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阿尔茨海默病、酒精使用障碍和双重诊断个体的认知功能障碍和脑容量缺陷。

Cognitive dysfunction and cerebral volumetric deficits in individuals with Alzheimer's disease, alcohol use disorder, and dual diagnosis.

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.

Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06519, USA.

出版信息

Psychiatry Res Neuroimaging. 2021 Nov 30;317:111380. doi: 10.1016/j.pscychresns.2021.111380. Epub 2021 Aug 29.

DOI:10.1016/j.pscychresns.2021.111380
PMID:34482052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8579376/
Abstract

Epidemiological surveys suggest that excessive drinking is associated with higher risk of Alzheimer's disease (AD). The present study utilized data from the National Alzheimer's Coordinating Center to examine cognition as well as gray/white matter and ventricular volumes among participants with AD and alcohol use disorder (AD/AUD, n = 52), AD only (n = 701), AUD only (n = 67), and controls (n = 1283). AUD diagnosis was associated with higher Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) in AD than in non-AD. AD performed worse on semantic fluency and Trail Making Test A + B (TMT A + B) and showed smaller total GMV, WMV, and larger ventricular volume than non-AD. AD had smaller regional GMV in the inferior/superior parietal cortex, hippocampal formation, occipital cortex, inferior frontal gyrus, posterior cingulate cortex, and isthmus cingulate cortex than non-AD. AUD had significantly smaller somatomotor cortical GMV and showed a trend towards smaller volume in the hippocampal formation, relative to non-AUD participants. Misuse of alcohol has an additive effect on dementia severity among AD participants. Smaller hippocampal volume is a common feature of both AD and AUD. Although AD is associated with more volumetric deficits overall, AD and AUD are associated with atrophy in largely distinct brain regions.

摘要

流行病学调查表明,过量饮酒与阿尔茨海默病(AD)的风险增加有关。本研究利用国家阿尔茨海默病协调中心的数据,检查了 AD 患者和酒精使用障碍(AD/AUD,n=52)、仅有 AD(n=701)、仅有 AUD(n=67)和对照组(n=1283)参与者的认知以及灰质/白质和脑室体积。与非 AD 相比,AD 患者的 AUD 诊断与更高的临床痴呆评定量表总和评分(CDR-SB)相关。AD 在语义流畅性和 Trail Making Test A+B(TMT A+B)方面表现更差,总 GMV、WMV 较小,脑室体积较大。AD 在顶下/上皮质、海马结构、枕叶皮质、额下回、后扣带回和峡部扣带回的皮质下 GMV 明显小于非 AD。与非 AUD 参与者相比,AUD 的躯体感觉皮质 GMV 明显较小,且海马结构体积较小。滥用酒精会加重 AD 患者的痴呆严重程度。较小的海马体积是 AD 和 AUD 的共同特征。尽管 AD 总体上与更大的体积缺陷相关,但 AD 和 AUD 与大脑中差异很大的区域萎缩有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d9/8579376/4e4a7cf9a670/nihms-1739837-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d9/8579376/4e4a7cf9a670/nihms-1739837-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9d9/8579376/4e4a7cf9a670/nihms-1739837-f0001.jpg

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