摘要
目的探讨脂蛋白脂酶基因第8内含子HindⅢ和第6内含子PvuⅡ酶切位点多态性与2型糖尿病及其胰岛素抵抗的发生之间是否有关联。方法选取78例2型糖尿病患者为病例组,49例正常人为正常对照组,分别对第8号内含子HindⅢ酶切位点(H)及第6号内含子PvuⅡ酶切位点(P)进行多态性分析。结果病例组等位基因"H+"和基因型H+H+分布频率分别高于正常对照组(P<0.05)。病例组中并发高甘油三酯血症组等位基因H+和基因型H+H+分布频率均高于正常甘油三酯血症患者组(P<0.05)。病例组中P+P+组高密度脂蛋白胆固醇水平低于P-P-组(P<0.05),而低密度脂蛋白胆固醇、胰岛素抵抗指数水平高于P-P-组(P<0.05)。结论脂蛋白脂酶HindⅢ酶切位点多态性与2型糖尿病及其胰岛素抵抗有关。PvuⅡ酶切位点多态性与2型糖尿病中胰岛素抵抗有关。
Objective To investigate the frequencies of variant of lipoprotein lipase (LPL) gene, HindⅢ site at intron 8 and PvuⅡ site at intron 6, and its relation with type 2 diabetes mellitus and insulin resistance (IR). Methods PCR-RFLP method was used to determine the DNA polymorphism of 8 th intron and 6 th intron of LPL gene in 78 T2DM patients and 49 controls. Results (1) Compared with control group, the frequencies of H+H+ genotypes and alleles "H^+" was significantly higher in type 2 diabetes patients (P〈0.05). (2) In type 2 diabetes patients, the H^+H^+ genotype and allele H^+ frequency of the hypertriglyeeridemia group was significantly higher than that of normal triglycerides control group (P〈0.05). (3) The levels of LDL-C and IR in P^+ P^+ genotype were higher than those in P-P- genotype (P〈0.05), but HDL-C was lower (P〈0.05). Conclusion The polymorphism of LPL-Hind Ⅲ site is significantly associated with type 2 diabetes mellitus and insulin resistance. The polymorphism of LPL- PvuⅡ site is significantly associated with insulin resistance in type 2 diabetes.
出处
《中国慢性病预防与控制》
CAS
2007年第6期529-532,共4页
Chinese Journal of Prevention and Control of Chronic Diseases
关键词
糖尿病
2型
胰岛素抵抗
脂蛋白脂酶基因
限制性片段长度多态性
Type 2 diabetes mellitus
Insulin resistance
Lipoprotein lipase gene
Restriction fragment length polymorphism