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Neurodegeneration: 2023 update. | LitMetric

Neurodegeneration: 2023 update.

Free Neuropathol

Department of Pathology, Nash Family Department of Neuroscience, Department of Artificial Intelligence & Human Health, Neuropathology Brain Bank & Research CoRE, Ronald M. Loeb Center for Alzheimer's Disease, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Published: January 2023

AI Article Synopsis

  • The paper reviews ten important studies from the past year in neurodegenerative neuropathology, focusing on research involving human tissue.
  • It highlights various disease categories and methods, showcasing research like a combined proteomic and transcriptomic study on Alzheimer's disease and new diagnostic criteria for progressive supranuclear palsy.
  • Significant findings include studies on TDP-43, cryogenic electron microscopy findings related to prion protein structures, and advancements in understanding microglial gene expression and chronic traumatic encephalopathy through innovative technologies.

Article Abstract

This paper reviews ten highly impactful studies published in the previous year selected by the author from the neurodegenerative neuropathology literature. As in previous years, the focus is to highlight human tissue-based experimentation most relevant to neuropathologists. A concerted effort was made to balance the selected studies across disease categories, approaches, and methodologies to capture the breadth of the research landscape. Studies include an integrated proteomic and transcriptomic study of Alzheimer disease (AD) and new consensus diagnostic neuropathological criteria for progressive supranuclear palsy. A number of studies looking at TAR DNA-binding protein 43 (TDP-43) are highlighted. One examined interaction between AD and limbic age-related TDP-43 encephalopathy (LATE) and yet another demonstrated how TDP-43 represses cryptic exon inclusion in , suggesting a novel pathogenic mechanism. Most surprisingly, three cryogenic electron microscopy (cryo-EM) studies showed that filaments form the core of TDP-43-positive inclusions. Cryo-EM revealed a prion protein amyloid structure from aggregates in Gerstmann-Sträussler-Scheinker disease. There was an elegant functional genomic study cataloging microglial gene expression in the human brain. A study shed light on how influences chronic traumatic encephalopathy. A pathoanatomical study tested the dual hit hypothesis of Lewy body progression throughout the nervous system. And finally, deep learning continues to show its promise with application of a weakly supervised multiple instance learning paradigm to assess aging post-mortem brains.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484115PMC
http://dx.doi.org/10.17879/freeneuropathology-2023-4899DOI Listing

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