Association of HIV Infection and Incident Abdominal Aortic Aneurysm Among 143 001 Veterans

Author:

Filipkowski Alexandra M.1,Kundu Suman2ORCID,Eden Svetlana K.3,Alcorn Charles W.4ORCID,Justice Amy C.56,So-Armah Kaku A.7,Tindle Hilary A.8,Wells Quinn S.2ORCID,Beckman Joshua A.2ORCID,Freiberg Matthew S.29ORCID,Aday Aaron W.2ORCID

Affiliation:

1. Mailman School of Public Health, Columbia University, New York, NY (A.M.F.).

2. Vanderbilt Translational and Clinical Cardiovascular Research Center, Division of Cardiovascular Medicine (S.K., Q.S.W., J.A.B., M.S.F., A.W.A.), Vanderbilt University Medical Center, Nashville, TN.

3. Department of Biostatistics (S.K.E.), Vanderbilt University Medical Center, Nashville, TN.

4. University of Pittsburgh School of Public Health, PA (C.W.A.).

5. Veterans Affairs Connecticut Healthcare System, West Haven (A.C.J.).

6. Department of Internal Medicine, Yale School of Medicine, West Haven, CT (A.C.J.).

7. Division of General Internal Medicine, Boston University School of Medicine, MA (K.A.S.-A.).

8. Department of Medicine (H.A.T.), Vanderbilt University Medical Center, Nashville, TN.

9. Veterans Affairs Tennessee Valley Healthcare System, Nashville (M.S.F.).

Abstract

Background: People with HIV (PWH) have an increased risk of cardiovascular disease. Previous cross-sectional data suggest there is a higher prevalence of abdominal aortic aneurysm (AAA) in PWH than in those without HIV. Whether PWH have an increased risk of incident AAA compared with those without HIV is unknown. Methods: We analyzed data among participants without prevalent AAA from the Veterans Aging Cohort Study, a prospective, observational, longitudinal cohort of veterans with HIV matched 1:2 with veterans without HIV infection. We calculated AAA rates by HIV status and assessed the association between HIV infection and incident AAA using Cox proportional hazards models. We defined AAA using the International Classification of Diseases, 9th or 10th revision, or Current Procedural Terminology codes and adjusted all models for demographic characteristics, cardiovascular disease risk factors, and substance use. Secondary analyses examined the association between time-varying CD4+ T-cell count or HIV viral load and incident AAA. Results: Among 143 001 participants (43 766 with HIV), over a median follow-up of 8.7 years, there were 2431 incident AAA events (26.4% among PWH). Rates of incident AAA per 1000 person-years were similar among PWH (2.0 [95% CI, 1.9–2.2]) and people without HIV (2.2 [95% CI, 2.1–2.3]). There was no evidence that HIV infection increased the risk of incident AAA compared with no HIV infection (adjusted hazard ratio, 1.02 [95% CI, 0.92–1.13]). In adjusted analyses with time-varying CD4+ T-cell counts or HIV viral load, PWH with CD4+ T-cell counts <200 cells/mm 3 (adjusted hazard ratio, 1.29 [95% CI, 1.02–1.65]) or HIV viral load ≥500 copies/mL (adjusted hazard ratio, 1.29 [95% CI, 1.09–1.52]) had an increased risk of AAA compared with those without HIV. Conclusions: HIV infection is associated with an increased risk of AAA among those with low CD4+ T-cell counts or elevated HIV viral load over time.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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