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Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?

BACKGROUND: Gestational diabetes mellitus (GDM) occurs in 3–5% of all pregnancies. GDM increases both maternal and fetal risks, causes fetal macrosomia, and hence increases the rates of caesarean sections and delivery complications such as shoulder dystocia. An early predictive marker and consequent...

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Autores principales: Stein, Roland Gregor, Meinusch, Malgorzata, Diessner, Joachim, Dietl, Johannes, Hönig, Arnd, Zollner, Ursula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907493/
https://www.ncbi.nlm.nih.gov/pubmed/24423633
http://dx.doi.org/10.12659/MSM.889503
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author Stein, Roland Gregor
Meinusch, Malgorzata
Diessner, Joachim
Dietl, Johannes
Hönig, Arnd
Zollner, Ursula
author_facet Stein, Roland Gregor
Meinusch, Malgorzata
Diessner, Joachim
Dietl, Johannes
Hönig, Arnd
Zollner, Ursula
author_sort Stein, Roland Gregor
collection PubMed
description BACKGROUND: Gestational diabetes mellitus (GDM) occurs in 3–5% of all pregnancies. GDM increases both maternal and fetal risks, causes fetal macrosomia, and hence increases the rates of caesarean sections and delivery complications such as shoulder dystocia. An early predictive marker and consequent early treatment could be beneficial, so amniotic fluid insulin and C-peptide have been examined in several studies. Increased amniotic fluid insulin in early amniocentesis between the 14(th) and 20(th) gestational week predicted a later GDM. A potential direct association with fetal macrosomia remains to be determined. MATERIAL/METHODS: This retrospective study investigated amniotic fluid insulin/C-peptide from amniocenteses between 14 and 20 weeks of gestation in correlation with fetal birth weight, type of delivery, and complications. To focus on effects of fetal hyperinsulinism apart from therapeutic confounders, we included patients who did not participate in GDM screening. Insulin and C-peptide were measured in 144 samples of frozen amniotic fluid. Birth weight, type of delivery, complications, and birth injuries were noted. RESULTS: Birth weights ranged from 760 g to 4410 g with a mean weight of 3424 g at an average of 40 weeks gestation. The mean amniotic fluid insulin was 4.36 μU/ml and the mean C-peptide concentration was 0.076 ng/ml. There was no correlation between amniotic fluid insulin or C peptide and birth weight, type of delivery, complications, and birth injuries. CONCLUSIONS: Amniotic fluid insulin and C-peptide are unsuitable as predictive marker for fetal macrosomia, type of delivery, complications, or birth injuries.
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spelling pubmed-39074932014-01-31 Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications? Stein, Roland Gregor Meinusch, Malgorzata Diessner, Joachim Dietl, Johannes Hönig, Arnd Zollner, Ursula Med Sci Monit Clinical Research BACKGROUND: Gestational diabetes mellitus (GDM) occurs in 3–5% of all pregnancies. GDM increases both maternal and fetal risks, causes fetal macrosomia, and hence increases the rates of caesarean sections and delivery complications such as shoulder dystocia. An early predictive marker and consequent early treatment could be beneficial, so amniotic fluid insulin and C-peptide have been examined in several studies. Increased amniotic fluid insulin in early amniocentesis between the 14(th) and 20(th) gestational week predicted a later GDM. A potential direct association with fetal macrosomia remains to be determined. MATERIAL/METHODS: This retrospective study investigated amniotic fluid insulin/C-peptide from amniocenteses between 14 and 20 weeks of gestation in correlation with fetal birth weight, type of delivery, and complications. To focus on effects of fetal hyperinsulinism apart from therapeutic confounders, we included patients who did not participate in GDM screening. Insulin and C-peptide were measured in 144 samples of frozen amniotic fluid. Birth weight, type of delivery, complications, and birth injuries were noted. RESULTS: Birth weights ranged from 760 g to 4410 g with a mean weight of 3424 g at an average of 40 weeks gestation. The mean amniotic fluid insulin was 4.36 μU/ml and the mean C-peptide concentration was 0.076 ng/ml. There was no correlation between amniotic fluid insulin or C peptide and birth weight, type of delivery, complications, and birth injuries. CONCLUSIONS: Amniotic fluid insulin and C-peptide are unsuitable as predictive marker for fetal macrosomia, type of delivery, complications, or birth injuries. International Scientific Literature, Inc. 2014-01-15 /pmc/articles/PMC3907493/ /pubmed/24423633 http://dx.doi.org/10.12659/MSM.889503 Text en © Med Sci Monit, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Clinical Research
Stein, Roland Gregor
Meinusch, Malgorzata
Diessner, Joachim
Dietl, Johannes
Hönig, Arnd
Zollner, Ursula
Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title_full Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title_fullStr Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title_full_unstemmed Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title_short Amniotic fluid insulin and C-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
title_sort amniotic fluid insulin and c-peptide as predictive markers for fetal macrosomia, birth injuries, and delivery complications?
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3907493/
https://www.ncbi.nlm.nih.gov/pubmed/24423633
http://dx.doi.org/10.12659/MSM.889503
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