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Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study

机译:收缩压和2型糖尿病风险:孟德尔随机研究

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摘要

Observational studies have shown that elevated systolic blood pressure (SBP) is associated with future onset of type 2 diabetes, but whether this association is causal is not known. We applied the Mendelian randomization framework to evaluate the causal hypothesis that elevated SBP increases risk for type 2 diabetes. We used 28 genetic variants associated with SBP and evaluated their impact on type 2 diabetes using a European-centric meta-analysis comprising 37,293 case and 125,686 control subjects. We found that elevation of SBP levels by 1 mmHg due to our genetic score was associated with a 2% increase in risk of type 2 diabetes (odds ratio 1.02, 95% Cl 1.01-1.03, P = 9.05 × 10~(-5)). To limit confounding, we constructed a second score based on 13 variants exclusively associated with SBP and found a similar increase in type 2 diabetes risk per 1 mmHg of genetic elevation in SBP (odds ratio 1.02, 95% Cl 1.01-1.03, P = 1.48 × 10~(-3)). Sensitivity analyses using multiple, alternative causal inference measures and simulation studies demonstrated consistent association, suggesting robustness of our primary observation. In line with previous reports from observational studies, we found that genetically elevated SBP was associated with increased risk for type 2 diabetes. Further work will be required to elucidate the biological mechanism and translational implications.
机译:观察性研究表明,收缩压升高(SBP)与2型糖尿病的未来发作有关,但尚不清楚这种关联是否是因果关系。我们应用孟德尔随机框架来评估因SBP升高而增加2型糖尿病风险的因果假设。我们使用了28个与SBP相关的遗传变异,并使用以欧洲为中心的荟萃分析(包括37,293个病例和125,686个对照受试者)评估了它们对2型糖尿病的影响。我们发现,由于我们的遗传评分导致SBP水平升高1 mmHg与2型糖尿病风险增加2%相关(几率1.02,95%Cl 1.01-1.03,P = 9.05×10〜(-5) )。为了限制混淆,我们基于13个仅与SBP相关的变异体构建了第二个评分,发现每1 mmHg的SBP遗传升高,2型糖尿病风险也有类似的增加(赔率1.02,95%Cl 1.01-1.03,P = 1.48 ×10〜(-3))。使用多种替代性因果推断方法进行的敏感性分析和模拟研究显示出一致的关联性,表明我们初步观察的稳健性。与之前的观察性研究结果一致,我们发现基因升高的SBP与2型糖尿病的风险增加相关。需要进一步的工作来阐明生物学机制和翻译意义。

著录项

  • 来源
    《Diabetes》 |2017年第2期|543-550|共8页
  • 作者单位

    Department of Biology, Swarthmore College, Swarthmore, PA;

    Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA;

    Translational Medicine and Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA ,Center for Non-Communicable Diseases, Karachi, Pakistan ,Department of Biostatistics and Epidemiology, Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA;

    Cardiology Division, Department of Medicine, and the Irving Institute for Clinical and Translational Research, Columbia University, New York, NY;

    MedStar Heart & Vascular Institute, MedStar Washington Hospital Center, Washington, DC;

    Department of Public Health, University of Helsinki, Helsinki, Finland ,Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland;

    National Institute for Health and Welfare, Department of Health, Helsinki, Finland;

    Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA ,Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA ,Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:46:07

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