Risk of Myocardial Infarction and Abacavir Therapy: No Increased Risk Across 52 GlaxoSmithKline-Sponsored Clinical Trials in Adult Subjects

被引:128
作者
Brothers, Cindy H. [1 ]
Hernandez, Jaime E. [1 ]
Cutrell, Amy G. [2 ]
Curtis, Lloyd [3 ]
Ait-Khaled, Mounir [4 ]
Bowlin, Steve J. [5 ]
Hughes, Sara H. [6 ]
Yeo, Jane M. [4 ]
Lapierre, Didier H. [4 ]
机构
[1] GlaxoSmithKline Infect Dis Med Dev Ctr, Res Triangle Pk, NC USA
[2] GlaxoSmithKline Infect Dis Med Dev Ctr Biometr, Res Triangle Pk, NC USA
[3] GlaxoSmithKline Global Clin Safety & Pharmacovigi, Middlesex, England
[4] GlaxoSmithKline Infect Dis Med Dev Ctr, Middlesex, England
[5] GlaxoSmithKline Worldwide Epidemiol, Upper Providence, PA USA
[6] GlaxoSmithKline Infect Dis Med Dev Ctr Biometr, Middlesex, England
关键词
abacavir; coronary artery disease; myocardial infarction; ANTIRETROVIRAL THERAPY; PROTEASE INHIBITORS; NUCLEOSIDE ANALOG; HIV-INFECTION; AIDS; COMBINATION; REGIMENS; POTENT; EUROPE; DEATH;
D O I
10.1097/QAI.0b013e31819ff0e6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Recently, the Data collection of Adverse events of Anti-HIV Drugs Group (D:A:D) described results from their international observational cohort of 33,347 HIV-1-infected individuals, Suggesting unexpected increased risk of myocardial infarction (MI) associated with abacavir (ABC) therapy [relative rate 1.9, 95% confidence interval (CI): 1.47 to 2.45; P = 0.0001]. To contribute to the scientific question, we summarized GlaxoSmithKline HIV clinical trial data to determine if a similar signal emerged. Methods: We compiled data from GlaxoSmithKline-sponsored clinical trials with >= 24 weeks of combination antiretroviral therapy comprising 14,174 HIV-infected adults who received ABC (n = 9502; 7641 person-years) or not (n = 4672; 4267 person-years). Findings: Baseline demographics and HIV disease characteristics, including lipids and glucose values, were similar. MI rates were comparable among Subjects exposed [n = 16 (0.168%; CI: 0.096 to 0.273; 2.09 per 1000 person-years)] or not [n = 11 (0.235%; CI: 0.118 to 0.421; 2.57 per 1000 person-years)] to ABC-containing therapy. Results of 12 trials with randomization to ABC or not were consistent (2.15 per 1000 person-years vs. 4.10 per 1000 person-years). Interpretations: In this pooled summary, we observed few MI events overall and no excess risk of MI with ABC therapy. It is unclear why results from this data set seem discrepant to the Data collection of Adverse events of Anti-MV Drugs data set, particularly, as the non-ABC MI event rate is similar. Further data are needed to evaluate any association between ABC and increased risk of MI.
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页码:20 / 28
页数:9
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