Department of Occupational and Environmental Health and State Key Laboratory of Environmental Health for Incubating, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
School of Public Health, Shenzhen University Medical School, Shenzhen University, Shenzhen, Guangdong, 518055, China.
Environ Pollut. 2024 Dec 1;362:125008. doi: 10.1016/j.envpol.2024.125008. Epub 2024 Sep 21.
The aim of this study was to explore the association between phthalates (PAEs) exposure and all-cause mortality among diabetic cases, and potential molecular mechanisms of the effect. We followed 2806 diabetes cases from 2008 to the end of 2018 based on the Dongfeng-Tongji study, of which 446 cases died. We measured serum levels of six PAEs (DMP, DEP, DiBP, DnBP, BBP, and DEHP). Cox models were used to investigate the associations between PAEs and all-cause mortality. Genes related to PAEs are obtained from the Comparative Toxicogenomics Database. We constructed polygenic scores for sex hormone-binding globulin (SHBG) and testosterone, and functional SNPs for IL-6, PPARG, and GPX1 from genotyping data, and further analyzed the environment-gene interactions. The positive associations of PAEs (DMP, DiBP, DnBP, DEHP) with mortality were only observed in males but not in females. Comparing with the extreme quartile 1, the HRs (95% CI) for quartile 4 were 1.63 (0.17, 2.26) for DMP, 1.82 (1.29, 2.56) for DiBP, 1.68 (1.18, 2.40) for DnBP, 1.66 (1.17, 2.36) for DEHP. Enrichment analysis showed that PAEs-related genes were mainly associated with hormones and IL-6-related pathways. Genetic variants of SHBG, testosterone, and IL-6 modified the association between PAEs mixture and all-cause mortality. PAEs exposure are associated with all-cause mortality among diabetic cases, and PAE exposure increases the risk of all-cause mortality only in males. Effects on the hormonal system and IL6-related pathways may be potential mechanisms.
本研究旨在探讨邻苯二甲酸酯(PAEs)暴露与糖尿病患者全因死亡率之间的关联,以及这种效应的潜在分子机制。我们基于东风-同济研究,对 2008 年至 2018 年底的 2806 例糖尿病患者进行了随访,其中 446 例死亡。我们测量了血清中 6 种 PAEs(DMP、DEP、DiBP、DnBP、BBP 和 DEHP)的水平。Cox 模型用于研究 PAEs 与全因死亡率之间的关系。我们从比较毒理学基因组数据库中获得了与 PAEs 相关的基因。我们从基因分型数据中构建了性激素结合球蛋白(SHBG)和睾酮的多基因评分,以及白细胞介素 6(IL-6)、过氧化物酶体增殖物激活受体(PPARG)和谷胱甘肽过氧化物酶 1(GPX1)的功能 SNP,进一步分析了环境-基因相互作用。PAEs(DMP、DiBP、DnBP、DEHP)与死亡率的正相关仅在男性中观察到,而在女性中未观察到。与极端四分位 1 相比,四分位 4 的 HR(95%CI)分别为 DMP 的 1.63(0.17,2.26)、DiBP 的 1.82(1.29,2.56)、DnBP 的 1.68(1.18,2.40)和 DEHP 的 1.66(1.17,2.36)。富集分析表明,PAEs 相关基因主要与激素和白细胞介素 6 相关途径有关。SHBG、睾酮和白细胞介素 6 的遗传变异修饰了 PAEs 混合物与全因死亡率之间的关联。PAEs 暴露与糖尿病患者的全因死亡率相关,PAEs 暴露仅增加男性全因死亡率的风险。对激素系统和白细胞介素 6 相关途径的影响可能是潜在的机制。