摘要
目的:探讨白介素6(IL-6)基因启动子-572C/G多态性与非酒精性脂肪肝炎(NASH)相关性.方法:应用聚合酶联反应-限制性片段长度多态性(PCR-RFLP)方法,分别检测NASH患者78例和正常者104例IL-6基因启动子-572C/G多态性的变异.采用ELISA法检测NASH患者组IL-6血清含量.结果:IL-6基因启动子-572位点的C等位基因频率高于健康对照组,两组基因分布频率有显著统计学差异(0.564 vs 0.404,P<0.05):NASH患者组中CC基因型携带者IL-6血清含量显著高于其他基因型携带者(6.54±4.21 vs 4.68±2.88,P<0.05),但HOMA-IR及BMI与其他两组基因型相比较并无显著统计学差异.结论:IL-6基因启动子-572位点的C等位基因与NASH发病具有一定程度相关性.
AIM:To investigate the relationship between the C/G genotypes of interleukin-6(IL-6)single nucleotide polymorphism(SNP)at 572 and the development of nonalcoholic steatohepatitis (NASH). METHODS:Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) was used to determine a common polymorphism of the human IL-6 gene-572C/G in 104 controls and NASH 78 patients.Enzyme linked immunosorbent assay(ELISA)was used to determine the concentration of serum IL-6 in 78 patients with NASH. RESULTS:Homozygotes for-572C of IL-6 gene were more frequent in NASH patients than in controls(0.564 vs 0.404,P〈0.05).Level of IL-6 was significantly higher in NASH patients with IL-6-572C/C genotype than that in NASH patients with other genotypes(6.54±4.21 vs 4.68±2.88,P〈0.05).The significant difference in HOMA-IR was not seen in three genotypes. CONCLUSION:The C/G homozygotes of IL-6 single nucleotide polymorphism at-572 have something to do with the pathogenesis of NASH.
出处
《世界华人消化杂志》
CAS
北大核心
2008年第6期635-639,共5页
World Chinese Journal of Digestology