Scientific Basis of Tolerable Daily Intake Derivation in Japan: Analysis of Study Types, Uncertainty Factors, and Critical Effect Levels in FSCJ Risk Assessment Reports.

Food safety (Tokyo, Japan) Pub Date : 2026-06-26 eCollection Date: 2026-06-01 DOI:10.14252/foodsafetyfscj.D-26-00004
Satoko Iwasawa, Kento Hoshino, Tomohiro Ohno, Itsumi Hashimoto, Yuka Miyoshi, Takahiro Sakamoto, Kenta Ito, Satoko Suzuki, Noriyuki Yoshioka, Masashi Tsunoda
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Abstract

This study aimed to clarify the scientific basis for deriving Tolerable Daily Intake (TDI) values in risk assessments conducted by the Food Safety Commission of Japan (FSCJ), with a particular focus on the types of studies used, uncertainty factors (UFs), and critical effect levels (No-Observed-Adverse-Effect Levels and Lowest-Observed-Adverse-Effect Levels). We reviewed 77 chemical risk assessment reports published by the FSCJ as of October 2022. Using a standardized data extraction template developed with reference to the ATSDR and IRIS formats, ten trained reviewers examined and coded relevant toxicological information. In total, 46 reports were included in the final analysis. Most TDI values (73.9%) were derived from animal studies and were typically accompanied by large UFs ranging from 100 to 1000. Human-based TDIs derived from human observational (15.2%) and human intervention (10.9%) studies accounted for a smaller proportion but were generally associated with higher TDI values and smaller UFs. The examination of the NOAEL and LOAEL distributions indicated that lower exposure thresholds were primarily based on human study, whereas higher thresholds predominantly relied on animal studies. The derivation of TDI in Japan relies predominantly on animal study. Enhancing the availability of high-quality human data and improving consistency in the application of UFs may strengthen the transparency and scientific validity of health-based guidance in the future.

日本每日可耐受摄入量来源的科学依据:FSCJ风险评估报告中的研究类型、不确定性因素和临界影响水平分析。
本研究旨在阐明日本食品安全委员会(FSCJ)进行的风险评估中得出每日可耐受摄入量(TDI)值的科学依据,特别关注所使用的研究类型、不确定性因素(UFs)和关键影响水平(无观察到的不良影响水平和最低观察到的不良影响水平)。我们回顾了截至2022年10月FSCJ发布的77份化学品风险评估报告。使用参照ATSDR和IRIS格式开发的标准化数据提取模板,10名训练有素的审查员检查并编码了相关毒理学信息。最后分析共包括46份报告。大多数TDI值(73.9%)来自动物研究,通常伴有100至1000的大UFs。来自人类观察研究(15.2%)和人类干预研究(10.9%)的基于人类的TDI所占比例较小,但通常与较高的TDI值和较小的UFs相关。对NOAEL和LOAEL分布的检查表明,较低的暴露阈值主要基于人类研究,而较高的阈值主要依赖于动物研究。在日本,TDI的推导主要依赖于动物研究。提高高质量人体数据的可得性和改进综合指标应用的一致性,可在未来加强基于健康的指导的透明度和科学有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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