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A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model
Mycotoxins, such as ochratoxin A (OTA), can occur from fungal growth on foods. OTA is considered a possible risk factor for adverse renal effects in humans based on renal tumors in male rats. For risk mitigation. Health Canada proposed maximum limits (MLs) for OTA based largely on a comparative risk...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Informa Healthcare
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310481/ https://www.ncbi.nlm.nih.gov/pubmed/22276591 http://dx.doi.org/10.3109/10408444.2011.636342 |
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author | Haighton, Lois A Lynch, Barry S Magnuson, Bernadene A Nestmann, Earle R |
author_facet | Haighton, Lois A Lynch, Barry S Magnuson, Bernadene A Nestmann, Earle R |
author_sort | Haighton, Lois A |
collection | PubMed |
description | Mycotoxins, such as ochratoxin A (OTA), can occur from fungal growth on foods. OTA is considered a possible risk factor for adverse renal effects in humans based on renal tumors in male rats. For risk mitigation. Health Canada proposed maximum limits (MLs) for OTA based largely on a comparative risk assessment conducted by Health Canada (Kuiper-Goodman et al., 2010), in which analytical data of OTA in foods were used to determine the possible impact adopting MLs may have on OTA risks. The EU MLs were used for comparison and resultant risk was determined based on age–sex strata groups. These data were reevaluated here to determine comparative risk on a lifetime basis instead of age strata. Also, as there is scientific disagreement over the mechanism of OTA-induced renal tumors, mechanistic data were revisited. On a lifetime basis, risks associated with dietary exposure were found to be negligible, even without MLs, with dietary exposures to OTA three to four orders of magnitude below the pivotal animal LOAEL and the TD(05). Our review of the mechanistic data supported a threshold-based mechanism as the most plausible. In particular, OTA was negative in genotoxicity assays with the highest specificity and levels of DNA adducts were very low and not typical of genotoxic carcinogens. In conclusion, OTA exposures from Canadian foods do not present a significant cancer risk. |
format | Online Article Text |
id | pubmed-3310481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Informa Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-33104812012-04-03 A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model Haighton, Lois A Lynch, Barry S Magnuson, Bernadene A Nestmann, Earle R Crit Rev Toxicol Review Article Mycotoxins, such as ochratoxin A (OTA), can occur from fungal growth on foods. OTA is considered a possible risk factor for adverse renal effects in humans based on renal tumors in male rats. For risk mitigation. Health Canada proposed maximum limits (MLs) for OTA based largely on a comparative risk assessment conducted by Health Canada (Kuiper-Goodman et al., 2010), in which analytical data of OTA in foods were used to determine the possible impact adopting MLs may have on OTA risks. The EU MLs were used for comparison and resultant risk was determined based on age–sex strata groups. These data were reevaluated here to determine comparative risk on a lifetime basis instead of age strata. Also, as there is scientific disagreement over the mechanism of OTA-induced renal tumors, mechanistic data were revisited. On a lifetime basis, risks associated with dietary exposure were found to be negligible, even without MLs, with dietary exposures to OTA three to four orders of magnitude below the pivotal animal LOAEL and the TD(05). Our review of the mechanistic data supported a threshold-based mechanism as the most plausible. In particular, OTA was negative in genotoxicity assays with the highest specificity and levels of DNA adducts were very low and not typical of genotoxic carcinogens. In conclusion, OTA exposures from Canadian foods do not present a significant cancer risk. Informa Healthcare 2012-02 2012-01-25 /pmc/articles/PMC3310481/ /pubmed/22276591 http://dx.doi.org/10.3109/10408444.2011.636342 Text en © 2012 by Informa Healthcare USA, Inc http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Haighton, Lois A Lynch, Barry S Magnuson, Bernadene A Nestmann, Earle R A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title | A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title_full | A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title_fullStr | A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title_full_unstemmed | A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title_short | A reassessment of risk associated with dietary intake of ochratoxin A based on a lifetime exposure model |
title_sort | reassessment of risk associated with dietary intake of ochratoxin a based on a lifetime exposure model |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3310481/ https://www.ncbi.nlm.nih.gov/pubmed/22276591 http://dx.doi.org/10.3109/10408444.2011.636342 |
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