Association between CSF biomarkers of Alzheimer's disease and neuropsychiatric symptoms: Mayo Clinic Study of Aging
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
K01 MH068351
NIMH NIH HHS - United States
R01 AG041851
NIA NIH HHS - United States
R01 AG069453
NIA NIH HHS - United States
R01 AG034676
NIA NIH HHS - United States
P50 AG016574
NIA NIH HHS - United States
P30 AG072980
NIA NIH HHS - United States
R01 AG011378
NIA NIH HHS - United States
R33 AG058738
NIA NIH HHS - United States
R01 AG057708
NIA NIH HHS - United States
P30 AG019610
NIA NIH HHS - United States
U01 AG006786
NIA NIH HHS - United States
R01 NS097495
NINDS NIH HHS - United States
P30 AG062677
NIA NIH HHS - United States
PubMed
35142047
PubMed Central
PMC10433790
DOI
10.1002/alz.12557
Knihovny.cz E-zdroje
- Klíčová slova
- Alzheimer's disease, CSF amyloid beta 42, CSF phosphorylated tau, CSF total tau, cerebrospinal fluid biomarkers, neuropsychiatric symptoms, non-demented,
- MeSH
- Alzheimerova nemoc * mozkomíšní mok MeSH
- amyloidní beta-protein mozkomíšní mok MeSH
- biologické markery mozkomíšní mok MeSH
- kognitivní dysfunkce * diagnóza MeSH
- lidé MeSH
- longitudinální studie MeSH
- peptidové fragmenty mozkomíšní mok MeSH
- proteiny tau mozkomíšní mok MeSH
- senioři MeSH
- stárnutí MeSH
- Check Tag
- lidé MeSH
- senioři MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- amyloidní beta-protein MeSH
- biologické markery MeSH
- peptidové fragmenty MeSH
- proteiny tau MeSH
INTRODUCTION: We examined the association between cerebrospinal fluid (CSF)-derived biomarkers of Alzheimer's disease and neuropsychiatric symptoms (NPS) in older non-demented adults. METHODS: We included 784 persons (699 cognitively unimpaired, 85 with mild cognitive impairment) aged ≥ 50 years who underwent CSF amyloid beta (Aβ42), hyperphosphorylated tau 181 (p-tau), and total tau (t-tau) as well as NPS assessment using Beck Depression and Anxiety Inventories (BDI-II, BAI), and Neuropsychiatric Inventory Questionnaire (NPI-Q). RESULTS: Lower CSF Aβ42, and higher t-tau/Aβ42 and p-tau/Aβ42 ratios were associated with BDI-II and BAI total scores, clinical depression (BDI-II ≥ 13), and clinical anxiety (BAI ≥ 10), as well as NPI-Q-assessed anxiety, apathy, and nighttime behavior. DISCUSSION: CSF Aβ42, t-tau/Aβ42, and p-tau/Aβ42 ratios were associated with NPS in community-dwelling individuals free of dementia. If confirmed by a longitudinal cohort study, the findings have clinical relevance of taking into account the NPS status of individuals with abnormal CSF biomarkers.
Alzheimer Center Department of Neurology Vrije Universiteit Amsterdam Amsterdam the Netherlands
Department of Neurology Barrow Neurological Institute Phoenix Arizona USA
Department of Neurology Mayo Clinic Rochester Minnesota USA
Department of Neurology University Medical Centre Maribor Maribor Slovenia
Department of Quantitative Health Sciences Mayo Clinic Rochester Minnesota USA
Department of Radiology Mayo Clinic Rochester Minnesota USA
Institute of Sports and Sports Science Karlsruhe Institute of Technology Karlsruhe Germany
International Clinical Research Center St Anne's Hospital Brno Czech Republic
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