Intrinsic Functional Network Connectivity Is Associated With Clinical Symptoms and Cognition in Late-Life Depression.

Biol Psychiatry Cogn Neurosci Neuroimaging

Center for Cognitive Medicine, Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tennessee; Geriatric Research, Education and Clinical Center, Department of Veterans Affairs Medical Center, Tennessee Valley Healthcare System, Nashville, Tennessee. Electronic address:

Published: February 2019

AI Article Synopsis

  • The study investigates how late-life depression (LLD) affects brain connectivity in older adults, focusing on specific brain networks like the default mode network (DMN) and cognitive control network (CCN).
  • The researchers analyzed data from 100 older adults, comparing those with LLD to nondepressed individuals, and found that LLD was linked to reduced DMN connectivity, particularly to a region in the frontal pole.
  • Increased connectivity in the CCN was correlated with more severe depression symptoms and poorer cognitive performance in areas such as memory and executive function among those with LLD.

Article Abstract

Background: Late-life depression (LLD) has been associated with alterations in intrinsic functional networks, best characterized in the default mode network (DMN), cognitive control network (CCN), and salience network. However, these findings often derive from small samples, and it is not well understood how network findings relate to clinical and cognitive symptomatology.

Methods: We studied 100 older adults (n = 79 with LLD, n = 21 nondepressed) and collected resting-state functional magnetic resonance imaging, clinical measures of depression, and performance on cognitive tests. We selected canonical network regions for each intrinsic functional network (DMN, CCN, and salience network) as seeds in seed-to-voxel analysis. We compared connectivity between the depressed and nondepressed groups and correlated connectivity with depression severity among depressed subjects. We then investigated whether the observed connectivity findings were associated with greater severity of common neuropsychiatric symptoms or poorer cognitive performance.

Results: LLD was characterized by decreased DMN connectivity to the frontal pole, a CCN region (Wald χ = 22.33, p < .001). No significant group differences in connectivity were found for the CCN or salience network. However, in the LLD group, increased CCN connectivity was associated with increased depression severity (Wald χ > 20.14, p < .001), greater anhedonia (Wald χ = 7.02, p = .008) and fatigue (Wald χ = 6.31, p = .012), and poorer performance on tests of episodic memory (Wald χ > 4.65, p < .031), executive function (Wald χ = 7.18, p = .007), and working memory (Wald χ > 4.29, p < .038).

Conclusions: LLD is characterized by differences in DMN connectivity, while CCN connectivity is associated with LLD symptomology, including poorer performance in several cognitive domains.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368882PMC
http://dx.doi.org/10.1016/j.bpsc.2018.09.003DOI Listing

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