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The association between urinary polycyclic aromatic hydrocarbon metabolites and liver function among US population: a
Manthar Ali Mallah1, Zhu Ying2, Mukhtiar Ali3
1Department of Toxicology, College of Public Health, Zhengzhou University, 100 Kexue Ave, Zhongyuan District, Zhengzhou, 450001, People's Republic of China.
Urinary polycyclic aromatic hydrocarbons (PAHs) are linked to elevated liver enzymes, specifically gamma-glutamyl transferase (GGT). 9-hydroxyfluorene showed the strongest association, with its effect on GGT levels potentially modified by other PAHs.
Area of Science:
- Environmental Health
- Toxicology
- Hepatology
Background:
- Pulmonary toxicity of polycyclic aromatic hydrocarbons (PAHs) is well-documented.
- Hepatotoxic effects of PAHs remain largely unknown.
- Urinary PAH metabolites serve as biomarkers for exposure.
Purpose of the Study:
- To investigate the association between urinary PAH levels and liver function parameters in the US population.
- To identify specific PAH metabolites linked to abnormal liver function.
- To assess the impact of PAHs on liver health beyond pulmonary effects.
Main Methods:
- Utilized data from the National Health and Nutritional Examination Survey (NHANES) 2003-2016.
- Included 2515 adult participants.
- Employed logistic regression to analyze associations between urinary PAHs and elevated gamma-glutamyl transferase (GGT), adjusting for confounders.
Main Results:
- Increased levels of 9-hydroxyfluorene, 2-hydroxyfluorene, and 3-hydroxyfluorene were significantly associated with elevated GGT.
- 9-hydroxyfluorene demonstrated the strongest association with elevated GGT (OR = 2.11, P < 0.001).
- The influence of 9-hydroxyfluorene on GGT levels was observed to be modified by the presence of other PAHs.
Conclusions:
- Urinary 9-hydroxyfluorene is significantly associated with elevated GGT levels, indicating potential hepatotoxicity.
- The combined presence of multiple PAHs may potentiate the effect of 9-hydroxyfluorene on liver function.
- Further research is warranted to elucidate the mechanisms of PAH-induced liver injury.
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