Slow twitch paraspinal muscle dysregulation in adolescent idiopathic scoliosis exhibiting HIF‐2α misexpression

• Published in: JOR-spine 2022-12, Vol.5 (4), p.e1227-n/a
• Main Authors: Tam, Wai Kit, Cheung, Jason P. Y., Koljonen, Paul A., Kwan, Kenny Y. H., Cheung, Kenneth M.C., Leung, Victor Y. L.
• Format: Article
• Language: English
• Subjects: adolescent idiopathic scoliosis; Antibodies; Back pain; Biopsy; Gene expression; Hypoxia; hypoxia inducible factors; Musculoskeletal system; Myogenesis; paraspinal muscle; Physiology; Protein expression; Proteins; Scoliosis; Software
• ISSN: 2572-1143; 2572-1143
• DOI: 10.1002/jsp2.1227

Background Adolescent idiopathic scoliosis (AIS) refers to a three‐dimensional spinal deformity which has a typical onset during adolescence. In most cases, the cause of the deformity cannot be clearly identified. Unbalanced paraspinal muscle activity in AIS patients was reported and hypoxia was implicated to regulate myogenesis. This study aims to investigate the association between myogenesis/muscle toning and HIF‐αs activity in the pathogenesis of AIS. Methods HIF‐αs expression was examined by enzyme‐linked immunosorbent assay and western blot in paraspinal myoblasts isolated from 18 subjects who underwent deformity correction surgery. QPCR was conducted to measure the gene expression levels of perinatal muscle fiber markers MYH3, MYH8; slow twitch muscle fiber markers MHY7; fast twitch muscle fiber markers MYH4; and myogenic regulatory factors MYF5 and MYOG. Slow and fast twitch muscle fiber composition in concave/convex paraspinal musculature of AIS subjects was evaluated by immunostaining of myosin heavy chain type I (MyHC I) and myosin heavy chain type II (MyHC II). Results Reduced HIF‐2α induction under hypoxia was found in paraspinal myoblast culture of 33% AIS subjects. We detected a suppression of perinatal and slow twitch muscle fiber associated genes, but not fast twitch muscle fiber‐associated genes and myogenic regulatory factors in HIF‐2α misexpressed AIS myoblasts. Distinct reduction of slow twitch muscle fiber was evidenced in convex paraspinal musculature, suggesting an asymmetric expression of slow twitch muscle fiber in HIF‐2α misexpressed AIS patients. Conclusions This study indicates an association of abnormal HIF‐2α expression in paraspinal myoblasts and a disproportionate slow twitch muscle fiber content in the convexity of the curvature in a subset of AIS subjects, suggesting HIF‐2α dysregulation as a possible risk factor for AIS. The role of HIF‐2α in paraspinal muscle function during spinal growth and its relevance in AIS prognosis warrants further investigation. This study indicates an association of abnormal HIF‐2α expression in paraspinal myoblasts and a disproportionate slow twitch muscle fiber content in the convexity of the curvature in a sub‐set of AIS subjects, suggesting HIF‐2α dysregulation as a possible risk factor for AIS. The role of HIF‐2α in paraspinal muscle function during spinal growth and its relevance in AIS prognosis warrants further investigation.