Cross-sectional and longitudinal associations of PAHs exposure with serum uric acid and hyperuricemia among Chinese urban residents: The potential role of oxidative damage

被引:2
|
作者
Ding, Xuejie [1 ,2 ,3 ]
Liu, Yang [1 ,2 ,3 ]
Wan, Shuhui [1 ,2 ,3 ]
Yang, Yueru [1 ,2 ,3 ]
Liang, Ruyi [1 ,2 ,3 ]
Yang, Shijie [4 ]
Zhang, Jiake [1 ,2 ,3 ]
Cao, Xiuyu [1 ,2 ,3 ]
Zhou, Min [1 ,2 ,3 ]
Chen, Weihong [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, Dept Occupat & Environm Hlth, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Key Lab Environm & Hlth, Minist Educ, Wuhan 430030, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Med Coll, Sch Publ Hlth, State Key Lab Environm Hlth Incubating, Wuhan 430030, Hubei, Peoples R China
[4] Hubei Prov Ctr Dis Control & Prevent, Hubei Prov Key Lab Appl Toxicol, Wuhan 430079, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Polycyclic aromatic hydrocarbons; Uric acid; Hyperuricemia; 8-Hydroxy-deoxyguanosine; General Chinese population; POLYCYCLIC AROMATIC-HYDROCARBONS; EPITHELIAL-CELLS; METABOLITES; STRESS; POPULATION; POLLUTION; ADULTS; RISK; GOUT; INFLAMMATION;
D O I
10.1016/j.envpol.2024.124664
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A few studies found polycyclic aromatic hydrocarbons (PAHs) were associated with serum uric acid (SUA) or hyperuricemia (HUA). However, the longitudinal study is vacant, and the underlying mechanisms remain unclear. We aimed to assess the cross-sectional and longitudinal associations of urinary PAHs metabolites with SUA levels and HUA risk, and explore the mediating effects of oxidative stress and inflammation. 10 urinary monohydroxylated PAHs metabolites and SUA levels were measured among 4047 Chinese urban residents at baseline and 1496 individuals at 6-year follow-up. Biomarkers of oxidative damage and inflammation in urine/plasma were determined at baseline. We adopted generalized linear mixed models and logistic regression to assess the associations of PAHs metabolites with SUA and HUA, weighted quantile sum regression and adaptive elastic net regression to evaluate the overall effects of multi-PAHs mixture, and mediation analysis to estimate the mediating roles of the biomarkers. In the cross-sectional study, each 1-unit increase in the ln-transformed values of 2OHNa, 2-OHFlu, 4-OHPh, 9-OHPh, 3-OHPh, 2-OHPh, EOHNa, EOHPh, and EOHPAHs was associated with a 4.10-, 3.90-, 6.42-, 7.33-, 4.85-, 5.43-, 4.47-, 7.67-, and 5.22-mu mol/L increase in SUA, respectively. Meanwhile, each 1-unit increase in the ln-transformed values of 1-OHNa, 2-OHNa, 4-OHPh, 9-OHPh, 3-OHPh, 2-OHPh, EOHNa, EOHPh, and EOHPAHs was associated with a 17, 14, 15, 22, 14, 19, 18, 27, and 21% increment in HUA risk, respectively. After 6 years, individuals with persistent high level of 9-OHPh had a 12.5 mu mol/L increase in SUA compared with those with persistent low level. The overall effects of multi-PAHs mixture on SUA and HUA remain positive. 8-hydroxy-deoxyguanosine mediated the associations of PAHs metabolites with SUA and HUA, and the mediated proportion ranged from 5.39% to 15.34%. PAHs exposure was associated with the elevated SUA levels and increased HUA risk, and oxidative DNA damage may be one of the underlying mechanisms.
引用
收藏
页数:12
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