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Confounding factors of Alzheimer's disease plasma biomarkers and their impact on clinical performance.
Pichet Binette, Alexa; Janelidze, Shorena; Cullen, Nicholas; Dage, Jeffrey L; Bateman, Randall J; Zetterberg, Henrik; Blennow, Kaj; Stomrud, Erik; Mattsson-Carlgren, Niklas; Hansson, Oskar.
Afiliação
  • Pichet Binette A; Clinical Memory Research Unit, Faculty of Medicine, Lund University, Lund, Sweden.
  • Janelidze S; Clinical Memory Research Unit, Faculty of Medicine, Lund University, Lund, Sweden.
  • Cullen N; Clinical Memory Research Unit, Faculty of Medicine, Lund University, Lund, Sweden.
  • Dage JL; Department of Neurology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • Bateman RJ; Department of Neurology, Washington University School of Medicine, St Louis, Missouri, USA.
  • Zetterberg H; Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden.
  • Blennow K; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Stomrud E; Department of Neurodegenerative Disease, UCL Institute of Neurology, Queen Square, London, UK.
  • Mattsson-Carlgren N; UK Dementia Research Institute at UCL, London, UK.
  • Hansson O; Hong Kong Center for Neurodegenerative Diseases, Hong Kong, China.
Alzheimers Dement ; 19(4): 1403-1414, 2023 04.
Article em En | MEDLINE | ID: mdl-36152307
INTRODUCTION: Plasma biomarkers will likely revolutionize the diagnostic work-up of Alzheimer's disease (AD) globally. Before widespread use, we need to determine if confounding factors affect the levels of these biomarkers, and their clinical utility. METHODS: Participants with plasma and CSF biomarkers, creatinine, body mass index (BMI), and medical history data were included (BioFINDER-1: n = 748, BioFINDER-2: n = 421). We measured beta-amyloid (Aß42, Aß40), phosphorylated tau (p-tau217, p-tau181), neurofilament light (NfL), and glial fibrillary acidic protein (GFAP). RESULTS: In both cohorts, creatinine and BMI were the main factors associated with NfL, GFAP, and to a lesser extent with p-tau. However, adjustment for BMI and creatinine had only minor effects in models predicting either the corresponding levels in CSF or subsequent development of dementia. DISCUSSION: Creatinine and BMI are related to certain plasma biomarkers levels, but they do not have clinically relevant confounding effects for the vast majority of individuals. HIGHLIGHTS: Creatinine and body mass index (BMI) are related to certain plasma biomarker levels. Adjusting for creatinine and BMI has minor influence on plasma-cerebrospinal fluid (CSF) associations. Adjusting for creatinine and BMI has minor influence on prediction of dementia using plasma biomarkers.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Alzheimers Dement Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Alzheimers Dement Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Suécia