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Estrogen Receptor 1 gene (ESR1) variants in Alzheimer's disease. Results of a meta-analysis.

机译:阿尔茨海默氏病中的雌激素受体1基因(ESR1)变体。荟萃分析的结果。

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BACKGROUND AND AIMS: There is some disagreement between clinical and basic science as to the benefit of estrogen in preventing cognitive decline. For cardiovascular disease, estrogen effects have been shown to vary with estrogen receptor (ESR) genotype. The present study was conceived to review evidence of ESR association with Alzheimer's disease (AD) which could account for the variability observed in estrogen treatment outcome. METHODS: A meta-analysis was performed on data from 8288 cases and controls, controlling for ethnicity (Asian vs European). To explore the specificity of our findings further, a second meta-analysis of association studies was then appended, addressing non-AD forms of dementia or cognitive impairment (total n=11036). RESULTS: A significant overall association of AD with two neighboring ESR1 variants located in a transcription-enhancing region (p=0.015) was noted. The genotypic effect was driven by the minor alleles in Asian populations, and did not reach significance in European samples (OR=1.1, p>0.267). When the phenotype was extended to other forms of dementia or cognitive impairment, the association was no longer observed. CONCLUSIONS: ESR1 variability was confirmed to modulate susceptibility to AD in Asian individuals, but not in Europeans. More research is required to address possible clinical implications, e.g., for hormone replacement therapy in early stages of AD.
机译:背景与目的:在临床和基础科学之间,关于雌激素在预防认知功能减退方面的益处存在分歧。对于心血管疾病,已显示雌激素作用随雌激素受体(ESR)基因型而异。本研究旨在审查ESR与阿尔茨海默氏病(AD)相关性的证据,这可以解释在雌激素治疗结果中观察到的变异性。方法:对来自8288例病例和对照者的数据进行了荟萃分析,以控制种族(亚洲人与欧洲人)。为了进一步探讨我们研究结果的特异性,然后附加了关联研究的第二次荟萃分析,以解决非AD形式的痴呆或认知障碍(总n = 11036)。结果:注意到AD与位于转录增强区(p = 0.015)的两个相邻ESR1变体的显着整体关联。基因型效应是由亚洲人群中的次要等位基因驱动的,在欧洲样本中没有达到显着性(OR = 1.1,p> 0.267)。当表型扩展到其他形式的痴呆或认知障碍时,不再观察到这种关联。结论:ESR1变异性被证实可以调节亚洲人对AD的易感性,而欧洲人则不然。需要进行更多的研究来解决可能的临床意义,例如,在AD早期进行激素替代治疗。

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