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全国在线调查使基于不良反应频率对提取物摄入的安全性进行重新评估成为可能。

Nationwide Online Survey Enables the Reevaluation of the Safety of Extract Intake Based on the Adverse Event Frequencies.

机构信息

Department of Food Function and Labeling, National Institute of Health and Nutrition, National Institutes of Biomedical Innovation, Health and Nutrition, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8636, Japan.

Department of Food Safety and Management, Showa Women's University, 1-7-57 Taishido, Setagaya-ku, Tokyo 154-8533, Japan.

出版信息

Nutrients. 2019 Apr 17;11(4):866. doi: 10.3390/nu11040866.

Abstract

The formulations of the functional ingredients of dietary supplements was studied with a small number of subjects, with a particular focus on their effectiveness, but not enough to evaluate their safety. In this regard, the reevaluation and estimation of the safe use of marketed products, with regards to their adverse event (AE) frequencies, are important. To address this issue, a post-marketing nationwide online survey was conducted for the herbal ingredient extract (CFE), a popular weight-loss ingredient. The questionnaire included product names, adherence to the claimed amount, and AE experiences. The safe intake amount was estimated by the relationship between the claimed amount of CFE and the frequencies of AEs of each product. The number of users who experienced AEs was 75 (10.5% of all users). Gastrointestinal symptoms accounted for 92.0% ( = 69) of all AEs, and diarrhea alone accounted for 81.3% ( = 61). The amount of CFE was significantly associated with the occurrence of diarrhea ( = 0.005). The fitted curve showed that the safe intake amount of CFE was less than 250 mg/day; however, considering its effectiveness, 500 mg/day of CFE might be acceptable. In conclusion, nationwide online surveys of users enable us to confirm and reevaluate the safety of herbal supplements.

摘要

对膳食补充剂的功能性成分进行了配方研究,研究对象数量较少,主要关注其有效性,但不足以评估其安全性。在这方面,重新评估和估计市售产品的安全使用非常重要,要考虑其不良反应 (AE) 的频率。为了解决这个问题,对一种流行的减肥成分草药成分提取物 (CFE) 进行了全国范围的在线上市后调查。问卷包括产品名称、对声称量的遵守情况以及 AE 经历。通过每个产品的 CFE 声称量与 AE 频率之间的关系来估计安全摄入量。经历不良反应的用户数量为 75 人(所有用户的 10.5%)。胃肠道症状占所有不良反应的 92.0%(=69),单独腹泻占 81.3%(=61)。CFE 量与腹泻的发生显著相关(=0.005)。拟合曲线表明,CFE 的安全摄入量小于 250mg/天;然而,考虑到其有效性,每天 500mg 的 CFE 可能是可以接受的。总之,对用户进行全国范围的在线调查使我们能够确认和重新评估草药补充剂的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55fd/6521622/4682bb6418bc/nutrients-11-00866-g001.jpg

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