Cited by 383Stress Responses and CortisolChild Abuse and TraumaTreatment of Major Depression

Hippocampal changes associated with early-life adversity and vulnerability to depression

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Rao, Uma, Chen, Li-Ann, Bidesi, Anup S., Shad, Mujeeb U., Thomas, M. Albert, Hammen, Constance L.·2010·Biological Psychiatry

Abstract

Background Smaller hippocampal volume has been reported in some adult and pediatric studies of unipolar major depressive disorder. It is not clear whether the smaller hippocampal volume precedes or is a consequence of the illness. Early-life adversity is associated with both smaller hippocampal volume and increased vulnerability to depressive disorder. Hippocampal changes may mediate the relationship between early-life adversity and depressive illness in a subset of patients. However, there are no reports of longitudinal clinical studies that have examined this issue.Methods Thirty adolescents with unipolar major depressive disorder, 22 adolescent volunteers with no personal history of a psychiatric illness including depression but who were at high risk for developing depression by virtue of parental depression (high-risk group), and 35 adolescent volunteers with no personal or family history of a psychiatric disorder (control subjects) underwent volumetric magnetic resonance imaging studies. Information was also gathered on early and recent adverse experiences with standard interviews. The participants were followed for up to 5 years to assess the onset and clinical course of depression.Results Depressed and high-risk groups had significantly smaller left and right hippocampal volumes than control subjects. Higher levels of early-life adversity were associated with smaller hippocampal volumes. Smaller hippocampal volume partially mediated the effect of early-life adversity on depression during longitudinal follow-up.Conclusions Smaller hippocampal volume in adolescents at high risk for depression suggests that it may be a vulnerability marker for the illness. Early-life adversity may interact with genetic vulnerability to induce hippocampal changes, potentially increasing the risk for depressive disorder.

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Crossref · 10.1016/j.biopsych.2009.10.017

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  • Some studies indicate that these structural changes may represent a pre-existing vulnerability to a major depressive episode, especially in people with particular genetic profiles or early life stress histories.

    “several other studies have found that these structural changes may reflect a pre-existing vulnerability to a MDE, particularly for individuals with certain genetic profiles and/or early life stress (ELS) histories (39–45).”

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References 74 · Cited by 383

Authors
Rao, U., Chen, L.-A., Bidesi, A. S., Shad, M. U., Thomas, M. A., & Hammen, C. L.
Affiliations
  • The University of Texas Southwestern Medical Center (US)
  • University of California, Los Angeles (US)
Corresponding author
Rao, Uma
Venue
Biological Psychiatry
Publisher
Elsevier BV
Published
2010-02
Volume
67
Issue
4
Pages
357-364
ISSN
0006-3223 (ISSN-L)
OpenAlex
W2018031501
Cited by
383
References
74
Citations by year
2026: 11 · 2025: 13 · 2024: 17 · 2023: 19 · 2022: 20 · 2021: 54 · 2020: 23 · 2019: 24 · 2018: 26 · 2017: 21 · 2016: 28 · 2015: 28 · 2014: 27 · 2013: 11 · 2012: 19
FWCI
7.49
Type
journal article
Language
en
Open access
Locations
  • Biological Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health (DA14037, DA15131, DA17804, DA17805, MH01419, MH62464, MH68391)
  • National Alliance for Research on Schizophrenia and Affective Disorders
Topics
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Social Sciences › Psychology › Clinical Psychology › Child Abuse and Trauma
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
Keywords
hippocampal volume, childhood adversity, depression vulnerability, unipolar major depression, adolescents, parental depression, high-risk group, genetic susceptibility, mediation, longitudinal follow-up, neuroimaging biomarkers
MeSH terms
Adolescent, Analysis of Variance, Child, Major Depressive Disorder, Female, Follow-Up Studies, Hippocampus, Humans, Functional Laterality, Life Change Events, Magnetic Resonance Imaging, Male, Chi-Square Distribution, Young Adult

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