Institute of Medical Science, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Transl Psychiatry. 2023 Aug 19;13(1):284. doi: 10.1038/s41398-023-02584-2.
Most patients with late-life depression (LLD) have cognitive impairment, and at least one-third meet diagnostic criteria for mild cognitive impairment (MCI), a prodrome to Alzheimer's dementia (AD) and other neurodegenerative diseases. However, the mechanisms linking LLD and MCI, and brain alterations underlying impaired cognition in LLD and LLD + MCI remain poorly understood.
To address this knowledge gap, we conducted a systematic review of studies of brain-cognition relationships in LLD or LLD + MCI to identify circuits underlying impaired cognition in LLD or LLD + MCI. We searched MEDLINE, PsycINFO, EMBASE, and Web of Science databases from inception through February 13, 2023. We included studies that assessed cognition in patients with LLD or LLD + MCI and acquired: (1) T1-weighted imaging (T1) measuring gray matter volumes or thickness; or (2) diffusion-weighted imaging (DWI) assessing white matter integrity. Due to the heterogeneity in studies, we only conducted a descriptive synthesis.
Our search identified 51 articles, resulting in 33 T1 studies, 17 DWI studies, and 1 study analyzing both T1 and DWI. Despite limitations, reviewed studies suggest that lower thickness or volume in the frontal and temporal regions and widespread lower white matter integrity are associated with impaired cognition in LLD. Lower white matter integrity in the posterior cingulate region (precuneus and corpus callosum sub-regions) was more associated with impairment executive function and processing speed than with memory.
Future studies should analyze larger samples of participants with various degrees of cognitive impairment and go beyond univariate statistical models to assess reliable brain-cognition relationships in LLD.
大多数老年期抑郁症(LLD)患者存在认知障碍,至少有三分之一的患者符合轻度认知障碍(MCI)的诊断标准,MCI 是阿尔茨海默病(AD)和其他神经退行性疾病的前驱症状。然而,将 LLD 与 MCI 联系起来的机制,以及 LLD 和 LLD+MCI 中认知障碍的大脑改变仍知之甚少。
为了解决这一知识空白,我们对 LLD 或 LLD+MCI 中与大脑认知关系的研究进行了系统回顾,以确定 LLD 或 LLD+MCI 中认知障碍的潜在回路。我们检索了 MEDLINE、PsycINFO、EMBASE 和 Web of Science 数据库,检索时间从建库到 2023 年 2 月 13 日。我们纳入了评估 LLD 或 LLD+MCI 患者认知的研究,并获取了:(1)T1 加权成像(T1)测量灰质体积或厚度;或(2)弥散加权成像(DWI)评估白质完整性。由于研究之间存在异质性,我们仅进行了描述性综合分析。
我们的检索共识别出 51 篇文章,其中包括 33 项 T1 研究、17 项 DWI 研究和 1 项同时分析 T1 和 DWI 的研究。尽管存在局限性,但回顾性研究表明,额叶和颞叶区域的厚度或体积较低,以及广泛的白质完整性较低与 LLD 中的认知障碍相关。后扣带回区域(楔前叶和胼胝体子区域)的白质完整性较低与执行功能和处理速度障碍的相关性大于与记忆障碍的相关性。
未来的研究应该分析更多不同程度认知障碍的参与者样本,并超越单变量统计模型来评估 LLD 中可靠的大脑-认知关系。