Histopathologic brain age estimation via multiple instance learning.
Gabriel A MarxJustin KauffmanAndrew T McKenzieDaniel G KoenigsbergCory T McMillanSusan MorgelloEsma KarlovichRicardo InsaustiTimothy E RichardsonJamie M WalkerCharles L WhiteBergan M BabrowiczLi ShenAnn C McKeeThor D Steinnull nullKurt FarrellJohn F CraryPublished in: Acta neuropathologica (2023)
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.
Keyphrases
- resting state
- white matter
- deep learning
- cerebral ischemia
- functional connectivity
- endothelial cells
- type diabetes
- metabolic syndrome
- machine learning
- multiple sclerosis
- neoadjuvant chemotherapy
- dna methylation
- working memory
- radiation therapy
- convolutional neural network
- locally advanced
- adipose tissue
- brain injury
- subarachnoid hemorrhage
- artificial intelligence