Evaluating the Cardiovascular Risk in an Aging Population of People With HIV: The Impact of Hepatitis C Virus Coinfection

Author:

Lang Raynell12ORCID,Humes Elizabeth2ORCID,Hogan Brenna2,Lee Jennifer2,D'Agostino Ralph3,Massaro Joseph4,Kim Arthur56ORCID,Meigs James B.67ORCID,Borowsky Leila7ORCID,He Wei7,Lyass Asya3,Cheng David8,Kim H. Nina9,Klein Marina B.10,Cachay Edward R.11ORCID,Bosch Ronald J.12,Gill M. John1,Silverberg Michael J.13,Thorne Jennifer E.14,McGinnis Kathleen15,Horberg Michael A.16,Sterling Timothy R.17,Triant Virginia A.57,Althoff Keri N.2ORCID

Affiliation:

1. Department of Medicine University of Calgary Calgary Alberta Canada

2. Department of Epidemiology Johns Hopkins Bloomberg School of Public Health Baltimore MD

3. Department of Mathematics and Statistics Boston University Boston MA

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

5. Division of Infectious Diseases Massachusetts General Hospital Boston MA

6. Harvard Medical School Boston MA

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

8. Biostatistics Center Massachusetts General Hospital Boston MA

9. University of Washington Seattle WA

10. McGill University Health Centre Montreal QC Canada

11. Department of Medicine, Division of Infectious Diseases and Global Public Health University of California San Diego CA

12. Harvard T.H. Chan School of Public Health Boston MA

13. Kaiser Permanente Northern California Oakland CA

14. Johns Hopkins University School of Medicine Baltimore MD

15. Veterans Affairs Connecticut Healthcare System West Haven CT

16. Kaiser Permanente Mid‐Atlantic States Rockville MD

17. Vanderbilt University School of Medicine Nashville TN

Abstract

Background People with HIV (PWH) are at an increased risk of cardiovascular disease (CVD) with an unknown added impact of hepatitis C virus (HCV) coinfection. We aimed to identify whether HCV coinfection increases the risk of type 1 myocardial infarction (T1MI) and if the risk differs by age. Methods and Results We used data from NA‐ACCORD (North American AIDS Cohort Collaboration on Research and Design) from January 1, 2000, to December 31, 2017, PWH (aged 40–79 years) who had initiated antiretroviral therapy. The primary outcome was an adjudicated T1MI event. Those who started direct‐acting HCV antivirals were censored at the time of initiation. Crude incidence rates per 1000 person‐years were calculated for T1MI by calendar time. Discrete time‐to‐event analyses with complementary log–log models were used to estimate adjusted hazard ratios and 95% CIs for T1MI among those with and without HCV. Among 23 361 PWH, 4677 (20%) had HCV. There were 89 (1.9%) T1MIs among PWH with HCV and 314 (1.7%) among PWH without HCV. HCV was not associated with increased T1MI risk in PWH (adjusted hazard ratio, 0.98 [95% CI, 0.74–1.30]). However, the risk of T1MI increased with age and was amplified in those with HCV (adjusted hazard ratio per 10‐year increase in age, 1.85 [95% CI, 1.38–2.48]) compared with those without HCV (adjusted hazard ratio per 10‐year increase in age,1.30 [95% CI, 1.13–1.50]; P <0.001, test of interaction). Conclusions HCV coinfection was not significantly associated with increased T1MI risk; however, the risk of T1MI with increasing age was greater in those with HCV compared with those without, and HCV status should be considered when assessing CVD risk in aging PWH.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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