Laboratory of Toxicology, Department of Environmental Veterinary Sciences, Faculty of Veterinary Medicine, Hokkaido University, Kita 18 Nishi 9, Kita-Ku, Sapporo, 060-0818, Japan.
Department of Chemistry, College of Natural and Computational Science, University of Gondar, P.O. Box 196, Gondar, Ethiopia.
Environ Sci Pollut Res Int. 2022 Jan;29(5):6622-6632. doi: 10.1007/s11356-021-16098-1. Epub 2021 Aug 28.
Interindividual genetic variations determine human's susceptibility to heavy metal-induced toxicity. Thus, we analyzed blood concentrations of lead (Pb) and cadmium (Cd) in 140 lead-exposed children. Genotyping of the glutathione S-transferase (GST) genes, GSTM1, GSTT1, and GSTP1 genes, was carried out to investigate their possible association with heavy metal concentrations and the risk of susceptibility to Pb toxicity. Exposure to both heavy metals was prevalent among the children. The blood Pb level ranged from 3.30 to 74.0 μg dL with an average value of 26.8 μg dL that is five times above its reference level. The average Cd level (0.22 μg L) was below its reference level. The metal-gene interaction showed positive correlation between GSTT1 null genotype and Pb and Cd levels (β = 0.11; p = 0.02 and β = 0.10; p = 0.01, respectively). More pronounced effects (β = 0.19; p < 0.01 and β = 0.25; p = 0.04) were found for the mixture of the three putative genes with blood Pb concentration. The susceptibility analysis using 10 μg dL as blood Pb cutoff level showed a high risk of Pb toxicity (OR = 2.54; 95% CI: 1.02-6.32, p = 0.04) for children carrying the GSTP1 Ile/Val genotype. Further, the combined effect of GSTP1 Ile/Val with GSTT1 null genotype was more pronounced and showed an increased risk of susceptibility to Pb toxicity (OR = 11.7; 95% CI: 1.36-102.1, p = 0.02). In summary, this study suggests that GSTT1 null and GSTP1 Ile/Val genotypes are the main genetic factors, and individual and specific combinations of GSTP1 Ile/Val with GSTM1 and GSTT1 GST polymorphisms are associated with susceptibility to Pb toxicity.
个体遗传变异决定了人类对重金属诱导毒性的易感性。因此,我们分析了 140 名铅暴露儿童的血液铅(Pb)和镉(Cd)浓度。进行谷胱甘肽 S-转移酶(GST)基因,GSTM1、GSTT1 和 GSTP1 基因的基因分型,以研究它们与重金属浓度和易感性铅毒性的风险之间的可能关联。儿童普遍存在两种重金属暴露。血铅水平范围为 3.30 至 74.0μg/dL,平均为 26.8μg/dL,是参考水平的五倍。平均 Cd 水平(0.22μg/L)低于参考水平。金属-基因相互作用显示 GSTT1 缺失基因型与 Pb 和 Cd 水平呈正相关(β=0.11;p=0.02 和 β=0.10;p=0.01)。对于与血 Pb 浓度混合的三个假定基因,发现更明显的影响(β=0.19;p<0.01 和 β=0.25;p=0.04)。使用 10μg/dL 作为血 Pb 截断值进行易感性分析显示,携带 GSTP1 Ile/Val 基因型的儿童患 Pb 毒性的风险很高(OR=2.54;95%CI:1.02-6.32,p=0.04)。此外,GSTP1 Ile/Val 与 GSTT1 缺失基因型的联合作用更为明显,并且显示出对 Pb 毒性易感性增加的风险(OR=11.7;95%CI:1.36-102.1,p=0.02)。总之,这项研究表明,GSTT1 缺失和 GSTP1 Ile/Val 基因型是主要的遗传因素,GSTP1 Ile/Val 与 GSTM1 和 GSTT1 GST 多态性的个体和特定组合与对 Pb 毒性的易感性有关。