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Individualized prognosis of cognitive decline and dementia in mild cognitive impairment based on plasma biomarker combinations.
Cullen, Nicholas C; Leuzy, Antoine; Palmqvist, Sebastian; Janelidze, Shorena; Stomrud, Erik; Pesini, Pedro; Sarasa, Leticia; Allué, José Antonio; Proctor, Nicholas K; Zetterberg, Henrik; Dage, Jeffrey L; Blennow, Kaj; Mattsson-Carlgren, Niklas; Hansson, Oskar.
  • Cullen NC; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
  • Leuzy A; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
  • Palmqvist S; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
  • Janelidze S; Memory Clinic, Skåne University Hospital, Lund, Sweden.
  • Stomrud E; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
  • Pesini P; Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden.
  • Sarasa L; Memory Clinic, Skåne University Hospital, Lund, Sweden.
  • Allué JA; Araclon Biotech, Zaragoza, Spain.
  • Proctor NK; Araclon Biotech, Zaragoza, Spain.
  • Zetterberg H; Araclon Biotech, Zaragoza, Spain.
  • Dage JL; Eli Lilly and Company, Indianapolis, IN, USA.
  • Blennow K; Department of Psychiatry and Neurochemistry, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
  • Mattsson-Carlgren N; Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
  • Hansson O; Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
Nat Aging ; 1(1): 114-123, 2021 01.
Article en En | MEDLINE | ID: mdl-37117993
ABSTRACT
We developed models for individualized risk prediction of cognitive decline in mild cognitive impairment (MCI) using plasma biomarkers of ß-amyloid (Aß), tau and neurodegeneration. A total of 573 patients with MCI from the Swedish BioFINDER study and the Alzheimer's Disease Neuroimaging Initiative (ADNI) were included in the study. The primary outcomes were longitudinal cognition and conversion to Alzheimer's disease (AD) dementia. A model combining tau phosphorylated at threonine 181 (P-tau181) and neurofilament light (NfL), but not Aß42/Aß40, had the best prognosis performance of all models (area under the curve = 0.88 for 4-year conversion to AD in BioFINDER, validated in ADNI), was stronger than a basic model of age, sex, education and baseline cognition, and performed similarly to cerebrospinal fluid biomarkers. A publicly available online tool for individualized prognosis in MCI based on our combined plasma biomarker models is introduced. Combination of plasma biomarkers may be of high value to identify individuals with MCI who will progress to AD dementia in clinical trials and in clinical practice.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Alzheimer / Disfunción Cognitiva Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article