DNA Methylation and Protein Markers of Chronic Inflammation and Their Associations With Brain and Cognitive Aging

Background and Objective To investigate chronic inflammation in relation cognitive ageing by comparison of an epigenetic and serum biomarker of C-Reactive Protein and their associations with neuroimaging and cognitive outcomes. Methods At baseline, participants (N = 521) were cognitively normal, around 73 years of age (M = 72.4, SD = 0.716), and had inflammation, vascular risk (cardiovascular disease history, hypertension, diabetes, smoking, alcohol consumption and BMI) and neuroimaging (structural and diffusion MRI) data available. Baseline inflammatory status was quantified by a traditional measure of peripheral inflammation - serum C-Reactive Protein (serum CRP) - and an epigenetic measure (DNA methylation signature of CRP; DNAm CRP). Linear models were used to examine the inflammation-brain health associations; mediation analyses were performed to interrogate the relationship between chronic inflammation, brain structure and cognitive functioning. Results We demonstrate that DNAm CRP shows significantly (on average 6.4-fold) stronger associations with brain health outcomes than serum CRP. DNAm CRP is associated with total brain volume (beta = -0.197, 95% CI [-0.28, -0.12], p(FDR) = 8.42 x 10(-6)), grey matter volume (beta = -0.200, 95% CI [-0.28, -0.12], p(FDR) = 1.66 x 10(-5)) and white matter volume (beta = -0.150, 95% CI [-0.23, -0.07], p(FDR) = 0.001) and regional brain atrophy. We additionally find that DNAm CRP has an inverse association with global and domain-specific (speed, visuospatial and memory) cognitive functioning, and that brain structure partially mediates this CRP-cognitive association (up to 29.7%), dependent on lifestyle and health factors. Conclusions These results support the hypothesis that chronic inflammation may contribute to neurodegenerative brain changes which underlie differences in cognitive ability in later life and highlight the potential of DNA methylation proxies for indexing chronic inflammatory status. Classification of Evidence This study provides Class II evidence that a DNA methylation signature of CRP levels is more strongly associated with brain health outcomes than serum CRP levels.

Automated summary

The study shows that DNA methylation of C-Reactive Protein is more strongly associated with brain health outcomes than serum CRP, with significant associations with total brain volume, grey matter volume, white matter volume, and regional brain atrophy. Additionally, DNAm CRP has an inverse association with global and domain-specific cognitive functioning, and brain structure partially mediates this CRP-cognitive association depending on lifestyle and health factors.