Incidence of non-AIDS defining comorbidities among young adults with perinatally acquired HIV in North America

Author:

Haw Nel Jason L.1,Lesko Catherine R.1,Ng Derek K.1,Lam Jennifer2,Lang Raynell3,Kitahata Mari M.4,Crane Heidi4,Eron Joseph5,Gill M. John36,Horberg Michael A.7,Karris Maile8,Loutfy Mona910,McGinnis Kathleen A.11,Moore Richard D.12,Althoff Keri1,Agwu Allison1213

Affiliation:

1. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland

2. Division of Research, Kaiser Permanente, Oakland, California, USA

3. Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

4. Department of Medicine, University of Washington School of Medicine, Seattle, Washington

5. Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA

6. Southern Alberta Clinic, Calgary, Alberta, Canada

7. Kaiser Permanente Mid-Atlantic Permanente Research Institute, Rockville, Maryland

8. Department of Medicine, University of California, San Diego, San Diego, California, USA

9. Department of Medicine, University of Toronto

10. Maple Leaf Medical Clinic, Toronto, Ontario, Canada

11. Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut

12. Department of Medicine

13. Department of Pediatrics, Johns Hopkins Medicine, Baltimore, Maryland, USA.

Abstract

Objective: The aim of this study is to describe the incidence of diabetes mellitus type 2 (T2DM), hypercholesterolemia, hypertriglyceridemia, hypertension, and chronic kidney disease (CKD) from 2000 to 2019 among North American adults with perinatally acquired HIV (PHIV) aged 18–30 years. Design: Description of outcomes based on electronic health records for a cohort of 375 young adults with PHIV enrolled in routine HIV care at clinics contributing data to the North American AIDS Cohort Collaboration on Research and Design (NA-ACCORD). Methods: We estimated overall, sex, and race-stratified cumulative incidences using Turnbull estimation, and incidence rates using quasi-Poisson regression. T2DM was defined as glycosylated hemoglobin more than 6.5% or based on clinical diagnosis and medication use. Hypercholesterolemia was based on medication use or total cholesterol at least 200 mg/dl. Hypertriglyceridemia was based on medication use or fasting triglyceride at least 150 mg/dl or nonfasting at least 200 mg/dl. Hypertension was based on clinical diagnosis. CKD was defined as estimated glomerular filtration rates less than 90 ml/mi|1.73 m2 for at least 3 months. Results: Cumulative incidence by age 30 and incidence rates from age 18 to 30 (per 100 person-years) were T2DM: 19%, 2.9; hypercholesterolemia: 40%, 4.6; hypertriglyceridemia: 50%, 5.6; hypertension: 22%, 2.0; and CKD: 25%, 3.3. Non-Black women had the highest incidence of hypercholesterolemia and hypertriglyceridemia, Black adults had the highest hypertension incidence, and Black men had the highest CKD incidence. Conclusion: There was a high incidence of five chronic comorbidities among people with PHIV. Earlier screening at younger ages might be considered for this unique population to strengthen prevention strategies and initiate treatment in a timely way.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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