Abstract
Mycotoxins are fungal toxins that may trigger adverse health effects in pregnant women and their unborn children. Yet, data is scarce on the dynamic exposure patterns of mycotoxins in pregnant women, especially in the United States. This study assessed mycotoxin exposure profiles in women (n = 50) from the Yale Pregnancy Outcome Prediction Study (YPOPS) cohort at four distinct time points. Multi-analyte human biomonitoring assays based on liquid chromatography tandem mass spectrometry (LC-MS/MS), were developed for human serum and plasma matrices. The serum method was applied, together with an established urine method, to quantify mycotoxin levels in longitudinally collected matched serum (n = 200) and spot urine (n = 200) samples throughout pregnancy. The serum samples were mostly contaminated by the potential carcinogen ochratoxin A (detection rate: 46 %; median: 0.09 ng/mL), the hepato- and nephrotoxic citrinin (detection rate: 32 %; median: 0.02 ng/mL) and two enniatins (EnnB; detection rate: 97 %; median: 0.01 ng/mL and EnnB1; detection rate: 12 %; median: 0.003 ng/mL) which may act as immunotoxins. The most prevalent mycotoxins quantified in urine included deoxynivalenol (detection rate: 99 %; median: 23 ng/mL), alternariol monomethyl ether (detection rate: 69 %; median: 0.04 ng/mL), and zearalenone (detection rate: 63 %; median: 0.16 ng/mL). Seven other biomarkers of exposure including the highly estrogenic α-zearalenol and genotoxic Alternaria toxins, were also determined. Carcinogenic aflatoxins were not detected in any of the samples. Exposure assessment was based on the urinary data and performed by calculating probable daily intakes and comparing the human biomonitoring guidance value (HBM-GV) for deoxynivalenol. The results showed that the individuals exceeded the tolerable daily intake for deoxynivalenol and zearalenone on average at 28 % and 2 % over the different time points. Using the HBM-GV approach, the average exceedances for deoxynivalenol increased to 48 % indicating high exposure. For all the samples in which ochratoxin A was quantified, the estimated margin of exposure for neoplastic effects was below 10,000, indicating possible health concerns. Overall, this study showed that pregnant women were exposed to several regulated and emerging mycotoxins and that exposome-scale assessment should be a future priority in susceptible populations to better characterize xenobiotic exposure.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 109081 |
| Fachzeitschrift | Environment International |
| Jahrgang | 194 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - Dez. 2024 |
Fördermittel
We would like to thank all the women for participating and providing blood and urine samples. Prof. Doris Marko and Dr. Dominik Braun are acknowledged for critical feedback during the design and evaluation stages of the project. This research was supported by the FWF project P33188-B and the Yale University Reproductive Sciences Data and Specimen Biorepository, HIC#1309012696, a component of the Department of Obstetrics, Gynecology & Reproductive Sciences, Yale School of Medicine, New Haven, CT. We would like to acknowledge the Mass Spectrometry Centre of the Faculty of Chemistry at the University of Vienna and the Exposome Austria Research Infrastructure. The University of Vienna, the Austrian Federal Ministry of Education, Science and Research (project DigiOmics4AT), and the Austrian Federal Ministry for Climate Protection, Environment, Energy, Mobility, Innovation and Technology (BMK) are acknowledged for their support of the Exposome Austria Research Infrastructure. For the purpose of Open Access, the author has applied a CC BY public copyright license to any Author Accepted Manuscript (AAM) version arising from this submission. We would like to thank all the women for participating and providing blood and urine samples. Prof. Doris Marko and Dr. Dominik Braun are acknowledged for critical feedback during the design and evaluation stages of the project. This research was supported by the FWF project P33188-B and the Yale University Reproductive Sciences Data and Specimen Biorepository, HIC #1309012696 , a component of the Department of Obstetrics, Gynecology & Reproductive Sciences, Yale School of Medicine , New Haven, CT. We would like to acknowledge the Mass Spectrometry Centre of the Faculty of Chemistry at the University of Vienna and the Exposome Austria Research Infrastructure. The University of Vienna, the Austrian Federal Ministry of Education, Science and Research (project DigiOmics4AT), and the Austrian Federal Ministry for Climate Protection, Environment, Energy, Mobility, Innovation and Technology ( BMK ) are acknowledged for their support of the Exposome Austria Research Infrastructure. For the purpose of Open Access, the author has applied a CC BY public copyright license to any Author Accepted Manuscript ( AAM ) version arising from this submission.
ÖFOS 2012
- 104023 Umweltchemie
- 106027 Ökotoxikologie