Lin W P, Lin J H, Chen X W, Wu C Y, Zhang L Q, Huang Z D, Lai J M
Department of Orthopedics, The First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, PR China.
Genet Mol Res. 2011;10(3):1719-27. doi: 10.4238/vol10-3gmr1283.
We investigated a possible association between interleukin (IL)-10 single nucleotide polymorphisms (SNPs) and susceptibility to and severity of lumbar disc degeneration (LDD) in a Chinese cohort of 320 patients with LDD and 269 gender- and age-matched controls. The degree of disc degeneration was determined by magnetic resonance imaging using Schneiderman's classification. Genetic analysis of IL-10 promoter polymorphisms (at -1082 A/G, -819 T/C, and -592 A/C) was carried out by PCR-RFLP. A total of 134 herniated lumbar intervertebral discs were collected during surgery for IL-10 mRNA detection. For SNPs at -592, the A allele and AA genotype frequencies were significantly higher in LDD patients than in controls. Similarly, the AA genotype and A allele frequencies at -1082 were significantly higher in cases than in controls. Among the LDD subjects, carriers of AA at -592 and GG at -1082 had significantly lower mean IL-10 mRNA expression than the other two genotypes. The SNPs at each locus were not significantly associated with severity grade in the LDD patients. Logistic regression analyses showed that the AA at -1082, AA at -592, and IL-10 mRNA expression level were independent risk factors for LDD. We conclude that the IL-10 SNPs at -1082 A/G and -592 A/C as well as IL-10 mRNA in the herniated lumbar intervertebral discs are associated with susceptibility to LDD in this Chinese cohort, but not with disease severity.
我们在一个由320例腰椎间盘退变(LDD)患者和269例性别及年龄匹配的对照组成的中国队列中,研究了白细胞介素(IL)-10单核苷酸多态性(SNP)与LDD易感性及严重程度之间的可能关联。采用施奈德曼分类法通过磁共振成像确定椎间盘退变程度。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对IL-10启动子多态性(-1082 A/G、-819 T/C和-592 A/C)进行基因分析。手术中收集了134个腰椎间盘突出症患者的椎间盘用于检测IL-10 mRNA。对于-592位点的SNP,LDD患者中A等位基因和AA基因型频率显著高于对照组。同样,-1082位点的AA基因型和A等位基因频率在病例组中也显著高于对照组。在LDD受试者中,-592位点为AA和-1082位点为GG的携带者的平均IL-10 mRNA表达水平显著低于其他两种基因型。每个位点的SNP与LDD患者的严重程度分级均无显著关联。逻辑回归分析显示,-1082位点的AA、-592位点的AA以及IL-10 mRNA表达水平是LDD的独立危险因素。我们得出结论,在这个中国队列中,-1082 A/G和-592 A/C位点的IL-10 SNP以及腰椎间盘突出症患者椎间盘内的IL-10 mRNA与LDD易感性相关,但与疾病严重程度无关。