Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population

被引:0
作者
Naoko Iwasaki
Yukio Horikawa
Takafumi Tsuchiya
Yutaka Kitamura
Takahiro Nakamura
Yukio Tanizawa
Yoshitomo Oka
Kazuo Hara
Takashi Kadowaki
Takuya Awata
Masashi Honda
Katsuko Yamashita
Naohisa Oda
Li Yu
Norihiro Yamada
Makiko Ogata
Naoyuki Kamatani
Yasuhiko Iwamoto
Laura del Bosque-Plata
M. Geoffrey Hayes
Nancy J. Cox
Graeme I. Bell
机构
[1] Tokyo Women’s Medical University,Diabetes Center
[2] Gunma University,Laboratory of Molecular Genetics, Department of Cell Biology, Institute for Molecular and Cellular Regulation
[3] The University of Chicago,Departments of Biochemistry and Molecular Biology, Human Genetics and Medicine
[4] Tokyo Women’s Medical University,Department of Statistical Genetics, Institute of Rheumatology
[5] Yamaguchi University Graduate School of Medicine,Division of Molecular Analysis of Human Disorders, Department of Bio
[6] Tohoku University,Signal Analysis
[7] University of Tokyo,Division of Molecular Metabolism and Diabetes, Department of Internal Medicine
[8] Saitama Medical School,Department of Metabolic diseases, Graduate School of Medicine and Faculty of Medicine
[9] Shiseikai Daini Hospital,Division of Endocrinology and Diabetes, Department of Medicine
[10] Seijin Igaku Medical Clinic,Department of Internal Medicine
[11] Fujita Health University School of Medicine,undefined
来源
Journal of Human Genetics | 2005年 / 50卷
关键词
Association study; Age-at-diagnosis; Calpain-10; Genetics; Polymorphism; Type 2 diabetes;
D O I
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学科分类号
摘要
Variation in the gene encoding the cysteine protease calpain-10 has been linked and associated with risk of type 2 diabetes. We have examined the effect of three polymorphisms in the calpain-10 gene (SNP-43, Indel-19, and SNP-63) on the development of type 2 diabetes in the Japanese population in a pooled analysis of 927 patients and 929 controls. We observed that SNP-43, Indel-19, and SNP-63 either individually or as a haplotype were not associated with altered risk of type 2 diabetes with the exception of the rare 111/221 haplogenotype (odds ratio (OR) =3.53, P=0.02). However, stratification based on the median age-at-diagnosis in the pooled study population (<50 and ≥50 years) revealed that allele 2 of Indel-19 and the 121 haplotype were associated with reduced risk in patients with later age-at-diagnosis (age-at-diagnosis ≥50 years OR=0.82 and 0.80, respectively; P=0.04 and 0.02). Thus, variation in the calpain-10 gene may affect risk of type 2 diabetes in Japanese, especially in older individuals.
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页码:92 / 98
页数:6
相关论文
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