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Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study

OBJECTIVE: To characterize birth size distribution in infants born to mothers with type 1 diabetes. In particular, the relationship between birth weight (BW) and length (BL) was studied because it may provide information on different causal pathways of fetal macrosomia commonly seen in diabetic preg...

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Detalles Bibliográficos
Autores principales: Persson, Martina, Pasupathy, Dharmintra, Hanson, Ulf, Norman, Mikael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114507/
https://www.ncbi.nlm.nih.gov/pubmed/21430084
http://dx.doi.org/10.2337/dc10-2406
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author Persson, Martina
Pasupathy, Dharmintra
Hanson, Ulf
Norman, Mikael
author_facet Persson, Martina
Pasupathy, Dharmintra
Hanson, Ulf
Norman, Mikael
author_sort Persson, Martina
collection PubMed
description OBJECTIVE: To characterize birth size distribution in infants born to mothers with type 1 diabetes. In particular, the relationship between birth weight (BW) and length (BL) was studied because it may provide information on different causal pathways of fetal macrosomia commonly seen in diabetic pregnancies. RESEARCH DESIGN AND METHODS: This was a population-based cohort study of 3,705 infants of type 1 diabetic mothers (1,876 boys), with a gestational age of 28–43 weeks, born in Sweden between 1998 and 2007. BW and BL were retrieved from the Medical Birth Registry and expressed as SD scores (SDS). Ponderal index (PI) was calculated as BW in g/length in cm(3). A BW >90th and a PI ≤90th percentile was defined as proportionate large-for-gestational age (LGA), whereas if both BW and PI >90th percentile, the infant was categorized as disproportionately large. Values are mean (SD). RESULTS: The BW distribution for offspring of type 1 diabetic mothers was bell-shaped, significantly broader, and markedly shifted to the right (BWSDS: 1.27 [1.48]) of the reference. Of the infants born to diabetic mothers, 47% were LGA, and among them, 46% were disproportionately large compared with 35% in nondiabetic LGA infants (P < 0.001). Female offspring of type 1 diabetic mothers had significantly higher BWSDS than males (1.34 vs. 1.20, P < 0.01), and preterm infants had higher BWSDS than term infants (1.41 vs. 1.23, P < 0.01) CONCLUSIONS: Fetal macrosomia in type 1 diabetic pregnancies is due to a right-shift and broadening of the entire BW distribution. The large number of disproportionate LGA infants born to type 1 diabetic mothers suggests an underlying metabolic problem. Fetal macrosomia was more pronounced in preterm and female offspring of type 1 diabetic mothers.
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spelling pubmed-31145072012-05-01 Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study Persson, Martina Pasupathy, Dharmintra Hanson, Ulf Norman, Mikael Diabetes Care Original Research OBJECTIVE: To characterize birth size distribution in infants born to mothers with type 1 diabetes. In particular, the relationship between birth weight (BW) and length (BL) was studied because it may provide information on different causal pathways of fetal macrosomia commonly seen in diabetic pregnancies. RESEARCH DESIGN AND METHODS: This was a population-based cohort study of 3,705 infants of type 1 diabetic mothers (1,876 boys), with a gestational age of 28–43 weeks, born in Sweden between 1998 and 2007. BW and BL were retrieved from the Medical Birth Registry and expressed as SD scores (SDS). Ponderal index (PI) was calculated as BW in g/length in cm(3). A BW >90th and a PI ≤90th percentile was defined as proportionate large-for-gestational age (LGA), whereas if both BW and PI >90th percentile, the infant was categorized as disproportionately large. Values are mean (SD). RESULTS: The BW distribution for offspring of type 1 diabetic mothers was bell-shaped, significantly broader, and markedly shifted to the right (BWSDS: 1.27 [1.48]) of the reference. Of the infants born to diabetic mothers, 47% were LGA, and among them, 46% were disproportionately large compared with 35% in nondiabetic LGA infants (P < 0.001). Female offspring of type 1 diabetic mothers had significantly higher BWSDS than males (1.34 vs. 1.20, P < 0.01), and preterm infants had higher BWSDS than term infants (1.41 vs. 1.23, P < 0.01) CONCLUSIONS: Fetal macrosomia in type 1 diabetic pregnancies is due to a right-shift and broadening of the entire BW distribution. The large number of disproportionate LGA infants born to type 1 diabetic mothers suggests an underlying metabolic problem. Fetal macrosomia was more pronounced in preterm and female offspring of type 1 diabetic mothers. American Diabetes Association 2011-05 2011-04-20 /pmc/articles/PMC3114507/ /pubmed/21430084 http://dx.doi.org/10.2337/dc10-2406 Text en © 2011 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Persson, Martina
Pasupathy, Dharmintra
Hanson, Ulf
Norman, Mikael
Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title_full Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title_fullStr Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title_full_unstemmed Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title_short Birth Size Distribution in 3,705 Infants Born to Mothers With Type 1 Diabetes: A population-based study
title_sort birth size distribution in 3,705 infants born to mothers with type 1 diabetes: a population-based study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114507/
https://www.ncbi.nlm.nih.gov/pubmed/21430084
http://dx.doi.org/10.2337/dc10-2406
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