4.7 Article

Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis

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DIABETES CARE
卷 44, 期 2, 页码 556-562

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AMER DIABETES ASSOC
DOI: 10.2337/dc20-1137

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资金

  1. Lady Davis Institute for Medical Research
  2. Department of Medicine, Jewish General Hospital
  3. UK Medical Research Council
  4. British Heart Foundation Intermediate Clinical Research Fellowship [FS/18/23/33512]
  5. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre
  6. Canadian Institutes of Health Research (CIHR)
  7. Lady Davis Institute of the Jewish General Hospital
  8. Canadian Foundation for Innovation
  9. NIH Foundation
  10. Cancer Research UK
  11. Fonds de Recherche Quebec Sante (FRQS)
  12. FRQS Clinical Research Scholarship
  13. Li Ka Shing Foundation
  14. NIHR Oxford Biomedical Research Centre, National Institutes of Health [CRR00070 CR00.01, 5P50-HD-028138-27]
  15. WT-SSI/John Fell funds
  16. University College London Hospitals NIHR Biomedical Research Centre
  17. British Heart Foundation
  18. Wellcome Trust [090532, 098381, 203141, 212259]
  19. National Institute of Diabetes and Digestive and Kidney Diseases [U01-DK-105535]
  20. UK Medical Research Council Population Health Scientist fellowship [MR/M014509/1]
  21. UK Medical Research Council Skills Development Fellowship [MR/P014550/1]
  22. Widenlife
  23. MRC [MR/M014509/1] Funding Source: UKRI

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The study found that genetic risk of type 2 diabetes affects the odds of coronary heart disease (CHD) similarly in both women and men, indicating no sex differential in the causal effect of diabetes on CHD risk. This suggests that prevention and management of type 2 diabetes for CHD risk reduction should be prioritized equally in both sexes.
OBJECTIVE Observational studies have demonstrated that type 2 diabetes is a stronger risk factor for coronary heart disease (CHD) in women compared with men. However, it is not clear whether this reflects a sex differential in the causal effect of diabetes on CHD risk or results from sex-specific residual confounding. RESEARCH DESIGN AND METHODS Using 270 single nucleotide polymorphisms (SNPs) for type 2 diabetes identified in a type 2 diabetes genome-wide association study, we performed a sex-stratified Mendelian randomization (MR) study of type 2 diabetes and CHD using individual participant data in UK Biobank (251,420 women and 212,049 men). Weighted median, MR-Egger, MR-pleiotropy residual sum and outlier, and radial MR from summary-level analyses were used for pleiotropy assessment. RESULTS MR analyses showed that genetic risk of type 2 diabetes increased the odds of CHD for women (odds ratio 1.13 [95% CI 1.08-1.18] per 1-log unit increase in odds of type 2 diabetes) and men (1.21 [1.17-1.26] per 1-log unit increase in odds of type 2 diabetes). Sensitivity analyses showed some evidence of directional pleiotropy; however, results were similar after correction for outlier SNPs. CONCLUSIONS This MR analysis supports a causal effect of genetic liability to type 2 diabetes on risk of CHD that is not stronger for women than men. Assuming a lack of bias, these findings suggest that the prevention and management of type 2 diabetes for CHD risk reduction is of equal priority in both sexes.

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