4.2 Article

Multimodal MRI markers support a model of small vessel ischemia for depressive symptoms in very old adults

Journal

PSYCHIATRY RESEARCH-NEUROIMAGING
Volume 224, Issue 2, Pages 73-80

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.pscychresns.2014.08.009

Keywords

MRI markers; Depression; Geriatric

Funding

  1. Healthy Brain and Resilience grant - National Institutes of Health/National Institutes of Aging [R01 AG29232-05, R01 AG037451-01]
  2. National Institute of Mental Health [R01 MH086498]

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In older adults, depressive symptoms are associated with lower quality of life, high morbidity and mortality. This study aims to identify brain magnetic resonance imaging (MRI) features associated with late-life depressive symptoms in the population. Older community-dwelling adults (n=314) from the Health ABC study underwent brain MRL Logistic regression was used to characterize the relationships between depressive symptoms (Center for Epidemiologic Studies of Depression scale, CES-D) and the following whole-brain variables: white matter hyperintensity (WMH) burden, fractional anisotropy (FA), and gray matter volume (GMV). Analyses examining possible regional differences between the CES-D groups controlled for Modified Mini-Mental State Examination score and diabetes status. The relative importance of localization of the markers was examined by comparing the distribution of significant peaks across the brain. Each whole-brain variable showed loss of integrity associated with high CES-D. For GMV, the odds ratio (OR)=0.84 (95% confidence interval (Cl) 0.74, 0.96); for FA, OR=0.714 (95% Cl 0.57, 0.88); for WMH, OR=1.89 (95%Cl 1.33, 2.69). Voxel-wise analyses and patterns of peak significance showed non-specific patterns for white matter measures. Loss of GMV was most significant in the bilateral insula and anterior cingulate cortex. This study supports a cerebrovascular pattern for depressive symptoms in older adults. The localization of gray matter changes to the insula, a watershed area and a hub of affective circuits, suggests an etiological pathway from ischemia to increased depressive burden. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

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