摘要
目的探讨TGF-β1-509C/T基因多态性与不同中医证型原发性膝骨关节炎(primary knee osteoarthritis,PKOA)遗传易感性的关系。方法采用关联分析,严格按照病例纳入标准,随机选取湖南地区PKOA患者88例(瘀血阻滞组52例,肾虚亏髓组36例),应用聚合酶链式反应-限制性片段长度多态性分析(PCR-RFLP)对所选对象TGF-β1-509位点基因和基因型进行检测。结果瘀血阻滞型PKOA组携带CC基因型的频率明显要高于对照组(50.0%vs 13.5%;χ~2=15.996,P〈0.05),差异有统计学意义;Logistic回归分析结果显示,与TGF-β1-509位点TT基因型相比,携带TGF-β1-509位点CC基因型有患瘀血阻滞型PKOA风险(OR=9.75,95%CI=7.10-13.46))。结论 TGF-β1-509位点与瘀血阻滞型PKOA相关,CC基因型是瘀血阻滞型PKOA易感基因型。
Objective To probe association of the promoter -509C/T gene polymorphisms of transforming growth factor-β1 (TGF-β1) with Common raditional Chinese medicine Syndromes primary knee osteoarthritis (PKOA). Methods the promoter - 509C/T gene polymorphisms were analysised by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in 88 patients with primary knee osteoarthritis (qi stagnation and blood stasis syndrome 52,Kidney empty marrow deficient syndrome36) from Affiliated Hospital to Hunan Insititute Chinese Medicine. Results Blood stasis type PH group carrying CC genotype frequency is significantly higher than the control(50.0% vs 13.5%;χ^2=15.996 ,P〈0.05),the difference was statistically significant; Logistic regression analysis showed that the TGF compared -β1-509 sites TF genotype,TGF-β1-509 locus genotype CC suffering from qi stagnation and blood stasis syndrome PKOA risk (OR=9.75,95%CI=7.10-13.46). Conclusion the promoter - 509C/T gene polymorphisms of transforming growth factor-β1 is associated with the PKOA patients. The CC genotype may be qi stagnation and blood stasis syndrome risk genotype.
出处
《江西医药》
CAS
2016年第2期134-136,共3页
Jiangxi Medical Journal
基金
湖南省科技厅课题(项目编号:2013FJ3152)
湖南省中医药研究院院级课题(编号:201224)
关键词
原发性膝骨关节炎
中医证型
转化生长因子Β1
基因多态性
聚合酶链式反应-限制性片段长度多态性
Primary knee osteoarthritis (PKOA)
Common TCM Syndromes
Transforming growth factor beta 1 (TGF-131)
Genetic polymorphism
Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP)