Genetic and epigenetic mechanisms influencing acute to chronic postsurgical pain transitions in pediatrics: Preclinical to clinical evidence

• Published in: Canadian Journal of Pain = Revue Canadienne de la Douleur Vol. 6; no. 2; pp. 85 - 107
• Main Authors: Dourson, Adam J., Willits, Adam, Raut, Namrata G.R., Kader, Leena, Young, Erin, Jankowski, Michael P., Chidambaran, Vidya
• Format: Journal Article Book Review
• Language: English
• Published: United States Taylor & Francis 2022; Taylor & Francis Ltd; Taylor & Francis Group
• Subjects: association studies; chronic postsurgical pain; clinical; CPSP; DNA methylation; Epigenetics; Genomics; GWAS; immunogenetics; nociception; Pediatrics; Review; rodent models; variants; chronic postsurgical pain; clinical; GWAS; association studies; CPSP; rodent models; DNA methylation; immunogenetics; nociception; variants; epigenetics
• ISSN: 2474-0527; 2474-0527
• DOI: 10.1080/24740527.2021.2021799

Chronic postsurgical pain (CPSP) in children remains an important problem with no effective preventive or therapeutic strategies. Recently, genomic underpinnings explaining additional interindividual risk beyond psychological factors have been proposed. We present a comprehensive review of current preclinical and clinical evidence for genetic and epigenetic mechanisms relevant to pediatric CPSP. Narrative review. Animal models are relevant to translational research for unraveling genomic mechanisms. For example, Cacng2, p2rx7, and bdnf mutant mice show altered mechanical hypersensitivity to injury, and variants of the same genes have been associated with CPSP susceptibility in humans; similarly, differential DNA methylation (H1SP) and miRNAs (miR-96/7a) have shown translational implications. Animal studies also suggest that crosstalk between neurons and immune cells may be involved in nociceptive priming observed in neonates. In children, differential DNA methylation in regulatory genomic regions enriching GABAergic, dopaminergic, and immune pathways, as well as polygenic risk scores for enhanced prediction of CPSP, have been described. Genome-wide studies in pediatric CPSP are scarce, but pathways identified by adult gene association studies point to potential common mechanisms. Bench-to-bedside genomics research in pediatric CPSP is currently limited. Reverse translational approaches, use of other -omics, and inclusion of pediatric/CPSP endophenotypes in large-scale biobanks may be potential solutions. Time of developmental vulnerability and longitudinal genomic changes after surgery warrant further investigation. Emergence of promising precision pain management strategies based on gene editing and epigenetic programing emphasize need for further research in pediatric CPSP-related genomics.