Huang Tengyang, Xu Xijin, Chen Shuqin, Liu Zhiping, Huang Yu, Huo Xia, Chen Guangcan
Laboratory of Environmental Medicine and Developmental Toxicology, Shantou University Medical College, Shantou 515041 Guangdong, PR China; Department of Digestive Surgery, the First Affiliated Hospital of Shantou University Medical College, Shantou 515000 Guangdong, PR China.
Laboratory of Environmental Medicine and Developmental Toxicology, Shantou University Medical College, Shantou 515041 Guangdong, PR China; Department of Cell Biology and Genetics, Shantou University Medical College, 515041 Shantou, Guangdong, PR China.
Environ Int. 2025 Jul;201:109549. doi: 10.1016/j.envint.2025.109549. Epub 2025 May 28.
Informal e-waste recycling releases airborne particulate matter (PM) and polycyclic aromatic hydrocarbons (PAHs), which are linked to intestinal barrier dysfunction and chronic inflammation. SIRT6, a histone deacetylase, modulates inflammation by suppressing NF-κB signaling, but its role in mitigating e-waste pollutant-induced childhood enteritis remains unclear. This cross-sectional study evaluated associations between e-waste exposure, intestinal inflammation, and SIRT6 levels in 217 preschool children from Guiyu (e-waste-exposed, n = 109) and Haojiang (non-exposed control, n = 108), China. Airborne pollutant exposure was quantified via the Air Quality Composite Index (AQCI) and average daily dose (ADD) for PM, PM, NO, and SO. Urinary PAH metabolites, serum SIRT6, inflammatory markers (GM-CSF, IL-10), and intestinal barrier biomarkers (IFABP, endotoxins) were measured using GC/MS, ELISA, and automated hematology analyzers. Dietary patterns, residential proximity to e-waste sites, and gastrointestinal symptoms were assessed via questionnaires. Statistical analyses included Spearman correlations, multivariate regression, and Bayesian kernel machine regression (BKMR) to evaluate pollutant effects on SIRT6 and inflammation. Children residing in Guiyu demonstrated significantly elevated urinary PAH metabolites and higher ADD of PM, PM, NO, and SO compared to reference populations. Concurrently, this cohort exhibited biomarker patterns indicative of intestinal barrier compromise, including elevated IFABP and systemic endotoxin levels. Serum analyses revealed quantifiable reductions in SIRT6 and GM-CSF concentrations, accompanied by increased circulating monocytes and lymphocytes. Notably, BKMR modeling identified non-linear U-shaped associations between mixed PM/PAH exposures and progressive SIRT6 suppression. Proximity to e-waste sites, lower parental education, and poor household ventilation correlated with heightened pollutant exposure and gastrointestinal morbidity. Chronic e-waste exposure was associated with decreased serum SIRT6 levels and concurrent elevation of intestinal inflammatory biomarkers in children. Our cross-sectional analysis revealed significant correlations between SIRT6 downregulation, altered GM-CSF/IL-10 signaling profiles, and disrupted macrophage-Treg homeostasis. These observational findings suggest SIRT6 may serve as a potential protective mediator in environmental enteritis.
非正规电子垃圾回收会释放空气颗粒物(PM)和多环芳烃(PAH),这些物质与肠道屏障功能障碍和慢性炎症有关。SIRT6是一种组蛋白脱乙酰酶,可通过抑制NF-κB信号传导来调节炎症,但其在减轻电子垃圾污染物诱发的儿童肠炎中的作用尚不清楚。这项横断面研究评估了来自中国贵屿(电子垃圾暴露组,n = 109)和濠江(非暴露对照组,n = 108)的217名学龄前儿童的电子垃圾暴露、肠道炎症和SIRT6水平之间的关联。通过空气质量综合指数(AQCI)以及PM、PM、NO和SO的日均剂量(ADD)对空气污染物暴露进行量化。使用气相色谱/质谱联用仪(GC/MS)、酶联免疫吸附测定(ELISA)和自动血液分析仪测量尿中PAH代谢物、血清SIRT6、炎症标志物(GM-CSF、IL-10)和肠道屏障生物标志物(IFABP、内毒素)。通过问卷调查评估饮食模式、居住地与电子垃圾场的距离以及胃肠道症状。统计分析包括Spearman相关性分析、多元回归分析和贝叶斯核机器回归(BKMR),以评估污染物对SIRT6和炎症的影响。与参照人群相比,居住在贵屿的儿童尿中PAH代谢物显著升高,PM、PM、NO和SO的ADD也更高。同时,该队列呈现出表明肠道屏障受损的生物标志物模式,包括IFABP升高和全身内毒素水平升高。血清分析显示SIRT6和GM-CSF浓度可量化降低,同时循环单核细胞和淋巴细胞增加。值得注意的是,BKMR模型确定了混合PM/PAH暴露与SIRT6逐渐受到抑制之间的非线性U形关联。居住地与电子垃圾场的距离、父母教育程度较低以及家庭通风不良与污染物暴露增加和胃肠道发病率升高相关。长期电子垃圾暴露与儿童血清SIRT6水平降低以及肠道炎症生物标志物同时升高有关。我们的横断面分析揭示了SIRT6下调、GM-CSF/IL-10信号谱改变与巨噬细胞-Treg稳态破坏之间存在显著相关性。这些观察结果表明,SIRT6可能是环境性肠炎的潜在保护性介质。