Volume 34, Issue 2 938267 pp. 113-120
Article
Open Access

Novel ERBB Receptor Feedback Inhibitor 1 (ERRFI1) + 808 T/G Polymorphism Confers Protective Effect on Diabetic Nephropathy in a Korean Population

Ihn Suk Lee

Ihn Suk Lee

Department of Internal Medicine The Catholic University College of Medicine Daejeon, Korea

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Ju Hee Lee

Ju Hee Lee

Department of Internal Medicine Chungnam National University School of Medicine Daejeon, Korea

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Hyun Jin Kim

Hyun Jin Kim

Department of Internal Medicine Chungnam National University School of Medicine Daejeon, Korea

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Jae Min Lee

Jae Min Lee

Department of Internal Medicine Eulji University School of Medicine Daejeon, Korea

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Seong Kyu Lee

Seong Kyu Lee

Department of Internal Medicine Eulji University School of Medicine Daejeon, Korea

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Hye Soo Kim

Hye Soo Kim

Department of Internal Medicine The Catholic University College of Medicine Daejeon, Korea

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Jong Min Lee

Jong Min Lee

Department of Internal Medicine The Catholic University College of Medicine Daejeon, Korea

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Kang Seo Park

Kang Seo Park

Department of Internal Medicine Eulji University School of Medicine Daejeon, Korea

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Bon Jeong Ku

Corresponding Author

Bon Jeong Ku

Department of Internal Medicine Chungnam National University School of Medicine Daejeon, Korea

Research Institute for Medical Sciences Chungnam National University School of Medicine Daejeon, Korea

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First published: 21 May 2013

Abstract

BACKGROUND: The identification and characterization of the gene, ERRFI1, in diabetes has not been reported. In this study, we evaluated the relationship between ERRFI1 polymorphism and characteristics of type 2 diabetes mellitus (T2DM) in Korea.

SUBJECTS AND METHODS: We conduct a case-control study involving T2DM patients (n=342) and controls (n=473).

RESULTS: A novel single nucleotide ERRFI1 gene polymorphism at +807(T/G) was found. G genotype frequency was 40.1% in the diabetic group and 42.7% in the control group; the difference was not significant (p=0.45). In the diabetic group, the urine albumin to creatinine ratio (ACR) was lower in the G genotype than in the T genotype (P=0.004). In males with T2DM, those with the G genotype displayed lower systolic blood pressure (P=0.01) and higher glomerular filtration rate (P=0.048) compare to those with the T genotype. In females with T2DM, urine ACR was low in those with the G genotype than in those with the T genotype (P=0.02). In the diabetic group, patients who harboring T allele had a 1.81 times higher risk of diabetic nephropathy than the G allele (95% CI 1.11–2.96, P=0.02). In females with T2DM, patients who harboring T allele had a 2.12 times higher risk of diabetic nephropathy (95% CI 1.07–4.1, P=0.03).

CONCLUSIONS: We identify new loci associated with glycemic traits in diabetes and this finding indicates the potential of ERRFI1 as a novel therapeutic target of diabetic nephropathy.

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