Plasma‐derived biomarkers of Alzheimer's disease and neuropsychiatric symptoms: A community‐based study

Author:

Krell‐Roesch Janina12,Zaniletti Isabella3,Syrjanen Jeremy A.2,Kremers Walter K.2,Algeciras‐Schimnich Alicia4,Dage Jeffrey L.5,van Harten Argonde C.6,Fields Julie A.7,Knopman David S.8,Jack Clifford R.9,Petersen Ronald C.28,Vassilaki Maria2,Geda Yonas E.10ORCID

Affiliation:

1. Institute of Sports and Sports Science Karlsruhe Institute of Technology Karlsruhe Germany

2. Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA

3. Department of Quantitative Health Sciences Mayo Clinic Scottsdale Arizona USA

4. Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota USA

5. Department of Neurology and Stark Neurosciences Research Institute Indiana University School of Medicine Indianapolis Indiana USA

6. Alzheimer Center, Department of Neurology Vrije Universiteit Amsterdam Amsterdam the Netherlands

7. Department of Psychiatry and Psychology Mayo Clinic Rochester Minnesota USA

8. Department of Neurology Mayo Clinic Rochester Minnesota USA

9. Department of Radiology Mayo Clinic Rochester Minnesota USA

10. Department of Neurology and the Franke Barrow Global Neuroscience Education Center Barrow Neurological Institute Phoenix Arizona USA

Abstract

AbstractINTRODUCTIONWe examined associations between plasma‐derived biomarkers of Alzheimer's disease (AD) and neuropsychiatric symptoms (NPS) in community‐dwelling older adults.METHODSCross‐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 [Aβ42]/Aβ40, phosphorylated tau 181 [p‐tau181], p‐tau217, total tau [t‐tau], neurofilament light [NfL]), and NPS assessment.RESULTSP‐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). Aβ42/Aβ40 and NfL were not associated with NPS.CONCLUSIONHigher 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 years Higher plasma tau levels are associated with increased neuropsychiatric symptoms Aβ42/Aβ40 and NfL are not associated with neuropsychiatric symptoms Clinicians should treat neuropsychiatric symptoms in persons with high plasma‐derived tau

Funder

National Institute on Aging

National Institute of Mental Health

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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