Report of an expert panel on the reanalysis by Seralini et al. (2007) of a 90-day study conducted by Monsanto in support of the safety of a genetically modified corn variety (MON 863)

被引:28
作者
Doull, J.
Gaylor, D.
Greim, H. A.
Lovell, D. P.
Lynch, B.
Munro, I. C.
机构
[1] Cantox Hlth Sci Inc, Mississauga, ON L5N 2X7, Canada
[2] Univ Kansas, Med Ctr, Dept Pharmacol, Div Toxicol, Kansas City, KS 66160 USA
[3] Gaylor & Assoc LLC, Eureka Springs, AR 72631 USA
[4] Tech Univ Munich, Inst Toxicol & Environm Hyg, D-85354 Freising Weihenstephan, Germany
[5] Univ Surrey, Postgrad Med Sch, Guildford GU2 7WG, Surrey, England
关键词
MON; 863; genetically modified organism; rat; subchronic toxicity; statistical analysis; European food safety authority (EFSA); liver kidney;
D O I
10.1016/j.fct.2007.08.033
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
MON 863, a genetically engineered corn variety that contains the gene for modified Bacillus thuringiensis Cry3Bb1 protein to protect against corn rootworm, was tested in a 90-day toxicity study as part of the process to gain regulatory approval. This study was reanalyzed by Seralini et al. who contended that the study showed possible hepatorenal effects of MON 863. An Expert Panel was convened to assess the original study results as analyzed by the Monsanto Company and the reanalysis conducted by Seralini et al. The Expert Panel concludes that the Seralini et al. reanalysis provided no evidence to indicate that MON 863 was associated with adverse effects in the 90-day rat study. In each case, statistical findings reported by both Monsanto and Seralini et al. were considered to be unrelated to treatment or of no biological or clinical importance because they failed to demonstrate a dose-response relationship, reproducibility over time, association with other relevant changes (e.g., histopathology), occurrence in both sexes, difference outside the normal range of variation, or biological plausibility with respect to cause-and-effect. The Seralini et al. reanalysis does not advance any new scientific data to indicate that MON 863 caused adverse effects in the 90-day rat study. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2073 / 2085
页数:13
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