Alpha 2-Macroglobulin Polymorphisms and Susceptibility to Alzheimer's Disease: A Comprehensive Meta-Analysis Based on 62 Studies.

IF 2.8 Q2 NEUROSCIENCES
Journal of Alzheimer's disease reports Pub Date : 2023-12-18 eCollection Date: 2023-01-01 DOI:10.3233/ADR-230131
Hongwei Zhang, Da Liu, Yuanyuan Duan, Yan Liu, Jianyu Liu, Na Bai, Qiang Zhou, Zhiyao Xu, Linyan Li, Hua Liu
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Abstract

Background: The relationship between alpha 2-macroglobulin (A2M) gene and Alzheimer's disease (AD) has been widely studied across populations; however, the results are inconsistent.

Objective: This study aimed to evaluate the association of A2M gene with AD by the application of meta-analysis.

Methods: Relevant studies were identified by comprehensive searches. The quality of each study was assessed using the Newcastle-Ottawa Scale. Allele and genotype frequencies were extracted from each of the included studies. Odds ratio (OR) with corresponding 95% confidence intervals (CI) was calculated using a random-effects or fixed-effects model. The Cochran Q statistic and I2 metric was used to evaluate heterogeneity, and Egger's test and Funnel plot were used to assess publication bias.

Results: A total of 62 studies were identified and included in the current meta-analysis. The G allele of rs226380 reduced AD risk (OR: 0.64, 95% CI: 0.47-0.87, pFDR = 0.012), but carrier with the TT genotype was more likely to develop AD in Asian populations (OR: 1.56, 95% CI: 1.12-2.19, pFDR = 0.0135). The V allele of the A2M-I/V (rs669) increased susceptibility to AD in female population (OR, 95% CI: 2.15, 1.38-3.35, pFDR = 0.0024); however, the II genotype could be a protective factor in these populations (OR, 95% CI: 0.43, 0.26-0.73, pFDR = 0.003). Sensitivity analyses confirmed the reliability of the original results.

Conclusions: Existing evidence indicate that A2M single nucleotide polymorphisms (SNPs) may be associated with AD risk in sub-populations. Future studies with larger sample sizes will be necessary to confirm the results.

α-2-巨球蛋白多态性与阿尔茨海默病的易感性:基于 62 项研究的综合元分析。
背景:α-2-巨球蛋白(A2M)基因与阿尔茨海默病(AD)的关系已在不同人群中被广泛研究,但结果并不一致:本研究旨在通过荟萃分析评估 A2M 基因与 AD 的关系:方法:通过全面检索确定相关研究。采用纽卡斯尔-渥太华量表评估每项研究的质量。从每项纳入的研究中提取等位基因和基因型频率。使用随机效应或固定效应模型计算患病率(OR)及相应的 95% 置信区间(CI)。Cochran Q 统计量和 I2 指标用于评估异质性,Egger 检验和 Funnel 图用于评估发表偏倚:结果:本次荟萃分析共确定并纳入了 62 项研究。rs226380的G等位基因可降低AD风险(OR:0.64,95% CI:0.47-0.87,pFDR = 0.012),但在亚洲人群中,TT基因型携带者更易患AD(OR:1.56,95% CI:1.12-2.19,pFDR = 0.0135)。A2M-I/V的V等位基因(rs669)增加了女性人群对AD的易感性(OR,95% CI:2.15,1.38-3.35,pFDR = 0.0024);然而,II基因型在这些人群中可能是一个保护因素(OR,95% CI:0.43,0.26-0.73,pFDR = 0.003)。敏感性分析证实了原始结果的可靠性:现有证据表明,A2M单核苷酸多态性(SNPs)可能与亚人群的AD风险有关。今后有必要进行样本量更大的研究,以确认研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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