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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

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....

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Autores principales: Xu, Guodong, You, Dingyun, Wong, Liping, Duan, Donghui, Kong, Fanqian, Zhang, Xiaohong, Zhao, Jinshun, Xing, Wenhua, Li, Li, Han, Liyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391911/
https://www.ncbi.nlm.nih.gov/pubmed/30668524
http://dx.doi.org/10.1530/EJE-18-0792
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author Xu, Guodong
You, Dingyun
Wong, Liping
Duan, Donghui
Kong, Fanqian
Zhang, Xiaohong
Zhao, Jinshun
Xing, Wenhua
Li, Li
Han, Liyuan
author_facet Xu, Guodong
You, Dingyun
Wong, Liping
Duan, Donghui
Kong, Fanqian
Zhang, Xiaohong
Zhao, Jinshun
Xing, Wenhua
Li, Li
Han, Liyuan
author_sort Xu, Guodong
collection PubMed
description 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 duration of follow-up was longer than 10 years and 1.10 in articles in which the duration of follow-up was less than 10 years. 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 approximately 17 and 97% greater, respectively, for women than for men.
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spelling pubmed-63919112019-03-04 Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis Xu, Guodong You, Dingyun Wong, Liping Duan, Donghui Kong, Fanqian Zhang, Xiaohong Zhao, Jinshun Xing, Wenhua Li, Li Han, Liyuan Eur J Endocrinol Clinical Study 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 duration of follow-up was longer than 10 years and 1.10 in articles in which the duration of follow-up was less than 10 years. 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 approximately 17 and 97% greater, respectively, for women than for men. Bioscientifica Ltd 2019-01-21 /pmc/articles/PMC6391911/ /pubmed/30668524 http://dx.doi.org/10.1530/EJE-18-0792 Text en © 2019 The authors http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Study
Xu, Guodong
You, Dingyun
Wong, Liping
Duan, Donghui
Kong, Fanqian
Zhang, Xiaohong
Zhao, Jinshun
Xing, Wenhua
Li, Li
Han, Liyuan
Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title_full Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title_fullStr Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title_full_unstemmed Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title_short Risk of all-cause and CHD mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
title_sort risk of all-cause and chd mortality in women versus men with type 2 diabetes: a systematic review and meta-analysis
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391911/
https://www.ncbi.nlm.nih.gov/pubmed/30668524
http://dx.doi.org/10.1530/EJE-18-0792
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