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<sub>GenPop</sub>) or for occupationally exposed adults (HBM-GV<sub>Worker</sub>) are derived for prioritized substances including...

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Main Authors: Farida Lamkarkach, Matthieu Meslin, Marike Kolossa-Gehring, Petra Apel, Robert Garnier
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:Toxics
Subjects:
Online Access:https://www.mdpi.com/2305-6304/10/6/298
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author Farida Lamkarkach
Matthieu Meslin
Marike Kolossa-Gehring
Petra Apel
Robert Garnier
author_facet Farida Lamkarkach
Matthieu Meslin
Marike Kolossa-Gehring
Petra Apel
Robert Garnier
author_sort Farida Lamkarkach
collection DOAJ
description Within the European Joint Program on Human Biomonitoring HBM4EU, human biomonitoring guidance values (HBM-GVs) for the general population (HBM-GV<sub>GenPop</sub>) or for occupationally exposed adults (HBM-GV<sub>Worker</sub>) 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<sub>Worker</sub>: 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<sub>Worker</sub> is 10 mg·L<sup>−1</sup> or 10 mg·g<sup>−1</sup> 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<sub>Worker</sub> 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 doaj.art-6889571ea9984db7a9676643a952f4612023-11-23T19:15:55ZengMDPI AGToxics2305-63042022-05-0110629810.3390/toxics10060298Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for DimethylformamideFarida Lamkarkach0Matthieu Meslin1Marike Kolossa-Gehring2Petra Apel3Robert Garnier4ANSES 14 Rue Pierre et Marie Curie, 94701 Maisons-Alfort, FranceANSES 14 Rue Pierre et Marie Curie, 94701 Maisons-Alfort, FranceGerman Environment Agency (UBA), Corrensplatz 1, 14195 Berlin, GermanyGerman Environment Agency (UBA), Corrensplatz 1, 14195 Berlin, GermanyParis Poison Centre, Toxicology Department (FeTox), APHP, Lariboisière-Fernand-Widal Hospital, 200 Rue du Faubourg Saint-Denis, 75010 Paris, FranceWithin the European Joint Program on Human Biomonitoring HBM4EU, human biomonitoring guidance values (HBM-GVs) for the general population (HBM-GV<sub>GenPop</sub>) or for occupationally exposed adults (HBM-GV<sub>Worker</sub>) 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<sub>Worker</sub>: 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<sub>Worker</sub> is 10 mg·L<sup>−1</sup> or 10 mg·g<sup>−1</sup> 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<sub>Worker</sub> 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.https://www.mdpi.com/2305-6304/10/6/298HBM4EUdimethylformamideDMFHBM-GVguidance valuebiomarker
spellingShingle Farida Lamkarkach
Matthieu Meslin
Marike Kolossa-Gehring
Petra Apel
Robert Garnier
Human Biomonitoring Initiative (HBM4EU): Human Biomonitoring Guidance Values Derived for Dimethylformamide
Toxics
HBM4EU
dimethylformamide
DMF
HBM-GV
guidance value
biomarker
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 HBM4EU
dimethylformamide
DMF
HBM-GV
guidance value
biomarker
url https://www.mdpi.com/2305-6304/10/6/298
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