Abstract
Exposure to metals may be associated with renal function impairment, but the effect modified by genetic polymorphisms was not considered in most studies. Epidermal growth factor receptor (EGFR) and tumor necrotic factor-α (TNF-α) play important roles in renal hemodynamics, and they have been reported to be associated with some renal diseases. The aim of our research is to explore whether genetic variations in EGFR and TNF-α have influence on renal function under exposure to various metals. This cross-sectional study consisted of 376 metal industrial workers, 396 participants of Taiwan Biobank, and 231 volunteers of health examinations. We identified 23 single nucleotide polymorphisms (SNPs) on the EGFR gene and 6 SNPs on the TNF-α gene, and we also measured their plasma concentration of cobalt, copper, zinc, selenium, arsenic, and lead. Multiple regression analysis was applied to investigate the association between various SNPs, metals, and renal function. Our results revealed some protective and susceptible genotypes under occupational or environmental exposure to metals. The individuals carrying EGFR rs2280653 GG might have declined renal function under excessive exposure to selenium, and those with EGFR rs3823585 CC, rs12671550 CC, and rs4947986 GG genotypes might be susceptible to lead nephrotoxicity. We suggest the high-risk population to prevent renal diseases.
Highlights
No significant difference was found in gender, age, uric acid, and estimated glomerular filtration rate (eGFR) between the two groups
We investigated the associations between Epidermal growth factor receptor (EGFR) and tumor necrotic factor-α (TNF-α) gene polymorphisms, plasma metal concentrations, and renal function
Our study showed that EGFR rs845561 and rs2075108 were associated with renal function
Summary
The aim of our research is to explore whether genetic variations in EGFR and TNF-α have influence on renal function under exposure to various metals.
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More From: International Journal of Environmental Research and Public Health
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