Genetic association of BIN1 and GAB2 in Alzheimer's disease: A meta-analysis and systematic review
| Autor: | Xiaoyan, Hao, Aijun, Wang, Chong, Li, Lufei, Shao, Yi, Li, Ping, Yang |
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| Rok vydání: | 2020 |
| Předmět: |
Tumor Suppressor Proteins
Nuclear Proteins Original Articles: Epidemiology Clinical Practice and Health Alzheimer's disease Polymorphism Single Nucleotide bridging integrator 1 White People GRB‐associated binding protein 2 Alzheimer Disease meta‐analysis Humans Genetic Predisposition to Disease Original Article linkage disequilibrium Adaptor Proteins Signal Transducing |
| Zdroj: | Geriatrics & Gerontology International |
| ISSN: | 1447-0594 |
| Popis: | Aim Heredity plays an important role in the pathogenesis of Alzheimer's disease (AD) especially for single‐nucleotide polymorphism (SNPs) of susceptible genes, which is one of the significant factors in the pathogenesis of AD. The SNPs of BIN1 rs744373, BIN1 rs7561528 and GAB2 rs2373115 are associated with AD in Asian and white people. Methods We included 34 studies with a total of 38 291 patients with AD and 55 538 controls of diverse races from four main databases. We used meta‐analysis to obtain I 2‐values and odds ratios of five genetic models in three SNPs. We carried out analysis of sensitivity, subgroup, publication bias and linkage disequilibrium test. Results The forest plots showed the odds ratio value of the three SNPs was >1 in white individuals, but not Asian individuals, in their genetic model. The funnel plot was symmetrical, and the D'‐value was 0.986 between rs744373 and rs7561528. Conclusions BIN1 rs744373, BIN1 rs7561528 and GAB2 rs2373115 are pathogenicity sites for AD in white people, and also rs7561528 belongs to a risk site in Asian people. The rs7561528 and rs744373 SNPs have strong linkage disequilibrium in Chinese people. In addition, apolipoprotein E ε4 status promotes them to result in the pathogenesis of AD. Geriatr Gerontol Int 2021; 21: 185–191. |
| Databáze: | OpenAIRE |
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