Background and objectives
While metabolic dysfunction-associated steatotic liver illness (MASLD) is associated pinch obesity, nan origin of its quickly rising prevalence is not good understood. In this study, we aimed to analyse nan relation betwixt arsenic vulnerability and MASLD successful humans.
Methods
Urinary inorganic arsenic information from nan National Health and Nutrition Examination Survey, 2011–2020, were used. These were mixed pinch decease certificate information from nan National Death Index of nan National Center for Health Statistics to ascertain mortality rates. Weighted linear regression and chi-squared study were performed.
Results
The study included 6,386 participants aft exclusions. The mean urinary arsenic level was 5.92 µg/L successful participants pinch MASLD versus 5.59 µg/L successful those without. Alanine aminotransferase levels exhibited a statistically important expanding inclination crossed some continuous arsenic levels and arsenic quintiles. A statistically important upward inclination was observed for nan income-to-poverty ratio and assemblage wide scale but not for acquisition status. MASLD prevalence was highest among nan achromatic population, while an expanding inclination was observed successful nan Hispanic organization complete nan years (p < 0.001). The proportionality of Mexican Americans accrued to 12.6% successful nan MASLD group versus 8.09% successful nan non-MASLD cohort (p < 0.001). There was a statistically important summation successful nan likelihood of MASLD crossed arsenic vulnerability levels, pinch individuals successful nan highest quintile having a 32% greater likelihood compared to those successful nan lowest quintile (p-trend = 0.002). The likelihood further accrued to 55% successful nan highest quintile (odds ratio 1.55, 95% assurance interval: 1.19–2.03; p-trend < 0.001). MASLD was much prevalent successful females than males (57.9% vs. 47.6%; p < 0.001), and nan mean property accrued from 46.9 years to 49.9 years (p = 0.016).
Conclusions
In this nationally typical study, higher urinary arsenic levels were importantly associated pinch a 55% accrued likelihood of MASLD (95% CI: 1.2–2.0) successful nan highest quintile, independent of accepted metabolic consequence factors. These findings persist crossed cardinal subgroups, suggesting arsenic whitethorn lend to hepatic steatosis moreover astatine mean vulnerability levels emblematic successful nan U.S. population. Screening for arsenic vulnerability (e.g., urinary biomarkers, well-water testing) successful high-risk regions (e.g., Southwest U.S.) could place populations for targeted liver illness prevention. Regulatory efforts to trim arsenic successful nutrient and h2o supplies (e.g., U.S. Food and Drug Administration limits for atom products) whitethorn concurrently mitigate nan MASLD burden.
Source:
Journal reference:
Choday, S. (2025). Urinary Arsenic Exposure and Metabolic Dysfunction-associated Steatotic Liver Disease: A NHANES Analysis. Journal of Translational Gastroenterology. doi.org/10.14218/jtg.2025.00019
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