Genetic Polymorphisms and Clopidogrel Efficacy for Acute Ischemic Stroke or Transient Ischemic Attack: A Systematic Review and Meta-analysis

BACKGROUND—The association of genetic polymorphisms and clopidogrel efficacy in patients with ischemic stroke or transient ischemic attack (TIA) remains controversial. We performed a systematic review and meta-analysis to assess the association between genetic polymorphisms, especially CYP2C19 genot...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2017-01, Vol.135 (1), p.21-33
Hauptverfasser: Pan, Yuesong, Chen, Weiqi, Xu, Yun, Yi, Xingyang, Han, Yan, Yang, Qingwu, Li, Xin, Huang, Li’an, Johnston, S Claiborne, Zhao, Xingquan, Liu, Liping, Zhang, Qi, Wang, Guangyao, Wang, Yongjun, Wang, Yilong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:BACKGROUND—The association of genetic polymorphisms and clopidogrel efficacy in patients with ischemic stroke or transient ischemic attack (TIA) remains controversial. We performed a systematic review and meta-analysis to assess the association between genetic polymorphisms, especially CYP2C19 genotype, and clopidogrel efficacy for ischemic stroke or TIA. METHODS—We conducted a comprehensive search of the PubMed and EMBASE from their inceptions to June 24, 2016. Studies that reported clopidogrel-treated patients with stroke or TIA and with information on genetic polymorphisms were included. The endpoints were stroke, composite vascular events and any bleeding. RESULTS—Among 15 studies of 4,762 patients with stroke or TIA treated with clopidogrel, carriers of CYP2C19 loss-of-function alleles (*2, *3 and/or *8) were at increased risk of stroke compared with non-carriers (12.0% vs. 5.8%; risk ratio (RR)1.92, 95% confidence interval [CI]1.57-2.35; p
ISSN:0009-7322
1524-4539
DOI:10.1161/CIRCULATIONAHA.116.024913