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评估非单调剂量-反应关系的证据:食品安全领域体内毒性数据的系统文献综述和(重新)分析。

Evaluating the evidence for non-monotonic dose-response relationships: A systematic literature review and (re-)analysis of in vivo toxicity data in the area of food safety.

机构信息

ANSES, Risk Assessment Department, Maisons-Alfort, France.

Institute of Environmental Medicine (IMM), Karolinska Institutet, Sweden.

出版信息

Toxicol Appl Pharmacol. 2018 Jan 15;339:10-23. doi: 10.1016/j.taap.2017.11.018. Epub 2017 Nov 24.

Abstract

This study aims to evaluate the evidence for the existence of non-monotonic dose-responses (NMDRs) of substances in the area of food safety. This review was performed following the systematic review methodology with the aim to identify in vivo studies published between January 2002 and February 2015 containing evidence for potential NMDRs. Inclusion and reliability criteria were defined and used to select relevant and reliable studies. A set of six checkpoints was developed to establish the likelihood that the data retrieved contained evidence for NMDR. In this review, 49 in vivo studies were identified as relevant and reliable, of which 42 were used for dose-response analysis. These studies contained 179 in vivo dose-response datasets with at least five dose groups (and a control group) as fewer doses cannot provide evidence for NMDR. These datasets were extracted and analyzed using the PROAST software package. The resulting dose-response relationships were evaluated for possible evidence of NMDRs by applying the six checkpoints. In total, 10 out of the 179 in vivo datasets fulfilled all six checkpoints. While these datasets could be considered as providing evidence for NMDR, replicated studies would still be needed to check if the results can be reproduced to rule out that the non-monotonicity was caused by incidental anomalies in that specific study. This approach, combining a systematic review with a set of checkpoints, is new and appears useful for future evaluations of the dose response datasets regarding evidence of non-monotonicity.

摘要

本研究旨在评估食品安全领域物质的非单调剂量反应(NMDR)证据。本综述采用系统综述方法进行,目的是确定 2002 年 1 月至 2015 年 2 月期间发表的含有潜在 NMDR 证据的体内研究。定义了纳入和可靠性标准,并用于选择相关和可靠的研究。制定了一套六个检查点来确定检索到的数据是否包含 NMDR 的证据。在本综述中,确定了 49 项相关且可靠的体内研究,其中 42 项用于剂量反应分析。这些研究包含 179 个体内剂量反应数据集,至少有五个剂量组(和一个对照组),因为较少的剂量不能提供 NMDR 的证据。这些数据集使用 PROAST 软件包进行提取和分析。通过应用这六个检查点,评估了由此产生的剂量反应关系是否存在 NMDR 的可能证据。在总共 179 个体内数据集中,有 10 个满足了所有六个检查点。虽然这些数据集可以被认为提供了 NMDR 的证据,但仍需要进行重复研究,以检查结果是否可以重现,以排除非单调是由该特定研究中的偶然异常引起的。这种结合系统综述和一套检查点的方法是新的,似乎对未来评估剂量反应数据集关于非单调的证据有用。

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