The influence of gender on the effects of aspirin in preventing myocardial infarction

<p>Abstract</p> <p>Background</p> <p>There is considerable variation in the effect of aspirin therapy reducing the risk of myocardial infarction (MI). Gender could be a potential explanatory factor for the variability. We conducted a systematic review and meta-analysis...

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Main Authors: Sin Don D, Gan Wen Q, Yerman Todd
Format: Article
Language:English
Published: BMC 2007-10-01
Series:BMC Medicine
Online Access:http://www.biomedcentral.com/1741-7015/5/29
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spelling doaj-12b3a6b865df4a0bb2afd0dcb1854b962020-11-25T00:18:44ZengBMCBMC Medicine1741-70152007-10-01512910.1186/1741-7015-5-29The influence of gender on the effects of aspirin in preventing myocardial infarctionSin Don DGan Wen QYerman Todd<p>Abstract</p> <p>Background</p> <p>There is considerable variation in the effect of aspirin therapy reducing the risk of myocardial infarction (MI). Gender could be a potential explanatory factor for the variability. We conducted a systematic review and meta-analysis to determine whether gender mix might play a role in explaining the large variation of aspirin efficacy across primary and secondary MI prevention trials.</p> <p>Methods</p> <p>Randomized placebo-controlled clinical trials that examined the efficacy of aspirin therapy on MI were identified by using the PUBMED database (1966 to October 2006). Weighted linear regression technique was used to determine the relationship between log-transformed relative risk (RR) of MI and the percentage of male participants in each trial. The reciprocal of the standard error of the RR in each trial (1/SE) was used as the weight.</p> <p>Results</p> <p>A total of 23 trials (n = 113 494 participants) were identified. Overall, compared with placebo, aspirin reduced the risk of non-fatal MI (RR = 0.72, 95% confidence interval (CI) 0.64–0.81, p < 0.001) but not of fatal MI (RR = 0.88, 95% CI 0.75–1.03, p = 0.120). A total of 27% of the variation in the non-fatal MI results could be accounted for by considering the gender mix of the trials (p = 0.017). Trials that recruited predominantly men demonstrated the largest risk reduction in non-fatal MI (RR = 0.62, 95% CI 0.54–0.71), while trials that contained predominately women failed to demonstrate a significant risk reduction in non-fatal MI (RR = 0.87, 95% CI 0.71–1.06).</p> <p>Conclusion</p> <p>Gender accounts for a substantial proportion of the variability in the efficacy of aspirin in reducing MI rates across these trials, and supports the notion that women might be less responsive to aspirin than men.</p> http://www.biomedcentral.com/1741-7015/5/29
collection DOAJ
language English
format Article
sources DOAJ
author Sin Don D
Gan Wen Q
Yerman Todd
spellingShingle Sin Don D
Gan Wen Q
Yerman Todd
The influence of gender on the effects of aspirin in preventing myocardial infarction
BMC Medicine
author_facet Sin Don D
Gan Wen Q
Yerman Todd
author_sort Sin Don D
title The influence of gender on the effects of aspirin in preventing myocardial infarction
title_short The influence of gender on the effects of aspirin in preventing myocardial infarction
title_full The influence of gender on the effects of aspirin in preventing myocardial infarction
title_fullStr The influence of gender on the effects of aspirin in preventing myocardial infarction
title_full_unstemmed The influence of gender on the effects of aspirin in preventing myocardial infarction
title_sort influence of gender on the effects of aspirin in preventing myocardial infarction
publisher BMC
series BMC Medicine
issn 1741-7015
publishDate 2007-10-01
description <p>Abstract</p> <p>Background</p> <p>There is considerable variation in the effect of aspirin therapy reducing the risk of myocardial infarction (MI). Gender could be a potential explanatory factor for the variability. We conducted a systematic review and meta-analysis to determine whether gender mix might play a role in explaining the large variation of aspirin efficacy across primary and secondary MI prevention trials.</p> <p>Methods</p> <p>Randomized placebo-controlled clinical trials that examined the efficacy of aspirin therapy on MI were identified by using the PUBMED database (1966 to October 2006). Weighted linear regression technique was used to determine the relationship between log-transformed relative risk (RR) of MI and the percentage of male participants in each trial. The reciprocal of the standard error of the RR in each trial (1/SE) was used as the weight.</p> <p>Results</p> <p>A total of 23 trials (n = 113 494 participants) were identified. Overall, compared with placebo, aspirin reduced the risk of non-fatal MI (RR = 0.72, 95% confidence interval (CI) 0.64–0.81, p < 0.001) but not of fatal MI (RR = 0.88, 95% CI 0.75–1.03, p = 0.120). A total of 27% of the variation in the non-fatal MI results could be accounted for by considering the gender mix of the trials (p = 0.017). Trials that recruited predominantly men demonstrated the largest risk reduction in non-fatal MI (RR = 0.62, 95% CI 0.54–0.71), while trials that contained predominately women failed to demonstrate a significant risk reduction in non-fatal MI (RR = 0.87, 95% CI 0.71–1.06).</p> <p>Conclusion</p> <p>Gender accounts for a substantial proportion of the variability in the efficacy of aspirin in reducing MI rates across these trials, and supports the notion that women might be less responsive to aspirin than men.</p>
url http://www.biomedcentral.com/1741-7015/5/29
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