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Plasma-derived biomarkers of Alzheimer's disease and neuropsychiatric symptoms: A community-based study.
Krell-Roesch, Janina; Zaniletti, Isabella; Syrjanen, Jeremy A; Kremers, Walter K; Algeciras-Schimnich, Alicia; Dage, Jeffrey L; van Harten, Argonde C; Fields, Julie A; Knopman, David S; Jack, Clifford R; Petersen, Ronald C; Vassilaki, Maria; Geda, Yonas E.
Afiliação
  • Krell-Roesch J; Institute of Sports and Sports Science Karlsruhe Institute of Technology Karlsruhe Germany.
  • Zaniletti I; Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA.
  • Syrjanen JA; Department of Quantitative Health Sciences Mayo Clinic Scottsdale Arizona USA.
  • Kremers WK; Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA.
  • Algeciras-Schimnich A; Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA.
  • Dage JL; Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota USA.
  • van Harten AC; Department of Neurology and Stark Neurosciences Research Institute Indiana University School of Medicine Indianapolis Indiana USA.
  • Fields JA; Alzheimer Center, Department of Neurology Vrije Universiteit Amsterdam Amsterdam the Netherlands.
  • Knopman DS; Department of Psychiatry and Psychology Mayo Clinic Rochester Minnesota USA.
  • Jack CR; Department of Neurology Mayo Clinic Rochester Minnesota USA.
  • Petersen RC; Department of Radiology Mayo Clinic Rochester Minnesota USA.
  • Vassilaki M; Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA.
  • Geda YE; Department of Neurology Mayo Clinic Rochester Minnesota USA.
Alzheimers Dement (Amst) ; 15(3): e12461, 2023.
Article em En | MEDLINE | ID: mdl-37529120
INTRODUCTION: We examined associations between plasma-derived biomarkers of Alzheimer's disease (AD) and neuropsychiatric symptoms (NPS) in community-dwelling older adults. METHODS: Cross-sectional study involving 1005 persons ≥50 years of age (mean 74 years, 564 male, 118 cognitively impaired), who completed plasma-derived biomarker (amyloid beta 42 [Aß42]/Aß40, phosphorylated tau 181 [p-tau181], p-tau217, total tau [t-tau], neurofilament light [NfL]), and NPS assessment. RESULTS: P-tau181 (odds ratio [OR] 2.06, 95% confidence interval [CI] 1.41-3.00, p < 0.001), p-tau217 (OR 1.70, 95% CI 1.10-2.61, p = 0.016), and t-tau (OR 1.44, 95% CI 1.08-1.92, p = 0.012) were associated with appetite change. We also found that p-tau181 and p-tau217 were associated with increased symptoms of agitation (OR 1.93, 95% CI 1.20-3.11, p = 0.007 and OR 2.04, 95% CI 1.21-3.42, p = 0.007, respectively), and disinhibition (OR 2.39, 95% CI 1.45-3.93, p = 0.001 and OR 2.30, 95% CI 1.33-3.98, p = 0.003, respectively). Aß42/Aß40 and NfL were not associated with NPS. CONCLUSION: Higher plasma-derived p-tau181 and p-tau217 levels are associated with increased symptoms of appetite change, agitation, and disinhibition. These findings may support the validity of plasma tau biomarkers for predicting behavioral symptoms that often accompany cognitive impairment. HIGHLIGHTS: We studied 1005 community-dwelling persons aged ≥ 50 yearsHigher plasma tau levels are associated with increased neuropsychiatric symptomsAß42/Aß40 and NfL are not associated with neuropsychiatric symptomsClinicians should treat neuropsychiatric symptoms in persons with high plasma-derived tau.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article