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Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark

PURPOSE: Inflammatory bowel disease (IBD) and autism spectrum disorders (ASD) may share genetic and environmental risk factors. We examined whether parental IBD is associated with an increased risk of ASD in offspring. METHODS: We conducted a registry-based nationwide cohort study including children...

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Autores principales: Andersen, Ane Birgitte Telén, Ehrenstein, Vera, Erichsen, Rune, Frøslev, Trine, Sørensen, Henrik Toft
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019630/
https://www.ncbi.nlm.nih.gov/pubmed/24855384
http://dx.doi.org/10.2147/CEG.S59360
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author Andersen, Ane Birgitte Telén
Ehrenstein, Vera
Erichsen, Rune
Frøslev, Trine
Sørensen, Henrik Toft
author_facet Andersen, Ane Birgitte Telén
Ehrenstein, Vera
Erichsen, Rune
Frøslev, Trine
Sørensen, Henrik Toft
author_sort Andersen, Ane Birgitte Telén
collection PubMed
description PURPOSE: Inflammatory bowel disease (IBD) and autism spectrum disorders (ASD) may share genetic and environmental risk factors. We examined whether parental IBD is associated with an increased risk of ASD in offspring. METHODS: We conducted a registry-based nationwide cohort study including children born alive in Denmark from January 1, 1994 to December 31, 2009, with follow-up throughout 2010. IBD in parents and ASD in offspring were identified using inpatient and outpatient hospital diagnoses. We computed risk of ASD and crude and adjusted incidence rate ratios (aIRRs) with 95% confidence intervals (CI) using Cox proportional-hazards regression. We evaluated the risk of ASD according to maternal and paternal IBD, and separately for maternal and paternal Crohn’s disease (CD) and ulcerative colitis (UC). Children with parents free of IBD were the comparison cohort. RESULTS: We identified 1,005,330 children during the study period. Among them, 11,888 (1.2%) had a parent with IBD and 8,087 (0.8%) had a diagnosis of ASD during up to 17 years of follow-up. The 10-year risks of ASD were 0.7% among children of parents with IBD and 0.9% among children of parents without IBD. The aIRR for ASD among children with parental IBD was 0.8 (95% CI: 0.6–1.0), and results were similar regardless of parent of IBD origin or whether a parent had CD or UC. The estimates were similar for different ASD subtypes. CONCLUSION: We found no evidence of an increased risk of ASD among children born to parents with IBD.
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spelling pubmed-40196302014-05-22 Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark Andersen, Ane Birgitte Telén Ehrenstein, Vera Erichsen, Rune Frøslev, Trine Sørensen, Henrik Toft Clin Exp Gastroenterol Original Research PURPOSE: Inflammatory bowel disease (IBD) and autism spectrum disorders (ASD) may share genetic and environmental risk factors. We examined whether parental IBD is associated with an increased risk of ASD in offspring. METHODS: We conducted a registry-based nationwide cohort study including children born alive in Denmark from January 1, 1994 to December 31, 2009, with follow-up throughout 2010. IBD in parents and ASD in offspring were identified using inpatient and outpatient hospital diagnoses. We computed risk of ASD and crude and adjusted incidence rate ratios (aIRRs) with 95% confidence intervals (CI) using Cox proportional-hazards regression. We evaluated the risk of ASD according to maternal and paternal IBD, and separately for maternal and paternal Crohn’s disease (CD) and ulcerative colitis (UC). Children with parents free of IBD were the comparison cohort. RESULTS: We identified 1,005,330 children during the study period. Among them, 11,888 (1.2%) had a parent with IBD and 8,087 (0.8%) had a diagnosis of ASD during up to 17 years of follow-up. The 10-year risks of ASD were 0.7% among children of parents with IBD and 0.9% among children of parents without IBD. The aIRR for ASD among children with parental IBD was 0.8 (95% CI: 0.6–1.0), and results were similar regardless of parent of IBD origin or whether a parent had CD or UC. The estimates were similar for different ASD subtypes. CONCLUSION: We found no evidence of an increased risk of ASD among children born to parents with IBD. Dove Medical Press 2014-05-07 /pmc/articles/PMC4019630/ /pubmed/24855384 http://dx.doi.org/10.2147/CEG.S59360 Text en © 2014 Andersen et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Andersen, Ane Birgitte Telén
Ehrenstein, Vera
Erichsen, Rune
Frøslev, Trine
Sørensen, Henrik Toft
Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title_full Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title_fullStr Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title_full_unstemmed Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title_short Autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in Denmark
title_sort autism spectrum disorders in children of parents with inflammatory bowel disease – a nationwide cohort study in denmark
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019630/
https://www.ncbi.nlm.nih.gov/pubmed/24855384
http://dx.doi.org/10.2147/CEG.S59360
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