A prospective cohort study of multimetal exposure and risk of gestational diabetes mellitus

妊娠期糖尿病 医学 前瞻性队列研究 糖尿病 队列研究 队列 内科学 产科 怀孕 妊娠期 内分泌学 遗传学 生物
作者
Jiajia Song,Yihui Wu,Yubing Ma,Juhui He,Shuqi Zhu,Yibo Tang,Jiayue Tang,Mengjia Hu,Luyao Hu,Lixia Zhang,Qi Wu,Jing Liu,Zhaoxia Liang
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:947: 174568-174568
标识
DOI:10.1016/j.scitotenv.2024.174568
摘要

The relationship between co-exposure to multiple metals and gestational diabetes mellitus (GDM) and the mechanisms involved are poorly understood. In this nested case-control study, 228 GDM cases and 456 matched controls were recruited, and biological samples were collected at 12–14 gestational weeks. The urinary concentrations of 10 metals and 8-hydroxydeoxyguanosine (8-OHdG) as well as the serum levels of malondialdehyde (MDA) and advanced glycation end products (AGEs) were determined to assess the association of metals with GDM risk and the mediating effects of oxidative stress. Urinary Ti concentration was significantly and positively associated with the risk of GDM (odds ratio [OR]:1.45, 95 % confidence interval [CI]: 1.12, 1.88), while Mn and Fe were negatively associated with GDM risk (OR: 0.67, 95 % CI: 0.50, 0.91 or OR: 0.61, 95 % CI: 0.47, 0.80, respectively). A significant negative association was observed between Mo and GDM risk, specifically in overweight and obese pregnant women. Bayesian kernel machine regression showed a significant negative joint effect of the mixture of 10 metals on GDM risk. The adjusted restricted cubic spline showed a protective role of Mn and Fe in GDM risk (P < 0.05). A significant negative association was observed between essential metals and GDM risk in quantile g-computation analysis (P < 0.05). Mediation analyses showed a mediating effect of MDA on the association between Ti and GDM risk, with a proportion of 8.7 % (P < 0.05), and significant direct and total effects on Ti, Mn, and Fe. This study identified Ti as a potential risk factor and Mn, Fe, and Mo as potential protective factors against GDM, as well as the mediating effect of lipid oxidation.
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