作者: Loo Keat Wei , Lyn R. Griffiths , Irene Looi , Cheah Wee Kooi , None
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摘要: Background and objectives: NOTCH3 gene variations play a significant role in cerebral autosomal dominant arteriopathy with subcortical infarcts leukoencephalopathy (CADASIL). However, the of polymorphisms risk ischemic stroke, its subtypes such as atherothrombotic or lacunar strokes, remains unclear. Aims: Hence, we carried out meta-analysis to examine whether rs1043994, rs1044009 rs3815188 are associated stroke major subtypes. Materials Methods: All relevant studies were systematically screened meta-analyzed using Review Manager (Revman) version 5.3. The strength association between measured odds ratios 95% confidence intervals, under different genetic models. Results: A total ten identified, five which considered rs1043994 (2077 cases/2147 controls), (2315 cases/3053 nine (2819 cases/2769 controls). These for their risk. Four (874 cases/2002 controls) polymorphism three (643 cases/1552 Three (1013 cases/1972 results showed lack all studied (i.e., lacunar). Conclusions: not significantly (p < 0.05).