Department of Public, College of Health Sciences, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Departments of Occupational Medicine and Family Medicine, Kaohsiung Municipal Siaogang Hospital, and Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Genes (Basel). 2021 Oct 2;12(10):1573. doi: 10.3390/genes12101573.
The results of many studies indicate that cadmium (Cd) exposure is harmful to humans, with the proximal tubule of the kidney being the main target of Cd accumulation and toxicity. Studies have also shown that Cd has the effect of activating the pathway of epidermal growth factor receptor (EGFR) signaling and cell growth. The EGFR is a family of transmembrane receptors, which are widely expressed in the human kidney. The aim of this study was to investigate the kidney function estimated glomerular filtration rate (eGFR), and its relationship with plasma Cd level and EGFR gene polymorphism. Using data from Academia Sinica Taiwan biobank, 489 subjects aged 30-70 years were analyzed. The demographic characteristics was determined from questionnaires, and biological sampling of urine and blood was determined from physical examination. Kidney function was assessed by the eGFR with CKD-EPI formula. Plasma Cd (ug/L) was measured by inductively coupled plasma mass spectrometry. A total of 97 single-nucleotide polymorphisms (SNPs) were identified in the EGFR on the Taiwan biobank chip, however 4 SNPs did not pass the quality control. Multiple regression analyses were performed to achieve the study aim. The mean (±SD) plasma Cd level of the study subjects was 0.02 (±0.008) ug/L. After adjusting for confounding variables, rs13244925 AA, rs6948867 AA, rs35891645 TT and rs6593214 AA types had higher eGFR (4.89 mL/min/1.73 m ( = 0.035), 5.54 mL/min/1.73 m ( = 0.03), 4.96 mL/min/1.73 m ( = 0.048) and 5.16 mL/min/1.73 m ( = 0.048), respectively). Plasma cadmium and rs845555 had an interactive effect on eGFR. In conclusion, EGFR polymorphisms could be modifiers of Cd kidney toxicity, in which rs13244925 AA, rs6948867 AA, rs35891645 TT and rs6593214 AA may be protective, and Cd interacting with rs845555 may affect kidney function.
许多研究的结果表明,镉(Cd)暴露对人类有害,肾脏的近曲小管是 Cd 蓄积和毒性的主要靶标。研究还表明,Cd 具有激活表皮生长因子受体(EGFR)信号通路和细胞生长的作用。EGFR 是一种跨膜受体家族,在人类肾脏中广泛表达。本研究旨在探讨估算肾小球滤过率(eGFR)与血浆 Cd 水平和 EGFR 基因多态性的关系。利用台湾生物银行的人群数据,对 489 名年龄在 30-70 岁之间的个体进行分析。通过问卷调查确定了人口统计学特征,通过体检确定了尿液和血液的生物采样。用 CKD-EPI 公式评估肾功能的 eGFR。用等离子体质谱法(ICP-MS)测量血浆 Cd(μg/L)。在台湾生物银行芯片上共鉴定出 EGFR 上的 97 个单核苷酸多态性(SNP),但 4 个 SNP 未通过质量控制。采用多元回归分析实现研究目的。研究对象的平均(±SD)血浆 Cd 水平为 0.02(±0.008)μg/L。在调整混杂变量后,rs13244925AA、rs6948867AA、rs35891645TT 和 rs6593214AA 基因型的 eGFR 较高(4.89mL/min/1.73m,=0.035)、5.54mL/min/1.73m(=0.03)、4.96mL/min/1.73m(=0.048)和 5.16mL/min/1.73m(=0.048)。血浆 Cd 和 rs845555 对 eGFR 有交互作用。结论:EGFR 多态性可能是 Cd 肾毒性的修饰因子,其中 rs13244925AA、rs6948867AA、rs35891645TT 和 rs6593214AA 可能具有保护作用,而 Cd 与 rs845555 相互作用可能影响肾功能。