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男性染色体 Y 的极度下调与阿尔茨海默病。

Extreme downregulation of chromosome Y and Alzheimer's disease in men.

机构信息

ISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red en Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.

CRG (Center for Genomics Regulation), Barcelona, Spain.

出版信息

Neurobiol Aging. 2020 Jun;90:150.e1-150.e4. doi: 10.1016/j.neurobiolaging.2020.02.003. Epub 2020 Feb 13.

Abstract

Research has revealed scarcely any biological factors of Alzheimer's disease (AD) that are specific to men. Here, we found that the extreme downregulation of chromosome Y (EDY) increases the age-related risk of AD in men. We considered that EDY was a possible male-specific pathway toward AD because EDY is the most likely consequence of the mosaic loss of chromosome Y, which has been recently associated with AD. We studied EDY in the undiseased brain of 371 individuals and observed that it co-occurred across multiple brain regions (p < 10) and associated with rs114241159 (p = 1.53 × 10) within ACSS3/PPFIA2, previously linked to amyloid beta concentrations. We also analyzed the 5 largest transcriptomic case-control studies, publicly available to date on AD (cases/controls = 556/462) and found a significant interaction with age (OR = 1.22, p = 0.0038). Our analyses suggest that aging men who live longer by avoiding EDY are more resilient to AD than those who do not.

摘要

研究几乎没有揭示出任何特定于男性的阿尔茨海默病(AD)的生物学因素。在这里,我们发现染色体 Y 的极度下调(EDY)会增加男性 AD 的年龄相关风险。我们认为 EDY 是 AD 的一种可能的男性特异性途径,因为 EDY 是染色体 Y 镶嵌丢失的最可能结果,而最近的研究表明,这种丢失与 AD 有关。我们研究了 371 名无疾病个体的大脑中的 EDY,并观察到它在多个大脑区域同时发生(p < 10),并且与 ACSS3/PPFIA2 内的 rs114241159 相关(p = 1.53 × 10),该基因先前与淀粉样β浓度有关。我们还分析了迄今为止在 AD 方面最大的 5 个转录组病例对照研究(病例/对照= 556/462),并发现与年龄存在显著交互作用(OR = 1.22,p = 0.0038)。我们的分析表明,与那些不避免 EDY 的男性相比,避免 EDY 的老年男性对 AD 的抵抗力更强。

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