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5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review

BACKGROUND: Acute interstitial nephritis (AIN) is an important cause of kidney injury accounting for up to 27% of unexplained renal impairment. In up to 70% of cases, drugs, including aminosalicylates, are reported as the underlying cause. Following two recent paediatric cases of suspected mesalazin...

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Autores principales: Moss, James G., Parry, Christopher M., Holt, Richard C. L., McWilliam, Stephen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052675/
https://www.ncbi.nlm.nih.gov/pubmed/35488310
http://dx.doi.org/10.1186/s40001-022-00687-y
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author Moss, James G.
Parry, Christopher M.
Holt, Richard C. L.
McWilliam, Stephen J.
author_facet Moss, James G.
Parry, Christopher M.
Holt, Richard C. L.
McWilliam, Stephen J.
author_sort Moss, James G.
collection PubMed
description BACKGROUND: Acute interstitial nephritis (AIN) is an important cause of kidney injury accounting for up to 27% of unexplained renal impairment. In up to 70% of cases, drugs, including aminosalicylates, are reported as the underlying cause. Following two recent paediatric cases of suspected mesalazine induced AIN within our own department, we performed a systematic review of the literature to address the following question: In patients with inflammatory bowel disease (IBD), is interstitial nephritis associated with 5-aminosalicylate (5-ASA) treatment? Our primary objective was to identify the number of cases reported in the literature of biopsy-proven 5-ASA induced interstitial nephritis, in children and adults with IBD. We also aimed to identify which variables influence the onset, severity and recovery of 5-ASA interstitial nephritis. METHODS: Embase and PubMed databases were searched from inception to 07/10/20. Search terms had three main themes: “inflammatory bowel disease”, “interstitial nephritis” and “aminosalicylates”. Studies were included if they reported an outcome of AIN, confirmed on biopsy, suspected to be secondary to a 5-ASA drug in those with IBD. A narrative synthesis was performed. RESULTS: Forty-one case reports were identified. Mesalazine was the most frequently reported aminosalicylate associated with AIN (95%). The median duration of treatment before AIN was diagnosed was 2.3 years (Interquartile Range (IQR) 12–48 months). The median rise in creatinine was 3.3 times the baseline measurement (IQR 2.5–5.5). Aminosalicylate withdrawal and steroids were the most frequently used treatments. Despite treatment, 15% of patients developed end-stage renal failure. CONCLUSIONS: AIN is a serious adverse drug reaction associated with aminosalicylates, with mesalazine accounting for most reports. The current guidance of annual monitoring of renal function may not be sufficient to identify cases early. Given the severity of AIN and reports in the literature that early treatment with steroids may be beneficial, we would recommend at least 6 monthly monitoring of renal function. PROSPERO registration number CRD42020205387. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-022-00687-y.
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spelling pubmed-90526752022-04-30 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review Moss, James G. Parry, Christopher M. Holt, Richard C. L. McWilliam, Stephen J. Eur J Med Res Review BACKGROUND: Acute interstitial nephritis (AIN) is an important cause of kidney injury accounting for up to 27% of unexplained renal impairment. In up to 70% of cases, drugs, including aminosalicylates, are reported as the underlying cause. Following two recent paediatric cases of suspected mesalazine induced AIN within our own department, we performed a systematic review of the literature to address the following question: In patients with inflammatory bowel disease (IBD), is interstitial nephritis associated with 5-aminosalicylate (5-ASA) treatment? Our primary objective was to identify the number of cases reported in the literature of biopsy-proven 5-ASA induced interstitial nephritis, in children and adults with IBD. We also aimed to identify which variables influence the onset, severity and recovery of 5-ASA interstitial nephritis. METHODS: Embase and PubMed databases were searched from inception to 07/10/20. Search terms had three main themes: “inflammatory bowel disease”, “interstitial nephritis” and “aminosalicylates”. Studies were included if they reported an outcome of AIN, confirmed on biopsy, suspected to be secondary to a 5-ASA drug in those with IBD. A narrative synthesis was performed. RESULTS: Forty-one case reports were identified. Mesalazine was the most frequently reported aminosalicylate associated with AIN (95%). The median duration of treatment before AIN was diagnosed was 2.3 years (Interquartile Range (IQR) 12–48 months). The median rise in creatinine was 3.3 times the baseline measurement (IQR 2.5–5.5). Aminosalicylate withdrawal and steroids were the most frequently used treatments. Despite treatment, 15% of patients developed end-stage renal failure. CONCLUSIONS: AIN is a serious adverse drug reaction associated with aminosalicylates, with mesalazine accounting for most reports. The current guidance of annual monitoring of renal function may not be sufficient to identify cases early. Given the severity of AIN and reports in the literature that early treatment with steroids may be beneficial, we would recommend at least 6 monthly monitoring of renal function. PROSPERO registration number CRD42020205387. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40001-022-00687-y. BioMed Central 2022-04-29 /pmc/articles/PMC9052675/ /pubmed/35488310 http://dx.doi.org/10.1186/s40001-022-00687-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Moss, James G.
Parry, Christopher M.
Holt, Richard C. L.
McWilliam, Stephen J.
5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title_full 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title_fullStr 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title_full_unstemmed 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title_short 5-ASA induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
title_sort 5-asa induced interstitial nephritis in patients with inflammatory bowel disease: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052675/
https://www.ncbi.nlm.nih.gov/pubmed/35488310
http://dx.doi.org/10.1186/s40001-022-00687-y
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