Cardiovascular Risk Estimation Is Suboptimal in People With HIV

Author:

Triant Virginia A.1234ORCID,Lyass Asya5ORCID,Hurley Leo B.6,Borowsky Leila H.1ORCID,Ehrbar Rachel Q.7ORCID,He Wei1,Cheng David84ORCID,Lo Janet94ORCID,Klein Daniel B.6ORCID,Meigs James B.14ORCID,Grinspoon Steven K.94,Plutzky Jorge104ORCID,Silverberg Michael J.6,LaValley Michael7ORCID,Massaro Joseph M.7,D'Agostino Ralph B.5

Affiliation:

1. Division of General Internal Medicine Massachusetts General Hospital Boston MA

2. Division of Infectious Diseases Massachusetts General Hospital Boston MA

3. Mongan Institute, Massachusetts General Hospital Boston MA

4. Harvard Medical School Boston MA

5. Department of Mathematics and Statistics Boston University Boston MA

6. Kaiser Permanente Northern California Oakland CA

7. Department of Biostatistics Boston University School of Public Health Boston MA

8. Biostatistics Center, Massachusetts General Hospital Boston MA

9. Metabolism Unit, Massachusetts General Hospital Boston MA

10. Division of Cardiovascular Medicine Brigham and Women’s Hospital Boston MA

Abstract

Background Established cardiovascular disease (CVD) risk prediction functions may not accurately predict CVD risk in people with HIV. We assessed the performance of 3 CVD risk prediction functions in 2 HIV cohorts. Methods and Results CVD risk scores were calculated in the Mass General Brigham and Kaiser Permanente Northern California HIV cohorts, using the American College of Cardiology/American Heart Association atherosclerotic CVD function, the FHS (Framingham Heart Study) hard coronary heart disease function and the Framingham Heart Study hard CVD function. Outcomes were myocardial infarction or coronary death for FHS hard coronary heart disease function; and myocardial infarction, stroke, or coronary death for American College of Cardiology/American Heart Association and FHS hard CVD function. We calculated regression coefficients and assessed discrimination and calibration by sex; predicted to observed risk of outcome was also compared. In the combined cohort of 9412, 158 (1.7%) had a coronary heart disease event, and 309 (3.3%) had a CVD event. Among women, CVD risk was generally underestimated by all 3 risk functions. Among men, CVD risk was underestimated by the American College of Cardiology/American Heart Association and FHS hard CVD function, but overestimated by the FHS hard coronary heart disease function. Calibration was poor for women using the FHS hard CVD function and for men using all functions. Discrimination in all functions was good for women (c‐statistics ranging from 0.78 to 0.90) and moderate for men (c‐statistics ranging from 0.71 to 0.72). Conclusions Established CVD risk prediction functions generally underestimate risk in people with HIV. Differences in model performance by sex underscore the need for both HIV‐specific and sex‐specific functions. Development of CVD risk prediction models tailored to HIV will enhance care for aging people with HIV.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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