Cardiovascular Disease Risk Factor Control in People With and Without Human Immunodeficiency Virus

Author:

Silverberg Michael J1ORCID,Levine Tory M1,Lea Alexandra N1,Williams Andrew E2,Alexeeff Stacey E1,Bryant Kendall3,Cavassini Matthias4,Flamm Jason A5,Hare C Bradley6,Ingle Suzanne M7,Justice Amy C8,Lam Jennifer O1,Sterling Stacy A1,Horberg Michael A9,Satre Derek D110

Affiliation:

1. Division of Research, Kaiser Permanente Northern California , Oakland, California , USA

2. Institute for Clinical Research and Health Policy Studies, Tufts Medical Center , Boston, Massachusetts , USA

3. National Institute on Alcohol Abuse and Alcoholism , Bethesda, Maryland , USA

4. Lausanne University Hospital, University of Lausanne , Lausanne , Switzerland

5. Kaiser Permanente Sacramento Medical Center , Sacramento, California , USA

6. Kaiser Permanente SanFrancisco Medical Center , San Francisco, California , USA

7. Population Health Sciences, Bristol Medical School, University of Bristol , Bristol , United Kingdom

8. VA Connecticut Healthcare System, Yale University Schools of Medicine and Public Health , New Haven, Connecticut , USA

9. Kaiser Permanente Mid-Atlantic Permanente Research Institute , Rockville, Maryland , USA

10. Department of Psychiatry, Weill Institute for Neurosciences, University of California , SanFrancisco, California , USA

Abstract

Abstract Background Management of hypertension, dyslipidemia, diabetes and other modifiable factors may mitigate the cardiovascular disease (CVD) risk in people with human immunodeficiency virus (HIV, PWH) compared with people without HIV (PWoH). Methods This was a retrospective cohort study of 8285 PWH and 170 517 PWoH from an integrated health system. Risk factor control was measured using a novel disease management index (DMI) accounting for amount/duration above treatment goals (0% to 100% [perfect control]), including 2 DMIs for hypertension (diastolic and systolic blood pressure), 3 for dyslipidemia (low-density lipoprotein, total cholesterol, triglycerides), and 1 for diabetes (HbA1c). CVD risk by HIV status was evaluated overall and in subgroups defined by DMIs, smoking, alcohol use, and overweight/obesity in adjusted Cox proportional hazards models. Results PWH and PWoH had similar DMIs (80%–100%) except for triglycerides (worse for PWH) and HbA1c (better for PWH). In adjusted models, PWH had an elevated risk of CVD compared with PWoH (hazard ratio [HR], 1.18; 95% confidence interval [CI], 1.07–1.31). This association was attenuated in subgroups with controlled dyslipidemia and diabetes but remained elevated for PWH with controlled hypertension or higher total cholesterol. The strongest HIV status association with CVD was seen in the subgroup with frequent unhealthy alcohol use (HR, 2.13; 95% CI, 1.04–4.34). Conclusions Control of dyslipidemia and diabetes, but not hypertension, attenuated the HIV status association with CVD. The strong association of HIV and CVD with frequent unhealthy alcohol use suggests enhanced screening and treatment of alcohol problems in PWH is warranted.

Funder

National Institute on Alcohol Abuse and Alcoholism

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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