Dong Xiaoliu, Zhang Li, Meng Qingling, Gao Qiuyan
Department of Neurology, Tangshan People's Hospital, Tangshan, 063000, China.
Department of Neurosurgery, Tangshan People's Hospital, Tangshan, 063000, China.
Mol Neurobiol. 2017 Jan;54(1):736-747. doi: 10.1007/s12035-015-9683-3. Epub 2016 Jan 15.
Alzheimer's disease (AD) has been one of the most prevalent health problems among senior population. Interleukin-1A (IL-1A) and IL-1B are two isoforms of IL-1. Recent studies suggested that certain polymorphisms on these two genes are associated with AD. Bridging integrator 1 (BIN1) is considered as common genetic risk factors for AD, whereas different studies have provided various conclusions regarding its role in AD. This study was designed to justify the association between multiple gene polymorphisms and AD through an evidence synthesis approach. We conducted a literature search to identify relevant articles published from 2000 to 2015 from PubMed, Embase, and Cochrane Library, in accordance with inclusion criteria. Pooled odds ratios (ORs) were calculated for the allele model. The effect estimates were summarized by both standard and cumulative meta-analysis. Finally, 54 articles with 88 independent studies were enrolled in this meta-analysis. Mutants in rs1800587 of IL-1A, rs1143634 of IL-1B, rs12989701, and rs744373 of BIN1 were significantly associated with AD onset. The difference effect of same single nucleotide polymorphisms (SNPs) on various ethnicities was also observed in our results. The present meta-analysis suggested that IL-1A, IL-1B, and BIN1 were candidate genes for AD pathogenesis. Polymorphisms of IL-1A, IL-1B, and BIN1 are associated with AD onset.
阿尔茨海默病(AD)一直是老年人群中最普遍的健康问题之一。白细胞介素-1A(IL-1A)和白细胞介素-1B(IL-1B)是白细胞介素-1(IL-1)的两种亚型。最近的研究表明,这两个基因上的某些多态性与AD相关。桥连整合器1(BIN1)被认为是AD常见的遗传风险因素,然而不同的研究对其在AD中的作用得出了各种不同结论。本研究旨在通过证据综合方法来验证多个基因多态性与AD之间的关联。我们按照纳入标准,在PubMed、Embase和Cochrane图书馆中进行文献检索,以识别2000年至2015年发表的相关文章。计算等位基因模型的合并比值比(OR)。效应估计通过标准和累积荟萃分析进行总结。最后,本荟萃分析纳入了54篇文章中的88项独立研究。IL-1A的rs1800587、IL-1B的rs1143634、BIN1的rs12989701和rs744373中的突变与AD发病显著相关。我们的结果还观察到相同单核苷酸多态性(SNP)在不同种族中的差异效应。本荟萃分析表明,IL-1A、IL-1B和BIN1是AD发病机制的候选基因。IL-1A、IL-1B和BIN1的多态性与AD发病相关。