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作 者:吴雪霁[1] 秦蕾[1] 周金意[1] 成金罗[2] 沈默宇[2] 王劲松[3] 周玲[1]
机构地区:[1]南京医科大学流行病与卫生统计学系,210029 [2]江苏省常州市第二人民医院内分泌科 [3]扬州大学医学院流行病学教研室
出 处:《中华医学遗传学杂志》2007年第6期656-659,共4页Chinese Journal of Medical Genetics
基 金:国家自然科学基金(30371241)
摘 要:目的探讨我国常州地区汉族家系2型糖尿病与尾加压素2(urotensinⅡ,UT-Ⅱ)基因rs228648多态性位点的关系。方法采用家系内外对照的病例对照研究,并设置无家族史的普通病例组,应用聚合酶链反应-限制性片段长度多态性技术,对rs228648(G/A)多态性进行基因分型。结果家系中携带AG和AA基因型者患病风险分别为GG型的1.98(95%可信区间=1.19~3.29)和2.46(95%可信区间=1.39~4.34)倍,家系病例组A等位基因频率高于内对照组及普通病例组(P=0.01)。内对照组A等位基因频率高于外对照组(P=0.001)。内对照组携带AG基因型者的胰岛素抵抗指数、胰岛素敏感指数以及胰岛初期分泌功能指数均高于GG基因型者(P〈0.05)。结论rs228648多态性位点变异可能是2型糖尿病的危险因素之一,家系人群该基因变异与其胰岛功能间存在关联。Objective To investigate the association between a polymorphism (rs228648) of urotensin Ⅱ (UTⅡ) gene and type 2 diabetes in pedigrees. Methods Patients and controls with/without familial history were enrolled in the same place. Results Carriers with AG or AA genotype from pedigrees had higher disease risk than those with GG genotype( OR = 1.98, 95% CI: 1.19-3.29, OR = 2.46,95% CI: 1.39-4.34), the frequency of A allele was higher in the patients from pedigrees than inner controls and patients who had no familial history( P = 0.01 ). The frequency of A allele was higher in the inner controls than outer ones( P = 0.001). The insulin resistance index, insulin sensitivity index and pancreatic secretion index of inner controls with AG genotype were higher than those with GG genotype(All P 〈 0.05). Conclusion This polymorphism of UT-Ⅱ gene might be a risk to type 2 diabetes, the insulin function of people from pedigrees is associated with the mutation.
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