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Gut microbiome composition may be an indicator of preclinical Alzheimer's disease.
Ferreiro, Aura L; Choi, JooHee; Ryou, Jian; Newcomer, Erin P; Thompson, Regina; Bollinger, Rebecca M; Hall-Moore, Carla; Ndao, I Malick; Sax, Laurie; Benzinger, Tammie L S; Stark, Susan L; Holtzman, David M; Fagan, Anne M; Schindler, Suzanne E; Cruchaga, Carlos; Butt, Omar H; Morris, John C; Tarr, Phillip I; Ances, Beau M; Dantas, Gautam.
Afiliación
  • Ferreiro AL; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Choi J; Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
  • Ryou J; Department of Pathology and Immunology, Division of Laboratory and Genomic Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Newcomer EP; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Thompson R; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Bollinger RM; Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Hall-Moore C; Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.
  • Ndao IM; Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Sax L; Program in Occupational Therapy, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Benzinger TLS; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Stark SL; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Holtzman DM; Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Fagan AM; Department of Radiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Schindler SE; Charles F. and Joanne Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Cruchaga C; Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Butt OH; Program in Occupational Therapy, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Morris JC; Charles F. and Joanne Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Tarr PI; Department of Neurology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Ances BM; Charles F. and Joanne Knight Alzheimer's Disease Research Center, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Dantas G; Hope Center for Neurological Disorders, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sci Transl Med ; 15(700): eabo2984, 2023 06 14.
Article en En | MEDLINE | ID: mdl-37315112
ABSTRACT
Alzheimer's disease (AD) pathology is thought to progress from normal cognition through preclinical disease and ultimately to symptomatic AD with cognitive impairment. Recent work suggests that the gut microbiome of symptomatic patients with AD has an altered taxonomic composition compared with that of healthy, cognitively normal control individuals. However, knowledge about changes in the gut microbiome before the onset of symptomatic AD is limited. In this cross-sectional study that accounted for clinical covariates and dietary intake, we compared the taxonomic composition and gut microbial function in a cohort of 164 cognitively normal individuals, 49 of whom showed biomarker evidence of early preclinical AD. Gut microbial taxonomic profiles of individuals with preclinical AD were distinct from those of individuals without evidence of preclinical AD. The change in gut microbiome composition correlated with ß-amyloid (Aß) and tau pathological biomarkers but not with biomarkers of neurodegeneration, suggesting that the gut microbiome may change early in the disease process. We identified specific gut bacterial taxa associated with preclinical AD. Inclusion of these microbiome features improved the accuracy, sensitivity, and specificity of machine learning classifiers for predicting preclinical AD status when tested on a subset of the cohort (65 of the 164 participants). Gut microbiome correlates of preclinical AD neuropathology may improve our understanding of AD etiology and may help to identify gut-derived markers of AD risk.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Microbiota / Microbioma Gastrointestinal Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Microbiota / Microbioma Gastrointestinal Tipo de estudio: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Sci Transl Med Asunto de la revista: CIENCIA / MEDICINA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos