Cited by 101Stress Responses and CortisolTreatment of Major DepressionNeural and Behavioral Psychology Studies

Hippocampal volume in vulnerability and resilience to depression

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Chan, Stella W.Y., Harmer, Catherine J., Norbury, Ray, O’Sullivan, Ursula, Goodwin, Guy M., Portella, Maria J.·2016·Journal of Affective Disorders

Abstract

Background Reduced hippocampal volume has been associated with clinical depression. However, it remains unclear whether these changes are a biological vulnerability marker or a consequence of this disorder. METHODS AND RESULTS (STUDY 1): We first compared hippocampal volumes between (i) never-depressed individuals with elevated risk for depression by virtue of high neuroticism (ii) recovered depressed individuals with matched levels of neuroticism; and (iii) individuals with low neuroticism and no history of depression. We replicated the finding of reduced hippocampal volume in the recovered group; unexpectedly however, the never-depressed high-risk group showed an increase in volume. One hypothesis is that this group had a mean age above the typical onset age for depression; hence, these participants who have remained euthymic despite their personality risk might in fact possess some resilience. METHODS AND RESULTS (STUDY 2): A subsequent study was therefore carried out to compare hippocampal volume between high-neurotic vs. low-neurotic volunteers in a younger sample. No group difference was found.Limitations The present findings are limited by a small sample size; the cross-sectional design precluded us from makineg definitive conclusions about causal effect.Conclusion Our overall results suggest that reduced hippocampal volumes is a neural marker for the scar effect of depression, although this structural impairment could also be seen as a vulnerability marker for the development of future recurrent episodes. By contrast, larger hippocampal volumes could be a biological marker of resilience. These findings have clinical implications regarding treatment development for the prevention of illness onset and recurrent depressive episodes.

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Crossref · 10.1016/j.jad.2015.09.021

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  • Previous studies suggest a strong impact of hippocampal structural alterations in the susceptibility to depression and an important contribution for recurrent episodes.

    “Importantly, previous studies also suggested a strong impact of hippocampal structural alterations in the susceptibility to depression40 and an important contribution for recurrent episodes.41”

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References 28 · Cited by 101

Authors
Chan, S. W. Y., Harmer, C. J., Norbury, R., O’Sullivan, U., Goodwin, G. M., & Portella, M. J.
Affiliations
Warneford Hospital (GB)
Corresponding author
Chan, Stella W.Y.
Venue
Journal of Affective Disorders
Publisher
Elsevier BV
Published
2016-01
Volume
189
Pages
199-202
ISSN
0165-0327 (ISSN-L)
OpenAlex
W2102182811
Cited by
101
References
28
Citations by year
2026: 6 · 2025: 7 · 2024: 15 · 2023: 8 · 2022: 5 · 2021: 7 · 2020: 11 · 2019: 11 · 2018: 12 · 2017: 16 · 2016: 3
FWCI
5.38
Type
journal article
Language
en
Open access
Locations
  • Journal of Affective Disorders (publishedVersion)
  • PubMed (publishedVersion)
  • Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
Funders
  • Ministerio de Ciencia e Innovación of the Spanish Government (CP10/00393)
  • European Regional Development Fund (ERDF) (2013-2016)
Topics
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords
hippocampal volume, depression, neuroticism, resilience, biomarkers, recurrent depression, depression prevention, brain structural changes
MeSH terms
Neuroticism, Adolescent, Adult, Anxiety Disorders, Atrophy, Cross-Sectional Studies, Depression, Female, Hippocampus, Humans, Hypertrophy, Magnetic Resonance Imaging, Male, Middle Aged, Risk Factors, Case-Control Studies, Resilience, Psychological, Young Adult, Neuroimaging

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