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Cortical Thickness and Hippocampal Volume in Vascular and Non-vascular Depressed Patients

Bibliographic Data

ID15520091
AuthorsDakota A Egglefield (0000-0003-1220-5559, The Graduate Center, CUNY, corresponding author), Sophie Schiff (0000-0002-3366-5311, The Graduate Center, CUNY), Jeffrey N Motter (0000-0002-7372-3424, Columbia University), Alice Grinberg (0000-0002-6682-6046, Albert Einstein College of Medicine), Bret R Rutherford (0000-0002-4660-119X, Columbia University), Joel R Sneed (0000-0003-1449-6839, The Graduate Center, CUNY)
Year2021
Volume12
Pages697489-697489
Publication date2021-07-14
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2021.697489
PMID34335333
OpenAlexW3178681460
LanguageEN
References cited37

Background: Reduced cortical thickness and hippocampal volume are prevalent markers of late life depression as well as mild cognitive impairment (MCI) but are conspicuously absent in the vascular depression (VD) literature. The present study aimed to determine differences in cortical thickness and hippocampal volume between VD and non-VD patients. Methods: Participants were enrolled in an 8-week open treatment antidepressant trial. Forty-one depressed individuals aged 50 and older underwent brain magnetic resonance imaging at baseline and were classified as VD or non-VD. Cortical thickness values for the left and right entorhinal, parahippocampal, and precuneal cortices, as well as left and right hippocampal volume, were linearly regressed on VD status to determine mean differences between VD and non-VD. Covariates included site, age, sex, and mean thickness or intracranial volume. Results: No statistical differences were found between VD and non-VD patients in cortical thickness of the bilateral precuneal, entorhinal, or parahippocampal cortices, or hippocampal volume ( p > 0.001). Conclusions: The absence of statistical differences in gray matter between VD and non-VD patients raises several diagnostic, etiological, and developmental possibilities, namely that VD may not be connected with other late-life psychiatric illnesses such as MCI or dementia and that vascular disease may not be a common etiological risk factor for depression and dementia. Larger datasets, prospective longitudinal studies, and cognitively intact controls are needed to further address these types of questions

Alzheimer's disease · Brain size · Cardiology · Dementia · Depression (economics · Disease · Entorhinal cortex · Etiology · Hippocampal formation · Late life depression · Magnetic resonance imaging · Radiology · Vascular dementia · Blood Pressure and Hypertension Studies · Dementia and Cognitive Impairment Research · Functional Brain Connectivity Studies · Medicine · Psychology · Internal Medicine

  • Multiple imputation

    Open Access•Joseph L Schafer•Statistical Methods in Medical…•1999

Highly citedNo

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