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雌激素受体β(ESR2)基因多态性与痴呆易感性。

Estrogen receptor beta (ESR2) gene polymorphism and susceptibility to dementia.

机构信息

Department of Biomedical Science, Faculty of Medicine and Health Sciences, Maulana Malik Ibrahim Islamic State University of Malang, Batu, East Java, 65151, Indonesia.

Department of General Surgery, Weston General Hospital, Grange Rd, Weston-super-Mare, BS23 4QT, UK.

出版信息

Acta Neurol Belg. 2021 Oct;121(5):1281-1293. doi: 10.1007/s13760-020-01360-z. Epub 2020 Apr 25.

Abstract

Strong evidence supports the involvement of sex steroid hormones in the development and progression of dementia. Attention has been largely focused on the association between genetic variants of estrogen receptor alpha (ERα, ESR1) with dementia, although several studies indicate that ERβ is predominantly expressed in the brain. Interestingly, however, a limited number of studies evaluate the role of ERβ (ESR2) in dementia. Therefore, a meta-analysis was conducted to clarify the association between ESR2 genetic polymorphisms and the risk of dementia. All the relevant studies evaluating ESR2 genetic polymorphisms and dementia were identified through online databases. In total, 14 studies including 20,609 subjects were analyzed. Collectively, it was found that a combined data set of ESR2 polymorphisms was not associated with dementia risk. Interestingly, ESR2 rs4986938 polymorphism is significantly associated with dementia in the Asian population (OR = 0.73, 95% CI 0.59-0.91, P = 0.006). The carrier of A allele in rs4986938 exhibits a protective effect against dementia (A vs. G, OR = 0.6633, P = 0.012; AA + GA vs. GG, OR = 0.6499, P = 0.014; GA vs. AA + GG, OR = 0.6672, P = 0.025; GA vs. GG, OR = 0.6617, P = 0.022). In conclusion, our study suggests that ESR2 genetic polymorphisms are not significantly associated with dementia risk. ESR2 rs4986938 may have potential as a genetic marker for dementia in the Asian population. However, further studies need to verify this conclusion.

摘要

大量证据支持性激素在痴呆的发生和发展中起作用。研究主要集中在雌激素受体 alpha(ERα,ESR1)的遗传变异与痴呆之间的关联上,尽管有几项研究表明 ERβ在大脑中表达更为丰富。然而,有趣的是,只有少数研究评估了 ERβ(ESR2)在痴呆中的作用。因此,进行了荟萃分析以阐明 ESR2 遗传多态性与痴呆风险之间的关系。通过在线数据库确定了所有评估 ESR2 遗传多态性与痴呆关系的相关研究。共有 14 项研究,共纳入 20609 例受试者。总的来说,发现 ESR2 多态性的综合数据集与痴呆风险无关。有趣的是,ESR2 rs4986938 多态性与亚洲人群的痴呆显著相关(OR=0.73,95%CI 0.59-0.91,P=0.006)。rs4986938 中的 A 等位基因携带者对痴呆有保护作用(A 与 G,OR=0.6633,P=0.012;AA+GA 与 GG,OR=0.6499,P=0.014;GA 与 AA+GG,OR=0.6672,P=0.025;GA 与 GG,OR=0.6617,P=0.022)。总之,我们的研究表明 ESR2 遗传多态性与痴呆风险无显著相关性。ESR2 rs4986938 可能是亚洲人群痴呆的潜在遗传标志物。然而,需要进一步的研究来验证这一结论。

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