4.5 Article

Associations of depression and regional brain structure across the adult lifespan: Pooled analyses of six population-based and two clinical cohort studies in the European Lifebrain consortium

期刊

NEUROIMAGE-CLINICAL
卷 36, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2022.103180

关键词

Neuroimaging; Depressive symptoms; Meta -analysis; Lifespan; Grey matter; Brain structure

资金

  1. EU [732592]
  2. LCBC: The European Research Council [283634, 725025, 313440]
  3. Norwegian Research Council
  4. National Association for Public Health's dementia research program, Norway
  5. Knut and Alice Wallenberg (KAW) foundation
  6. Spanish Ministry of Economy and Competitiveness (MINECO) grant [PSI2015-64227-R]
  7. California Walnut Commission, Sacramento, California [NCT01634841]
  8. ICREA Academia
  9. German Federal Ministry of Education and Research [16SV5537/16SV5837/16SV5538/16SV5536K/01UW0808/01UW0706/01GL1716A/01GL1716B]
  10. European Research Council [677804]
  11. UK Medical Research Council [G1001354]
  12. Wellcome Trust [203139/Z/16/Z]
  13. HDH Wills 1965 Charitable Trust [1117747]
  14. NIHR Oxford Health Biomedical Research Centre
  15. Geestkracht program of the Netherlands Organisation for Health Research and Development [10-000-1002]
  16. VU University Medical Center
  17. GGZ inGeest
  18. Leiden University Medical Center
  19. Leiden University
  20. GGZ Rivierduinen
  21. University Medical Center Groningen
  22. University of Groningen
  23. Lentis
  24. GGZ Friesland
  25. GGZ Drenthe
  26. Rob Giel Onderzoekscentrum
  27. NWO VICI [91811602]
  28. European Research Council (ERC) [283634, 725025, 677804] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

This study investigated the association between depressive symptoms and depression status with brain structures, and found that in clinical patient-control cohorts, both depressive symptoms and depression status were associated with lower thickness and volume of specific brain regions, while no such associations were observed in the general population.
Objective: Major depressive disorder has been associated with lower prefrontal thickness and hippocampal volume, but it is unknown whether this association also holds for depressive symptoms in the general population. We investigated associations of depressive symptoms and depression status with brain structures across population-based and patient-control cohorts, and explored whether these associations are similar over the lifespan and across sexes. Methods: We included 3,447 participants aged 18-89 years from six population-based and two clinical patient -control cohorts of the European Lifebrain consortium. Cross-sectional meta-analyses using individual person data were performed for associations of depressive symptoms and depression status with FreeSurfer-derived thickness of bilateral rostral anterior cingulate cortex (rACC) and medial orbitofrontal cortex (mOFC), and hippocampal and total grey matter volume (GMV), separately for population-based and clinical cohorts. Results: Across patient-control cohorts, depressive symptoms and presence of mild-to-severe depression were associated with lower mOFC thickness (rsymptoms =-0.15/ rstatus =-0.22), rACC thickness (rsymptoms =-0.20/ rstatus =-0.25), hippocampal volume (rsymptoms =-0.13/ rstatus = 0.13) and total GMV (rsymptoms =-0.21/ rstatus =-0.25). Effect sizes were slightly larger for presence of moderate-to-severe depression. Associations were similar across age groups and sex. Across population-based cohorts, no associations between depression and brain structures were observed. Conclusions: Fitting with previous meta-analyses, depressive symptoms and depression status were associated with lower mOFC, rACC thickness, and hippocampal and total grey matter volume in clinical patient-control cohorts, although effect sizes were small. The absence of consistent associations in population-based cohorts with mostly mild depressive symptoms, suggests that significantly lower thickness and volume of the studied brain structures are only detectable in clinical populations with more severe depressive symptoms.

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