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Common factor GWAS identifies shared risk loci between chronic widespread pain, atherosclerosis and arterial stiffness.

McGrath, D. P.; Kazemi Naeini, M.; Freydin, M. B.; Cecelja, M.; Compte, R.; Williams, F. M.

2025-09-12 public and global health
10.1101/2025.09.08.25331262 medRxiv
Show abstract

Chronic widespread pain (CWP) is a complex condition linked to impaired arterial health, including atherosclerosis and increased arterial stiffness. Epidemiological evidence suggests shared biological mechanisms, with strong associations between CWP and arterial dysfunction, However, the genetic basis remains largely unexplored. We conducted a common pathway genome-wide association study using genomic structural equation modeling (GenomicSEM) and GWAS summary statistics for CWP, atherosclerosis, and pulse wave velocity to identify shared genetic factors. This analysis revealed 53 genome-wide significant variants contributing to a shared latent factor, with opposing trait loadings suggestive of antagonistic pleiotropy. Lead loci included RNF123, ATP2C1, and COMT, with gene-level analysis implicating neurodevelopmental pathways and glycosaminoglycan degradation through hyaluronidase activity. Chromatin interaction and expression mapping supported regulatory links in relevant tissues. Our findings demonstrate that neurogenic and extracellular matrix-related processes, including glycan metabolism, contribute to the shared genetic architecture of CWP and cardiovascular traits, offering mechanistic insight into their comorbidity.

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