Dumitrescu Logan, Mayeda Elizabeth Rose, Sharman Kavya, Moore Annah M, Hohman Timothy J
Vanderbilt Memory and Alzheimer's Center, Vanderbilt University Medical Center, Nashville, TN.
Vanderbilt Genetics Institute, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Curr Genet Med Rep. 2019 Mar;7(1):13-21. doi: 10.1007/s40142-019-0157-1. Epub 2019 Jan 21.
Summarize sex-specific contributors to the genetic architecture of Alzheimer's disease (AD).
There are sex differences in the effects of Apolipoprotein E (), genes along the pathway, and genes along the neurotrophic signaling pathway in predicting AD. Reported sex differences are largely driven by stronger associations among females. Evidence also suggests that genetic predictors of amyloidosis are largely shared across sexes, while sex-specific genetic effects emerge downstream of amyloidosis and drive the clinical manifestation of AD.
There is a lack of comprehensive assessments of sex differences in genome-wide analyses of AD and a need for more systematic reporting a sex-stratified genetic effects. The emerging emphasis on sex as a biological variable provides an opportunity for transdisciplinary collaborations aimed at addressing major analytical challenges that have hampered advancements in the field. Ultimately, sex-specific genetic association studies represent a logical first step towards precision medicine.
总结阿尔茨海默病(AD)遗传结构中的性别特异性影响因素。
载脂蛋白E(ApoE)、淀粉样前体蛋白加工途径相关基因以及神经营养信号通路相关基因在预测AD方面存在性别差异。报告的性别差异主要由女性中更强的关联驱动。证据还表明,淀粉样变性的遗传预测因素在很大程度上在两性之间是共享的,而性别特异性遗传效应在淀粉样变性下游出现并驱动AD的临床表现。
在AD的全基因组分析中缺乏对性别差异的全面评估,并且需要更系统地报告性别分层的遗传效应。对性别作为生物学变量的新强调为跨学科合作提供了机会,旨在应对阻碍该领域进展的主要分析挑战。最终,性别特异性遗传关联研究是迈向精准医学的合理第一步。