Qiao Jun, Xiao Lingyan, Xu Leilei, Qian Bangping, Zhu Zezhang, Qiu Yong
Department of Spine Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School.
Intensive Care Unit, the Second Hospital of Nanjing, Nanjing, Jiangsu, China.
Clin Spine Surg. 2018 Apr;31(3):E193-E196. doi: 10.1097/BSD.0000000000000628.
This is a genetic association study.
To investigate association between suppressor of cytokine signaling-3 (SOCS3) gene polymorphisms and the onset and progression of lumbar adolescent idiopathic scoliosis (AIS) and to further clarify its role in the regulation of SOCS3 expression in AIS patients.
Some studies showed that muscle development imbalance may be responsible for onset and progression of lumbar AIS. SOCS3 is one of the significant regulators of skeletal muscle development, and in vitro study showed that SOCS3 influences myoblast differentiation.
Rs4969198 was genotyped in 476 lumbar AIS patients and 672 controls. The differences of genotype and allele distributions between patients and controls were calculated using the χ test. Paravertebral muscles were collected from 53 AIS, 23 congenital scoliosis, and 18 lumbar disk herniation patients. AIS patients were classified into 3 groups according to the genotypes of each single nucleotide polymorphisms, and 1-way analysis of variance test was used to compare SOCS3 expression among different groups and genotypes.
Patients were found to have a significantly higher frequency of GG than the controls (40.8% vs. 29.9%, odds ratio=1.36; P=0.000), and the frequency of allele G was found to be remarkably higher in the patients than the controls (65.3% vs. 56.7%, odds ratio=1.15; P=0.000). AIS patients had significantly less muscle expression of the SOCS3 than the congenital scoliosis patients (2.73±2.17 vs. 4.62±2.41; P=0.006) and the lumbar disk herniation patients (2.73±2.17 vs. 4.12±2.93; P=0.009). The SOCS3 expression was significantly correlated with the curve severity (r=0.472; P=0.014).
The SOCS3 gene is significantly associated with the development of lumbar AIS in Chinese population. Decreased expression of SOCS3 is associated with larger severity of lumbar AIS.
Level III.
这是一项基因关联研究。
探讨细胞因子信号转导抑制因子3(SOCS3)基因多态性与青少年特发性脊柱侧凸(AIS)腰椎发病及进展的关系,并进一步阐明其在AIS患者中对SOCS3表达的调控作用。
一些研究表明,肌肉发育不平衡可能是青少年特发性脊柱侧凸腰椎发病及进展的原因。SOCS3是骨骼肌发育的重要调节因子之一,体外研究表明SOCS3影响成肌细胞分化。
对476例青少年特发性脊柱侧凸腰椎患者和672例对照进行Rs4969198基因分型。采用χ检验计算患者与对照之间基因型和等位基因分布的差异。收集53例青少年特发性脊柱侧凸、23例先天性脊柱侧凸和18例腰椎间盘突出症患者的椎旁肌。根据每个单核苷酸多态性的基因型将青少年特发性脊柱侧凸患者分为3组,采用单因素方差分析比较不同组和基因型之间的SOCS3表达。
发现患者中GG基因型频率显著高于对照组(40.8%对29.9%,比值比=1.36;P=0.000),且患者中等位基因G的频率显著高于对照组(65.3%对56.7%,比值比=1.15;P=0.000)。青少年特发性脊柱侧凸患者的SOCS3肌肉表达明显低于先天性脊柱侧凸患者(2.73±2.17对4.62±2.41;P=0.006)和腰椎间盘突出症患者(2.73±2.17对4.12±2.93;P=0.009)。SOCS3表达与侧弯严重程度显著相关(r=0.472;P=0.014)。
在中国人群中,SOCS3基因与青少年特发性脊柱侧凸腰椎的发生显著相关。SOCS3表达降低与青少年特发性脊柱侧凸腰椎严重程度增加有关。
三级。