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炎症性肠病患者食用食物污染物和药物的不良反应风险升高:综述

Elevated risk of adverse effects from foodborne contaminants and drugs in inflammatory bowel disease: a review.

机构信息

Division of Toxicology, Wageningen University and Research, Wageningen, The Netherlands.

Department of Metabolic Health Research, Netherlands Organization for Applied Scientific Research (TNO), Leiden, The Netherlands.

出版信息

Arch Toxicol. 2024 Nov;98(11):3519-3541. doi: 10.1007/s00204-024-03844-w. Epub 2024 Sep 9.

DOI:10.1007/s00204-024-03844-w
PMID:39249550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11489187/
Abstract

The global burden of Inflammatory bowel disease (IBD) has been rising over the last decades. IBD is an intestinal disorder with a complex and largely unknown etiology. The disease is characterized by a chronically inflamed gastrointestinal tract, with intermittent phases of exacerbation and remission. This compromised intestinal barrier can contribute to, enhance, or even enable the toxicity of drugs, food-borne chemicals and particulate matter. This review discusses whether the rising prevalence of IBD in our society warrants the consideration of IBD patients as a specific population group in toxicological safety assessment. Various in vivo, ex vivo and in vitro models are discussed that can simulate hallmarks of IBD and may be used to study the effects of prevalent intestinal inflammation on the hazards of these various toxicants. In conclusion, risk assessments based on healthy individuals may not sufficiently cover IBD patient safety and it is suggested to consider this susceptible subgroup of the population in future toxicological assessments.

摘要

过去几十年,炎症性肠病(IBD)的全球负担一直在增加。IBD 是一种肠道疾病,病因复杂,很大程度上尚不明确。该疾病的特征为慢性肠道炎症,伴有间歇性加重和缓解。这种受损的肠道屏障可能会促进、加重甚至使药物、食物来源的化学物质和颗粒物质的毒性作用增强。本综述讨论了我们社会中 IBD 的患病率不断上升是否表明需要将 IBD 患者视为毒理学安全性评估中的一个特定人群。讨论了各种体内、体外和离体模型,这些模型可以模拟 IBD 的特征,并可用于研究常见肠道炎症对这些各种毒物危害的影响。总之,基于健康个体的风险评估可能无法充分涵盖 IBD 患者的安全性,因此建议在未来的毒理学评估中考虑这一易患人群亚组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/06b0b7e6a80e/204_2024_3844_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/e683c06b48d4/204_2024_3844_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/ab6fda8b6f67/204_2024_3844_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/d49c945adf12/204_2024_3844_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/06b0b7e6a80e/204_2024_3844_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/e683c06b48d4/204_2024_3844_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/ab6fda8b6f67/204_2024_3844_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/d49c945adf12/204_2024_3844_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e71/11489187/06b0b7e6a80e/204_2024_3844_Fig4_HTML.jpg

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本文引用的文献

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