Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Background Depression diagnosis is associated with decreased prefrontal thickness and hippocampal volume. Less is known about these associations in the general population and across the lifespan. We investigate associations between (subclinical) depression and brain structure, and moderating effects of age and sex. Methods We included 1870 participants between 18 and 85 years old from 3 sites (UK, Norway, Netherlands) of the European Lifebrain consortium. Meta-analyses were performed, calculating per-site and pooled effect sizes for associations between mild/moderate depression and FreeSurfer-derived rACC, mOFC thickness or hippocampal volume. In ongoing analyses, we include additional cohorts (Spain, Germany, Sweden, UK, Denmark; final N∼3500) and explore the effects of age and sex. Results 374 participants met criteria for mild-to-moderate depression, with 181 meeting criteria for moderate depression. Mild-to-moderate depression (vs. no depression) was not significantly associated with rACC (Cohen’s d=-0.090) or mOFC (d=-0.114) thickness, or hippocampal volume (d=0.018). Similarly, moderate depression was not significantly associated with rACC (d=-0.164) or mOFC thickness (d=-0.088), or hippocampal volume (d=-0.012). Conclusions Mild or moderate depression was not associated with medial prefrontal thickness, or hippocampal volume, although effect-sizes for medial prefrontal areas were similar to previous observations in the ENIGMA consortium. However, associations with hippocampal volume were not in line with earlier ENIGMA findings, potentially due to few participants with moderate depression. Of relevance, earlier studies often had a more limited age range, and associations might change across the lifespan. Therefore, in ongoing analyses we investigate potential moderating effects of age which will be presented at the conference.

Original publication

DOI

10.1016/j.biopsych.2021.02.680

Type

Conference paper

Publisher

Society of Biological Psychiatry

Publication Date

01/05/2021

Volume

89

Pages

S272 - S272