» Articles » PMID: 19282778

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

Overview
Date 2009 Mar 14
PMID 19282778
Citations 61
Authors
Affiliations
Soon will be listed here.
Abstract

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 > or = 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-HIV 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.

Citing Articles

Direct and indirect cardiovascular and cardiometabolic sequelae of the combined anti-retroviral therapy on people living with HIV.

Batta Y, King C, Cooper F, Johnson J, Haddad N, Boueri M Front Physiol. 2023; 14:1118653.

PMID: 37078025 PMC: 10107050. DOI: 10.3389/fphys.2023.1118653.


Abacavir antiretroviral therapy and indices of subclinical vascular disease in persons with HIV.

Martinez C, Rikhi R, Pester M, Parker M, Gonzalez A, Larson M PLoS One. 2022; 17(3):e0264445.

PMID: 35271614 PMC: 8912137. DOI: 10.1371/journal.pone.0264445.


Relationship between Endothelial Function, Antiretroviral Treatment and Cardiovascular Risk Factors in HIV Patients of African Descent in South Africa: A Cross-Sectional Study.

Nkeh-Chungag B, Goswami N, Engwa G, Sewani-Rusike C, Mbombela V, Webster I J Clin Med. 2021; 10(3).

PMID: 33498530 PMC: 7864186. DOI: 10.3390/jcm10030392.


Do Combination Antiretroviral Therapy Regimens for HIV Infection Feature Diverse T-Cell Phenotypes and Inflammatory Profiles?.

Tincati C, Mondatore D, Bai F, Monforte A, Marchetti G Open Forum Infect Dis. 2020; 7(9):ofaa340.

PMID: 33005694 PMC: 7513927. DOI: 10.1093/ofid/ofaa340.


Cardiovascular disease among people living with HIV in Brazil.

Boettiger D, Escuder M, Law M, Veloso V, Souza R, Ikeda M Trop Med Int Health. 2020; 25(7):886-896.

PMID: 32306480 PMC: 7547667. DOI: 10.1111/tmi.13405.