Association between the ACE I/D polymorphism and risk of ischemic stroke: An updated meta-analysis of 47,026 subjects from 105 case–control studies

Abstract Background The association between the angiotensin-converting enzyme insertion/deletion ( ACE I/D) polymorphism and risk of ischemic stroke (IS) remains controversial and ambiguous. To clarify this association, a large meta-analysis was performed. Methods Electronic databases in both Englis...

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Veröffentlicht in:Journal of the neurological sciences 2014-10, Vol.345 (1), p.37-47
Hauptverfasser: Zhao, Jiangyang, Qin, Xue, Li, Shan, Zeng, Zhiyu
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Sprache:eng
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Zusammenfassung:Abstract Background The association between the angiotensin-converting enzyme insertion/deletion ( ACE I/D) polymorphism and risk of ischemic stroke (IS) remains controversial and ambiguous. To clarify this association, a large meta-analysis was performed. Methods Electronic databases in both English and Chinese were used to identify relevant studies (updated in February 2014). Odds ratios (ORs) and 95% confidence intervals (95% CIs) were used to describe the strength of the association. Results One hundred and fifty eligible studies, including 18,258 IS cases and 28,768 controls, were identified. Meta-analysis of these studies pointed to a significant association between the ACE I/D polymorphism and IS risk: (D vs. I: OR = 1.354, 95% CI = 1.272–1.440, P < 0.001; DD vs. II: OR = 1.755, 95% CI = 1.561–1.973, P < 0.001; ID vs. II: OR = 1.178, 95% CI = 1.098–1.263, P < 0.001; DD vs. ID/II: OR = 1.535, 95% CI = 1.399–1.684, P < 0.001; DD/ID vs. II: OR = 1.353, 95% CI = 1.251–1.463, P < 0.001). Subgroup analysis revealed a significantly elevated risk among Asians, but with borderline statistical significance among Caucasians. Conclusion This meta-analysis indicated that the ACE I/D polymorphism may be a genetic susceptibility factor for IS, especially among Asians, but with borderline statistical significance for Caucasians. Further investigations are needed to validate our conclusions.
ISSN:0022-510X
1878-5883
DOI:10.1016/j.jns.2014.07.023