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Sex differences in type 2 diabetes: focus on disease course and outcomes

BACKGROUND: Women with type 2 diabetes (T2D) are less likely to reach the goals for hemoglobin A(1c) compared with men, and have higher all-cause mortality. The risk of cardiovascular disease is elevated among both men and women with T2D, however, the risk has declined among men over recent years wh...

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Detalles Bibliográficos
Autores principales: Arnetz, Lisa, Ekberg, Neda Rajamand, Alvarsson, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172102/
https://www.ncbi.nlm.nih.gov/pubmed/25258546
http://dx.doi.org/10.2147/DMSO.S51301
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author Arnetz, Lisa
Ekberg, Neda Rajamand
Alvarsson, Michael
author_facet Arnetz, Lisa
Ekberg, Neda Rajamand
Alvarsson, Michael
author_sort Arnetz, Lisa
collection PubMed
description BACKGROUND: Women with type 2 diabetes (T2D) are less likely to reach the goals for hemoglobin A(1c) compared with men, and have higher all-cause mortality. The risk of cardiovascular disease is elevated among both men and women with T2D, however, the risk has declined among men over recent years while it remains stationary in women. Reasons for these sex differences remain unclear, and guidelines for diabetes treatment do not differentiate between sexes. Possible causes for varying outcome include differences in physiology, treatment response, and psychological factors. This review briefly outlines sex differences in hormonal pathophysiology, and thereafter summarizes the literature to date on sex differences in disease course and outcome. METHODS: Systematic searches were performed on PubMed using “sex”, “gender”, and various glucose-lowering therapies as keywords. Earlier reviews are summarized and results from individual studies are reported. Reference lists from studies were used to augment the search. RESULTS: There is an increased risk of missing the diagnosis of T2D when screening women with only fasting plasma glucose instead of with an oral glucose tolerance test. The impact of various risk factors for complications may differ by sex. Efficacy and side effects of some glucose-lowering drugs differ between men and women. Men with T2D appear to suffer more microvascular complications, while women have higher morbidity and mortality in cardiovascular disease and also fare worse psychologically. CONCLUSION: Few studies to date have focused on sex differences in T2D. Several questions demand further study, such as whether risk factors and treatment guidelines should be sex-specific. There is a need for clinical trials designed specifically to evaluate sex differences in efficacy and outcome of the available treatments.
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spelling pubmed-41721022014-09-25 Sex differences in type 2 diabetes: focus on disease course and outcomes Arnetz, Lisa Ekberg, Neda Rajamand Alvarsson, Michael Diabetes Metab Syndr Obes Review BACKGROUND: Women with type 2 diabetes (T2D) are less likely to reach the goals for hemoglobin A(1c) compared with men, and have higher all-cause mortality. The risk of cardiovascular disease is elevated among both men and women with T2D, however, the risk has declined among men over recent years while it remains stationary in women. Reasons for these sex differences remain unclear, and guidelines for diabetes treatment do not differentiate between sexes. Possible causes for varying outcome include differences in physiology, treatment response, and psychological factors. This review briefly outlines sex differences in hormonal pathophysiology, and thereafter summarizes the literature to date on sex differences in disease course and outcome. METHODS: Systematic searches were performed on PubMed using “sex”, “gender”, and various glucose-lowering therapies as keywords. Earlier reviews are summarized and results from individual studies are reported. Reference lists from studies were used to augment the search. RESULTS: There is an increased risk of missing the diagnosis of T2D when screening women with only fasting plasma glucose instead of with an oral glucose tolerance test. The impact of various risk factors for complications may differ by sex. Efficacy and side effects of some glucose-lowering drugs differ between men and women. Men with T2D appear to suffer more microvascular complications, while women have higher morbidity and mortality in cardiovascular disease and also fare worse psychologically. CONCLUSION: Few studies to date have focused on sex differences in T2D. Several questions demand further study, such as whether risk factors and treatment guidelines should be sex-specific. There is a need for clinical trials designed specifically to evaluate sex differences in efficacy and outcome of the available treatments. Dove Medical Press 2014-09-16 /pmc/articles/PMC4172102/ /pubmed/25258546 http://dx.doi.org/10.2147/DMSO.S51301 Text en © 2014 Arnetz et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Arnetz, Lisa
Ekberg, Neda Rajamand
Alvarsson, Michael
Sex differences in type 2 diabetes: focus on disease course and outcomes
title Sex differences in type 2 diabetes: focus on disease course and outcomes
title_full Sex differences in type 2 diabetes: focus on disease course and outcomes
title_fullStr Sex differences in type 2 diabetes: focus on disease course and outcomes
title_full_unstemmed Sex differences in type 2 diabetes: focus on disease course and outcomes
title_short Sex differences in type 2 diabetes: focus on disease course and outcomes
title_sort sex differences in type 2 diabetes: focus on disease course and outcomes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4172102/
https://www.ncbi.nlm.nih.gov/pubmed/25258546
http://dx.doi.org/10.2147/DMSO.S51301
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