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Author Notes:

Correspondence: A. C. Justice, VA Connecticut Healthcare System, Yale University School of Medicine, 950 Campbell Ave, Bldg 35a Rm 2-212 (11-ACSLG), West Haven, CT 06516 (amy.justice2@va.gov)

All authors contributed to study design.

A. C. J., J. L. S., C. R., and J. T. contributed to data collection; J. L. S., C. R., V. C. M., J. T., A. C. J., and D. R. contributed to data quality and analysis; all authors contributed to manuscript development and have critically reviewed the manuscript and approved the final version.

We are grateful to the patients and clinical staff at the Veteran Affairs clinical sites that were part of the Veterans Aging Cohort Study.

Potential conflicts of interest: A. A. B. has received investigator-initiated research grants (to the institution, unrelated to current work) from Gilead Sciences and AbbVie.

All other authors report no potential conflicts.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.

Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

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Research Funding:

This work was supported by the following: Agency for Healthcare Research and Quality (R01-HS018372); National Institute on Alcohol Abuse and Alcoholism (U24-AA020794;, U01-AA020790;, U01-AA020795;, U01-AA020799;, U24-AA022001;, U24 AA022007;, U10 AA013566-completed); National Heart, Lung, and Blood Institute (R01-HL095136;, R01-HL090342); National Institute of Allergy and Infectious Diseases (U01-A1069918); Fogarty International Center (R25TW009337); National Institute of Mental Health (P30-MH062294); National Institute on Drug Abuse (R01DA035616); National Cancer Institute (R01 CA173754), Veterans Health Administration Office of Research and Development (VA REA 08-266, VA IRR Merit Award), and Office of Academic Affiliations (Medical Informatics Fellowship).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Infectious Diseases
  • Microbiology
  • acute myocardial infarction
  • HIV
  • mortality
  • VACS Index
  • VETERANS AGING COHORT
  • COMBINATION ANTIRETROVIRAL THERAPY
  • CARDIOVASCULAR-DISEASE
  • INFECTED PATIENTS
  • RISK-FACTORS
  • INDEX
  • IMMUNODEFICIENCY
  • HOSPITALIZATION
  • INDIVIDUALS
  • VIREMIA

Baseline, Time-Updated, and Cumulative HIV Care Metrics for Predicting Acute Myocardial Infarction and All-Cause Mortality

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Journal Title:

Clinical Infectious Diseases

Volume:

Volume 63, Number 11

Publisher:

, Pages 1423-1430

Type of Work:

Article | Final Publisher PDF

Abstract:

Background. After adjustment for cardiovascular risk factors and despite higher mortality, those with human immunodeficiency virus (HIV+) have a greater risk of acute myocardial infarction (AMI) than uninfected individuals. Methods. We included HIV+ individuals who started combination antiretroviral therapy (cART) in the Veterans Aging Cohort Study (VACS) from 1996 to 2012. We fit multivariable proportional hazards models for baseline, time-updated and cumulative measures of HIV-1 RNA, CD4 counts, and the VACS Index. We used the trapezoidal rule to build the following cumulative measures: viremia copy-years, CD4-years, and VACS Index score-years, captured 180 days after cART initiation until AMI, death, last clinic visit, or 30 September 2012. The primary outcomes were incident AMI (Medicaid, Medicare, and Veterans Affairs International Classification of Diseases-9 codes) and death. Results. A total of 8168 HIV+ individuals (53 861 person-years) were analyzed with 196 incident AMIs and 1710 deaths. Controlling for known cardiovascular risk factors, 6 of the 9 metrics predicted AMI and all metrics predicted mortality. Time-updated VACS Index had the lowest Akaike information criterion among all models for both outcomes. A time-updated VACS Index score of 55+ was associated with a hazard ratio (HR) of 3.31 (95% confidence interval [CI], 2.11-5.20) for AMI and a HR of 31.77 (95% CI, 26.17-38.57) for mortality. Conclusions. Time-updated VACS Index provided better AMI and mortality prediction than CD4 count and HIV-1 RNA, suggesting that current health determines risk more accurately than prior history and that risk assessment can be improved by biomarkers of organ injury.

Copyright information:

© The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. This work is written by (a) US Government employee(s) and is in the public domain in the US.

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