DNA methylation signatures of C-reactive protein associations with structural neuroimaging measures and major depressive disorder

BackgroundInflammatory processes are implicated in the aetiology of Major Depressive Disorder (MDD); however, the relationship between peripheral inflammation, brain structure and depression remains unclear. This study investigates associations between depression, structural neuroimaging measures and two measures of inflammation: serum-based C-reactive protein (CRP) and a methylation-based score for CRP (DNAm CRP) in a large community-based sample. MethodsSerum CRP and DNAm CRP were assessed for participants in Generation Scotland (NMDD cases = 240, Ncontrols = 558) alongside structural brain scans (T1 and diffusion MRI). Linear regression was used to investigate associations between (i) both CRP measures and depressive symptoms, (ii) both CRP measures and structural imaging variables and (iii) inflammation x MDD interaction effects (for both CRP measures) with imaging measures. ResultsIncreased serum CRP was significantly associated with overall MDD symptom severity and specifically with somatic symptoms-general interest ({beta}= 0.145, PFDR = 6x10-4) and energy levels ({beta}= 0.101, PFDR = 0.027) and also reduced entorhinal cortex thickness ({beta}= - 0.095, PFDR = 0.037). DNAm CRP was significantly associated with reduced global grey matter/cortical volume and reduced integrity of 16 white matter tracts and showed larger effect sizes ({beta}average = -0.15) compared to serum CRP across all measures ({beta}average = 0.01). ConclusionsAcute measures of CRP were related to current depression symptoms, specifically somatic symptoms, whereas methylation signatures of inflammation demonstrated greater differences in global and regional brain structure. This study highlights the utility of combining serological and methylation markers to study chronic inflammation effects on the brain in psychiatric disorders.