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Cortical Thickness and Hippocampal Volume in Vascular and Non-vascular Depressed Patients.
Egglefield, Dakota A; Schiff, Sophie; Motter, Jeffrey N; Grinberg, Alice; Rutherford, Bret R; Sneed, Joel R.
Afiliação
  • Egglefield DA; The Graduate Center, City University of New York, New York, NY, United States.
  • Schiff S; Queens College, City University of New York, Queens, NY, United States.
  • Motter JN; The Graduate Center, City University of New York, New York, NY, United States.
  • Grinberg A; Queens College, City University of New York, Queens, NY, United States.
  • Rutherford BR; Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, NY, United States.
  • Sneed JR; Division of Geriatric Psychiatry, New York State Psychiatric Institute, New York, NY, United States.
Front Psychiatry ; 12: 697489, 2021.
Article em En | MEDLINE | ID: mdl-34335333
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Revista: Front Psychiatry Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Revista: Front Psychiatry Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos