Liu Shengyuan, Zeng Fangfang, Wang Changyi, Chen Zhongwei, Zhao Bin, Li Keshen
Guangdong Key Laboratory of Age-Related Cardiac and Cerebral Diseases, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, China.
Department of Chronic Disease, Shenzhen Nanshan Center for Chronic Disease Control, Shenzhen 518054, China.
Sci Rep. 2015 Sep 4;5:13598. doi: 10.1038/srep13598.
The association between the G894T polymorphism (Glu298Asp) of nitric oxide synthase 3 (NOS3) and risk of Alzheimer's disease (AD) was explored by performing a meta-analysis of case-control studies. Bibliographical searches were conducted in the MEDLINE, EMBASE, and China National Knowledge Infrastructure (CNKI) databases without any language limitations. Two investigators independently assessed abstracts for relevant studies, and reviewed all eligible studies. We adopted regrouping in accordance with the most probably appropriate genetic model. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of this association. We performed a meta-analysis including 21 published articles with 23 case-control studies (5,670 cases and 5,046 controls). In the analyses, we found significant association between G894T polymorphism and AD risk under a complete overdominant model (GG + TT vs. GT) (OR = 1.18; 95%CI, 1.04-1.35; P = 0.010). When stratified by time of AD onset, we found the association between this polymorphism and AD susceptibility to be more substantial among late onset patients than among early onset patients (OR for late vs. early onset: 1.33 vs. 1.02, P interaction = 0.049). The meta-analysis showed that the polymorphism G894T of NOS3 was associated with risk of AD.
通过对病例对照研究进行荟萃分析,探讨一氧化氮合酶3(NOS3)的G894T多态性(Glu298Asp)与阿尔茨海默病(AD)风险之间的关联。在MEDLINE、EMBASE和中国知网(CNKI)数据库中进行文献检索,无任何语言限制。两名研究者独立评估相关研究的摘要,并对所有符合条件的研究进行审查。我们根据最可能合适的遗传模型进行重新分组。采用比值比(OR)和95%置信区间(CI)来评估这种关联的强度。我们进行了一项荟萃分析,纳入了21篇已发表文章中的23项病例对照研究(5670例病例和5046例对照)。在分析中,我们发现在完全显性模型(GG + TT与GT)下,G894T多态性与AD风险之间存在显著关联(OR = 1.18;95%CI,1.04 - 1.35;P = 0.010)。按AD发病时间分层时,我们发现这种多态性与AD易感性之间的关联在晚发型患者中比早发型患者中更显著(晚发型与早发型的OR:1.33对1.02,P交互作用 = 0.049)。荟萃分析表明,NOS3的G894T多态性与AD风险相关。