2016
DOI: 10.2903/sp.efsa.2016.en-1027
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Review of non‐monotonic dose‐responses of substances for human risk assessment

Abstract: In this project, the evidence for the non-monotonic dose-response (NMDR) hypothesis was evaluated by critically reviewing the scientific peer-reviewed literature in the last decade (from 2002 onwards) for substances in the area of food safety. The project was performed according to the systematic review methodology. After a detailed analysis of previous reports published on the issue of NMDRs, a literature search was performed to identify in vivo, in vitro and epidemiological/human studies containing eviden… Show more

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Cited by 25 publications
(67 citation statements)
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“…In these published in vivo rodent studies on Dibutyl phthalate, the test concentration range for different endpoints is 0.01-1000 mg/kg/day across compiled studies in DEDuCT 2.0, the lowest dose at which an adverse effect is observed in any of these studies is 0.01 mg/kg/day, and the highest dose at which no adverse effects are observed in any of the studies is 125 mg/kg/day ( Supplementary Table S4). We remark that the compiled dosage information for Dibutyl phthalate in DEDuCT 2.0 is compatible with previous reports suggesting possible non-monotonic dose response for this chemical (Beausoleil et al, 2016).…”
Section: A Case Study Of Deduct 20 In Risk Assessment Of Edcssupporting
confidence: 90%
“…In these published in vivo rodent studies on Dibutyl phthalate, the test concentration range for different endpoints is 0.01-1000 mg/kg/day across compiled studies in DEDuCT 2.0, the lowest dose at which an adverse effect is observed in any of these studies is 0.01 mg/kg/day, and the highest dose at which no adverse effects are observed in any of the studies is 125 mg/kg/day ( Supplementary Table S4). We remark that the compiled dosage information for Dibutyl phthalate in DEDuCT 2.0 is compatible with previous reports suggesting possible non-monotonic dose response for this chemical (Beausoleil et al, 2016).…”
Section: A Case Study Of Deduct 20 In Risk Assessment Of Edcssupporting
confidence: 90%
“…Chemicals with non-monotonic dose responses not only have increasing effects with increasing dose but may also have effects in the low-dose range [15,19]. A study commissioned by the European Food Safety Authority concluded that non-monotonic dose responses for several food-related chemicals (such as FCCs) could neither be confirmed nor rejected, and further investigation has been recommended [118]. Guidance for addressing this difficulty in chemical risk assessment has been published [119].…”
Section: Using Generic Thresholds For the Safety Assessment Of Fccs Imentioning
confidence: 99%
“…Finally, neurotoxicological studies on EDCs have brought to the attention of scientists and regulators three important issues that are usually underestimated and, in general, not properly addressed in other contexts: (i) the impact of low doses, (ii) long-term effects, and (iii) interactions occurring because of mixtures of compounds. It was observed, indeed, that EDC doses similar to environmental levels can have significant effects in experimental models, showing peculiar dose-response patterns that are not monotonic [119], even if this phenomenon has yet to be validated in other settings [120]. Moreover, EDCs can cause effects that only manifest much later in life than the period of exposure [121], most likely because of epigenetic mechanisms of information transmission: the exposure to the chemical could result in epigenetic modifications of the genome that can be inherited by future generations [122].…”
Section: Endocrine Disruptorsmentioning
confidence: 99%