Serum protein α-klotho mediates the association between lead, mercury, and kidney function in middle-aged and elderly populations.
- Author:
Lin JIANG
1
;
Tingting GUO
2
;
Xin ZHONG
3
;
Yini CAI
2
;
Wanyu YANG
2
;
Jun ZHANG
2
Author Information
- Publication Type:Journal Article
- Keywords: Estimated glomerular filtration; Kidney function; Lead; Mediation; Mercury; α-Klotho
- MeSH: Humans; Middle Aged; Lead/blood*; Female; Klotho Proteins; Male; Aged; Adult; Mercury/blood*; Glomerular Filtration Rate; Nutrition Surveys; United States; Kidney/physiology*; Glucuronidase/blood*; Environmental Pollutants/blood*
- From:Environmental Health and Preventive Medicine 2025;30():10-10
- CountryJapan
- Language:English
-
Abstract:
BACKGROUND:Heavy metals are significant risk factors for kidney function. Numerous studies have shown that exposure to heavy metals negatively correlates with kidney function through oxidative stress pathways, and serum α-klotho is linked to oxidative stress. However, the role of α-klotho in the relationship between blood lead, mercury, and kidney function remains unclear.
METHOD:This study evaluated the mediating role of alpha-klotho in the relationship between lead, mercury and renal function, using data from the 2007-2016 National Health and Nutrition Examination Survey (NHANES) in U.S. adults aged 40-79. The sample included 11,032 participants, with blood lead, mercury, α-klotho, and other relevant covariates measured. Inductively coupled plasma mass spectrometry was used to assess blood lead and mercury levels, and enzyme-linked immunosorbent assay (ELISA) was employed to measure serum α-klotho. Kidney function was evaluated using estimated glomerular filtration rate (eGFR) based on creatinine levels. Multivariable linear regression was conducted to analyze the relationships between blood lead, mercury, α-klotho, and eGFR. A mediation analysis model was used to assess whether α-klotho influenced these associations.
RESULTS:We observed a significant association between blood lead and eGFR. Mediation analysis revealed that α-klotho accounted for 12.76% of the relationship between serum lead and eGFR in the NHANES population. Subgroup analysis showed that α-klotho mediated 12.43%, 6.87%, 21.50% and 5.44% of the relationship between blood lead and eGFR in women, middle-aged adults (40-59 years old), without cardiovascular disease and hypertension, respectively. However, α-klotho did not mediate the relationship between blood mercury and eGFR in terms of gender or age. This newly identified pathway may provide valuable insights for the prevention and treatment mechanisms related to kidney function impairment.
CONCLUSION:We found that blood lead was associated with renal function. According to the results of subgroup analysis, for blood lead, serum α-klotho mediated the association in females, middle aged 60-79 years. The relationship between blood mercury and renal function was not clinically significant, and serum α-Klotho mediated the relationship between blood mercury and renal function without significant clinical significance.
