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Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk

AIMS: The cumulative effect of gestational diabetes mellitus (GDM) and hypertensive disorders of pregnancy (HDP) on postpartum cardio-metabolic diseases is equivocal. We aimed to assess the associations of GDM and HDP’s individual and synergic contribution to risks of postpartum cardio-metabolic dis...

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Autores principales: Li, Ling-Jun, Aris, Izzuddin M, Su, Lin Lin, Chong, Yap Seng, Wong, Tien Yin, Tan, Kok Hian, Wang, Jie Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834770/
https://www.ncbi.nlm.nih.gov/pubmed/29444890
http://dx.doi.org/10.1530/EC-17-0359
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author Li, Ling-Jun
Aris, Izzuddin M
Su, Lin Lin
Chong, Yap Seng
Wong, Tien Yin
Tan, Kok Hian
Wang, Jie Jin
author_facet Li, Ling-Jun
Aris, Izzuddin M
Su, Lin Lin
Chong, Yap Seng
Wong, Tien Yin
Tan, Kok Hian
Wang, Jie Jin
author_sort Li, Ling-Jun
collection PubMed
description AIMS: The cumulative effect of gestational diabetes mellitus (GDM) and hypertensive disorders of pregnancy (HDP) on postpartum cardio-metabolic diseases is equivocal. We aimed to assess the associations of GDM and HDP’s individual and synergic contribution to risks of postpartum cardio-metabolic diseases (metabolic syndrome (MetS), abnormal glucose metabolism and hypertension (HTN)). METHODS: Of participants from a Singapore birth cohort, 276 mothers attending the 5-year postpartum visit were included in this study. During this visit, we collected mothers’ history of GDM and HDP in all live births in a chronicle sequence and assessed the cardio-metabolic risks based on blood pressure, anthropometry and a panel of serum biomarkers. We diagnosed MetS, abnormal glucose metabolism and HTN according to Adult Treatment Panel III 2000 and World Health Organization guidelines. RESULTS: Of 276 mothers, 157 (56.9%) had histories of GDM while 23 (8.3%) had histories of HDP. After full adjustment, we found associations of GDM episodes with postpartum abnormal glucose metabolism (single episode: relative risk (RR) 2.9 (95% CI: 1.7, 4.8); recurrent episodes (≥2): RR = 3.8 (2.1–6.8)). Also, we found association between histories of HDP and HTN (RR = 3.6 (1.5, 8.6)). Having either (RR 2.6 (1.7–3.9)) or both gestational complications (RR 2.7 (1.6–4.9)) was associated with similar risk of postpartum cardio-metabolic disease. CONCLUSIONS: Mothers with GDM or HDP had a threefold increased risk of postpartum abnormal glucose metabolism or HTN, respectively. Having both GDM and HDP during past pregnancies was not associated with additional risk of postpartum cardio-metabolic diseases beyond that associated with either complication alone.
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spelling pubmed-58347702018-03-07 Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk Li, Ling-Jun Aris, Izzuddin M Su, Lin Lin Chong, Yap Seng Wong, Tien Yin Tan, Kok Hian Wang, Jie Jin Endocr Connect Research AIMS: The cumulative effect of gestational diabetes mellitus (GDM) and hypertensive disorders of pregnancy (HDP) on postpartum cardio-metabolic diseases is equivocal. We aimed to assess the associations of GDM and HDP’s individual and synergic contribution to risks of postpartum cardio-metabolic diseases (metabolic syndrome (MetS), abnormal glucose metabolism and hypertension (HTN)). METHODS: Of participants from a Singapore birth cohort, 276 mothers attending the 5-year postpartum visit were included in this study. During this visit, we collected mothers’ history of GDM and HDP in all live births in a chronicle sequence and assessed the cardio-metabolic risks based on blood pressure, anthropometry and a panel of serum biomarkers. We diagnosed MetS, abnormal glucose metabolism and HTN according to Adult Treatment Panel III 2000 and World Health Organization guidelines. RESULTS: Of 276 mothers, 157 (56.9%) had histories of GDM while 23 (8.3%) had histories of HDP. After full adjustment, we found associations of GDM episodes with postpartum abnormal glucose metabolism (single episode: relative risk (RR) 2.9 (95% CI: 1.7, 4.8); recurrent episodes (≥2): RR = 3.8 (2.1–6.8)). Also, we found association between histories of HDP and HTN (RR = 3.6 (1.5, 8.6)). Having either (RR 2.6 (1.7–3.9)) or both gestational complications (RR 2.7 (1.6–4.9)) was associated with similar risk of postpartum cardio-metabolic disease. CONCLUSIONS: Mothers with GDM or HDP had a threefold increased risk of postpartum abnormal glucose metabolism or HTN, respectively. Having both GDM and HDP during past pregnancies was not associated with additional risk of postpartum cardio-metabolic diseases beyond that associated with either complication alone. Bioscientifica Ltd 2018-02-14 /pmc/articles/PMC5834770/ /pubmed/29444890 http://dx.doi.org/10.1530/EC-17-0359 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Research
Li, Ling-Jun
Aris, Izzuddin M
Su, Lin Lin
Chong, Yap Seng
Wong, Tien Yin
Tan, Kok Hian
Wang, Jie Jin
Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title_full Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title_fullStr Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title_full_unstemmed Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title_short Effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
title_sort effect of gestational diabetes and hypertensive disorders of pregnancy on postpartum cardiometabolic risk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834770/
https://www.ncbi.nlm.nih.gov/pubmed/29444890
http://dx.doi.org/10.1530/EC-17-0359
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