Journal
PSYCHIATRY AND CLINICAL NEUROSCIENCES
Volume 74, Issue 12, Pages 645-651Publisher
WILEY
DOI: 10.1111/pcn.13150
Keywords
Alzheimer's disease; dementia; genes; longitudinal study; neuropsychiatric symptoms
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Funding
- Academia Sinica of Taiwan [AS-BD-108-2]
- Ministry of Science and Technology of Taiwan [106-2321-B-075-001-, 107-2321-B-075-001-, 107-2221-E-075-006-]
- Taipei Veterans General Hospital [V107C-032, V108C-113, V108D43-002-MY2-1]
- Kaohsiung Medical University Hospital [KMUH103-3R56]
- Brain Research Center, National Yang-Ming University from the Featured Areas Research Center Program within Ministry of Education in Taiwan
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Aim The aim of this study was to investigate the associations between candidate gene variants and domains of neuropsychiatric symptoms (NPS) and the changes in these associations over a 1-year period. Methods Seven hundred and ninety-three Taiwanese participants (47.8% female) with Alzheimer's disease (AD) were enrolled. Genes associated with a risk of developing AD were selected as candidate genes. NPS were assessed using the Neuropsychiatric Inventory Questionnaire (NPI-Q), and the NPI-Q total score and sub-scores for the Psychosis, Mood, and Frontal Syndrome domains were calculated. Results Patients with AD and theAPOE epsilon 4 allele exhibited more obvious symptoms of psychosis. Mood symptoms were associated withCD33rs3865444 andEPHA1rs11767557, and frontal symptoms were associated withSORL1rs3824968. A 1-year Time x Alleles interaction effect ofCD33rs3865444 on mood symptoms was discerned. Conclusion Risk genes of AD, which are also associated with NPS, areAPOE epsilon 4 for psychosis,CD33andEPHA1for mood symptoms, andSORL1for frontal symptoms. The association betweenCD33and mood symptoms is dynamic and could change over 1 year; however, the results should be interpreted with caution because corrections for multiple comparisons were not performed.
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