| Literature DB >> 26445159 |
Zhongwei Guo1,2, Xiaozheng Liu3, Xize Jia3, Hongtao Hou2, Yulin Cao2, Fuquan Wei2, Jiapeng Li2, Xingli Chen2, Yingchun Zhang1, Yuedi Shen4, Lili Wei1, Luoyi Xu1, Wei Chen1,5.
Abstract
Alzheimer's disease (AD) is characterized by progressive cognitive decline along with neuropsychiatric symptoms including depression and psychosis. Depression is a common psychiatric disorder occurring in people across the lifespan. Accumulating evidence indicates that depression may be a prodrome and/or a "risk factor" for AD. However, whether AD and depression share a common pathophysiological pathway is still unclear. The aim of this study was to identify regional alterations in brain function associated with depressive symptoms in mild AD patients. Thirty-two mild AD patients were evaluated using the Neuropsychiatric Inventory and Hamilton Depression Rating Scale, and were divided into two groups: 15 AD patients with depressive symptoms (D-AD) and 17 non-depressed AD (nD-AD) patients. Using the approach of regional homogeneity (ReHo), we characterized resting-state regional brain activity in D-AD and nD-AD patients. Compared with nD-AD patients, D-AD patients showed decreased ReHo in the right precentral gyrus, right superior frontal gyrus, right middle frontal gyrus, and right inferior frontal cortex. Our findings show regional brain activity alterations in D-AD patients. Thus, D-AD pathogenesis may be attributed to abnormal neural activity in multiple brain regions.Entities:
Keywords: Alzheimer’s disease; depressive symptoms; regional homogeneity; resting state functional magnetic resonance imaging
Mesh:
Year: 2015 PMID: 26445159 DOI: 10.3233/JAD-150460
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472