@article{8bdef9f49c244450b164a727532dc3c4,
title = "Recent abacavir use increases risk of type 1 and type 2 myocardial infarctions among adults with HIV",
abstract = "Background: There is persistent confusion as to whether abacavir (ABC) increases the risk of myocardial infarction (MI), and whether such risk differs by type 1 (T1MI) or 2 (T2MI) MI in adults with HIV. Methods: Incident MIs in North American Cohort Collaboration on Research and Design participants were identified from 2001 to 2013. Discrete time marginal structural models addressed channeling biases and time-dependent confounding to estimate crude hazard ratio (HR) and adjusted hazard ratio (aHR) and 95% confidence intervals; analyses were performed for T1MI and T2MI separately. A sensitivity analysis evaluated whether Framingham risk score (FRS) modified the effect of ABC on MI occurrence. Results: Eight thousand two hundred sixty-five adults who initiated antiretroviral therapy contributed 29,077 person-years and 123 MI events (65 T1MI and 58 T2MI). Median follow-up time was 2.9 (interquartile range 1.4-5.1) years. ABC initiators were more likely to have a history of injection drug use, hepatitis C virus infection, hypertension, diabetes, impaired kidney function, hyperlipidemia, low (,200 cells/mm3) CD4 counts, and a history of AIDS. The risk of the combined MI outcome was greater for persons who used ABC in the previous 6 months [aHR = 1.84 (1.17-2.91)]; and persisted for T1MI (aHR = 1.62 [1.01]) and T2MI [aHR = 2.11 (1.08-4.29)]. FRS did not modify the effect of ABC on MI (P = 0.14) and inclusion of FRS in the MSM did not diminish the effect of recent ABC use on the combined outcome. Conclusions: Recent ABC use was associated with MI after adjustment for known risk factors and for FRS. However, screening for T1MI risks may not identify all or even most persons at risk of ABC use-associated MIs.",
keywords = "Abacavir, Causal inference, HIV, Myocardial infarction",
author = "Elion, {Richard A.} and Althoff, {Keri N.} and Jinbing Zhang and Moore, {Richard D.} and Gange, {Stephen J.} and Kitahata, {Mari M.} and Crane, {Heidi M.} and Drozd, {Daniel R.} and Stein, {James H.} and Klein, {Marina B.} and Eron, {Joseph J.} and Silverberg, {Michael J.} and Mathews, {William C.} and Justice, {Amy C.} and Sterling, {Timothy R.} and Rabkin, {Charles S.} and Mayor, {Angel M.} and Klein, {Daniel B.} and Horberg, {Michael A.} and Bosch, {Ronald J.} and Oghenowede Eyawo and Palella, {Frank J.}",
note = "Funding Information: The NA-ACCORD is the largest consortium of HIV cohorts in the United States and Canada. It serves as the North American region of the International Epidemiology Databases to Evaluate AIDS project, supported by the National Institutes of Health. Details on this collaboration have been published previously.24 Briefly, NA-ACCORD consists of single and multisite clinical and interval cohort studies that accumulate data from adults ($18 years old) with HIV at $200 sites in the United States and Canada. Participating cohorts submit comprehensive data on enrolled participants to the Data Management Core (University of Washington, Seattle, WA), where data are harmonized across cohorts and transmitted to the Epidemiology/Biostatistics Core (Johns Hopkins University, Baltimore, MD), which conducted the analyses presented here. The human subject research activities of the NA-ACCORD and each of the participating cohort studies have been reviewed and approved by their respective local institutional review boards and by the Johns Hopkins University School of Medicine. Funding Information: Supported by National Institutes of Health grants U01AI069918, F31DA037788, G12MD007583, K01AI093197, K23EY013707, K24AI065298, K24AI118591, K24DA000432, KL2TR000421, M01RR000052, N01CP01004, N02CP055504, N02CP91027, P30AI027757, P30AI027763, P30AI027767, P30AI036219, P30AI050410, P30AI094189, P30AI110527, P30MH62246, R01AA016893, R01CA165937, R01DA011602, R01DA012568, R01 AG053100, R24AI067039, U01AA013566, U01AA020790, U01AI031834, U01AI034989, U01AI034993, U01AI034994, U01AI035004, U01AI035039, U01AI035040, U01AI035041, U01AI035042, U01AI037613, U01AI037984, U01AI038855, U01AI038858, U01AI042590, U01AI068634, U01AI068636, U01AI069432, U01AI069434, U01AI103390, U01AI103397, U01AI103401, U01AI103408, U01DA03629, U01DA036935, U01HD032632, U10EY008057, U10EY008052, U10EY008067, U24AA020794, U54MD007587, UL1RR024131, UL1TR000004, UL1TR000083, UL1TR000454, UM1AI035043, Z01CP010214, and Z01CP010176; contracts CDC-200-2006-18797 and CDC-200-2015-63931 from the Centers for Disease Control and Prevention, USA; contract 90047713 from the Agency for Healthcare Research and Quality, USA; contract 90051652 from the Health Resources and Services Administration, USA; grants CBR-86906, CBR-94036, HCP-97105 and TGF-96118 from the Canadian Institutes of Health Research, Canada; Ontario Ministry of Health and Long Term Care; and the Government of Alberta, Canada. Additional support was provided by the National Cancer Institute, National Institute for Mental Health, and National Institute on Drug Abuse. Publisher Copyright: {\textcopyright} 2018 Wolters Kluwer Health, Inc.",
year = "2018",
doi = "10.1097/QAI.0000000000001642",
language = "English (US)",
volume = "78",
pages = "62--72",
journal = "Journal of Acquired Immune Deficiency Syndromes",
issn = "1525-4135",
publisher = "Lippincott Williams and Wilkins",
number = "1",
}