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Racial differences in longitudinal Alzheimer's disease biomarkers among cognitively normal adults.
Xiong, Chengjie; Luo, Jingqin; Schindler, Suzanne E; Fagan, Anne M; Benzinger, Tammie; Hassenstab, Jason; Balls-Berry, Joyce E; Agboola, Folasade; Grant, Elizabeth; Moulder, Krista L; Morris, John C.
Afiliación
  • Xiong C; Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Luo J; Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Schindler SE; Division of Biostatistics, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Fagan AM; Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Benzinger T; Siteman Cancer Center Biostatistics Core, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Hassenstab J; Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Balls-Berry JE; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Agboola F; Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Grant E; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Moulder KL; Knight Alzheimer Disease Research Center, Washington University School of Medicine, St. Louis, Missouri, USA.
  • Morris JC; Department of Radiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Alzheimers Dement ; 18(12): 2570-2581, 2022 12.
Article en En | MEDLINE | ID: mdl-35218143
INTRODUCTION: Longitudinal changes in Alzheimer's disease (AD) biomarkers, including cerebrospinal fluid (CSF) analytes, amyloid uptakes from positron emission tomography (PET), structural outcomes from magnetic resonance imaging (MRI), and cognition, have not been compared between Blacks and Whites. METHODS: A total of 179 Blacks and 1180 Whites who were cognitively normal at baseline and had longitudinal data from at least one biomarker modality were analyzed for the annual rates of change. RESULTS: CSF amyloid beta (Aß)42/Aß40 declined more slowly (P = .0390), and amyloid (PET) accumulated more slowly (P = .0157), in Blacks than Whites. CSF Aß42 changed in opposite directions over time between Blacks and Whites (P = .0039). The annual increase in CSF total tau and phosphorylated tau181 for Blacks was about half of that for Whites. DISCUSSION: Longitudinal racial differences in amyloid biomarkers are observed. It will be important to comprehensively and prospectively examine the effects of apolipoprotein E genotype and sociocultural factors on these differences.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer Límite: Adult / Humans Idioma: En Revista: Alzheimers Dement Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer Límite: Adult / Humans Idioma: En Revista: Alzheimers Dement Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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