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2型糖尿病遗传因素评估。

Assessment of genetic factors for type 2 diabetes mellitus.

作者信息

Yamada Yoshiji, Matsuo Hitoshi, Segawa Tomonori, Watanabe Sachiro, Kato Kimihiko, Kameyama Takashi, Yokoi Kiyoshi, Ichihara Sahoko, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Nozawa Yoshinori

机构信息

Department of Human Functional Genomics, Life Science Research Center, Mie University, Mie 514-8507, Japan.

出版信息

Int J Mol Med. 2006 Aug;18(2):299-308.

Abstract

The purpose of the present study was to identify gene polymorphisms for reliable assessment of genetic factors for type 2 diabetes mellitus. The study population comprised 4853 unrelated Japanese individuals (2688 men, 2165 women), including 1489 subjects with type 2 diabetes mellitus (969 men, 520 women) and 3364 controls (1719 men, 1645 women). The genotypes for 148 polymorphisms of 124 candidate genes were determined with a method that combines polymerase chain reaction and sequence-specific oligonucleotide probes with suspension array technology. Sixteen polymorphisms were related (p<0.05) to the prevalence of type 2 diabetes mellitus as determined by the chi-square test. Multivariable logistic regression analysis with adjustment for age, sex, and the prevalence of smoking revealed that, among these polymorphisms, the -603A --> G polymorphism of the gene for coagulation factor III (F3) was significantly (p<0.001) associated with the prevalence of type 2 diabetes mellitus, with the -603G allele representing a risk factor for this condition. A stepwise forward selection procedure demonstrated that F3 genotype (GG versus AA + AG) significantly (p<0.001) and independently affected the prevalence of type 2 diabetes mellitus. Genotype for F3 may prove reliable for assessment of genetic factors for type 2 diabetes mellitus. Determination of the genotype for this gene may contribute to personalized prevention of this condition.

摘要

本研究的目的是鉴定基因多态性,以便可靠地评估2型糖尿病的遗传因素。研究人群包括4853名无亲缘关系的日本人(2688名男性,2165名女性),其中有1489名2型糖尿病患者(969名男性,520名女性)和3364名对照者(1719名男性,1645名女性)。采用聚合酶链反应和序列特异性寡核苷酸探针相结合的悬浮芯片技术,对124个候选基因的148个多态性进行基因分型。通过卡方检验确定,有16个多态性与2型糖尿病的患病率相关(p<0.05)。在对年龄、性别和吸烟率进行调整的多变量逻辑回归分析中发现,在这些多态性中,凝血因子III(F3)基因的-603A→G多态性与2型糖尿病的患病率显著相关(p<0.001),-603G等位基因是这种疾病的一个危险因素。逐步向前选择程序表明,F3基因型(GG与AA+AG)显著(p<0.001)且独立地影响2型糖尿病的患病率。F3基因型可能被证明对评估2型糖尿病的遗传因素是可靠的。测定该基因的基因型可能有助于对这种疾病进行个性化预防。

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