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Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide

Within the European Joint Program on Human Biomonitoring HBM4EU, human biomonitoring guidance values (HBM-GVs) for the general population (HBM-GV(GenPop)) or for occupationally exposed adults (HBM-GV(Worker)) are derived for prioritized substances including dimethylformamide (DMF). The methodology t...

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Autores principales: Lamkarkach, Farida, Meslin, Matthieu, Kolossa-Gehring, Marike, Apel, Petra, Garnier, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230076/
https://www.ncbi.nlm.nih.gov/pubmed/35736906
http://dx.doi.org/10.3390/toxics10060298
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author Lamkarkach, Farida
Meslin, Matthieu
Kolossa-Gehring, Marike
Apel, Petra
Garnier, Robert
author_facet Lamkarkach, Farida
Meslin, Matthieu
Kolossa-Gehring, Marike
Apel, Petra
Garnier, Robert
author_sort Lamkarkach, Farida
collection PubMed
description Within the European Joint Program on Human Biomonitoring HBM4EU, human biomonitoring guidance values (HBM-GVs) for the general population (HBM-GV(GenPop)) or for occupationally exposed adults (HBM-GV(Worker)) are derived for prioritized substances including dimethylformamide (DMF). The methodology to derive these values that was agreed upon within the HBM4EU project was applied. A large database on DMF exposure from studies conducted at workplaces provided dose–response relationships between biomarker concentrations and health effects. The hepatotoxicity of DMF has been identified as having the most sensitive effect, with increased liver enzyme concentrations serving as biomarkers of the effect. Out of the available biomarkers of DMF exposure studied in this paper, the following were selected to derive HBM-GV(Worker): total N-methylformamide (tNMF) (sum of N-hydroxymethyl-N-methylformamide and NMF) and N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC) in urine. The proposed HBM-GV(Worker) is 10 mg·L(−1) or 10 mg·g(−1) creatinine for both biomarkers. Due to their different half-lives, tNMF (representative of the exposure of the day) and AMCC (representative of the preceding days’ exposure) are complementary for the biological monitoring of workers exposed to DMF. The levels of confidence for these HBM-GV(Worker) are set to “high” for tNMF and “medium-low” for AMCC. Therefore, further investigations are required for the consolidation of the health-based HBM-GV for AMCC in urine.
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spelling pubmed-92300762022-06-25 Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide Lamkarkach, Farida Meslin, Matthieu Kolossa-Gehring, Marike Apel, Petra Garnier, Robert Toxics Article Within the European Joint Program on Human Biomonitoring HBM4EU, human biomonitoring guidance values (HBM-GVs) for the general population (HBM-GV(GenPop)) or for occupationally exposed adults (HBM-GV(Worker)) are derived for prioritized substances including dimethylformamide (DMF). The methodology to derive these values that was agreed upon within the HBM4EU project was applied. A large database on DMF exposure from studies conducted at workplaces provided dose–response relationships between biomarker concentrations and health effects. The hepatotoxicity of DMF has been identified as having the most sensitive effect, with increased liver enzyme concentrations serving as biomarkers of the effect. Out of the available biomarkers of DMF exposure studied in this paper, the following were selected to derive HBM-GV(Worker): total N-methylformamide (tNMF) (sum of N-hydroxymethyl-N-methylformamide and NMF) and N-acetyl-S-(N-methylcarbamoyl)cysteine (AMCC) in urine. The proposed HBM-GV(Worker) is 10 mg·L(−1) or 10 mg·g(−1) creatinine for both biomarkers. Due to their different half-lives, tNMF (representative of the exposure of the day) and AMCC (representative of the preceding days’ exposure) are complementary for the biological monitoring of workers exposed to DMF. The levels of confidence for these HBM-GV(Worker) are set to “high” for tNMF and “medium-low” for AMCC. Therefore, further investigations are required for the consolidation of the health-based HBM-GV for AMCC in urine. MDPI 2022-05-31 /pmc/articles/PMC9230076/ /pubmed/35736906 http://dx.doi.org/10.3390/toxics10060298 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lamkarkach, Farida
Meslin, Matthieu
Kolossa-Gehring, Marike
Apel, Petra
Garnier, Robert
Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title_full Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title_fullStr Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title_full_unstemmed Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title_short Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
title_sort human biomonitoring initiative (hbm4eu): human biomonitoring guidance values derived for dimethylformamide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230076/
https://www.ncbi.nlm.nih.gov/pubmed/35736906
http://dx.doi.org/10.3390/toxics10060298
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