Atherosclerotic Cardiovascular Events in Patients Infected With Human Immunodeficiency Virus and Hepatitis C Virus
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Published on: September 11, 2019
Boun Kim Tan1,2,3, Mathieu Chalouni4, Dominique Salmon Ceron2,3
1Assistance Publique des Hôpitaux de Paris, Hôpitaux Universitaires Paris Centre, Department of Internal Medicine, Hôpital Cochin, Paris, France.
Insights
Patients with HIV and HCV coinfection face a high risk of atherosclerotic cardiovascular disease (ASCVD). Key factors include aging, prior CVD, cholesterol levels, statin use, and alcohol intake. Managing these can reduce ASCVD events.
Area of Science:
- Cardiology
- Infectious Diseases
- Epidemiology
Background:
- Patients coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) exhibit an elevated risk of cardiovascular disease (CVD).
- However, specific factors contributing to atherosclerotic cardiovascular disease (ASCVD) events in this population remain underexplored.
Purpose of the Study:
- To investigate the incidence of ASCVD events in HIV-HCV coinfected patients.
- To identify factors associated with ASCVD events in this cohort.
Main Methods:
- The study utilized data from the nationwide Agence Nationale de Recherches sur le Sida et les hépatites virales (ANRS) CO13 HEPAVIH cohort.
- Aalen-Johansen method estimated incidences of total, coronary/cerebral, and peripheral artery disease (PAD) ASCVD events.
- Cause-specific Cox proportional hazards models identified associated factors.
Main Results:
- The incidence rates per 1000 person-years were 6.98 for total ASCVD, 4.01 for coronary/cerebral ASCVD, and 3.17 for PAD ASCVD events.
- Independent predictors of total ASCVD included aging, prior CVD, high total cholesterol, low high-density lipoprotein cholesterol, statin use, and high alcohol intake.
- Undetectable baseline HIV RNA was associated with fewer coronary/cerebral events.
Conclusions:
- HIV-HCV coinfected individuals experience a substantial burden of ASCVD events.
- Traditional cardiovascular risk factors significantly influence ASCVD development in this group.
- Effective management strategies should focus on controlling cholesterol and maintaining undetectable HIV viral load to mitigate cardiovascular risk.
Background:
An increased risk of cardiovascular disease (CVD) was reported in patients coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV), without identifying factors associated with atherosclerotic CVD (ASCVD) events.
Methods:
HIV-HCV coinfected patients were enrolled in the Agence Nationale de Recherches sur le Sida et les hépatites virales (ANRS) CO13 HEPAVIH nationwide cohort. Primary outcome was total ASCVD events. Secondary outcomes were coronary and/or cerebral ASCVD events, and peripheral artery disease (PAD) ASCVD events. Incidences were estimated using the Aalen-Johansen method. Factors associated with ASCVD were identified using cause-specific Cox proportional hazards models.
Results:
At baseline, median age of the study population (N = 1213) was 45.4 (interquartile range [IQR] 42.1-49.0) years and 70.3% were men. After a median follow-up of 5.1 (IQR 3.9-7.0) years, the incidence was 6.98 (95% confidence interval [CI], 5.19-9.38) per 1000 person-years for total ASCVD events, 4.01 (2.78-6.00) for coronary and/or cerebral events, and 3.17 (2.05-4.92) for PAD ASCVD events. Aging (hazard ratio [HR] 1.06; 95% CI, 1.01-1.12), prior CVD (HR 8.48; 95% CI, 3.14-22.91), high total cholesterol (HR 1.43; 95% CI, 1.11-1.83), high-density lipoprotein cholesterol (HR 0.22; 95% CI, 0.08-0.63), statin use (HR 3.31; 95% CI, 1.31-8.38), and high alcohol intake (HR 3.18; 95% CI, 1.35-7.52) were independently associated with total ASCVD events, whereas undetectable baseline viral load (HR 0.41, 95% CI, 0.18-0.96) was associated with coronary and/or cerebral events.
Conclusions:
HIV-HCV coinfected patients experienced a high incidence of ASCVD events. Some traditional cardiovascular risk factors were the main determinants of ASCVD. Controlling cholesterol abnormalities and maintaining undetectable HIV RNA are essential to control cardiovascular risk.
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