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首页> 外文期刊>Human Molecular Genetics >Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes
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Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes

机译:ABO血型区域的遗传变异,血浆可溶性E-选择素水平和2型糖尿病的风险

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摘要

Blood soluble E-selectin (sE-selectin) levels have been related to various conditions such as type 2 diabetes. We performed a genome-wide association study among women of European ancestry from the Nurses' Health Study, and identified genome-wide significant associations between a cluster of markers at the ABO locus (9q34) and plasma sE-selectin concentration. The strongest association was with rs651007, which explained ∼9.71% of the variation in sE-selectin concentrations. SNP rs651007 was also nominally associated with soluble intracellular cell adhesion molecule-1 (sICAM-1) (P = 0.026) and TNF-R2 levels (P = 0.018), independent of sE-selectin. In addition, the genetic-inferred ABO blood group genotypes were associated with sE-selectin concentrations (P = 3.55 × 10−47). Moreover, we found that the genetic-inferred blood group B was associated with a decreased risk (OR = 0.44, 0.27–0.70) of type 2 diabetes compared with blood group O, adjusting for sE-selectin, sICAM-1, TNF-R2 and other covariates. Our findings indicate that the genetic variants at ABO locus affect plasma sE-selectin levels and diabetes risk. The genetic associations with diabetes risk were independent of sE-selectin levels.
机译:血液可溶性E-选择素(sE-selectin)的水平与各种疾病(例如2型糖尿病)有关。我们从“护士健康研究”中对欧洲血统的女性进行了全基因组关联研究,并确定了ABO位点(9q34)处的一组标记与血浆sE-选择素浓度之间的全基因组显着关联。与rs651007的关联最强,这解释了sE-选择素浓度变异的〜9.71%。 SNP rs651007在名义上也与可溶性细胞内细胞粘附分子1(sICAM-1)(P = 0.026)和TNF-R2水平(P = 0.018)相关,独立于sE-选择素。另外,遗传推断的ABO血型基因型与sE-选择素浓度有关(P = 3.55×10 -47 )。此外,我们发现,与O型血型相比,B型血型与2型糖尿病的风险降低(OR = 0.44,0.27–0.70)相关,并调整了sE-选择素,sICAM-1,TNF-R2和其他协变量。我们的发现表明,ABO位点的遗传变异会影响血浆sE-选择素水平和糖尿病风险。与糖尿病风险的遗传关联与sE-选择素水平无关。

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  • 来源
    《Human Molecular Genetics 》 |2010年第9期| p.1856-1862| 共7页
  • 作者单位

    Department of Nutrition and|Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA,;

    Department of Nutrition and;

    Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA,;

    Department of Nutrition and;

    Department of Nutrition and|Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA,|Channing Laboratory, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA,;

    Department of Nutrition and;

    Department of Epidemiology, Merck Research Labs, 305 S Sumneytown Pike, North Wales, PA 19454, USA,;

    Department of Biostatistics, University of Washington, Seattle, WA 98195, USA and;

    Center for Genotyping and Analysis, Broad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, MA 02142, U;

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