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在日本人群中,早发型2型(非胰岛素依赖型)糖尿病与葡萄糖激酶基因座相关,但与腺苷脱氨酶基因座无关。

Early-onset type 2 (non-insulin-dependent) diabetes mellitus is associated with glucokinase locus, but not with adenosine deaminase locus, in the Japanese population.

作者信息

Takekawa K, Ikegami H, Fukuda M, Ueda H, Kawaguchi Y, Fujioka Y, Fujisawa T, Ogihara T

机构信息

Department of Geriatric Medicine, Osaka University Medical School, Japan.

出版信息

Diabetes Res Clin Pract. 1994 Apr;23(3):141-6. doi: 10.1016/0168-8227(94)90097-3.

Abstract

To investigate the possible contribution of glucokinase (GCK) and adenosine deaminase (ADA) loci to the genetic susceptibility to type 2 (non-insulin-dependent) diabetes mellitus, we studied the association of these loci with type 2 diabetes in the Japanese population. Fifty patients with type 2 diabetes and 50 control subjects were analyzed for microsatellite polymorphism 3' to the GCK gene and PstI polymorphism in the ADA gene by polymerase chain reaction. The frequency of the most common GCK allele (Z) was significantly lower in type 2 diabetic patients than that in control subjects and a longer Z + 2 allele was more common in type 2 diabetic patients (26% vs. 15%, P = 0.053), particularly in those with younger age of onset (33% vs. 15%, younger onset type 2 diabetes vs. control, P = 0.014). The frequency of genotypes containing at least one Z + 2 allele was significantly more common in type 2 diabetic patients (46% vs. 28%, P < 0.05), particularly in those with younger age of onset (61% vs. 28%, relative risk 4.00, P < 0.01). In contrast, there was no difference in allelic or genotypic frequencies of PstI polymorphism in the ADA gene between the two groups. Despite the association between the GCK locus and type 2 diabetes, none of the patients had known mutations (Glu265-->AM265, Glu279-->AM279, Gly299-->Arg299, Glu300-->Gln300, Leu309-->Pro309). These results suggest that the GCK locus, but not the ADA locus, contributes to the genetic susceptibility to type 2 diabetes in Japanese.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为研究葡萄糖激酶(GCK)和腺苷脱氨酶(ADA)基因座对2型(非胰岛素依赖型)糖尿病遗传易感性的可能作用,我们在日本人群中研究了这些基因座与2型糖尿病的关联。通过聚合酶链反应分析了50例2型糖尿病患者和50例对照者的GCK基因3'端微卫星多态性以及ADA基因的PstI多态性。2型糖尿病患者中最常见的GCK等位基因(Z)频率显著低于对照者,且较长的Z + 2等位基因在2型糖尿病患者中更常见(26%对15%,P = 0.053),尤其是在发病年龄较轻的患者中(33%对15%,早发型2型糖尿病对对照,P = 0.014)。在2型糖尿病患者中,至少含有一个Z + 2等位基因的基因型频率显著更高(46%对28%,P < 0.05),尤其是在发病年龄较轻的患者中(61%对28%,相对风险4.00,P < 0.01)。相比之下,两组间ADA基因PstI多态性的等位基因频率或基因型频率无差异。尽管GCK基因座与2型糖尿病有关联,但所有患者均未发现已知突变(Glu265→AM2, Glu279→AM279, Gly299→Arg299, Glu300→Gln300, Leu309→Pro309)。这些结果表明,在日本人中,GCK基因座而非ADA基因座对2型糖尿病的遗传易感性有影响。(摘要截短于250字)

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