Comparative analysis of paraspinal muscle imbalance between idiopathic scoliosis and congenital scoliosis from the transcriptome aspect

Author:

Wang Zhen12ORCID,Zhao Junduo1,Tan Haining3,Jiao Yang1,Chen Xin1,Shen Jianxiong1

Affiliation:

1. Department of Orthopedics Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences Beijing China

2. Department of Orthopedics The First Affiliated Hospital of Nanjing Medical University Nanjing China

3. Department of Orthopedics Beijing Friendship Hospital, Capital Medical University Beijing China

Abstract

AbstractBackgroundPrevious studies have analyzed paraspinal muscle imbalance in idiopathic scoliosis (IS) with methods including imaging, histology and electromyography. However, whether paraspinal muscle imbalance is the cause or the consequence of spinal deformities in IS remains unclear. Comparison of paraspinal muscle imbalance between IS and congenital scoliosis (CS) may shed some light on the causality of paraspinal muscle imbalance and IS. This study aimed to elucidate the generality and individuality of paraspinal muscle imbalance between IS and CS from gene expression.MethodsFive pairs of surgical‐treated IS and CS patients were matched. Bilateral paraspinal muscles at the apex were collected for transcriptome sequencing. Differentially expressed genes (DEGs) between the convexity and concavity in both IS and CS were identified. Comparison of DEGs between IS and CS was conducted to discriminate IS‐specific DEGs from DEGs shared by both IS and CS. Bioinformatics analysis was performed. The top 10 hub genes in the protein–protein interaction (PPI) network of IS‐specific DEGs were validated by quantitative PCR (qPCR) in 10 pairs of IS and CS patients.ResultsA total of 370 DEGs were identified in IS, whereas 380 DEGs were identified in CS. Comparison of DEGs between IS and CS identified 59 DEGs shared by IS and CS, along with 311 DEGs specific for IS. These IS‐specific DEGs were enriched in response to external stimulus and signaling receptor binding in GO terms and calcium signaling pathway in KEGG pathways. The top 10 hub genes in the PPI network of IS‐specific DEGs include BDKRB1, PRH1‐TAS2R14, CNR2, NPY4R, HTR1E, CXCL3, ICAM1, ALB, ADIPOQ, and GCGR. Among these hub genes, the asymmetrical expression of PRH1‐TAS2R14 and ADIPOQ in IS but not CS were validated by qPCR.ConclusionsTranscriptomic differences in bilateral paraspinal muscles between the convexity and concavity in IS share few similarities with those in CS.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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