在遗传驱动的亚群中发现具有不同预后影响的精准AD生物标志物。

Brian N Lee, Junwen Wang, Kwangsik Nho, Andrew J Saykin, Li Shen
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摘要

阿尔茨海默病(AD)是一种高度遗传性的神经退行性疾病,以记忆障碍为特征。了解遗传因素对阿尔茨海默病病理的影响可以为干预措施提供信息,以减缓或预防阿尔茨海默病的进展。我们对1574名阿尔茨海默病神经影像学倡议(ADNI)参与者进行了分层遗传分析,以检查数量性状(QT)水平与未来诊断之间的关系。Chow试验用于确定个体的遗传特征是否影响QT综合征与未来诊断之间的预测关系。我们的chow测试分析发现,认知和基于pet的生物标志物在对AD基因座的等位基因剂量进行分层时预测未来诊断的差异。生物标志物的事后自举和关联分析证实了差异效应,强调了分层模型实现个体化AD诊断预测的必要性。这种新应用的Chow测试允许定量和直接比较基于遗传的差异。我们的发现,以及确定的qt -未来诊断关系,保证了未来从生物学背景下的调查。
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Discovering Precision AD Biomarkers with Varying Prognosis Effects in Genetics Driven Subpopulations.

Alzheimer's Disease (AD) is a highly heritable neurodegenerative disorder characterized by memory impairments. Understanding how genetic factors contribute to AD pathology may inform interventions to slow or prevent the progression of AD. We performed stratified genetic analyses of 1,574 Alzheimer's Disease Neuroimaging Initiative (ADNI) participants to examine associations between levels of quantitative traits (QT's) and future diagnosis. The Chow test was employed to determine if an individual's genetic profile affects identified predictive relationships between QT's and future diagnosis. Our chow test analysis discovered that cognitive and PET-based biomarkers differentially predicted future diagnosis when stratifying on allelic dosage of AD loci. Post-hoc bootstrapped and association analyses of biomarkers confirmed differential effects, emphasizing the necessity of stratified models to realize individualized AD diagnosis prediction. This novel application of the Chow test allows for the quantification and direct comparison of genetic-based differences. Our findings, as well as the identified QT-future diagnosis relationships, warrant future investigation from a biological context.

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