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Cadmium exposure associated with altered liver function biomarkers in middle-aged and older adultsHeavy Metal Exposure Linked to Liver Changes in Older Adults

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Key Takeaway
Note associations between blood cadmium and liver biomarkers in a cross-sectional cohort; causality not established.

This cross-sectional study evaluated 451 participants from the general middle-aged and older adults population in the Dongdagou Xinglong cohort in Northwest China. The primary exposure was co-exposure to multiple heavy metals, specifically cadmium and others. Liver function biomarkers served as the primary outcomes.

The analysis revealed that gamma-glutamyl transferase (GGT) was positively correlated with blood cadmium (β = 0.236, P < 0.05). Total bile acids (TBA) showed a positive correlation (β = 0.162, P < 0.05), as did alanine aminotransferase (ALT) (β = 0.142, P < 0.05) and aspartate aminotransferase (AST) (β = 0.114, P < 0.05). Conversely, direct bilirubin (DBil) was negatively correlated (β = −0.207, P < 0.05), along with total bilirubin (TBil) (β = −0.166, P < 0.05) and indirect bilirubin (IBil) (β = −0.157, P < 0.05).

Animal model findings indicated that cadmium exposure led to elevated serum GGT and ALP levels and induced histopathological alterations in the liver. No adverse events, serious adverse events, discontinuations, or tolerability data were reported. The study notes that evidence regarding the hepatotoxic effects of co-exposure to multiple heavy metals in this population remains limited.

A new study from Northwest China looked at 451 middle-aged and older adults to see if heavy metals in the blood are linked to liver health. Researchers measured levels of several heavy metals, including cadmium, and checked liver function through blood tests.

The study found that higher blood cadmium levels were linked to higher levels of certain liver enzymes (GGT, TBA, ALT, AST) and lower levels of bilirubin. When looking at the combined effect of multiple heavy metals, the pattern was similar. In animal tests, cadmium exposure caused liver damage and raised enzyme levels.

This is a cross-sectional study, meaning it shows a link but cannot prove that heavy metals caused the liver changes. The study was also relatively small and only looked at one region in China. More research is needed to confirm these findings and understand the long-term effects.

For now, the results suggest that exposure to heavy metals like cadmium may affect liver function in older adults. However, this is early evidence and should not cause alarm. If you are concerned about heavy metal exposure, talk to your doctor.

What this means for you:
Heavy metals in blood are linked to liver enzyme changes, but more research is needed.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedApr 2026
View Original Abstract ↓
BackgroundEvidence regarding the hepatotoxic effects of co-exposure to multiple heavy metals in the general middle-aged and older adults population remains limited. This study aimed to investigate the association between heavy metal mixtures and liver function in the population of Northwest China, with key findings supported using an animal model.MethodsWe conducted a cross-sectional study involving 451 participants from the Dongdagou Xinglong cohort. Concentrations of heavy metals and liver function indices were measured. Multiple linear regression, Bayesian kernel machine regression (BKMR), weighted quantile sum (WQS), and quantile-based g-computation (Qgcomp) regression were employed to evaluate the combined effects of co-exposure to multiple heavy metals on liver function. A sub-chronic cadmium (Cd) exposure rat model was further established to validate population-based findings.ResultsMultiple linear regression analysis revealed that blood Cd was positively correlated with GGT (β = 0.236), TBA (β = 0.162), ALT (β = 0.142) and AST (β = 0.114), while negatively correlated with DBil (β = −0.207), TBil (β = −0.166) and IBil (β = −0.157) (all P < 0.05). Similarly, other heavy metals also exhibited significant associations with liver function indicators. BKMR analysis showed that heavy metal mixture exposure was positively associated with ALT, AST, ALP, GGT, CHE, and TBA, but negatively associated with TBil, DBil, and IBil; WQS regression indicated that positive associations between the metal mixture and GGT as well as CHE; and the Qgcomp model demonstrated that the metal mixture was positively associated with ALT, GGT, and TBA, and negatively associated with TBil, DBil, and IBil. Notably, all three statistical models consistently identified Cd as the factor associated with liver function biomarkers. Furthermore, animal experiments provided experimental evidence consistent with the human findings: Cd exposure led to elevated serum GGT and ALP levels and induced histopathological alterations in the liver. Transcriptomic sequencing suggested that hepatic lipid metabolism pathways may be involved in Cd-induced liver injury.ConclusionsOverall, our study shows that co-exposure to heavy metals is associated with liver function biomarkers in middle-aged and older adults, with Cd identified as the predominant factor associated with liver function biomarkers.
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