Histopathologic brain age estimation via multiple instance learning.

TitleHistopathologic brain age estimation via multiple instance learning.
Publication TypeJournal Article
Year of Publication2023
AuthorsMarx, GA, Kauffman, J, McKenzie, AT, Koenigsberg, DG, McMillan, CT, Morgello, S, Karlovich, E, Insausti, R, Richardson, TE, Walker, JM, White, CL, Babrowicz, BM, Shen, L, McKee, AC, Stein, TD, Farrell, K, Crary, JF
Corporate AuthorsPART Working Group
JournalActa Neuropathol
Volume146
Issue6
Pagination785-802
Date Published2023 Dec
ISSN1432-0533
KeywordsAcceleration, Aging, Autopsy, Brain, Child, Preschool, DNA Methylation, Epigenesis, Genetic, Epigenomics, Humans
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.

DOI10.1007/s00401-023-02636-3
Alternate JournalActa Neuropathol
PubMed ID37815677
PubMed Central IDPMC10627911
Grant ListR01NS086736 / NS / NINDS NIH HHS / United States
U24 MH100931 / MH / NIMH NIH HHS / United States
R01 AG062348 / AG / NIA NIH HHS / United States
R01AG062348 / AG / NIA NIH HHS / United States
R01 NS086736 / NS / NINDS NIH HHS / United States
R01 NS095252 / NS / NINDS NIH HHS / United States
K01 AG070326 / AG / NIA NIH HHS / United States
P30AG066514 / AG / NIA NIH HHS / United States
U24MH100931 / MH / NIMH NIH HHS / United States
RF1 AG060961 / AG / NIA NIH HHS / United States
K01AG070326 / AG / NIA NIH HHS / United States
R01AG054008 / NS / NINDS NIH HHS / United States
R01NS095252 / NS / NINDS NIH HHS / United States
R01 AG054008 / AG / NIA NIH HHS / United States
R01AG060961 / AG / NIA NIH HHS / United States
P30 AG066514 / AG / NIA NIH HHS / United States