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      Plasma Resistin Is Associated With Single Nucleotide Polymorphisms of a Possible Resistin Receptor, the Decorin Gene, in the General Japanese Population

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          Abstract

          Resistin is an adipokine secreted from adipocytes in mice. We previously reported that a single nucleotide polymorphism (SNP) –420 (rs1862513) in the human resistin gene ( RETN), is correlated with plasma resistin. Decorin is a multifunctional proteoglycan, and its isoform, lacking 14 amino acids from the N terminal region of mature core decorin, recently was identified as a resistin receptor in mice. To examine whether SNPs in the vicinity of the human decorin gene ( DCN) are associated with plasma resistin, we cross-sectionally analyzed six tag SNPs selected around DCN in the same linkage disequilibrium block in 2,078 community-dwelling Japanese subjects. Plasma resistin was associated with the rs7139228, rs7956537, rs516115, and rs3138167 genotypes in DCN. A multiple regression analysis revealed that the genotype of rs7308752 (G/G) or rs516115 (C/C) was associated with decreased plasma resistin after adjusted for age, sex, BMI, and the RETN SNP rs1862513. The effect of rs7139228 and rs1862513 seemed to be additive without synergistic interaction. Therefore, plasma resistin was associated with some tag SNPs around DCN in the general Japanese population. The possibility that human decorin is a human resistin receptor should be pursued.

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          Author and article information

          Journal
          Diabetes
          Diabetes
          diabetes
          diabetes
          Diabetes
          Diabetes
          American Diabetes Association
          0012-1797
          1939-327X
          February 2013
          17 January 2013
          : 62
          : 2
          : 649-652
          Affiliations
          [1] 1Department of Molecular and Genetic Medicine, Ehime University Graduate School of Medicine, Ehime, Japan
          [2] 2Department of Anti-Aging and Genetics, Ehime Proteo-Medicine Research Center, Ehime University, Ehime, Japan
          [3] 3Translational Research Center, Ehime University Hospital, Ehime, Japan
          [4] 4Doctoral Program in Life System Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Ibaraki, Japan
          [5] 5Department of Community Medicine, Ehime University Graduate School of Medicine, Ehime, Japan
          [6] 6Department of Geriatric Medicine, Ehime University Graduate School of Medicine, Ehime, Japan
          Author notes
          Corresponding authors: Hiroshi Onuma, onuma@ 123456m.ehime-u.ac.jp , and Haruhiko Osawa, harosawa@ 123456m.ehime-u.ac.jp .

          H. Onuma and Y. Tabara contributed equally to this study.

          Article
          0058
          10.2337/db12-0058
          3554371
          23193185
          60a4004c-69d4-4c53-a89b-af91d2ce7060
          © 2013 by the American Diabetes Association.

          Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.

          History
          : 23 January 2012
          : 14 August 2012
          Page count
          Pages: 4
          Categories
          Original Research
          Genetics/Genomes/Proteomics/Metabolomics

          Endocrinology & Diabetes
          Endocrinology & Diabetes

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