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Association between urinary cadmium exposure and metabolic syndrome and the mediating role of thyroid dysfunction: NHANES 2007 to 2012  ( SCI-EXPANDED收录)  

文献类型:期刊文献

英文题名:Association between urinary cadmium exposure and metabolic syndrome and the mediating role of thyroid dysfunction: NHANES 2007 to 2012

作者:Peng, Jie[1];Wang, Sijiong[2];Liu, Ye[1];Zhu, Lichao[1];Zhao, Yating[1]

第一作者:Peng, Jie

通信作者:Zhao, YT[1]

机构:[1]North China Univ Sci & Technol, Affiliated Hosp, Breast Dis Treatment Ctr, Tangshan 063000, Hebei, Peoples R China;[2]Gansu Univ Chinese Med, Clin Med Coll 1, Lanzhou, Peoples R China

第一机构:North China Univ Sci & Technol, Affiliated Hosp, Breast Dis Treatment Ctr, Tangshan 063000, Hebei, Peoples R China

通信机构:[1]corresponding author), North China Univ Sci & Technol, Affiliated Hosp, Breast Dis Treatment Ctr, Tangshan 063000, Hebei, Peoples R China.

年份:2026

卷号:105

期号:15

起止页码:e48230

外文期刊名:MEDICINE

收录:;Scopus(收录号:2-s2.0-105035470602);WOS:【SCI-EXPANDED(收录号:WOS:001737488300001)】;

语种:英文

外文关键词:metabolic syndrome; NHANES; T4; thyroid function; TSH; urinary cadmium

摘要:This study aims to examine the association between urinary cadmium (U-Cd) exposure and metabolic syndrome (MetS) in U.S. adults and evaluate whether thyroid function (TSH/T4) mediates this relationship. We analyzed National Health and Nutrition Examination Survey 2007-2012 data (n = 4869; age >= 18) to assess the relationship between U-Cd and MetS. U-Cd was measured by ICP-MS, adjusted for creatinine, and log-transformed. We employed weighted logistic regression, restricted cubic splines for nonlinearity, and multivariable models for U-Cd-TSH/T4 relations, with causal mediation analysis for indirect effects, considering demographics and lifestyle factors. Higher U-Cd was associated with greater MetS risk in a dose-response fashion: versus Q1, OR (95% CI) for Q2, Q3, Q4 were 1.84 (1.49-2.26), 2.36 (1.92-2.89), and 2.49 (2.04-3.06); P-trend <.0001. Restricted cubic splines showed a significant overall and nonlinear association (P_overall = .006; P_nonlinear = .036), with relatively flat risk at low exposure and steeper increases beyond a turning point. U-Cd correlated positively with T4 (fully adjusted beta approximate to 0.26 ng/dL per unit increase; P <.001) and inversely with TSH. Mediation indicated a small but significant indirect effect via T4 (indirect effect approximate to 0.003; 95% CI, 0.001-0.005; proportion mediated approximate to 8.3%), while TSH and TSH/T4 showed negligible or negative indirect effects; the direct path from U-Cd to MetS predominated. Findings were generally stronger in women, younger adults (<40 years), and those with higher physical activity, and were robust across chronic-disease strata. In a nationally representative sample, U-Cd exposure is positively - and nonlinearly - associated with MetS; this relationship is driven mainly by a direct effect with a modest mediating role of T4, underscoring the metabolic implications of environmental cadmium and the relevance of thyroid pathways.

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