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Histopathologic brain age estimation via multiple instance learning.
Marx, Gabriel A; Kauffman, Justin; McKenzie, Andrew T; Koenigsberg, Daniel G; McMillan, Cory T; Morgello, Susan; Karlovich, Esma; Insausti, Ricardo; Richardson, Timothy E; Walker, Jamie M; White, Charles L; Babrowicz, Bergan M; Shen, Li; McKee, Ann C; Stein, Thor D; Farrell, Kurt; Crary, John F.
Afiliación
  • Marx GA; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Kauffman J; Department of Artificial Intelligence and Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank and Research CoRE, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York,
  • McKenzie AT; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Koenigsberg DG; Department of Artificial Intelligence and Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank and Research CoRE, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York,
  • McMillan CT; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Morgello S; Department of Artificial Intelligence and Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank and Research CoRE, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York,
  • Karlovich E; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Insausti R; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Richardson TE; Department of Artificial Intelligence and Human Health, Nash Family Department of Neuroscience, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Neuropathology Brain Bank and Research CoRE, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, Box 1194, New York,
  • Walker JM; Frontotemporal Degeneration Center, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • White CL; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Babrowicz BM; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Shen L; Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, New York, NY, USA.
  • McKee AC; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Stein TD; Human Neuroanatomy Laboratory, School of Medicine, University of Castilla-La Mancha, Albacete, Spain.
  • Farrell K; Department of Pathology, Icahn School of Medicine at Mount Sinai, Friedman Brain Institute, 1 Gustave L. Levy Place, Box 1194, New York, NY, 10029, USA.
  • Crary JF; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Acta Neuropathol ; 146(6): 785-802, 2023 12.
Article en En | MEDLINE | ID: mdl-37815677
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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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Envejecimiento Tipo de estudio: Prognostic_studies Límite: Child, preschool / Humans Idioma: En Revista: Acta Neuropathol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Encéfalo / Envejecimiento Tipo de estudio: Prognostic_studies Límite: Child, preschool / Humans Idioma: En Revista: Acta Neuropathol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos