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Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis

期刊

EUROPEAN JOURNAL OF ENDOCRINOLOGY
卷 180, 期 4, 页码 243-255

出版社

OXFORD UNIV PRESS
DOI: 10.1530/EJE-18-0792

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资金

  1. Natural Science Foundation of Zhejiang Province [LY17H260002]
  2. K C Wong Magna Fund in Ningbo University
  3. China Postdoctoral Science Foundation [156458]
  4. Jiangsu Postdoctoral Science Foundation [1601121B]
  5. Natural Science Foundation of Ningbo [2016A610169]
  6. Public welfare technology and policy science (soft science) application research of Zhejiang Province [2017C35006]
  7. Ningbo Scientific Innovation Team for Environmental Hazardous Factor Control and Prevention [2016C51001]
  8. Project of Science and Technology Innovation for College Students in Zhejiang Province [2018R405092]
  9. Sanming Project of Medicine in Shenzhen [SZSM201803080]

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Objective: Previous studies have shown sex-specific differences in all-cause and CHD mortality in type 2 diabetes. We performed a systematic review and meta-analysis to provide a global picture of the estimated influence of type 2 diabetes on the risk of all-cause and CHD mortality in women vs men. Methods: We systematically searched PubMed, EMBASE and Web of Science for studies published from their starting dates to Aug 7, 2018. The sex-specific hazard ratios (HRs) and their pooled ratio (women vs men) of all-cause and CHD mortality associated with type 2 diabetes were obtained through an inverse variance-weighted random-effects meta-analysis. Subgroup analyses were used to explore the potential sources of heterogeneity. Results: The 35 analyzed prospective cohort studies included 2 314 292 individuals, among whom 254 038 all-cause deaths occurred. The pooled women vs men ratio of the HRs for all-cause and CHD mortality were 1.17 (95% CI: 1.12-1.23, I-2 = 81.6%) and 1.97 (95% CI: 1.49-2.61, I-2 = 86.4%), respectively. The pooled estimate of the HR for all-cause mortality was approximately 1.30 in articles in which the durat ion of follow-up was longer than 10 years and 1.10 in articles in which the duration of follow-up was less than 10 ye ars. The pooled HRs for all-cause mortality in patients with type 2 diabetes was 2.33 (95% CI: 2.02-2.69) in women and 1.91 (95% CI: 1.72-2.12) in men, compared with their healthy counterparts. Conclusions: The effect of diabetes on all-cause and CHD mortality is approx imately 17 and 97% greater, respectively, for women than for men.

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