Risk of adverse cardiovascular outcomes among people with HIV and nonalcoholic fatty liver disease

Author:

Krishnan Arunkumar1,Sims Omar T.23,Surapaneni Phani Keerthi4,Woreta Tinsay A.5,Alqahtani Saleh A.56

Affiliation:

1. Section of Gastroenterology and Hepatology, West Virginia University School of Medicine, Morgantown, West Virginia

2. Department of Gastroenterology, Hepatology and Nutrition

3. Department of Quantitative Health Sciences, Cleveland Clinic Foundation, Cleveland, Ohio

4. Section of Nutrition and Metabolic Diseases, Department of Internal Medicine, West Virginia University School of Medicine, Morgantown, West Virginia

5. Division of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

6. Liver Transplant Center, King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.

Abstract

Objective: To examine and compare the risk of major adverse cardiovascular events (MACEs) between people with HIV (PWH) with and without nonalcoholic fatty liver disease (NAFLD). Design: Population-based, multicenter, retrospective cohort study. Methods: Data on PWH between January 1, 2008, and December 31, 2020 were extracted from the TriNetX database. Primary outcomes were defined as the first incidence of myocardial infarction (MI), MACE, new-onset heart failure (HF), and a composite of cerebrovascular disease. Cox models were used to obtain hazard ratios (HRs) and 95% confidence intervals (CIs). Results: A total of 151 868 patients were identified as having HIV. After exclusions, 4969 patients were identified as having NAFLD. Of them, 4463 (90%) were propensity matched to a non-NAFLD control. Patients with NAFLD were older (42.9 versus 40.8 years). Among the NAFLD cohort, most participants were male and had a smoking history (12.3 versus 9.8%) than non-NAFLD. The mean follow-up was 4.8 ± 1.1 years for the NAFLD group and 5.3 ± 1.2 years for the non-NAFLD group. The risk of all outcomes was statistically significantly higher in NAFLD patients compared to those without NAFLD: MI (HR, 1.49; 95% CI, 1.11–2.01) MACE (HR, 1.49; 95% CI, 1.25–1.79), HF (HR, 1.73; 95% CI 1.37–2.19) and, cerebrovascular diseases (HR, 1.25; 95% CI, 1.05–1.48) and sensitivity analysis showed similar magnitude to the one generated in the primary analysis. Conclusions: Patients with NAFLD have an elevated risk of adverse cardiovascular events (CVEs). The results indicate the need for targeted efforts to improve awareness of risks factors associated with adverse CVEs risk in PWH with NAFLD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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