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Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk

OBJECTIVE: Genes associated with cardiovascular disease may also be risk factors for congenital cerebral palsy (CP) and these associations may be modified by sex, since there is an increased risk of CP in male children. We investigated the association between CP of the child with cardiovascular dise...

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Autores principales: Streja, Elani, Wu, Chunsen, Uldall, Peter, Grove, Jakob, Arah, Onyebuchi, Olsen, Jørn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815096/
https://www.ncbi.nlm.nih.gov/pubmed/24223882
http://dx.doi.org/10.1371/journal.pone.0079071
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author Streja, Elani
Wu, Chunsen
Uldall, Peter
Grove, Jakob
Arah, Onyebuchi
Olsen, Jørn
author_facet Streja, Elani
Wu, Chunsen
Uldall, Peter
Grove, Jakob
Arah, Onyebuchi
Olsen, Jørn
author_sort Streja, Elani
collection PubMed
description OBJECTIVE: Genes associated with cardiovascular disease may also be risk factors for congenital cerebral palsy (CP) and these associations may be modified by sex, since there is an increased risk of CP in male children. We investigated the association between CP of the child with cardiovascular disease in parents, taking sex of the child into consideration. METHODS: All parents of non-adopted singletons born in Denmark between 1973 and 2003 were included. Parents of a child with CP, confirmed by the Danish National CP registry, were considered exposed. Cox proportional hazards regressions were used to model risk of cardiovascular outcomes for exposed parents compared to all other parents beginning at the child’s 10(th) birthday. RESULTS: We identified 733,730 mothers and 666,652 fathers among whom 1,592 and 1,484, respectively, had a child with CP. The mean age for mothers at end of follow up was 50±8 years. After adjustment for maternal age, parental education, child’s sex, child’s residence, child being small for gestational age and maternal hypertensive disorder during pregnancy, mothers of CP male children had an excess risk of cardiovascular disease (HR: 1.52, 95% CI: 1.16-2.00), attributable mostly to an increased incidence of hypertension and cerebrovascular disease. After additional adjustment for preterm birth, the association was markedly attenuated for cardiovascular disease (1.34, 95%CI: 1.02 - 1.76), became nonsignificant for hypertension, but remained significant for cerebrovascular disease (HR: 2.73, 95% CI: 1.45- 5.12). There was no increased risk of cardiovascular events in mothers of female CP children, or fathers of CP children of any sex. CONCLUSIONS: Women that have a male child with CP are at increased risk for premature cardiovascular disease. Part of this association may be related to risk factors for preterm births.
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spelling pubmed-38150962013-11-09 Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk Streja, Elani Wu, Chunsen Uldall, Peter Grove, Jakob Arah, Onyebuchi Olsen, Jørn PLoS One Research Article OBJECTIVE: Genes associated with cardiovascular disease may also be risk factors for congenital cerebral palsy (CP) and these associations may be modified by sex, since there is an increased risk of CP in male children. We investigated the association between CP of the child with cardiovascular disease in parents, taking sex of the child into consideration. METHODS: All parents of non-adopted singletons born in Denmark between 1973 and 2003 were included. Parents of a child with CP, confirmed by the Danish National CP registry, were considered exposed. Cox proportional hazards regressions were used to model risk of cardiovascular outcomes for exposed parents compared to all other parents beginning at the child’s 10(th) birthday. RESULTS: We identified 733,730 mothers and 666,652 fathers among whom 1,592 and 1,484, respectively, had a child with CP. The mean age for mothers at end of follow up was 50±8 years. After adjustment for maternal age, parental education, child’s sex, child’s residence, child being small for gestational age and maternal hypertensive disorder during pregnancy, mothers of CP male children had an excess risk of cardiovascular disease (HR: 1.52, 95% CI: 1.16-2.00), attributable mostly to an increased incidence of hypertension and cerebrovascular disease. After additional adjustment for preterm birth, the association was markedly attenuated for cardiovascular disease (1.34, 95%CI: 1.02 - 1.76), became nonsignificant for hypertension, but remained significant for cerebrovascular disease (HR: 2.73, 95% CI: 1.45- 5.12). There was no increased risk of cardiovascular events in mothers of female CP children, or fathers of CP children of any sex. CONCLUSIONS: Women that have a male child with CP are at increased risk for premature cardiovascular disease. Part of this association may be related to risk factors for preterm births. Public Library of Science 2013-11-01 /pmc/articles/PMC3815096/ /pubmed/24223882 http://dx.doi.org/10.1371/journal.pone.0079071 Text en © 2013 Streja 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
Streja, Elani
Wu, Chunsen
Uldall, Peter
Grove, Jakob
Arah, Onyebuchi
Olsen, Jørn
Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title_full Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title_fullStr Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title_full_unstemmed Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title_short Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk
title_sort congenital cerebral palsy, child sex and parent cardiovascular risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815096/
https://www.ncbi.nlm.nih.gov/pubmed/24223882
http://dx.doi.org/10.1371/journal.pone.0079071
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