Association of functional connectivity of the executive control network or default mode network with cognitive impairment in older adults with remitted major depressive disorder or mild cognitive impairment

默认模式网络 重性抑郁障碍 心理学 认知 痴呆 工作记忆 联想(心理学) 精神科 睡眠剥夺对认知功能的影响 执行职能 临床心理学 神经科学 听力学 内科学 医学 疾病 心理治疗师
作者
Neda Rashidi‐Ranjbar,Tarek K. Rajji,Colin Hawco,Sanjeev Kumar,Nathan Herrmann,Linda Mah,Alastair J. Flint,Corinne E. Fischer,Meryl A. Butters,Bruce G. Pollock,Erin W. Dickie,Christopher R. Bowie,Matan Soffer,Benoit H. Mulsant,Aristotle N. Voineskos
出处
期刊:Neuropsychopharmacology [Springer Nature]
卷期号:48 (3): 468-477 被引量:2
标识
DOI:10.1038/s41386-022-01308-2
摘要

Major depressive disorder (MDD) is associated with an increased risk of developing dementia. The present study aimed to better understand this risk by comparing resting state functional connectivity (rsFC) in the executive control network (ECN) and the default mode network (DMN) in older adults with MDD or mild cognitive impairment (MCI). Additionally, we examined the association between rsFC in the ECN or DMN and cognitive impairment transdiagnostically. We assessed rsFC alterations in ECN and DMN in 383 participants from five groups at-risk for dementia-remitted MDD with normal cognition (MDD-NC), non-amnestic mild cognitive impairment (naMCI), remitted MDD + naMCI, amnestic MCI (aMCI), and remitted MDD + aMCI-and from healthy controls (HC) or individuals with Alzheimer's dementia (AD). Subject-specific whole-brain functional connectivity maps were generated for each network and group differences in rsFC were calculated. We hypothesized that alteration of rsFC in the ECN and DMN would be progressively larger among our seven groups, ranked from low to high according to their risk for dementia as HC, MDD-NC, naMCI, MDD + naMCI, aMCI, MDD + aMCI, and AD. We also regressed scores of six cognitive domains (executive functioning, processing speed, language, visuospatial memory, verbal memory, and working memory) on the ECN and DMN connectivity maps. We found a significant alteration in the rsFC of the ECN, with post hoc testing showing differences between the AD group and the HC, MDD-NC, or naMCI groups, but no significant alterations in rsFC of the DMN. Alterations in rsFC of the ECN and DMN were significantly associated with several cognitive domain scores transdiagnostically. Our findings suggest that a diagnosis of remitted MDD may not confer functional brain risk for dementia. However, given the association of rs-FC with cognitive performance (i.e., transdiagnostically), rs-FC may help in stratifying this risk among people with MDD and varying degrees of cognitive impairment.

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