检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:韩存芝[1] 石璟[2] 杜丽莉[1] 荆洁线[1] 赵先文[1] 田保国[1] 田富国[1] 刘秀英[1] 张中书[1] 张进[1]
机构地区:[1]山西省肿瘤研究所,太原030013 [2]山西医科大学
出 处:《中华流行病学杂志》2007年第2期136-140,共5页Chinese Journal of Epidemiology
基 金:基金项目:山西省自然科学基金资助项目(2006011129).
摘 要:目的探讨瘦素及其瘦素受体基因多态性与乳腺癌发生的关系。方法采用PCR—RFLP对94例乳腺癌患者、128例健康对照者进行瘦素受体基因Gln223Arg多态性检测;ELISA分析法测定瘦索水平。结果乳腺癌组瘦索受体基因Gln223Arg的GG、GA和AA基因型表达频率分别为69.15%、17.02%和13.83%;等位基因G和A为77.66%和22.34%与对照组82.03%、15.63%和2.34%及等位基因的89.84%和10.16%相比较,差异有统计学意义(P=0.004,P=0.001)。乳腺癌组瘦素水平,腰臀比(WHR)明显高于对照组,差异均有统计学意义(P〈0.01,P〈0.001)。非条件logistic回归多因素分析表明,瘦素受体基因多态性、瘦素水平及WHR升高,与乳腺癌发生的相关危险度分别为:OR=4.87,95%CI:1.30~1822,P=0.019;OR=1.53,95%CI:1.13~2.07,P=0.006;OR=3.68,95%CI:1.34~10.11,P=0.011。结论瘦素受体基因Gln223Arg多态性、瘦素及WHR升高,可能增加乳腺癌发生的风险性。Objective To evaluate the association between serum level of leptin and leptin receptor gene(LEPR) polymorphism and patients with breast cancer, Methods LEPR Gln223Arg polymorphism was detected by polymerase chain reaction restriction fragment length polymorphism in 94 patients with breast cancer and 128 healthy controls. The level of leptin were analyzed by enzyme linked immunosorbent assay. Results In univariate regression analyses, we found serum level of leptin and LEPR Gin223Arg genotype polymorphism were significantly higrer than those of the controls (P 〈 0.05-0.001, respectively). Through rnultivariable analyses, we found that increased risk estimates for breast cancer were among those with leptin level( OR = 1.53,95 % CI : 1.13-2.07, P = 0. 006 ), LEPR Gin223Arg genotype ( OR = 4,87, 95 96 CI ; 1.30- 18,22, P = 0.019 ), WHR ( OR - 3.68, 95 % CI : 1.34- 10.11, P = 0.011 ). Conclusion Results from this study suggested that LEPR Gln233Agr polymorphism, the elevated WHR and serum level of leptin might be correlated with increased risk of breast cancer.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.28