NHANES survey who were 20 years or older in the US community, and whose estimated glomerular filtration rate (eGFR) values were calculated using CKD Epidemiology Collaborative equation formula.[17] According to Supplementary Figure 1 and Supplementary Materials, http://links.lww.com/CM9/C291, NHANES participants in the US community, who were 20 years or older (n = 35,922), were included. We excluded those with missing CVH data (n = 6087) and eGFR data (n = 107). Also, 46 potential participants were lost to follow-up. Thus, 29,682 individuals (17,297 with normal renal function, 9502 with mild renal insufficiency, and 2883 with moderate to severe renal insufficiency) were eventually enrolled in the study.

Patient and public involvement statement

The project was authorized by the National Center for Health Statistics Research Ethics Review Board (Protocol #2005-06, Protocol #2011-17, and Protocol #2018-01). Written informed consent was obtained from all participants.

CVH measurements and classification

The CVH concept was updated in the latest 2022 AHA recommendations, Life’s Essential 8.[11] Currently, four health behaviors (diet, physical activity, nicotine exposure, and sleep) and four health factors (body mass index [BMI], cholesterol, blood glucose, and blood pressure) have been identified. CVH measurement details are shown in Supplementary Table 1, http://links.lww.com/CM9/C291. The total CVH score was the average of the eight health index scores, and the range was 0–100. An individual with CVH score of <50 was poor; while 50–79 and ≥80 scores were intermediate and ideal, respectively.

Defining variables of interest

Age, sex, race, education level, alcohol use, and CVD history (congestive heart failure, coronary heart disease, stroke, heart attack, and angina), as well as family histories of CVD and diabetes, were self-reported. We performed analyses using eGFR values, which were calculated using the CKD Epidemiology Collaborative equation.[17] We divided participants into three eGFR categories:[18] (1) normal renal function with eGFR ≥90 mL·min−1·m−2; (2) mild renal insufficiency with eGFR 60–89 mL·min−1·m−2; and (3) moderate to severe renal insufficiency with eGFR <60 mL·min−1·m−2.

Mortality outcomes

Mortality information was collected by the National Center for Health Statistics and was based on several population surveys and death certificate records from the National Death Index. The primary study outcome was cardiovascular mortality. Cause of death was categorized using the International Classification of Diseases 10th edition (ICD-10) codes I00–I078. The secondary study outcome was all-cause mortality. Mortality follow-up data for NHANES participants from 2007 to 2018 were available as of December 31, 2019.

Statistical analysis

Analyses were performed using NHANES-recommended weights. Continuous variables were expressed as the mean ± standard error (SE) and statistically analyzed using one-way analysis of variance tests. Categorical variables were expressed as percentages and tested using the chi-squared method.

Cox proportional hazard models after recommended weighting were used to calculate hazard ratios (HRs) and 95% confidence intervals (CI) for cardiovascular or all-cause mortality, with multivariable adjustments for age, sex, race, alcohol consumption, education, CVD, family history of diabetes and CVD. Cardiovascular and all-cause mortality risks were assessed based on individual ICVHMs, combined health behaviors, combined health indicators, and combined CVH scores in participants with renal insufficiency. By analyzing the associations between ICVHMs components and cardiovascular and all-cause mortality, we adjusted for all other cardiovascular indicators. Additional analyses on the number of ideal health behaviors, ideal health indicators, and ICVHMs were performed to assess cardiovascular risk and all-cause mortality. We also conducted the subgroup analyses. Moreover, restricted cubic spline plots were used to explore health behavior, health scores, and CVH score associations with cardiovascular risk and all-cause mortality.

In supplementary analyses, we also analyzed cardiovascular risk and all-cause mortality according to combined health behaviors, combined health factors, combined CVH scores, individual ICVHMs, the number of health behaviors, health factors, and combined ICVHMs in participants with mild or moderate to severe renal insufficiency vs. individuals with normal renal function. Participants were stratified into subgroups according to age and sex; associations between health behaviors, health factors, and combined CVH scores, and cardiovascular or all-cause mortality in participants with mild renal insufficiency or moderate to severe renal insufficiency were examined and compared to participants with normal renal function in each age or sex subgroup. CVH distribution and trend levels in patients with renal insufficiency (from 2007 to 2018) were explored. A two-sided P-value <0.05 indicated statistically significant difference. The data analyses were performed using R software (version 4.2.0; R Foundation for Statistical Computing, Vienna, Austria).

Results

Of 29,682 participants, 17,297 (weighted rate, 59.0%) had normal renal function, 9502 (weighted rate, 33.3%) had mild renal insufficiency, and 2883 (weighted rate, 7.6%) had moderate to severe renal insufficiency. The mean age ranged from 40.2 ± 0.2 years to 71.6 ± 0.4 years. Baseline characteristics of study participants according to renal function status are shown in Table 1. When compared to participants with normal renal function, those with mild renal insufficiency had the highest percentages of males, while the moderate to severe category had the lowest education levels. Participants with mild or moderate to severe renal insufficiency were older, had lower health factor scores, lower CVH scores, and fewer ICVHMs.

Table 1.

Baseline characteristics of participants with normal renal function, mild renal insufficiency, and moderate to severe renal insufficiency (n = 29,682)*.

Baseline characteristics Normal renal function Mild renal insufficiency Moderate to severe renal insufficiency P-values
Participants 17,297 (59.0) 9502 (33.3) 2883 (7.6)
Age (years) 40.2 ± 0.2 57.8 ± 0.3 71.6 ± 0.4 <0.001
Men 8113 (47.6) 5043 (51.4) 1394 (43.2) <0.001
Race <0.001
Mexican American 3357 (11.8) 998 (4.3) 230 (3.4)
Non-Hispanic Black 3671 (12.2) 1832 (8.2) 647 (10.8)
Non-Hispanic White 5965 (59.6) 4898 (77.4) 1644 (78.4)
Other Hispanic 2024 (7.2) 911 (3.9) 197 (2.9)
Other race 2280 (9.2) 863 (6.2) 165 (4.5)
Education level 0.013
<12 grades 4194 (16.0) 2196 (13.7) 860 (20.9)
12 grades 3895 (23.2) 2159 (22.5) 733 (26.3)
>12 grades 9201 (60.8) 5135 (63.8) 1287 (52.8)
Drinking status <0.001
Non-drinker 4184 (20.9) 2989 (25.9) 1313 (43.7)
Low to moderate drinker 4863 (32.1) 3482 (44. 6) 935 (41.3)
Heavy drinker 6943 (46.9) 2315 (29.6) 355 (15.1)
Self-reported CVD 905 (4.4) 1657 (13.9) 1132 (35.7) <0.001
Family history of CVD 1966 (11.6) 1328 (14.9) 451 (15.8)
Family history of diabetes 7599 (41.2) 4139 (40.1) 1382 (44.0) 0.102
Healthy diet 4056 (23.8) 2810 (29.8) 789 (27.9) <0.001
PA at goal 12,226 (74.6) 6045 (69.9) 1255 (48.6) <0.001
Smoking status at goal 10,033 (56.2) 4991 (54.5) 1432 (51.3) <0.001
Sleeping at goal 10,388 (63.5) 5922 (66.6) 1749 (64.1) <0.001
BMI (kg/m2) 29.2 ± 0.1 29.3 ± 0.1 30.7 ± 0.2 <0.001
Non-high cholesterol (mg/dL) 139.1 ± 0.7 142.4 ± 0.8 132.1 ± 1.4 0.371
Systolic BP (mm Hg) 119.4 ± 0.2 125.2 ± 0.3 132.1 ± 0.8 <0.001
Diastolic BP (mm Hg) 71.1 ± 0.2 71.3 ± 0.2 64.9 ± 0.5 <0.001
Glycated HbA1c (%) 5.6 ± 0.0 5.8 ± 0.0 6.3 ± 0.0 <0.001
CVH sore 69.6 ± 0.3 67.1 ± 0.3 60.5 ± 0.5 <0.001
Health behavior score 67.1 ± 0.4 69.0 ± 0.4 64.0 ± 0.6 0.852
Health factor score 72.1 ± 0.3 65.1 ± 0.4 56.9 ± 0.6 <0.001
ICVHMs <0.001
≤1 989 (5.0) 855 (7.0) 343 (10.2)
2 2212 (11.1) 1654 (14.2) 667 (21.6)
3 3549 (18.4) 2351 (22.8) 862 (29.5)
4 3913 (23.3) 2212 (23.8) 579 (19. 9)
5 3262 (20.0) 1419 (17.2) 291 (11.5)
6 2127 (13.4) 702 (9.7) 115 (6.0)
≥7 1245 (8.7) 309 (5.3) 26 (1.3)

Values were shown as mean ± SE or n (%). *All estimates accounted for complex survey designs. All the rates in Table 1 indicate the weighted rates. BP: Blood pressure; BMI: Body mass index; CVD: Cardiovascular disease; CVH: Cardiovascular health; HbA1c: Hemoglobin A1c; HEI-2015: Healthy Eating Index 2015; ICVHMs: Ideal cardiovascular health metrics; PA: Physical activity; SE: Standard error; –: Not applicable.

Overall, the ideal CVH status, ideal health behaviors, and health factors were observed in a lower proportion of participants with renal insufficiency [Supplementary Figure 2, http://links.lww.com/CM9/C291]. Moreover, the overall trend in individual or combined ICVHMs from 2007 to 2018 was different. The ideal status proportion was an increasing trend in glucose level and smoking level, and was a downward trend in BMI level [Supplementary Figure 3, http://links.lww.com/CM9/C291]. However, both individual and combined ICVHMs remained mostly stable.

As indicated in Table 2, the associations were identified between each ICVHM component and cardiovascular mortality and all-cause mortality. During a mean follow-up of 6.58 years, an ideal CVH and ideal health behaviors reduced cardiovascular mortality (ideal CVH: HR = 0.42; 95% CI: 0.25–0.70; ideal health behaviors: HR = 0.53; 95% CI: 0.39–0.73), and all-cause mortality (ideal CVH: HR = 0.58; 95% CI: 0.45–0.76; ideal health behaviors: HR = 0.55; 95% CI: 0.46–0.65) in participants with renal insufficiency. When compared with participants who had one ideal metric or none, for participants who had two to five and at least six ideal metrics, the cardiovascular mortality HR was 0.83 (95% CI: 0.51–1.35), 0.56 (95% CI: 0.36–0.86), 0.43 (95% CI: 0.29–0.62), 0.44 (95% CI: 0.27–0.70), and 0.25 (95% CI: 0.13–0.50), respectively [Table 3]. For each one ICVHM increment, a 25% reduction in cardiovascular mortality (95% CI: 0.69–0.82) was recorded. A similar HR pattern was observed for desirable health behavior metrics in participants with renal insufficiency; each increment in health behavior was associated with an HR = 0.68 (95% CI: 0.61–0.77) for cardiovascular mortality. The result of all-cause mortality was similar to cardiovascular mortality. In subgroup analyses, cardiovascular and all-cause mortality continued to decrease as each ICVHM, ideal health behavior, and ideal health factor increased [Figure 1]. Moreover, restricted cubic spline analyses showed that relationships between CVH, health behavior, and health factor scores, and all-cause mortality appeared to be non-linear (All P for non-linear <0.001; Supplementary Figure 4A, http://links.lww.com/CM9/C291). However, the relationship between CVH scores and cardiovascular mortality appeared to be linear (P for non-linear = 0.071; Supplementary Figure 4B, http://links.lww.com/CM9/C291).

Table 2.

HR (95% CI) of all-cause mortality and cardiovascular mortality according to individual ICVHMs among participants with renal insufficiency*.

Categories All-cause mortality Cardiovascular mortality
Person-years No. of cases HR (95% CI) Person-years No. of cases HR (95% CI)
Diet
Non-ideal 56,276 1760 1 [Reference] 56,276 476 1 [Reference]
Ideal 24,026 617 0.91 (0.78–1.07) 24,026 165 0.86 (0.61–1.22)
PA
Non-ideal 31,753 1390 1 [Reference] 31,753 392 1 [Reference]
Ideal 48,549 897 0.60 (0.52–0.69) 48,549 249 0.54 (0.41–0.70)
Smoking
Non-ideal 38,271 1349 1 [Reference] 38,271 343 1 [Reference]
Ideal 42,031 938 0.63 (0.56–0.72) 42,031 298 0.79 (0.60–1.04)
Sleeping
Non-ideal 31,089 942 1 [Reference] 31,089 272 1 [Reference]
Ideal 49,214 1345 0.78 (0.70–0.88) 49,214 369 0.75 (0.61–0.92)
BMI
Non-ideal 62,015 1669 1 [Reference] 62,015 492 1 [Reference]
Ideal 18,287 618 1.33 (1.15–1.54) 18,287 149 1.16 (0.91–1.48)
Total cholesterol
Non-ideal 45,641 1044 1 [Reference] 45,641 287 1 [Reference]
Ideal 34,661 1243 1.13 (0.98–1.31) 34,661 354 0.99 (0.77–1.27)
Glycated HbA1c
Non-ideal 46,957 1677 1 [Reference] 46,957 487 1 [Reference]
Ideal 33,346 610 0.83 (0.71–0.97) 33,346 154 0.76 (0.57–1.02)
BP
Non-ideal 11,973 763 1 [Reference] 11,973 239 1 [Reference]
Ideal 4,727 263 0.85 (0.66–1.09) 4727 75 0.75 (0.45–1.26)
Health behavior score
Non-ideal 55,562 1881 1 [Reference] 55,562 528 1 [Reference]
Ideal 24,740 406 0.55 (0.46–0.65) 24,740 113 0.53 (0.39–0.73)
Health factor score
Non-ideal 66,371 2032 1 [Reference] 66,371 581 1 [Reference]
Ideal 13,932 255 0.94 (0.79–1.12) 13,932 60 0.72 (0.51–1.03)
CVH score
Non-ideal 69,433 2146 1 [Reference] 69,433 608 1 [Reference]
Ideal 10,869 141 0.58 (0.45–0.76) 10,869 33 0.42 (0.25–0.70)

*12,385 participants (9502 with mild renal insufficiency, and 2883 with moderate to severe renal insufficiency) were included in the analysis. All analysis adjusted for age, sex, race, education level, alcohol drinking, family history of diabetes (yes or no), family history of CVD (yes or no) and self-reported CVD (congestive heart failure, coronary heart disease, stroke, heart attack, and angina). Individual CVH metrics were mutually adjusted. BP: Blood pressure; BMI: Body mass index; CI: Confidence interval; CVD: Cardiovascular disease; CVH: Cardiovascular health; HbA1c: Hemoglobin A1c; HR: Hazard ratio; ICVHMs: Ideal cardiovascular health metrics; PA: Physical activity.

Table 3.

HR (95% CI) of all-cause mortality and cardiovascular mortality according to the number of combined ICVHMs in participants with renal insufficiency.

Categories All-cause mortality Cardiovascular mortality
Person-years No. of cases HR (95% CI) Person-years No. of cases HR (95% CI)
No. of ICVHMs
≤1 7587 315 1 [Reference] 7587 99 1 [Reference]
2 14,639 671 0.87 (0.68–1.12) 14,639 157 0.83 (0.51–1.35)
3 20,644 619 0.69 (0.53–0.90) 20,644 169 0.56 (0.36–0.86)
4 18,191 437 0.64 (0.49–0.82) 18,191 121 0.43 (0.29–0.62)
5 11,321 248 0.53 (0.41–0.70) 11,321 73 0.44 (0.27–0.70)
≥6 7921 97 0.38 (0.27–0.53) 7921 22 0.25 (0.13–0.50)
No. of health behaviors
≤1 24,879 1050 1 [Reference] 24,879 288 1 [Reference]
2 28,639 759 0.68 (0.59–0.79) 28,639 220 0.70 (0.56–0.88)
3 20,427 402 0.53 (0.46–0.62) 20,427 109 0.46 (0.33–0.63)
4 6367 76 0.26 (0.19–0.37) 6367 24 0.32 (0.19–0.53)
No. of health factors
≤1 30,417 909 1 [Reference] 30,417 274 1 [Reference]
2 22,430 685 0.98 (0.83–1.16) 22,430 181 0.78 (0.61–0.98)
3 9275 207 0.93 (0.74–1.16) 9275 49 0.65 (0.43–0.99)
4 2554 37 1.54 (0.92–2.59) 2554 5 0.47 (0.16–1.35)
Each 1-number increment in ideal health behaviors NA NA 0.70 (0.65–0.74) NA NA 0.68 (0.61–0.77)
Each 1-number increment in ideal health factors NA NA 1.02 (0.92–1.12) NA NA 0.79 (0.67–0.94)
Each 1-number increment in ICVHMs NA NA 0.83 (0.79–0.87) NA NA 0.75 (0.69–0.82)

*12,385 participants (9502 with mild renal insufficiency, and 2883 with moderate to severe renal insufficiency) were included. All analyses were adjusted for age, sex, race, education level, alcohol consumption, family history of diabetes (yes or no), family history of CVD (yes or no), and self-reported CVD (congestive heart failure, coronary heart disease, stroke, heart attack, and angina. CI: Confidence interval; CVD: Cardiovascular disease; HR: Hazard ratio; ICVHMs: Ideal cardiovascular health metrics; NA: Not applicable.

Figure 1.

Figure 1

HR (95% CI) of all-cause mortality and cardiovascular mortality according to each 1-number increment in combined ICVHMs in participants with renal insufficiency, according to age and sex categories. CI: Confidence interval; HR: Hazard ratio; ICVHMs: Ideal cardiovascular health metrics.

As shown in Table 4, when compared to participants with normal renal function, participants with mild renal insufficiency who had ideal CVH reduced cardiovascular mortality (HR = 0.34; 95% CI: 0.14–0.81). In participants with moderate to severe renal insufficiency, the HR for cardiovascular mortality decreased gradually from 8.41 (95% CI: 3.35–21.12) for poor CVH to 2.10 (95% CI: 0.81–5.43) for an ideal CVH (P for trend <0.001). Similar results were observed in health behavior and all-cause mortality scores. In participants with mild renal insufficiency and younger than 75 years, an ideal CVH significantly reduced cardiovascular and all-cause mortality. In men and women participants, an ideal CVH or ideal health behaviors significantly reduced cardiovascular mortality [Supplementary Figure 5A, http://links.lww.com/CM9/C291]. A similar association was not observed in participants with moderate to severe renal insufficiency [Supplementary Figure 5B, http://links.lww.com/CM9/C291]. However, the HR for cardiovascular or all-cause mortality was not increased when compared to participants with normal renal function.

Table 4.

HR (95% CI) of all-cause mortality and cardiovascular mortality according to individual and combined ICVHMs in participants with mild renal insufficiency or moderate to severe renal insufficiency when compared to participants with normal renal function*.

Categories All-cause mortality Cardiovascular mortality
Person-years No. of cases HR (95% CI) P for trend Person-years No. of cases HR (95% CI) P for trend
Normal renal function 121,909 366 1 [Reference] 121,909 84 1 [Reference]
Mild renal insufficiency
Healthy diet 19,074 352 0.94 (0.73–1.21) 19,074 84 1.01 (0.64–1.59)
PA at goal 40,963 591 0.73 (0.59–0.90) 40,963 151 0.87 (0.53–1.43)
Ideal smoking 33,520 490 0.63 (0.49–0.81) 33,520 146 0.98 (0.58–1.64)
Sleeping at goal 38,941 738 0.77 (0.63–0.96) 38,941 178 0.90 (0.55–1.46)
Ideal BMI 15,120 367 1.11 (0.84–1.47) 15,120 79 1.08 (0.62–1.90)
Ideal blood cholesterol 25,936 668 1.05 (0.84–1.32) 25,936 160 1.05 (0.65–1.69)
Idea blood glucose 29,159 395 0.73 (0.56–0.94) 29,159 90 0.91 (0.55–1.51)
Ideal BP 22,297 314 0.84 (0.66–1.07) 22,297 71 0.87 (0.53–1.43)
Health behaviors score <0.001 0.010
Poor 12,026 381 1.29 (1.02–1.63) 12,026 211 1.47 (0.92–2.36)
Intermediate 30,684 603 0.69 (0.57–0.84) 30,684 87 0.86 (0.52–1.41)
Ideal 20,892 277 0.52 (0.40–0.69) 20,892 29 0.77 (0.44–1.36)
Health factors score 0.440 0.080
Poor 15,018 317 0.73 (0.59–0.91) 15,018 94 1.10 (0.68–1.79)
Intermediate 36,062 770 0.75 (0.60–0.93) 36,062 201 0.98 (0.59–1.61)
Ideal 12,522 174 0.75 (0.57–0.99) 12,522 32 0.60 (0.31–1.15)
CVH score <0.001 <0.001
Poor 9489 300 1.16 (0.93–1.46) 9489 89 1.70 (1.01–2.85)
Intermediate 44,350 858 0.70 (0.57–0.86) 44,350 220 0.88 (0.55–1.40)
Ideal 9763 103 0.47 (0.33–0.69) 9763 18 0.34 (0.14–0.81)
Moderate to severe renal insufficiency
Healthy diet 4952 265 1.87 (1.19–2.93) 4952 81 4.14 (1.10–15.51)
PA at goal 7586 306 1.31 (0.96–1.77) 7586 98 2.41 (1.23–4.72)
Ideal smoking 8511 448 1.38 (0.99–1.92) 8511 152 2.49 (1.39–4.48)
Sleeping at goal 10,273 607 1.69 (1.24–2.31) 10,273 191 3.80 (1.57–9.19)
Ideal BMI 3167 251 2.30 (1.57–3.38) 3167 70 3.78 (2.02–7.09)
Ideal blood cholesterol 8725 575 1.87 (1.43–2.46) 8725 194 3.23 (1.86–5.60)
Idea blood glucose 4187 215 1.51 (1.13–2.02) 4187 64 3.33 (1.84–6.03)
Ideal BP 4727 263 1.54 (1.15–2.06) 4727 75 2.42 (1.28–4.57)
Health behaviors score <0.001 <0.001
Poor 4061 354 2.86 (2.11–3.87) 4061 103 7.45 (3.42–16.24)
Intermediate 8791 549 1.71 (1.24–2.36) 8791 169 3.90 (1.64–9.26)
Ideal 3849 129 0.91 (0.61–1.35) 3849 42 1.56 (0.68–3.59)
Health factors score 0.040 0.080
Poor 5995 386 2.09 (1.50–2.92) 5995 125 5.62 (2.27–13.95)
Intermediate 9296 559 1.58 (1.19–2.11) 9296 161 3.16 (1.50–6.65)
Ideal 1410 81 1.43 (0.98–2.09) 1410 28 3.90 (1.71–8.91)
CVH score
Poor 4044 319 2.79 (1.97–3.95) <0.001 4044 107 8.41 (3.35–21.12) <0.001
Intermediate 11,551 669 1.53 (1.14–2.04) 11,551 192 2.76 (1.32–5.74)
Ideal 1106 38 0.85 (0.54–1.32) 1106 15 2.10 (0.81–5.43)

*29,682 participants (17,297 with normal renal function, 9502 with mild renal insufficiency, and 2883 with moderate to severe renal insufficiency) were included. All analyses were adjusted for age, sex, race, education level, alcohol consumption, family history of diabetes (yes or no), family history of CVD (yes or no), and self-reported CVD (congestive heart failure, coronary heart disease, stroke, heart attack, and angina). Individual CVH metrics were mutually adjusted. BP: Blood pressure; BMI: Body mass index; CI: Confidence interval; CVD: Cardiovascular disease; CVH: Cardiovascular health; HR: Hazard ratio; ICVHMs: Ideal cardiovascular health metrics; PA: Physical activity.

Furthermore, when compared to participants with normal renal function, in participants with mild renal insufficiency, the HR for cardiovascular mortality gradually decreased from 1.47 (95% CI: 0.85–2.52) in those who had ≤1 ICVHMs to 0.30 (95% CI: 0.12–0.77) in participants who had >6 ICVHMs [Supplementary Table 2, http://links.lww.com/CM9/C291]. All-cause mortality and cardiovascular mortality decreased with increasing ICVHMs. Similar trends were observed in participants with increased ICVHMs or increased healthy behaviors in participants with mild and moderate to severe renal insufficiency. The magnitude of incremental risks for cardiovascular mortality associated with fewer ICVHMs was greatest among participants who were younger than 75 years (≥6 ICVHMs: HR = 0.02; 95% CI: 0.00–0.16; ≤1 ICVHMs: HR = 1.75; 95% CI: 0.87–3.53; Supplementary Figure 6A, http://links.lww.com/CM9/C291) and greatest in female participants (≥6 ICVHMs: HR = 0.87; 95% CI: 0.30–2.51; ≤1 ICVHMs: HR = 3.67; 95% CI: 1.69–7.98). Similar healthy behavior and health factor results were also observed in participants with mild renal insufficiency. In participants with moderate to severe renal insufficiency, similar correlations between ICVHMs, health factors, and health behaviors with age and sex were observed [Supplementary Figure 6B, http://links.lww.com/CM9/C291].

Discussion

In this retrospective cohort study, ideal CVH ratios in participants with renal insufficiency were <20% over 10 years. For each ICVHM increment, cardiovascular mortality risk in renal insufficiency populations decreased by >20%. Furthermore, when compared with individuals with normal renal function, increased ICVHMs mitigated adverse risks associated with renal impairment.

Evidence for a relationship between renal dysfunction and adverse cardiovascular events was first recognized in dialysis populations; approximately 50% of individuals with ESRD die from a cardiovascular event.[19,20] Many studies have reported that relationships between renal impairment and increased CVD morbidity and mortality extend across the renal insufficiency spectrum, including the mildest degrees of renal impairment.[21,22] However, approximately half of individuals with severely reduced renal function and most individuals with renal damage or mildly reduced renal function were unaware of having CKD—this situation leads to a lack of treatment and partly explains the severe adverse outcomes due to renal impairment.[23] Additionally, kidney disease usually degenerates over time, and in some patients, the disease progresses to kidney failure even with proper treatment.[23] Therefore, in addition to monitoring and treatment strategies, controllable risk prevention and intervention approaches are highly advantageous when managing individuals with renal insufficiency. A retrospective cohort study of 837 Chinese individuals reported that positive changes in ICVHMs exerted favorable effects on renal function.[24] However, few further trials investigating ideal CVH benefits in reducing poor prognoses during renal impairment have been conducted, especially in the field of cardiovascular. Our results suggest that individuals with renal insufficiency should continuously strive for ideal AHA CVH metrics to improve cardiovascular event outcomes. Furthermore, maintaining the highest possible CVH metric levels will generate the best outcomes; however, if more than one metric is suboptimal or trending badly, they do not all need to be addressed simultaneously as the AHA suggested.[11] Our study emphasized that individuals with renal insufficiency should maintain more healthy behaviors than healthy factors, and that improving health factors alone does not provide ideal benefits.

In 2020, the AHA released their 2030 Impact Goals, which was to achieve CVH for all.[25] However, in 2020, <1% of US adults had all ideal metric levels and only 13% had five metrics in the ideal range.[26] Recent studies also highlighted the need to focus on ICVHMs in specific groups.[14] In a renal insufficiency cohort, analyses indicated that only the ratios of ideal smoking status and glycated hemoglobin A1c are over 50%. Meanwhile, the prevalence of individual ICVHMs did not have a significant increasing tendency during our study period. Our data should encourage the AHA to meet the 2030 goals in their drive to achieve CVH for all and help renal insufficiency and other chronic disease advocacy groups refine CVH definitions and reduce the global CVD burden in the future. It is important to adopt this approach when formulating future public policies and implementing effective population-based prevention and management strategies.

Using newly updated CVH information, we analyzed cardiovascular risk factor profiles to ascertain the cardiovascular benefit of CVH in a population with renal insufficiency. Importantly, regardless of gender, age, and renal function severity, the cardiovascular benefits of ideal CVH were extremely high in renal insufficiency populations. Additionally, we observed that participants with mild renal insufficiency, who had a greater number of ICVHMs, appeared to have a lower risk of cardiovascular mortality risk, and this counteracted the adverse risk of renal impairment in patients with moderate to severe renal function insufficiency when compared with the overall population with normal renal function. Our study also had several limitations. Firstly, as a retrospective cohort study, robust causal inferences were difficult to establish. Secondly, individual CVH’s were self-reported and subjected to misclassification and recall bias and may have led to an over- or under-estimation of our results. Thirdly, when investigating whether ICVHMs could offset the risks posed by renal insufficiency, we did not consider the CVH status of the reference population. However, factoring in the CVH of the general population for analysis would be both complex and challenging. Finally, the competing risk of cardiovascular mortality was not accounted for in our models. Using NHANES and weighting, it was difficult to balance them at the same time, therefore, we performed all-cause mortality analyses to support cardiovascular mortality results.

In conclusion, with a redefined CVH, we observed that benefits, especially cardiovascular, increased with ICVHMs in all patients with renal insufficiency, and an increased number of ICVHMs counteracted renal impairment harm when compared with the normal population. Our observations showed that effective CVH interventions in populations with renal insufficiency may promote higher CVH levels, help formulate public health policies, and reduce the burden of cardiovascular illness in this population.

Acknowledgements

The authors thank the participants and staff of the NHANES database for their valuable contributions.

Funding

This work was partially supported by the Leading Talents Plan, Beijing Municipal Health Commission (No. LJRC20240306).

Conflicts of interest

None.

Supplementary Material

cm9-138-2824-s001.docx (976.6KB, docx)

Footnotes

How to cite this article: Chen WH, Xiao GT, Ding S, Shi SS, Pan YX, Tu JB, Zhang YB, Liao Y, Chen LL, Chen KH, Huang RC. Life’s Essential 8 metrics and prognosis in patients with renal insufficiency: Results from the National Health and Nutrition Examination Survey, 2007–2018. Chin Med J 2025;138:2824–2831. doi: 10.1097/CM9.0000000000003461

References

  • 1.Ortiz A Covic A Fliser D Fouque D Goldsmith D Kanbay M, et al. Epidemiology, contributors to, and clinical trials of mortality risk in chronic kidney failure. Lancet 2014;383:1831–1843. doi: 10.1016/s0140-6736(14)60384-6. [DOI] [PubMed] [Google Scholar]
  • 2.Rewa O, Bagshaw S. Acute kidney injury-epidemiology, outcomes and economics. Nat Rev Nephrol 2014;10:193–207. doi: 10.1038/nrneph.2013.282. [DOI] [PubMed] [Google Scholar]
  • 3.Wijayaratne D, Beligaswatta C, Harber M. Acute kidney injury epidemiology and causes. Primer Nephrol 2022;159:153–180. doi: 10.1007/978-3-030-76419-7_8. [Google Scholar]
  • 4.Lameire N Bagga A Cruz D De Maeseneer J Endre Z Kellum J, et al. Acute kidney injury: An increasing global concern. Lancet 2013;382:170–179. doi: 10.1016/s0140-6736(13)60647-9. [DOI] [PubMed] [Google Scholar]
  • 5.Kalantar-Zadeh K, Jafar T, Nitsch D, Neuen B, Perkovic V. Chronic kidney disease. Lancet 2021;398:786–802. doi: 10.1016/s0140-6736(21)00519-5. [DOI] [PubMed] [Google Scholar]
  • 6.Gansevoort R Correa-Rotter R Hemmelgarn B Jafar T Heerspink H Mann J, et al. Chronic kidney disease and cardiovascular risk: Epidemiology, mechanisms, and prevention. Lancet 2013;382:339–352. doi: 10.1016/s0140-6736(13)60595-4. [DOI] [PubMed] [Google Scholar]
  • 7.Levin A, Foley R. Cardiovascular disease in chronic renal insufficiency. Am J Kidney Dis 2000;36:S24–S30. doi: 10.1053/ajkd.2000.19928. [DOI] [PubMed] [Google Scholar]
  • 8.Hostetter T. Prevention of the development and progression of renal disease. J Am Soc Nephrol 2003;14:S144–S147. doi: 10.1097/01.asn.0000070150.60928.06. [DOI] [PubMed] [Google Scholar]
  • 9.Zoccali C. Traditional and emerging cardiovascular and renal risk factors: An epidemiologic perspective. Kidney Int 2006;70:26–33. doi: 10.1038/sj.ki.5000417. [DOI] [PubMed] [Google Scholar]
  • 10.Lloyd-Jones D Hong Y Labarthe D Mozaffarian D Appel L Van Horn L, et al. Defining and setting national goals for cardiovascular health promotion and disease reduction: The American Heart Association’s strategic Impact Goal through 2020 and beyond. Circulation 2010;121:586–613. doi: 10.1161/circulationaha.109.192703. [DOI] [PubMed] [Google Scholar]
  • 11.Lloyd-Jones D Allen N Anderson C Black T Brewer L Foraker R, et al. Life’s Essential 8: Updating and enhancing the American Heart Association’s construct of cardiovascular health: A presidential advisory From the American Heart Association. Circulation 2022;146:e18–e43. doi: 10.1161/cir.0000000000001078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Yang Q Cogswell ME Flanders WD Hong Y Zhang Z Loustalot F, et al. Trends in cardiovascular health metrics and associations with all-cause and CVD mortality among US adults. JAMA 2012;307:1273–1283. doi: 10.1001/jama.2012.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Han QL Wu SL Liu XX An SS Wu YT Gao JS, et al. Ideal cardiovascular health score and incident end-stage renal disease in a community-based longitudinal cohort study: The Kailuan Study. BMJ Open 2016;6:e012486. doi: 10.1136/bmjopen-2016-012486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Wang T Lu J Su Q Chen Y Bi Y Mu Y, et al. Ideal cardiovascular health metrics and major cardiovascular events in patients with prediabetes and diabetes. JAMA Cardiol 2019;4:874–883. doi: 10.1001/jamacardio.2019.2499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Matsushita K van der Velde M Astor B Woodward M Levey A de Jong P, et al. Association of estimated glomerular filtration rate and albuminuria with all-cause and cardiovascular mortality in general population cohorts: A collaborative meta-analysis. Lancet 2010;375:2073–2081. doi: 10.1016/s0140-6736(10)60674-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.van der Velde M Matsushita K Coresh J Astor BC Woodward M Levey A, et al. Lower estimated glomerular filtration rate and higher albuminuria are associated with all-cause and cardiovascular mortality. A collaborative meta-analysis of high-risk population cohorts. Kidney Int 2011;79:1341–1352. doi: 10.1038/ki.2010.536. [DOI] [PubMed] [Google Scholar]
  • 17.Levey AS Stevens LA Schmid CH Zhang YL Castro AF 3rd Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med 2009;150:604–612. doi: 10.7326/0003-4819-150-9-200905050-00006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Stevens PE Levin A, Kidney Disease: Improving Global Outcomes Chronic Kidney Disease Guideline Development Work Group Members . Evaluation and management of chronic kidney disease: Synopsis of the kidney disease: Improving global outcomes 2012 clinical practice guideline. Ann Intern Med 2013;158:825–830. doi: 10.7326/0003-4819-158-11-201306040-00007. [DOI] [PubMed] [Google Scholar]
  • 19.Tonelli M Wiebe N Culleton B House A Rabbat C Fok M, et al. Chronic kidney disease and mortality risk: A systematic review. J Am Soc Nephrol 2006;17:2034–2047. doi: 10.1681/asn.2005101085. [DOI] [PubMed] [Google Scholar]
  • 20.Schiffrin EL, Lipman ML, Mann JF. Chronic kidney disease: Effects on the cardiovascular system. Circulation 2007;116:85–97. doi: 10.1161/CIRCULATIONAHA.106.678342. [DOI] [PubMed] [Google Scholar]
  • 21.Coresh J, Astor B, Sarnak M. Evidence for increased cardiovascular disease risk in patients with chronic kidney disease. Curr Opin Nephrol Hypertens 2004;13:73–81. doi: 10.1097/00041552-200401000-00011. [DOI] [PubMed] [Google Scholar]
  • 22.Pinkau T, Hilgers K, Veelken R, Mann J. How does minor renal dysfunction influence cardiovascular risk and the management of cardiovascular disease? J Am Soc Nephrol 2004;15:517–523. doi: 10.1097/01.asn.0000107565.17553.71. [DOI] [PubMed] [Google Scholar]
  • 23.Stats F. National chronic kidney disease fact sheet, 2017. US Department of Health and Human Services, Centers for Disease Control and Prevention; Atlanta, GA: 2017. [Google Scholar]
  • 24.Wang Y, Yang P, Cao X, Wu L, Chen Z. Association between the changes in ideal cardiovascular health status and the decline of glomerular filtration rates in medical examination people (in Chinese). J Central South Univ (Med Sci) 2017;42:681–686. doi: 10.11817/j.issn.1672-7347.2017.06.014. [DOI] [PubMed] [Google Scholar]
  • 25.Angell SY McConnell MV Anderson CAM Bibbins-Domingo K Boyle DS Capewell S, et al. The American Heart Association 2030 impact goal: A presidential advisory from the American Heart Association. Circulation 2020;141:e120–e138. doi: 10.1161/cir.0000000000000758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Virani SS Alonso A Benjamin EJ Bittencourt MS Callaway CW Carson AP, et al. Heart disease and stroke statistics-2020 update: A report from the American Heart Association. Circulation 2020;141:e139–e596. doi: 10.1161/cir.0000000000000757. [DOI] [PubMed] [Google Scholar]

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