Author:
Parisien Marc,van Reij Roel R.I.,Khoury Samar,Koseli Eda,Karaky Mohamad,van den Hoogen Nynke J.,Peng Garrie,Allegri Massimo,de Gregori Manuela,Chelly Jacques E.,Rakel Barbara A.,Aasvang Eske K.,Kehlet Henrik,Buhre Wolfgang F.F.A.,Bryant Camron D.,Damaj M. Imad,King Irah L.,Mogil Jeffrey S.,Joosten Elbert A.J.,Diatchenko Luda
Abstract
ABSTRACTChronic post-surgical pain affects a large proportion of people undergoing surgery, delaying recovery time and worsening quality of life. Although many environmental variables have been established as risk factors, less is known about genetic risk. To uncover genetic risk factors we performed genome-wide association studies in post-surgical cohorts of five surgery types— hysterectomy, mastectomy, abdominal, hernia, and knee— totaling 1350 individuals. Genetic associations between post-surgical chronic pain levels on a numeric rating scale (NRS) and additive genetic effects at common SNPs were evaluated. We observed genome-wide significant hits in almost all cohorts that displayed significance at the SNP, gene, and pathway levels. The cohorts were then combined via a GWAS meta-analysis framework for further analyses. Using partitioned heritability, we found that loci at genes specifically expressed in the immune system carried enriched heritability, especially genes related to B and T cells. The relevance of B cells in particular was then demonstrated in mouse postoperative pain assays. Taken altogether, our results suggest a role for the adaptive immune system in chronic post-surgical pain.
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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