Frontiers in Aging Neuroscience (Feb 2018)

Depressive Symptom Dimensions and Their Association with Hippocampal and Entorhinal Cortex Volumes in Community Dwelling Older Adults

  • Deirdre M. O’Shea,
  • Deirdre M. O’Shea,
  • Deirdre M. O’Shea,
  • Vonetta M. Dotson,
  • Vonetta M. Dotson,
  • Vonetta M. Dotson,
  • Adam J. Woods,
  • Adam J. Woods,
  • Adam J. Woods,
  • Eric C. Porges,
  • Eric C. Porges,
  • Eric C. Porges,
  • John B. Williamson,
  • John B. Williamson,
  • John B. Williamson,
  • Andrew O’Shea,
  • Andrew O’Shea,
  • Ronald Cohen,
  • Ronald Cohen,
  • Ronald Cohen

DOI
https://doi.org/10.3389/fnagi.2018.00040
Journal volume & issue
Vol. 10

Abstract

Read online

Objective: Research has shown that depression is a risk factor for Alzheimer’s disease (AD) and subsequent cognitive decline. This is compounded by evidence showing an association between depression and reduced hippocampal volumes; a primary structure implicated in the pathogenesis of the disease. Less is known about the relationship between depression and other AD vulnerable regions such as the entorhinal cortex. Given the heterogeneity of depressive symptom presentation, we examined whether symptom dimensions were associated with hippocampal and entorhinal cortex volumes in community dwelling older adults.Methods: Eighty-one community dwelling adults completed the Beck Depression Inventory – second edition and underwent structural neuroimaging. Measures of hippocampal and entorhinal cortex volumes were obtained using FreeSurfer software. Linear regression models included regions of interest as dependent variables, with depressive symptom dimensions, as independent variables, controlling for total intracranial volumes, age, education, and gender.Results: Somatic symptoms were negatively associated with total, right, and left hippocampal volumes. Affective symptoms were negatively associated with total entorhinal cortex volumes, with a marginal main effect on left entorhinal cortex volumes.Conclusion: Our findings provide support for examining depressive symptoms and their association with AD vulnerable regions along subdimensions of affective, cognitive, and somatic symptoms to better understand profiles of symptoms most associated with these regions. Conceptualizing depressive symptoms in this way may also better inform treatment approaches in terms of targeting types of symptoms that may be more closely linked to poorer brain and cognitive health outcomes.

Keywords