학술논문

Psychosocial factors and hippocampal subfields: The Medea‐7T study
Document Type
Report
Source
Human Brain Mapping. March 2023, Vol. 44 Issue 5, p1964, 21 p.
Subject
Psychological aspects
Social aspects
Analysis
Depression (Mood disorder) -- Social aspects -- Psychological aspects -- Analysis
Dementia -- Analysis -- Social aspects -- Psychological aspects
Nervous system diseases -- Social aspects -- Psychological aspects -- Analysis
Anxiety -- Psychological aspects -- Analysis -- Social aspects
Stress (Psychology) -- Psychological aspects -- Social aspects -- Analysis
Depression, Mental -- Social aspects -- Psychological aspects -- Analysis
Language
English
ISSN
1065-9471
Abstract
INTRODUCTION The hippocampus is implicated in many neuropsychiatric diseases, such as depression, schizophrenia, and dementia, where frequently a smaller hippocampal volume has been observed in comparing cases to controls. Based [...]
: Specific subfields within the hippocampus have shown vulnerability to chronic stress, highlighting the importance of looking regionally within the hippocampus to understand the role of psychosocial factors in the development of neurodegenerative diseases. A systematic review on psychosocial factors and hippocampal subfield volumes was performed and showed inconsistent results, highlighting the need for future studies to explore this relationship. The current study aimed to explore the association of psychosocial factors with hippocampal (subfield) volumes, using high‐field 7T MRI. Data were from the Memory Depression and Aging (Medea)‐7T study, which included 333 participants without dementia. Hippocampal subfields were automatically segmented from T2‐weighted images using ASHS software. Generalized linear models accounting for correlated outcomes were used to assess the association between subfields (i.e., entorhinal cortex, subiculum, Cornu Ammonis [CA]1, CA2, CA3, dentate gyrus, and tail) and each psychosocial factor (i.e., depressive symptoms, anxiety symptoms, childhood maltreatment, recent stressful life events, and social support), adjusted for age, sex, and intracranial volume. Neither depression nor anxiety was associated with specific hippocampal (subfield) volumes. A trend for lower total hippocampal volume was found in those reporting childhood maltreatment, and a trend for higher total hippocampal volume was found in those who experienced a recent stressful life event. Among subfields, low social support was associated with lower volume in the CA3 (B = −0.43, 95% CI: −0.72; −0.15). This study suggests possible differential effects among hippocampal (subfield) volumes and psychosocial factors.