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Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome
BACKGROUND/AIMS: Little is known about the association between infantile colic and the later onset of irritable bowel syndrome (IBS). METHODS: This study examined all 917 707 children who were born in Korea between 2007 and 2008. Infantile colic was defined with 1 or more diagnoses of ICD-10 code R1...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Neurogastroenterology and Motility
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577576/ https://www.ncbi.nlm.nih.gov/pubmed/36250369 http://dx.doi.org/10.5056/jnm21181 |
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author | Kim, Ju Hee Lee, Seung Won Kwon, Yoowon Ha, Eun Kyo An, Jaewoo Cha, Hye Ryeong Jeong, Su Jin Han, Man Yong |
author_facet | Kim, Ju Hee Lee, Seung Won Kwon, Yoowon Ha, Eun Kyo An, Jaewoo Cha, Hye Ryeong Jeong, Su Jin Han, Man Yong |
author_sort | Kim, Ju Hee |
collection | PubMed |
description | BACKGROUND/AIMS: Little is known about the association between infantile colic and the later onset of irritable bowel syndrome (IBS). METHODS: This study examined all 917 707 children who were born in Korea between 2007 and 2008. Infantile colic was defined with 1 or more diagnoses of ICD-10 code R10.4 or R68.1 at the age of 5 weeks to 4 months, and infants with a diagnosis of infantile colic and without were allocated into the infantile colic group and the control group. IBS was defined as 2 or more diagnoses of ICD-10 code K58.X after 4 years of age. Each child was traced until 2017. The risk of IBS with infantile colic was evaluated using a Cox proportional hazards model with propensity score inverse probability of treatment weighting (IPTW). RESULTS: After IPTW, 363 528 and 359 842 children were allocated to the control group and the infantile colic group, respectively. The infantile colic group had a higher risk of developing IBS in childhood (hazard ratio [95% CI], 1.12 [1.10 to 1.13]) than the control group. Moreover, the subgroup analyses according to the feeding status, birth weight, sex, or economic status, showed that the risk of IBS with former infantile colic remained statistically significant. CONCLUSIONS: Children with a diagnosis of infantile colic during the infant period had a significant risk of developing IBS after 4 years of age. Understanding the pathogenesis of infantile colic in the neonatal period may reduce the prevalence and severity of functional gastrointestinal disorders from childhood to adolescence to adulthood. |
format | Online Article Text |
id | pubmed-9577576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society of Neurogastroenterology and Motility |
record_format | MEDLINE/PubMed |
spelling | pubmed-95775762022-10-30 Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome Kim, Ju Hee Lee, Seung Won Kwon, Yoowon Ha, Eun Kyo An, Jaewoo Cha, Hye Ryeong Jeong, Su Jin Han, Man Yong J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: Little is known about the association between infantile colic and the later onset of irritable bowel syndrome (IBS). METHODS: This study examined all 917 707 children who were born in Korea between 2007 and 2008. Infantile colic was defined with 1 or more diagnoses of ICD-10 code R10.4 or R68.1 at the age of 5 weeks to 4 months, and infants with a diagnosis of infantile colic and without were allocated into the infantile colic group and the control group. IBS was defined as 2 or more diagnoses of ICD-10 code K58.X after 4 years of age. Each child was traced until 2017. The risk of IBS with infantile colic was evaluated using a Cox proportional hazards model with propensity score inverse probability of treatment weighting (IPTW). RESULTS: After IPTW, 363 528 and 359 842 children were allocated to the control group and the infantile colic group, respectively. The infantile colic group had a higher risk of developing IBS in childhood (hazard ratio [95% CI], 1.12 [1.10 to 1.13]) than the control group. Moreover, the subgroup analyses according to the feeding status, birth weight, sex, or economic status, showed that the risk of IBS with former infantile colic remained statistically significant. CONCLUSIONS: Children with a diagnosis of infantile colic during the infant period had a significant risk of developing IBS after 4 years of age. Understanding the pathogenesis of infantile colic in the neonatal period may reduce the prevalence and severity of functional gastrointestinal disorders from childhood to adolescence to adulthood. The Korean Society of Neurogastroenterology and Motility 2022-10-30 2022-10-30 /pmc/articles/PMC9577576/ /pubmed/36250369 http://dx.doi.org/10.5056/jnm21181 Text en © 2022 The Korean Society of Neurogastroenterology and Motility https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Ju Hee Lee, Seung Won Kwon, Yoowon Ha, Eun Kyo An, Jaewoo Cha, Hye Ryeong Jeong, Su Jin Han, Man Yong Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title | Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title_full | Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title_fullStr | Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title_full_unstemmed | Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title_short | Infantile Colic and the Subsequent Development of the Irritable Bowel Syndrome |
title_sort | infantile colic and the subsequent development of the irritable bowel syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577576/ https://www.ncbi.nlm.nih.gov/pubmed/36250369 http://dx.doi.org/10.5056/jnm21181 |
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