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Parental inflammatory bowel disease and autism in children
Evidence linking parental inflammatory bowel disease (IBD) with autism in children is inconclusive. We conducted four complementary studies to investigate associations between parental IBD and autism in children, and elucidated their underlying etiology. Conducting a nationwide population-based coho...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307481/ https://www.ncbi.nlm.nih.gov/pubmed/35654906 http://dx.doi.org/10.1038/s41591-022-01845-9 |
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author | Sadik, Aws Dardani, Christina Pagoni, Panagiota Havdahl, Alexandra Stergiakouli, Evie Khandaker, Golam M. Sullivan, Sarah A. Zammit, Stan Jones, Hannah J. Davey Smith, George Dalman, Christina Karlsson, Håkan Gardner, Renee M. Rai, Dheeraj |
author_facet | Sadik, Aws Dardani, Christina Pagoni, Panagiota Havdahl, Alexandra Stergiakouli, Evie Khandaker, Golam M. Sullivan, Sarah A. Zammit, Stan Jones, Hannah J. Davey Smith, George Dalman, Christina Karlsson, Håkan Gardner, Renee M. Rai, Dheeraj |
author_sort | Sadik, Aws |
collection | PubMed |
description | Evidence linking parental inflammatory bowel disease (IBD) with autism in children is inconclusive. We conducted four complementary studies to investigate associations between parental IBD and autism in children, and elucidated their underlying etiology. Conducting a nationwide population-based cohort study using Swedish registers, we found evidence of associations between parental diagnoses of IBD and autism in children. Polygenic risk score analyses of the Avon Longitudinal Study of Parents and Children suggested associations between maternal genetic liability to IBD and autistic traits in children. Two-sample Mendelian randomization analyses provided evidence of a potential causal effect of genetic liability to IBD, especially ulcerative colitis, on autism. Linkage disequilibrium score regression did not indicate a genetic correlation between IBD and autism. Triangulating evidence from these four complementary approaches, we found evidence of a potential causal link between parental, particularly maternal, IBD and autism in children. Perinatal immune dysregulation, micronutrient malabsorption and anemia may be implicated. |
format | Online Article Text |
id | pubmed-9307481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-93074812022-07-24 Parental inflammatory bowel disease and autism in children Sadik, Aws Dardani, Christina Pagoni, Panagiota Havdahl, Alexandra Stergiakouli, Evie Khandaker, Golam M. Sullivan, Sarah A. Zammit, Stan Jones, Hannah J. Davey Smith, George Dalman, Christina Karlsson, Håkan Gardner, Renee M. Rai, Dheeraj Nat Med Article Evidence linking parental inflammatory bowel disease (IBD) with autism in children is inconclusive. We conducted four complementary studies to investigate associations between parental IBD and autism in children, and elucidated their underlying etiology. Conducting a nationwide population-based cohort study using Swedish registers, we found evidence of associations between parental diagnoses of IBD and autism in children. Polygenic risk score analyses of the Avon Longitudinal Study of Parents and Children suggested associations between maternal genetic liability to IBD and autistic traits in children. Two-sample Mendelian randomization analyses provided evidence of a potential causal effect of genetic liability to IBD, especially ulcerative colitis, on autism. Linkage disequilibrium score regression did not indicate a genetic correlation between IBD and autism. Triangulating evidence from these four complementary approaches, we found evidence of a potential causal link between parental, particularly maternal, IBD and autism in children. Perinatal immune dysregulation, micronutrient malabsorption and anemia may be implicated. Nature Publishing Group US 2022-06-02 2022 /pmc/articles/PMC9307481/ /pubmed/35654906 http://dx.doi.org/10.1038/s41591-022-01845-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sadik, Aws Dardani, Christina Pagoni, Panagiota Havdahl, Alexandra Stergiakouli, Evie Khandaker, Golam M. Sullivan, Sarah A. Zammit, Stan Jones, Hannah J. Davey Smith, George Dalman, Christina Karlsson, Håkan Gardner, Renee M. Rai, Dheeraj Parental inflammatory bowel disease and autism in children |
title | Parental inflammatory bowel disease and autism in children |
title_full | Parental inflammatory bowel disease and autism in children |
title_fullStr | Parental inflammatory bowel disease and autism in children |
title_full_unstemmed | Parental inflammatory bowel disease and autism in children |
title_short | Parental inflammatory bowel disease and autism in children |
title_sort | parental inflammatory bowel disease and autism in children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307481/ https://www.ncbi.nlm.nih.gov/pubmed/35654906 http://dx.doi.org/10.1038/s41591-022-01845-9 |
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