Late-life onset psychotic symptoms and incident cognitive impairment in people without dementia: Modification by genetic risk for Alzheimer's disease

被引:13
|
作者
Creese, Byron [1 ,11 ]
Arathimos, Ryan [2 ]
Aarsland, Dag [3 ,4 ]
Ballard, Clive [1 ]
Brooker, Helen [5 ]
Hampshire, Adam [6 ]
Corbett, Anne [7 ]
Ismail, Zahinoor [8 ,9 ,10 ]
机构
[1] Univ Exeter, Fac Hlth & Life Sci, Dept Clin & Biomed Sci, Exeter, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Social Genet & Dev Psychiat Ctr, London, England
[3] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Old Age Psychiat, London, England
[4] Stavanger Univ Hosp, Ctr Age Related Med, Stavanger, Norway
[5] Univ Exeter, Fac Hlth & Life Sci, Dept Hlth & Community Sci, Exeter, England
[6] Imperial Coll London, Fac Med, Dept Brain Sci, London, England
[7] Univ Exeter, Fac Hlth & Life Sci, Dept Hlth & Community Sci, Exeter, England
[8] Univ Calgary, Hotchkiss Brain Inst, Dept Psychiat Clin Neurosci & Community Hlth Sci, Calgary, AB, Canada
[9] Univ Calgary, OBrien Inst Publ Hlth, Calgary, AB, Canada
[10] Univ Exeter, Fac Hlth & Life Sci, Dept Hlth & Community Sci, Exeter, England
[11] Univ Exeter, Fac Hlth & Life Sci, RILD Bldg,Barrack Rd, Exeter EX2 5AX, England
基金
加拿大健康研究院;
关键词
APOE; cognition; mild behavioral impairment; neuropsychiatric symptoms; psychosis; MILD BEHAVIORAL IMPAIRMENT; NEUROPSYCHIATRIC SYMPTOMS; NEURODEGENERATION; SCHIZOPHRENIA; ASSOCIATION; DISORDERS; CHECKLIST; CRITERIA;
D O I
10.1002/trc2.12386
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
IntroductionLate-life onset psychosis is associated with faster progression to dementia in cognitively normal people, but little is known about its relationship with cognitive impairment in advance of dementia. MethodsClinical and genetic data from 2750 people >= 50 years of age without dementia were analyzed. Incident cognitive impairment was operationalized using the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) and psychosis was rated using the Mild Behavioral Impairment Checklist (henceforth MBI-psychosis). The whole sample was analyzed before stratification on apolipoprotein E (APOE) epsilon 4 status. ResultsIn Cox proportional hazards models, MBI-psychosis had a higher hazard for cognitive impairment relative to the No Psychosis group (hazard ratio [HR]: 3.6, 95% confidence interval [CI]: 2.2-6, p < 0.0001). The hazard for MBI-psychosis was higher in APOE epsilon 4 carriers and there was an interaction between the two (HR for interaction: 3.4, 95% CI: 1.2-9.8, p = 0.02). DiscussionPsychosis assessment in the MBI framework is associated with incident cognitive impairment in advance of dementia. These symptoms may be particularly important in the context of APOE genotype.
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页数:12
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