Genome-wide Association Study of Multisite Chronic Pain in UK Biobank

Johnston, K. J. A.; Adams, M. J.; Nicholl, B. I.; Ward, J.; Strawbridge, R.; Ferguson, A.; McIntosh, A.; Bailey, M. E. S.; Smith, D. J.

doi:10.1101/502807

bioRxiv · 10.1101/502807

Genome-wide Association Study of Multisite Chronic Pain in UK Biobank

Johnston, K. J. A.·Adams, M. J.·Nicholl, B. I.·Ward, J.·Strawbridge, R.·Ferguson, A.·McIntosh, A.·Bailey, M. E. S.·Smith, D. J.

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Abstract

Chronic pain is highly prevalent worldwide, contributing a significant socioeconomic and public health burden. Several aspects of chronic pain, for example back pain and a severity-related phenotype, chronic pain grade, have been shown to be complex, heritable traits with a polygenic component. Additional pain-related phenotypes capturing aspects of an individuals overall sensitivity to experiencing and reporting chronic pain have also been suggested. We have here made use of a measure of the number of sites of chronic pain in individuals within the general UK population. This measure, termed Multisite Chronic Pain (MCP), is also a complex trait, but its genetic architecture has not previously been investigated. To address this, a large-scale genome-wide association study (GWAS) of MCP was carried out in ~380,000 UK Biobank participants to identify associated genetic variants. Findings were consistent with MCP having a significant polygenic component with a SNP heritability of 10.2%, and 76 independent lead single nucleotide polymorphisms (SNPs) at 39 risk loci were identified. Additional gene-level association analyses identified neurogenesis, synaptic plasticity, nervous system development, cell-cycle progression and apoptosis genes as being enriched for genetic association with MCP. Genetic correlations were observed between MCP and a range of psychiatric, autoimmune and anthropometric traits including major depressive disorder (MDD), asthma and BMI. Furthermore, in Mendelian randomisation (MR) analyses a bi-directional causal relationship was observed between MCP and MDD. A polygenic risk score (PRS) for MCP was found to significantly predict chronic widespread pain (pain all over the body), indicating the existence of genetic variants contributing to both of these pain phenotypes. These findings support the proposition that chronic pain involves a strong nervous system component and have implications for our understanding of the physiology of chronic pain and for the development of novel treatment strategies.

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Johnston, K. J. A., Adams, M. J., Nicholl, B. I., Ward, J., Strawbridge, R., Ferguson, A., McIntosh, A., Bailey, M. E. S., Smith, D. J.. 2018-12-20. Genome-wide Association Study of Multisite Chronic Pain in UK Biobank. https://doi.org/10.1101/502807

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