摘要
目的:分析半胱氨酸蛋白酶8(CASP8)基因-6526NI/D多态性与2型糖尿痛(T2DM)易感性的关系。方法:采用PCR—RFLP技术结合DNA测序检测414例正常人和410例2型糖尿患者CASP8基因-6526NI/D的多态性。结果:对照组和糖尿病组I/I、I/D和D/D的基因型频率分别为56.5%、38.9%、4.6%和58.0%、32.9%、9.0%.差异有统计学意义(P〈0.05)。D/D基因型发生T2DM的风险为I/I基因型的1.916倍(95%CI=1.199-3.054,P〈0.05)。D/D基因型的空腹血糖高于I/D和I/I基因型(P〈0.05)。结论:CASP8基因-6526NI/D多态性与2型糖尿病的发生相关。
Objective To investigate the association of cysteine aspartic acid specific protease 8 (CASP 8) gene-652 6N Insertion/Deletion polymorphisms and susceptibility of type 2 diabetes meUitus (T2DM). Methods CASP 8 gene -652 6N I/D polymorphisms were detected by polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing in 414 controls and 410 patients with T2DM. Results I/I, I/D and D/D genotype frequency were 56.5%, 38.9%, 4.6% in controls and 58.0%, 32.9%, 9.0% in T2DM group respectively (P 〈 0.05). The risk in D/D genotype people was 1.916 times than I/I genotype (adjusted OR = 1.916, 95%CI = 1.199 - 3.054, P 〈 0.05). The fasting blood sugar of D/D genotype people was significantly higher than that of I/D and I/I genotype people (P 〈 0.05). Conclusions CASP 8 gene -652 6N I/D polymorphisms are associated with T2DM outbreak.
出处
《实用医学杂志》
CAS
北大核心
2014年第19期3073-3075,共3页
The Journal of Practical Medicine
基金
中华医学会临床医学科研专项资金项目(编号:12020160276)
四川省卫生厅科研项目(编号:120348)
关键词
糖尿病
2型
半胱氨酸蛋白酶8
多态性
Diabetes mellitus,type 2
Cysteine aspartic acid specific protease 8
Polymorphism