病态的
背景(考古学)
海马结构
生物年龄
脑老化
人脑
神经科学
公制(单位)
病理
神经影像学
疾病
医学
生理学
生物
心理学
老年学
古生物学
运营管理
经济
作者
Gabriel A. Marx,Justin Kauffman,Andrew McKenzie,Daniel Koenigsberg,Cory T. McMillan,Susan Morgello,Esma Karlovich,Ricardo Insausti,Timothy E. Richardson,Jamie M. Walker,Charles L. White,Bergan Babrowicz,Li Shen,Ann C. McKee,Thor D. Stein,Kurt Farrell,John F. Crary
标识
DOI:10.1007/s00401-023-02636-3
摘要
Abstract Understanding age acceleration, the discordance between biological and chronological age, in the brain can reveal mechanistic insights into normal physiology as well as elucidate pathological determinants of age-related functional decline and identify early disease changes in the context of Alzheimer’s and other disorders. Histopathological whole slide images provide a wealth of pathologic data on the cellular level that can be leveraged to build deep learning models to assess age acceleration. Here, we used a collection of digitized human post-mortem hippocampal sections to develop a histological brain age estimation model. Our model predicted brain age within a mean absolute error of 5.45 ± 0.22 years, with attention weights corresponding to neuroanatomical regions vulnerable to age-related changes. We found that histopathologic brain age acceleration had significant associations with clinical and pathologic outcomes that were not found with epigenetic based measures. Our results indicate that histopathologic brain age is a powerful, independent metric for understanding factors that contribute to brain aging.
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