Associations between mercury exposure and the risk of nonalcoholic fatty liver disease (NAFLD) in US adolescents

非酒精性脂肪肝 全国健康与营养检查调查 优势比 脂肪肝 体重不足 体质指数 横断面研究 人口 丙氨酸转氨酶 医学 内科学 四分位数 环境卫生 置信区间 疾病 胃肠病学 超重 病理
作者
Runsen Chen,Yang Xu,Cheng Xu,Yaqin Shu,Siyu Ma,Changgui Lu,Xuming Mo
出处
期刊:Environmental Science and Pollution Research [Springer Nature]
卷期号:26 (30): 31384-31391 被引量:31
标识
DOI:10.1007/s11356-019-06224-5
摘要

Little is known regarding the effects of environmental mercury (Hg) exposure on liver dysfunction in adolescents. We aimed to explore the association between Hg exposure and the risk of nonalcoholic fatty liver disease (NAFLD) in the adolescent population. The cross-sectional associations between blood Hg concentrations and serum alanine aminotransferase (ALT) levels, a surrogate for suspected NAFLD, were evaluated using data from adolescents (aged 12–17 years old) who participated in the National Health and Nutrition Examination Survey (NHANES), 1999–2014. A final sample of 6389 adolescents was analysed. Elevated ALT was defined as > 25 IU/L and > 22 IU/L for boys and girls ≤ 17 years old, respectively. Odds ratios (ORs) of Hg levels in association with serum ALT levels were estimated using a logistic regression after adjusting for gender, age, ethnicity, serum cotinine, body mass index, the poverty income ratio, and NHANES cycles. The median blood Hg level was 0.73 ± 0.91 μg/L amongst US adolescents. In the adjusted model, the ORs of elevated ALT levels of those in the 4th quartile were higher amongst non-Hispanic white adolescents (OR = 1.76, 95% CI 1.20, 2.59; P = 0.035) and those who were normal or underweight (OR = 1.41, 95% CI 1.08, 1.85; P = 0.020). No association was observed for the other variables. Our results indicate that the positive association between blood Hg exposure and the risk of NAFLD in US adolescents is the highest amongst non-Hispanic white and those who are normal or underweight, regardless of ethnicity. More research is necessary to confirm this association and to clarify the potential mechanisms.
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