Neuropsychiatric symptoms, APOE ε4, and the risk of incident dementia: a population-based study
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 AG028573
NIA NIH HHS - United States
K01 MH068351
NIMH NIH HHS - United States
U01 AG006786
NIA NIH HHS - United States
UL1 TR000135
NCATS NIH HHS - United States
PubMed
25653291
PubMed Central
PMC4351664
DOI
10.1212/wnl.0000000000001307
PII: WNL.0000000000001307
Knihovny.cz E-zdroje
- MeSH
- apolipoprotein E4 genetika MeSH
- duševní poruchy diagnóza genetika psychologie MeSH
- incidence MeSH
- kognitivní dysfunkce diagnóza genetika psychologie MeSH
- kohortové studie MeSH
- lidé MeSH
- longitudinální studie MeSH
- následné studie MeSH
- neuropsychologické testy * MeSH
- prospektivní studie MeSH
- rizikové faktory MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- surveillance populace * metody MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- apolipoprotein E4 MeSH
OBJECTIVE: To investigate the population-based interaction between a biological variable (APOE ε4), neuropsychiatric symptoms, and the risk of incident dementia among subjects with prevalent mild cognitive impairment (MCI). METHODS: We prospectively followed 332 participants with prevalent MCI (aged 70 years and older) enrolled in the Mayo Clinic Study of Aging for a median of 3 years. The diagnoses of MCI and dementia were made by an expert consensus panel based on published criteria, after reviewing neurologic, cognitive, and other pertinent data. Neuropsychiatric symptoms were determined at baseline using the Neuropsychiatric Inventory Questionnaire. We used Cox proportional hazards models, with age as a time scale, to calculate hazard ratios (HRs) and 95% confidence intervals (CIs). Models were adjusted for sex, education, and medical comorbidity. RESULTS: Baseline agitation, nighttime behaviors, depression, and apathy significantly increased the risk of incident dementia. We observed additive interactions between APOE ε4 and depression (joint effect HR = 2.21; 95% CI = 1.24-3.91; test for additive interaction, p < 0.001); and between APOE ε4 and apathy (joint effect HR = 1.93; 95% CI = 0.93-3.98; test for additive interaction, p = 0.031). Anxiety, irritability, and appetite/eating were not associated with increased risk of incident dementia. CONCLUSIONS: Among prevalent MCI cases, baseline agitation, nighttime behaviors, depression, and apathy elevated the risk of incident dementia. There was a synergistic interaction between depression or apathy and APOE ε4 in further elevating the risk of incident dementia.
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A longitudinal investigation of Aβ, anxiety, depression, and mild cognitive impairment
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