Department of Food Technology, Safety, and Health, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Department of Translational Physiology, Infectiology and Public Health, Laboratory of Integrative Metabolomics, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Mycotoxin Res. 2024 Nov;40(4):681-691. doi: 10.1007/s12550-024-00558-x. Epub 2024 Sep 11.
To date, the changes in maternal metabolic response associated with prenatal aflatoxin exposure remain largely unknown. This study investigated the effects of prenatal aflatoxin exposure on the maternal serum metabolome in rural Ethiopia. A total of 309 pregnant women were enrolled prospectively, and their serum aflatoxin concentrations were measured using targeted liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Serum metabolic fingerprints were obtained using laser-assisted rapid evaporative ionization mass spectrometry (LA-REIMS), followed by combination of univariate and multivariate statistical modelling to evaluate changes in circulating metabolic features between aflatoxin-exposed and unexposed mothers and to select discriminatory metabolic features. The analysis revealed that 81.8% of women were exposed to aflatoxins, with a median concentration of 12.9 pg/mg albumin. The orthogonal partial least square discriminant analysis (OPLS-DA) regression model demonstrated significant disparities in the serum metabolome when comparing Ethiopian pregnant women with low vs high aflatoxin exposure. Thirty-two differentially expressed metabolic features were identified, affecting aminoacyl-tRNA biosynthesis pathway. Several discriminatory metabolites have been identified, including glutamine, tryptophan, tyrosine, carnosine, and 1-methylnicotinamide. In conclusion, our findings indicate that aflatoxin exposure during pregnancy have shown disparities in the maternal serum metabolome, primarily affecting protein synthesis. Further research is needed to identify specific metabolite biomarkers and elucidate the underlying mechanisms.
迄今为止,与产前黄曲霉毒素暴露相关的母体代谢反应变化在很大程度上仍不清楚。本研究调查了产前黄曲霉毒素暴露对埃塞俄比亚农村孕妇血清代谢组的影响。总共前瞻性地招募了 309 名孕妇,并使用靶向液相色谱-串联质谱(LC-MS/MS)测量了他们的血清黄曲霉毒素浓度。使用激光辅助快速蒸发电离质谱(LA-REIMS)获得血清代谢指纹图谱,然后结合单变量和多变量统计建模来评估暴露和未暴露于黄曲霉毒素的母亲之间循环代谢特征的变化,并选择有区别的代谢特征。分析表明,81.8%的女性接触过黄曲霉毒素,白蛋白中黄曲霉毒素的中位数浓度为 12.9 pg/mg。正交偏最小二乘判别分析(OPLS-DA)回归模型显示,在比较低暴露和高暴露的埃塞俄比亚孕妇的血清代谢组时存在显著差异。鉴定出 32 个差异表达的代谢特征,影响氨酰-tRNA 生物合成途径。已确定几种有区别的代谢物,包括谷氨酰胺、色氨酸、酪氨酸、肌肽和 1-甲基烟酰胺。总之,我们的研究结果表明,怀孕期间接触黄曲霉毒素会导致母体血清代谢组出现差异,主要影响蛋白质合成。需要进一步研究以确定特定的代谢物生物标志物并阐明潜在的机制。