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Comparative brain metabolomics reveals shared and distinct metabolic alterations in Alzheimer's disease and progressive supranuclear palsy.
Batra, Richa; Krumsiek, Jan; Wang, Xue; Allen, Mariet; Blach, Colette; Kastenmüller, Gabi; Arnold, Matthias; Ertekin-Taner, Nilüfer; Kaddurah-Daouk, Rima F.
Affiliation
  • Batra R; Department of Physiology and Biophysics, Institute for Computational Biomedicine, Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Krumsiek J; Department of Physiology and Biophysics, Institute for Computational Biomedicine, Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, USA.
  • Wang X; Department of Quantitative Health Sciences, Mayo Clinic Florida, Jacksonville, FL, USA.
  • Allen M; Department of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.
  • Blach C; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.
  • Kastenmüller G; Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.
  • Arnold M; Institute of Computational Biology, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.
  • Ertekin-Taner N; Department of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.
  • Kaddurah-Daouk RF; Department of Neuroscience, Mayo Clinic Florida, Jacksonville, FL, USA.
medRxiv ; 2023 Jul 27.
Article in En | MEDLINE | ID: mdl-37546878
Metabolic dysregulation is a hallmark of neurodegenerative diseases, including Alzheimer's disease (AD) and progressive supranuclear palsy (PSP). While metabolic dysregulation is a common link between these two tauopathies, a comprehensive brain metabolic comparison of the diseases has not yet been performed. We analyzed 342 postmortem brain samples from the Mayo Clinic Brain Bank and examined 658 metabolites in the cerebellar cortex and the temporal cortex between the two tauopathies. Our findings indicate that both diseases display oxidative stress associated with lipid metabolism, mitochondrial dysfunction linked to lysine metabolism, and an indication of tau-induced polyamine stress response. However, specific to AD, we detected glutathione-related neuroinflammation, deregulations of enzymes tied to purines, and cognitive deficits associated with vitamin B. Taken together, our findings underscore vast alterations in the brain's metabolome, illuminating shared neurodegenerative pathways and disease-specific traits in AD and PSP.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MedRxiv Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos