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载脂蛋白 E 基因多态性与阿尔茨海默病的关联:一项更新的荟萃分析证据。

Association of PICALM Gene Polymorphisms with Alzheimer's Disease: Evidence from an Updated Meta-Analysis.

机构信息

Department of Epidemiology, School of Medicine, Jinan University, Guangzhou 510630, China.

Department of preventive medicine laboratory, School of Public Health, Zunyi Medical University, Zunyi, 563006, China.

出版信息

Curr Alzheimer Res. 2019;16(13):1196-1205. doi: 10.2174/1567205016666190805165607.

Abstract

BACKGROUND

Previous studies have examined the roles of three polymorphisms (rs3851179, rs541458, and rs592297) of the PICALM gene in susceptibility to Alzheimer's disease (AD) with inconclusive findings.

OBJECTIVE

We performed a meta-analysis to explore whether these three polymorphisms in the PICALM gene were associated with susceptibility to AD.

METHODS

Bibliographical searches were conducted in the PubMed, Embase, Web of Science, and China National Knowledge Infrastructure (CNKI) databases. Summary Odds Ratios (ORs) with 95% Confidence Intervals (CIs) were used to assess the strength of association in a random effects model. Potential sources of heterogeneity were identified by subgroup and meta-regression analyses.

RESULTS

Twenty studies (9,017 cases and 15,448 controls) on rs3851179, 12 studies (8,077 cases and 12,022 controls) on rs541458, and 4 studies (2,106 cases and 2,234 controls) on rs592297 were considered eligible for meta-analyses. For both rs3851179 and rs541458, the overall ORs were significant under all genetic models with mild heterogeneity. Compared with G carriers, A carriers of rs3851179 were associated with a decreased risk of AD (OR = 0.88; 95% CI 0.84, 0.91, P for Z-test <0.001, I2 = 0.0%). Compared with T carriers, C carriers of rs541458 were inversely associated with AD risk (OR = 0.86; 95% CI 0.81, 0.92, P for Z-test <0.001, I2 = 39.5%). No association was observed for rs592297. Subgroup and meta-regression analyses indicated that the protective effect of the rs541458 C allele was observed only among Caucasians, not among Asians (P for interaction: 0.021~<0.001).

CONCLUSION

rs3851179 and rs541458 appear to be associated with decreased AD risk. The null associations for rs592297 with AD risk need further confirmation with a larger number of participants.

摘要

背景

先前的研究已经探讨了 PICALM 基因的三个多态性(rs3851179、rs541458 和 rs592297)在阿尔茨海默病(AD)易感性中的作用,但结果并不一致。

目的

我们进行了一项荟萃分析,以探讨 PICALM 基因中的这三个多态性是否与 AD 的易感性有关。

方法

在 PubMed、Embase、Web of Science 和中国知网(CNKI)数据库中进行文献检索。使用随机效应模型,采用汇总优势比(ORs)及其 95%置信区间(CIs)来评估关联强度。通过亚组和荟萃回归分析确定异质性的潜在来源。

结果

共纳入了 20 项关于 rs3851179(9017 例病例和 15448 例对照)、12 项关于 rs541458(8077 例病例和 12022 例对照)和 4 项关于 rs592297(2106 例病例和 2234 例对照)的研究,适合进行荟萃分析。在所有遗传模型下,rs3851179 和 rs541458 的总体 OR 均具有统计学意义,但存在轻度异质性。与 G 携带者相比,rs3851179 的 A 携带者患 AD 的风险降低(OR=0.88;95%CI 0.84,0.91,Z 检验 P<0.001,I2=0.0%)。与 T 携带者相比,rs541458 的 C 携带者患 AD 的风险呈反向关联(OR=0.86;95%CI 0.81,0.92,Z 检验 P<0.001,I2=39.5%)。rs592297 与 AD 风险无关。亚组和荟萃回归分析表明,rs541458 的 C 等位基因的保护作用仅在白种人中观察到,而在亚洲人中则没有(交互作用 P 值:0.021~<0.001)。

结论

rs3851179 和 rs541458 似乎与 AD 风险降低有关。rs592297 与 AD 风险的关联需要进一步通过更大的参与者数量来确认。

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