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Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes

OBJECTIVE: The aim of this study was to evaluate the relationship between inflammatory cytokines, placental weight, glycated hemoglobin and adverse perinatal outcomes (APOs) in women with gestational diabetes mellitus (GDM). SUBJECTS AND METHODS: This was a prospective, longitudinal and observationa...

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Autores principales: Braga, Fernanda Oliveira, Negrato, Carlos Antonio, da Matta, Maria de Fátima Bevilacqua, Carneiro, João Régis Ivar, Gomes, Marília Brito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Endocrinologia e Metabologia 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118841/
https://www.ncbi.nlm.nih.gov/pubmed/30864628
http://dx.doi.org/10.20945/2359-3997000000099
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author Braga, Fernanda Oliveira
Negrato, Carlos Antonio
da Matta, Maria de Fátima Bevilacqua
Carneiro, João Régis Ivar
Gomes, Marília Brito
author_facet Braga, Fernanda Oliveira
Negrato, Carlos Antonio
da Matta, Maria de Fátima Bevilacqua
Carneiro, João Régis Ivar
Gomes, Marília Brito
author_sort Braga, Fernanda Oliveira
collection PubMed
description OBJECTIVE: The aim of this study was to evaluate the relationship between inflammatory cytokines, placental weight, glycated hemoglobin and adverse perinatal outcomes (APOs) in women with gestational diabetes mellitus (GDM). SUBJECTS AND METHODS: This was a prospective, longitudinal and observational study conducted from April 2004 to November 2005 in Bauru, Brazil. Included patients had singleton pregnancies and performed a 100 g OGTT and had the levels of C-reactive protein (CRP), interleukin (IL)-6, TNF alfa and glycated hemoglobin (HbA1c) determined at 24-28(th) gestation weeks. RESULTS: A total of 176 patients were included, of whom 78 had the diagnosis of GDM (44.3%). Multivariate analysis demonstrated that HbA1c, age, body mass index (BMI) and previous history of GDM were independent predictors for GDM diagnosis. ROC curve indicated that HbA1C levels ≥ 5.1% at 24-28 weeks gestation were associated with GDM. No difference was found in IL-6, tumor necrosis factor alpha (TNF-alpha) and CRP serum levels in women with and without GDM. Multivariate analysis showed that placental weight was significantly associated with APOs (p < 0.005), with a cut-off value of 610 grams as demonstrated by the ROC curve. CONCLUSION: Placental weight ≥ 610 grams and HbA1C ≥ 5.1% were found to be associated with APOs and GDM, respectively, and their evaluation should be part of prenatal care routine.
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spelling pubmed-101188412023-04-21 Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes Braga, Fernanda Oliveira Negrato, Carlos Antonio da Matta, Maria de Fátima Bevilacqua Carneiro, João Régis Ivar Gomes, Marília Brito Arch Endocrinol Metab Original Article OBJECTIVE: The aim of this study was to evaluate the relationship between inflammatory cytokines, placental weight, glycated hemoglobin and adverse perinatal outcomes (APOs) in women with gestational diabetes mellitus (GDM). SUBJECTS AND METHODS: This was a prospective, longitudinal and observational study conducted from April 2004 to November 2005 in Bauru, Brazil. Included patients had singleton pregnancies and performed a 100 g OGTT and had the levels of C-reactive protein (CRP), interleukin (IL)-6, TNF alfa and glycated hemoglobin (HbA1c) determined at 24-28(th) gestation weeks. RESULTS: A total of 176 patients were included, of whom 78 had the diagnosis of GDM (44.3%). Multivariate analysis demonstrated that HbA1c, age, body mass index (BMI) and previous history of GDM were independent predictors for GDM diagnosis. ROC curve indicated that HbA1C levels ≥ 5.1% at 24-28 weeks gestation were associated with GDM. No difference was found in IL-6, tumor necrosis factor alpha (TNF-alpha) and CRP serum levels in women with and without GDM. Multivariate analysis showed that placental weight was significantly associated with APOs (p < 0.005), with a cut-off value of 610 grams as demonstrated by the ROC curve. CONCLUSION: Placental weight ≥ 610 grams and HbA1C ≥ 5.1% were found to be associated with APOs and GDM, respectively, and their evaluation should be part of prenatal care routine. Sociedade Brasileira de Endocrinologia e Metabologia 2019-02-01 /pmc/articles/PMC10118841/ /pubmed/30864628 http://dx.doi.org/10.20945/2359-3997000000099 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Braga, Fernanda Oliveira
Negrato, Carlos Antonio
da Matta, Maria de Fátima Bevilacqua
Carneiro, João Régis Ivar
Gomes, Marília Brito
Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title_full Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title_fullStr Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title_full_unstemmed Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title_short Relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
title_sort relationship between inflammatory markers, glycated hemoglobin and placental weight on fetal outcomes in women with gestational diabetes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118841/
https://www.ncbi.nlm.nih.gov/pubmed/30864628
http://dx.doi.org/10.20945/2359-3997000000099
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