Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes

ObjectivePregnancy is associated with an increase in total cholesterol, high density lipoproteins (HDL), and low-density lipoproteins (LDL). Postpartum, HDL and LDL decrease over the first 12 weeks postpartum. Oxidized LDL (ox-LDL) is a marker of oxidative stress-related inflammation, which is assoc...

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Main Authors: Oscar A. Viteri, Mary Alice Sallman, Pauline M. Berens, Pamela D. Berens, Farah H. Amro, Maria S. Hutchinson, Susan M. Ramin, Sean C. Blackwell, Jerrie S. Refuerzo, Judith. A. Smith
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-10-01
Series:Frontiers in Medicine
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmed.2017.00180/full
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spelling doaj-2bf3dda7d0fe48d7aa83d7ff6b12abe12020-11-24T20:53:04ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2017-10-01410.3389/fmed.2017.00180285986Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational DiabetesOscar A. Viteri0Mary Alice Sallman1Pauline M. Berens2Pamela D. Berens3Farah H. Amro4Maria S. Hutchinson5Susan M. Ramin6Sean C. Blackwell7Jerrie S. Refuerzo8Judith. A. Smith9Department of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesDepartment of Obstetrics, Gynecology and Reproductive Sciences, UTHealth McGovern Medical School, Houston, TX, United StatesObjectivePregnancy is associated with an increase in total cholesterol, high density lipoproteins (HDL), and low-density lipoproteins (LDL). Postpartum, HDL and LDL decrease over the first 12 weeks postpartum. Oxidized LDL (ox-LDL) is a marker of oxidative stress-related inflammation, which is associated with obesity and also with development of cardiovascular disease. Cardiovascular protection and weight loss are benefits from metformin, especially in women with diabetes. The objective of this study was to compare changes in lipid profiles and biomarkers for obesity during the initial 6 weeks postpartum between women with gestational diabetes mellitus (GDM) treated with metformin versus placebo.MethodsThis was a planned ancillary study of a randomized controlled trial compares metformin versus placebo in women with GDM for postpartum weight loss. Two 3 mL blood samples were collected within 24 h of delivery and 6 weeks postpartum immediately processed after collection then stored at −20°C until completion of clinical trial prior to analysis. Change in the median plasma concentrations of total cholesterol, HDL, ox-LDL, glucose, insulin, leptin, and unacylated ghrelin were compared between study groups.ResultsOf the 77 postpartum women were included, 35 received metformin and 42 received placebo. There was less of a reduction in HDL in the metformin group compared to placebo (−2.3 versus −7.5 mg/dL, p = 0.019). In addition, there was a greater reduction in ox-LDL in those receiving metformin (−12.2 versus −3.8 mg/dL, p = 0.038). No other differences were observed in the selected biomarkers evaluated.ConclusionBiomarker levels of HDL and ox-LDL were positively affected during the initial 6 weeks postpartum in GDM women treated with metformin. Additional studies with a longer duration of metformin treatment in the postpartum period are warranted to evaluate long-term potential benefits.http://journal.frontiersin.org/article/10.3389/fmed.2017.00180/fullmetforminhigh-density lipoproteinsoxidized-low-density lipoproteinsgestational diabetescardiac riskpostpartum
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language English
format Article
sources DOAJ
author Oscar A. Viteri
Mary Alice Sallman
Pauline M. Berens
Pamela D. Berens
Farah H. Amro
Maria S. Hutchinson
Susan M. Ramin
Sean C. Blackwell
Jerrie S. Refuerzo
Judith. A. Smith
spellingShingle Oscar A. Viteri
Mary Alice Sallman
Pauline M. Berens
Pamela D. Berens
Farah H. Amro
Maria S. Hutchinson
Susan M. Ramin
Sean C. Blackwell
Jerrie S. Refuerzo
Judith. A. Smith
Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
Frontiers in Medicine
metformin
high-density lipoproteins
oxidized-low-density lipoproteins
gestational diabetes
cardiac risk
postpartum
author_facet Oscar A. Viteri
Mary Alice Sallman
Pauline M. Berens
Pamela D. Berens
Farah H. Amro
Maria S. Hutchinson
Susan M. Ramin
Sean C. Blackwell
Jerrie S. Refuerzo
Judith. A. Smith
author_sort Oscar A. Viteri
title Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
title_short Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
title_full Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
title_fullStr Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
title_full_unstemmed Potential of Metformin to Improve Cardiac Risk in Postpartum Women with Gestational Diabetes
title_sort potential of metformin to improve cardiac risk in postpartum women with gestational diabetes
publisher Frontiers Media S.A.
series Frontiers in Medicine
issn 2296-858X
publishDate 2017-10-01
description ObjectivePregnancy is associated with an increase in total cholesterol, high density lipoproteins (HDL), and low-density lipoproteins (LDL). Postpartum, HDL and LDL decrease over the first 12 weeks postpartum. Oxidized LDL (ox-LDL) is a marker of oxidative stress-related inflammation, which is associated with obesity and also with development of cardiovascular disease. Cardiovascular protection and weight loss are benefits from metformin, especially in women with diabetes. The objective of this study was to compare changes in lipid profiles and biomarkers for obesity during the initial 6 weeks postpartum between women with gestational diabetes mellitus (GDM) treated with metformin versus placebo.MethodsThis was a planned ancillary study of a randomized controlled trial compares metformin versus placebo in women with GDM for postpartum weight loss. Two 3 mL blood samples were collected within 24 h of delivery and 6 weeks postpartum immediately processed after collection then stored at −20°C until completion of clinical trial prior to analysis. Change in the median plasma concentrations of total cholesterol, HDL, ox-LDL, glucose, insulin, leptin, and unacylated ghrelin were compared between study groups.ResultsOf the 77 postpartum women were included, 35 received metformin and 42 received placebo. There was less of a reduction in HDL in the metformin group compared to placebo (−2.3 versus −7.5 mg/dL, p = 0.019). In addition, there was a greater reduction in ox-LDL in those receiving metformin (−12.2 versus −3.8 mg/dL, p = 0.038). No other differences were observed in the selected biomarkers evaluated.ConclusionBiomarker levels of HDL and ox-LDL were positively affected during the initial 6 weeks postpartum in GDM women treated with metformin. Additional studies with a longer duration of metformin treatment in the postpartum period are warranted to evaluate long-term potential benefits.
topic metformin
high-density lipoproteins
oxidized-low-density lipoproteins
gestational diabetes
cardiac risk
postpartum
url http://journal.frontiersin.org/article/10.3389/fmed.2017.00180/full
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