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Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study
BACKGROUND: To examine whether prenatal exposure to parental type 1 diabetes, type 2 diabetes, or gestational diabetes is associated with an increased risk of malignant neoplasm or diseases of the circulatory system in the offspring. METHODS/PRINCIPAL FINDINGS: We conducted a population-based cohort...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359312/ https://www.ncbi.nlm.nih.gov/pubmed/22649497 http://dx.doi.org/10.1371/journal.pone.0036727 |
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author | Wu, Chun S. Nohr, Ellen A. Bech, Bodil H. Vestergaard, Mogens Olsen, Jørn |
author_facet | Wu, Chun S. Nohr, Ellen A. Bech, Bodil H. Vestergaard, Mogens Olsen, Jørn |
author_sort | Wu, Chun S. |
collection | PubMed |
description | BACKGROUND: To examine whether prenatal exposure to parental type 1 diabetes, type 2 diabetes, or gestational diabetes is associated with an increased risk of malignant neoplasm or diseases of the circulatory system in the offspring. METHODS/PRINCIPAL FINDINGS: We conducted a population-based cohort study of 1,781,576 singletons born in Denmark from 1977 to 2008. Children were followed for up to 30 years from the day of birth until the onset of the outcomes under study, death, emigration, or December 31, 2009, whichever came first. We used Cox proportional hazards model to estimate hazard ratios (HR) with 95% confidence intervals (95% CI) for the outcomes under study while adjusting for potential confounders. An increased risk of malignant neoplasm was found in children prenatally exposed to maternal type 2 diabetes (HR = 2.2, 95%CI: 1.5–3.2). An increased risk of diseases of the circulatory system was found in children exposed to maternal type 1 diabetes (HR = 2.2, 95%CI: 1.6–3.0), type 2 diabetes (HR = 1.4, 95%CI: 1.1–1.7), and gestational diabetes (HR = 1.3, 95%CI: 1.1–1.6), but results were attenuated after excluding children with congenital malformations. An increased risk of diseases of the circulatory system was also found in children exposed to paternal type 2 diabetes (HR = 1.5, 95%CI: 1.1–2.2) and the elevated risk remained after excluding children with congenital malformations. CONCLUSIONS: This study suggests that susceptibility to malignant neoplasm is modified partly by fetal programming. Diseases of the circulatory system may be modified by genetic factors, other time-stable family factors, or fetal programming. |
format | Online Article Text |
id | pubmed-3359312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33593122012-05-30 Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study Wu, Chun S. Nohr, Ellen A. Bech, Bodil H. Vestergaard, Mogens Olsen, Jørn PLoS One Research Article BACKGROUND: To examine whether prenatal exposure to parental type 1 diabetes, type 2 diabetes, or gestational diabetes is associated with an increased risk of malignant neoplasm or diseases of the circulatory system in the offspring. METHODS/PRINCIPAL FINDINGS: We conducted a population-based cohort study of 1,781,576 singletons born in Denmark from 1977 to 2008. Children were followed for up to 30 years from the day of birth until the onset of the outcomes under study, death, emigration, or December 31, 2009, whichever came first. We used Cox proportional hazards model to estimate hazard ratios (HR) with 95% confidence intervals (95% CI) for the outcomes under study while adjusting for potential confounders. An increased risk of malignant neoplasm was found in children prenatally exposed to maternal type 2 diabetes (HR = 2.2, 95%CI: 1.5–3.2). An increased risk of diseases of the circulatory system was found in children exposed to maternal type 1 diabetes (HR = 2.2, 95%CI: 1.6–3.0), type 2 diabetes (HR = 1.4, 95%CI: 1.1–1.7), and gestational diabetes (HR = 1.3, 95%CI: 1.1–1.6), but results were attenuated after excluding children with congenital malformations. An increased risk of diseases of the circulatory system was also found in children exposed to paternal type 2 diabetes (HR = 1.5, 95%CI: 1.1–2.2) and the elevated risk remained after excluding children with congenital malformations. CONCLUSIONS: This study suggests that susceptibility to malignant neoplasm is modified partly by fetal programming. Diseases of the circulatory system may be modified by genetic factors, other time-stable family factors, or fetal programming. Public Library of Science 2012-05-23 /pmc/articles/PMC3359312/ /pubmed/22649497 http://dx.doi.org/10.1371/journal.pone.0036727 Text en Wu et al. http://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 author and source are properly credited. |
spellingShingle | Research Article Wu, Chun S. Nohr, Ellen A. Bech, Bodil H. Vestergaard, Mogens Olsen, Jørn Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title | Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title_full | Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title_fullStr | Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title_full_unstemmed | Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title_short | Long-Term Health Outcomes in Children Born to Mothers with Diabetes: A Population-Based Cohort Study |
title_sort | long-term health outcomes in children born to mothers with diabetes: a population-based cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359312/ https://www.ncbi.nlm.nih.gov/pubmed/22649497 http://dx.doi.org/10.1371/journal.pone.0036727 |
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