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Prospective longitudinal voxel-based morphometry study of major depressive disorder in young individuals at high familial risk

Published online by Cambridge University Press:  10 June 2016

T. Nickson
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
S. W. Y. Chan
Affiliation:
Clinical Psychology, University of Edinburgh, Edinburgh, UK
M. Papmeyer
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK Translational Research Center, University Hospital of Psychiatry, University of Bern, Bern, Switzerland
L. Romaniuk
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
A. Macdonald
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
T. Stewart
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
S. Kielty
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
S. M. Lawrie
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
J. Hall
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK
J. E. Sussmann
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
A. M. McIntosh
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, Edinburgh, UK
H. C. Whalley*
Affiliation:
Division of Psychiatry, University of Edinburgh, Edinburgh, UK
*
*Address for correspondence: Heather Whalley, Ph.D., Division of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF, UK. (Email: heather.whalley@ed.ac.uk)

Abstract

Background

Previous neuroimaging studies indicate abnormalities in cortico-limbic circuitry in mood disorder. Here we employ prospective longitudinal voxel-based morphometry to examine the trajectory of these abnormalities during early stages of illness development.

Method

Unaffected individuals (16–25 years) at high and low familial risk of mood disorder underwent structural brain imaging on two occasions 2 years apart. Further clinical assessment was conducted 2 years after the second scan (time 3). Clinical outcome data at time 3 was used to categorize individuals: (i) healthy controls (‘low risk’, n = 48); (ii) high-risk individuals who remained well (HR well, n = 53); and (iii) high-risk individuals who developed a major depressive disorder (HR MDD, n = 30). Groups were compared using longitudinal voxel-based morphometry. We also examined whether progress to illness was associated with changes in other potential risk markers (personality traits, symptoms scores and baseline measures of childhood trauma), and whether any changes in brain structure could be indexed using these measures.

Results

Significant decreases in right amygdala grey matter were found in HR MDD v. controls (p = 0.001) and v. HR well (p = 0.005). This structural change was not related to measures of childhood trauma, symptom severity or measures of sub-diagnostic anxiety, neuroticism or extraversion, although cross-sectionally these measures significantly differentiated the groups at baseline.

Conclusions

These longitudinal findings implicate structural amygdala changes in the neurobiology of mood disorder. They also provide a potential biomarker for risk stratification capturing additional information beyond clinically ascertained measures.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2016 

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