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Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis
AIM: To investigate the effect of disease activity or thiopurine use on low birth weight and small for gestational age in women with inflammatory bowel disease (IBD). METHODS: Selection criteria included all relevant articles on the effect of disease activity or thiopurine use on the risk of low bir...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725303/ https://www.ncbi.nlm.nih.gov/pubmed/29259384 http://dx.doi.org/10.3748/wjg.v23.i45.8082 |
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author | Gonzalez-Suarez, Begoña Sengupta, Shreyashee Moss, Alan C |
author_facet | Gonzalez-Suarez, Begoña Sengupta, Shreyashee Moss, Alan C |
author_sort | Gonzalez-Suarez, Begoña |
collection | PubMed |
description | AIM: To investigate the effect of disease activity or thiopurine use on low birth weight and small for gestational age in women with inflammatory bowel disease (IBD). METHODS: Selection criteria included all relevant articles on the effect of disease activity or thiopurine use on the risk of low birth weight (LBW) or small for gestational age (SGA) among pregnant women with IBD. Sixty-nine abstracts were identified, 35 papers were full text reviewed and, only 14 of them met inclusion criteria. Raw data were extracted to generate the relative risk of LBW or SGA. Quality was assessed using the Newcastle Ottawa Scale. RESULTS: This meta-analysis is reported according to PRISMA guidelines. Fourteen studies met inclusion criteria, and nine reported raw data suitable for meta-analysis. We found an increased risk ratio of both SGA and LBW in women with active IBD, when compared with women in remission: 1.3 for SGA (4 studies, 95%CI: 1.0-1.6, P = 0.04) and 2.0 for LBW (4 studies, 95%CI: 1.5-2.7, P < 0.0001). Women on thiopurines during pregnancy had a higher risk of LBW (RR 1.4, 95%CI: 1.1-1.9, P = 0.007) compared with non-treated women, but when adjusted for disease activity there was no significant effect on LBW (RR 1.2, 95%CI: 0.6-2.2, P = 0.6). No differences were observed regarding SGA (2 studies; RR 0.9, 95%CI: 0.7-1.2, P = 0.5). CONCLUSION: Women with active IBD during pregnancy have a higher risk of LBW and SGA in their neonates. This should be considered in treatment decisions during pregnancy. |
format | Online Article Text |
id | pubmed-5725303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-57253032017-12-19 Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis Gonzalez-Suarez, Begoña Sengupta, Shreyashee Moss, Alan C World J Gastroenterol Meta-Analysis AIM: To investigate the effect of disease activity or thiopurine use on low birth weight and small for gestational age in women with inflammatory bowel disease (IBD). METHODS: Selection criteria included all relevant articles on the effect of disease activity or thiopurine use on the risk of low birth weight (LBW) or small for gestational age (SGA) among pregnant women with IBD. Sixty-nine abstracts were identified, 35 papers were full text reviewed and, only 14 of them met inclusion criteria. Raw data were extracted to generate the relative risk of LBW or SGA. Quality was assessed using the Newcastle Ottawa Scale. RESULTS: This meta-analysis is reported according to PRISMA guidelines. Fourteen studies met inclusion criteria, and nine reported raw data suitable for meta-analysis. We found an increased risk ratio of both SGA and LBW in women with active IBD, when compared with women in remission: 1.3 for SGA (4 studies, 95%CI: 1.0-1.6, P = 0.04) and 2.0 for LBW (4 studies, 95%CI: 1.5-2.7, P < 0.0001). Women on thiopurines during pregnancy had a higher risk of LBW (RR 1.4, 95%CI: 1.1-1.9, P = 0.007) compared with non-treated women, but when adjusted for disease activity there was no significant effect on LBW (RR 1.2, 95%CI: 0.6-2.2, P = 0.6). No differences were observed regarding SGA (2 studies; RR 0.9, 95%CI: 0.7-1.2, P = 0.5). CONCLUSION: Women with active IBD during pregnancy have a higher risk of LBW and SGA in their neonates. This should be considered in treatment decisions during pregnancy. Baishideng Publishing Group Inc 2017-12-07 2017-12-07 /pmc/articles/PMC5725303/ /pubmed/29259384 http://dx.doi.org/10.3748/wjg.v23.i45.8082 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Meta-Analysis Gonzalez-Suarez, Begoña Sengupta, Shreyashee Moss, Alan C Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title | Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title_full | Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title_fullStr | Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title_full_unstemmed | Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title_short | Impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: A meta-analysis |
title_sort | impact of inflammatory bowel disease activity and thiopurine therapy on birth weight: a meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725303/ https://www.ncbi.nlm.nih.gov/pubmed/29259384 http://dx.doi.org/10.3748/wjg.v23.i45.8082 |
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