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Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus

AIMS/INTRODUCTION: To determine whether maternal serum markers in the early second trimester are useful for prediction of gestational diabetes mellitus (GDM). MATERIALS AND METHODS: A total of 876 singleton pregnancies were recruited in the present study. Blood samples were collected during 16–20 ge...

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Autores principales: Zhao, Baihui, Han, Xiujun, Meng, Qing, Luo, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031488/
https://www.ncbi.nlm.nih.gov/pubmed/29288571
http://dx.doi.org/10.1111/jdi.12798
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author Zhao, Baihui
Han, Xiujun
Meng, Qing
Luo, Qiong
author_facet Zhao, Baihui
Han, Xiujun
Meng, Qing
Luo, Qiong
author_sort Zhao, Baihui
collection PubMed
description AIMS/INTRODUCTION: To determine whether maternal serum markers in the early second trimester are useful for prediction of gestational diabetes mellitus (GDM). MATERIALS AND METHODS: A total of 876 singleton pregnancies were recruited in the present study. Blood samples were collected during 16–20 gestational weeks. GDM women were diagnosed by an oral glucose tolerance test during 24–28 gestational weeks. A total of 56 women with GDM and 73 healthy pregnant women were selected. Maternal serum concentrations of placental protein 13 (PP13), pentraxin 3 (PTX3), soluble fms‐like tyrosine kinase‐1 (sFlt‐1), myostatin and follistatin (FST) were detected at 16–20 weeks’ gestation. All of these markers concentrations were expressed as multiples of the medians. The Mann–Whitney U‐test was used for comparison of the multiples of the medians of different concentrations of these five serum markers between the GDM group and the control group. Receiver operating characteristic curve analysis was applied to assess the sensitivity and specificity of significant serum markers from a Mann–Whitney U‐test comparison. RESULTS: Compared with healthy pregnancies, the serum levels of PP13, PTX3, sFlt‐1, myostatin and FST in the early second trimester were significantly increased in patients who had developed GDM late. In screening for GDM by PP13, PTX3, sFlt‐1, myostatin and FST, the detection rates were 92.3, 94.9, 94.9, 92.5 and 92.3%, respectively at 80% specificity. PTX3 and sFlt‐1 were the most sensitive markers. CONCLUSIONS: Maternal serum markers including PP13, PTX3, sFlt‐1, myostatin and FST increase in the early second trimester of women with GDM. These five markers, especially PTX3 and sFlt‐1, could have the value of prediction for those patients who would develop GDM in the late second trimester.
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spelling pubmed-60314882018-07-11 Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus Zhao, Baihui Han, Xiujun Meng, Qing Luo, Qiong J Diabetes Investig Articles AIMS/INTRODUCTION: To determine whether maternal serum markers in the early second trimester are useful for prediction of gestational diabetes mellitus (GDM). MATERIALS AND METHODS: A total of 876 singleton pregnancies were recruited in the present study. Blood samples were collected during 16–20 gestational weeks. GDM women were diagnosed by an oral glucose tolerance test during 24–28 gestational weeks. A total of 56 women with GDM and 73 healthy pregnant women were selected. Maternal serum concentrations of placental protein 13 (PP13), pentraxin 3 (PTX3), soluble fms‐like tyrosine kinase‐1 (sFlt‐1), myostatin and follistatin (FST) were detected at 16–20 weeks’ gestation. All of these markers concentrations were expressed as multiples of the medians. The Mann–Whitney U‐test was used for comparison of the multiples of the medians of different concentrations of these five serum markers between the GDM group and the control group. Receiver operating characteristic curve analysis was applied to assess the sensitivity and specificity of significant serum markers from a Mann–Whitney U‐test comparison. RESULTS: Compared with healthy pregnancies, the serum levels of PP13, PTX3, sFlt‐1, myostatin and FST in the early second trimester were significantly increased in patients who had developed GDM late. In screening for GDM by PP13, PTX3, sFlt‐1, myostatin and FST, the detection rates were 92.3, 94.9, 94.9, 92.5 and 92.3%, respectively at 80% specificity. PTX3 and sFlt‐1 were the most sensitive markers. CONCLUSIONS: Maternal serum markers including PP13, PTX3, sFlt‐1, myostatin and FST increase in the early second trimester of women with GDM. These five markers, especially PTX3 and sFlt‐1, could have the value of prediction for those patients who would develop GDM in the late second trimester. John Wiley and Sons Inc. 2018-01-28 2018-07 /pmc/articles/PMC6031488/ /pubmed/29288571 http://dx.doi.org/10.1111/jdi.12798 Text en © 2017 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Articles
Zhao, Baihui
Han, Xiujun
Meng, Qing
Luo, Qiong
Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title_full Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title_fullStr Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title_full_unstemmed Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title_short Early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
title_sort early second trimester maternal serum markers in the prediction of gestational diabetes mellitus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031488/
https://www.ncbi.nlm.nih.gov/pubmed/29288571
http://dx.doi.org/10.1111/jdi.12798
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