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Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester

OBJECTIVE: To analyse data from a randomised, controlled study of prandial insulin aspart versus human insulin, both with NPH insulin, in pregnant women with type 1 diabetes for potential factors predicting poor pregnancy outcomes. RESEARCH DESIGN/METHOD: Post hoc analysis including 91 subjects rand...

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Autores principales: Damm, Peter, Mersebach, Henriette, Råstam, Jacob, Kaaja, Risto, Hod, Moshe, McCance, David R., Mathiesen, Elisabeth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa UK Ltd. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877859/
https://www.ncbi.nlm.nih.gov/pubmed/23687948
http://dx.doi.org/10.3109/14767058.2013.806896
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author Damm, Peter
Mersebach, Henriette
Råstam, Jacob
Kaaja, Risto
Hod, Moshe
McCance, David R.
Mathiesen, Elisabeth R.
author_facet Damm, Peter
Mersebach, Henriette
Råstam, Jacob
Kaaja, Risto
Hod, Moshe
McCance, David R.
Mathiesen, Elisabeth R.
author_sort Damm, Peter
collection PubMed
description OBJECTIVE: To analyse data from a randomised, controlled study of prandial insulin aspart versus human insulin, both with NPH insulin, in pregnant women with type 1 diabetes for potential factors predicting poor pregnancy outcomes. RESEARCH DESIGN/METHOD: Post hoc analysis including 91 subjects randomised prior to pregnancy with known outcome in early pregnancy and 259 subjects randomised prior to pregnancy/during pregnancy of <10 weeks’ gestation with known late-pregnancy outcomes. Poor early-pregnancy outcomes included fetal loss <22 gestational weeks and/or congenital malformation (n = 18). Poor late-pregnancy outcomes included: composite endpoint including pre-eclampsia, preterm delivery and perinatal death (n = 78); preterm delivery (n = 63); and excessive fetal growth (n = 88). RESULTS: 18 patients experienced a malformed/lost fetus in early pregnancy – none preceded by severe hypoglycaemia. Albuminuria in early pregnancy was a significant predictor of poor late-pregnancy outcome (composite endpoint; p = 0.012). In the third trimester, elevated HbA(1c), ≥ 1 plasma glucose (PG) measurement >11 mmol/L (198 mg/dL) and %PG values outside 3.9–7.0 mmol/L (70–126 mg/dL) were significant predictors of poor late-pregnancy outcomes (all p < 0.05). CONCLUSIONS: Elevated HbA(1c), high glucose spikes and out-of-range %PG in the third trimester, and albuminuria in early pregnancy, are associated with poor late-pregnancy outcomes.
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spelling pubmed-38778592014-01-17 Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester Damm, Peter Mersebach, Henriette Råstam, Jacob Kaaja, Risto Hod, Moshe McCance, David R. Mathiesen, Elisabeth R. J Matern Fetal Neonatal Med Original Article OBJECTIVE: To analyse data from a randomised, controlled study of prandial insulin aspart versus human insulin, both with NPH insulin, in pregnant women with type 1 diabetes for potential factors predicting poor pregnancy outcomes. RESEARCH DESIGN/METHOD: Post hoc analysis including 91 subjects randomised prior to pregnancy with known outcome in early pregnancy and 259 subjects randomised prior to pregnancy/during pregnancy of <10 weeks’ gestation with known late-pregnancy outcomes. Poor early-pregnancy outcomes included fetal loss <22 gestational weeks and/or congenital malformation (n = 18). Poor late-pregnancy outcomes included: composite endpoint including pre-eclampsia, preterm delivery and perinatal death (n = 78); preterm delivery (n = 63); and excessive fetal growth (n = 88). RESULTS: 18 patients experienced a malformed/lost fetus in early pregnancy – none preceded by severe hypoglycaemia. Albuminuria in early pregnancy was a significant predictor of poor late-pregnancy outcome (composite endpoint; p = 0.012). In the third trimester, elevated HbA(1c), ≥ 1 plasma glucose (PG) measurement >11 mmol/L (198 mg/dL) and %PG values outside 3.9–7.0 mmol/L (70–126 mg/dL) were significant predictors of poor late-pregnancy outcomes (all p < 0.05). CONCLUSIONS: Elevated HbA(1c), high glucose spikes and out-of-range %PG in the third trimester, and albuminuria in early pregnancy, are associated with poor late-pregnancy outcomes. Informa UK Ltd. 2014-01 2013-06-20 /pmc/articles/PMC3877859/ /pubmed/23687948 http://dx.doi.org/10.3109/14767058.2013.806896 Text en © 2014 Informa UK Ltd. All rights reserved: reproduction in whole or part not permitted http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Original Article
Damm, Peter
Mersebach, Henriette
Råstam, Jacob
Kaaja, Risto
Hod, Moshe
McCance, David R.
Mathiesen, Elisabeth R.
Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title_full Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title_fullStr Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title_full_unstemmed Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title_short Poor pregnancy outcome in women with type 1 diabetes is predicted by elevated HbA(1c) and spikes of high glucose values in the third trimester
title_sort poor pregnancy outcome in women with type 1 diabetes is predicted by elevated hba(1c) and spikes of high glucose values in the third trimester
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877859/
https://www.ncbi.nlm.nih.gov/pubmed/23687948
http://dx.doi.org/10.3109/14767058.2013.806896
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