4.7 Article

Structural brain correlates of serum and epigenetic markers of inflammation in major depressive disorder

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 92, Issue -, Pages 39-48

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2020.11.024

Keywords

Major depressive disorder; Depression; Inflammation; C-reactive protein; CRP; Methylation; Brain morphology; Brain structure; White matter integrity; MRI

Funding

  1. Chief Scientist Office of the Scottish Government Health Directorates [CZD/16/6]
  2. Scottish Funding Council [HR03006]
  3. Wellcome Trust [216767/Z/19/Z, 104036/Z/14/Z]
  4. Medical Research Council UK
  5. Medical Research Council
  6. University of Edinburgh through the Precision Medicine Doctoral Training program
  7. UK Medical Research Council [MR/R024065/1]
  8. National Institutes of Health (NIH) [R01AG054628]
  9. MRC [MR/R024065/1, MR/J006971/1, UKDRI-4002] Funding Source: UKRI
  10. Wellcome Trust [216767/Z/19/Z] Funding Source: researchfish

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The study revealed associations between peripheral inflammation and depressive symptoms as well as brain structures, with methylation-based inflammation markers showing stronger connections to imaging metrics than serum-based CRP measures. These findings emphasize the importance of methylation-based measures for future studies on the relationship between peripheral inflammation and depressive symptoms.
Inflammatory processes are implicated in the aetiology of Major Depressive Disorder (MDD); however, the relationship between peripheral inflammation, brain structure and depression remains unclear, partly due to complexities around the use of acute/phasic inflammatory biomarkers. Here, we report the first large-scale study of both serological and methylomic signatures of CRP (considered to represent acute and chronic measures of inflammation respectively) and their associations with depression status/symptoms, and structural neuroimaging phenotypes (T1 and diffusion MRI) in a large community-based sample (Generation Scotland; N-MDD cases = 271, N-controls = 609). Serum CRP was associated with overall MDD severity, and specifically with current somatic symptoms-general interest (beta = 0.145, P-FDR = 6 x 10(-4)) and energy levels (beta = 0.101, P-FDR = 0.027), along with reduced entorhinal cortex thickness (beta = -0.095, P-FDR = 0.037)(.) DNAm CRP was significantly associated with reduced global grey matter/cortical volume and widespread reductions in integrity of 16/24 white matter tracts (with greatest regional effects in the external and internal capsules, beta(FA)= -0.12 to -0.14). In general, the methylation-based measures showed stronger associations with imaging metrics than serum-based CRP measures (beta average = -0.15 versus beta average = 0.01 respectively). These findings provide evidence for central effects of peripheral inflammation from both serological and epigenetic markers of inflammation, including in brain regions previously implicated in depression. This suggests that these imaging measures may be involved in the relationship between peripheral inflammation and somatic/depressive symptoms. Notably, greater effects on brain morphology were seen for methylation-based rather than serum-based measures of inflammation, indicating the importance of such measures for future studies.

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