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Plasma biomarkers predict cognitive trajectories in an ethnoracially and clinically diverse cohort: Mediation with hippocampal volume.
Sapkota, Shraddha; Erickson, Kelsey; Harvey, Danielle; Tomaszewski-Farias, Sarah E; Olichney, John M; Johnson, David K; Dugger, Brittany N; Mungas, Dan M; Fletcher, Evan; Maillard, Pauline; Seshadri, Sudha; Satizabal, Claudia L; Kautz, Tiffany; Parent, Danielle; Tracy, Russell P; Maezawa, Izumi; Jin, Lee-Way; DeCarli, Charles.
Afiliação
  • Sapkota S; Department of Neurology University of California Davis California USA.
  • Erickson K; Department of Pathology and Laboratory Medicine University of California Davis California USA.
  • Harvey D; Department of Public Health Sciences University of California Davis California USA.
  • Tomaszewski-Farias SE; Department of Neurology University of California Davis California USA.
  • Olichney JM; Department of Neurology University of California Davis California USA.
  • Johnson DK; Department of Neurology University of California Davis California USA.
  • Dugger BN; Department of Pathology and Laboratory Medicine University of California Davis California USA.
  • Mungas DM; Department of Neurology University of California Davis California USA.
  • Fletcher E; Department of Neurology University of California Davis California USA.
  • Maillard P; Department of Neurology University of California Davis California USA.
  • Seshadri S; Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases and Department of Population Health Sciences UT Health San Antonio San Antonio Texas USA.
  • Satizabal CL; Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases and Department of Population Health Sciences UT Health San Antonio San Antonio Texas USA.
  • Kautz T; Department of Neurology Boston University School of Medicine Boston Massachusetts USA.
  • Parent D; The Framingham Heart Study Framingham Massachusetts USA.
  • Tracy RP; Glenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases and Department of Population Health Sciences UT Health San Antonio San Antonio Texas USA.
  • Maezawa I; Department of Pathology and Laboratory Medicine University of Vermont Burlington Vermont USA.
  • Jin LW; Department of Pathology and Laboratory Medicine University of Vermont Burlington Vermont USA.
  • DeCarli C; Department of Pathology and Laboratory Medicine University of California Davis California USA.
Alzheimers Dement (Amst) ; 14(1): e12349, 2022.
Article em En | MEDLINE | ID: mdl-36092690
Introduction: We examine whether the association between key plasma biomarkers (amyloid ß [aß] 42/40, total tau (t-tau), neurofilament light [NfL]) and cognitive trajectories (executive function [EF] and episodic memory [EM]) is mediated through neurodegeneration. Methods: All participants were recruited from the University of California, Davis-Alzheimer's Disease Research Center (n = 473; baseline age range = 49-95 years, 60% women). We applied an accelerated longitudinal design to test latent growth models for EF and EM, and path and mediation analyses. Age was centered at 75 years, and all models were adjusted for sex, education, and ethnicity. Results: HV differentially mediated the association aß 42/40 and NfL on EF and EM level and change. Hippocampal volume (HV) did not mediate the association between t-tau and cognitive performance. Discussion: Neurodegeneration as represented with HV selectively mediates the association between key non-invasive plasma biomarkers and cognitive trajectories in an ethnoracially and clinically diverse community-based sample.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Alzheimers Dement (Amst) Ano de publicação: 2022 Tipo de documento: Article