环氧乙烷暴露增加美国普通人群葡萄糖代谢受损:一项全国性横断面研究。

IF 4 3区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Yuqi Zhao, Deliang Liu, Xiaogao Pan, Yuyong Tan
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引用次数: 0

摘要

背景:目前的实验证据支持环氧乙烷(EO)暴露相关的病理生理可能会影响葡萄糖代谢,但很少有基于人群的研究探讨其潜在联系:本研究使用了 2017 年至 2020 年美国国家健康与营养调查(NHANES)中 15560 名参与者的横截面数据。通过改良埃德曼反应检测环氧乙烷血红蛋白加合物(HbEO),计算环氧乙烷暴露水平。我们重点研究了环氧乙烷暴露与糖尿病前期和糖尿病以及糖代谢受损指标的关联,并进一步分析了潜在的致病机制。统计方法包括逻辑回归、广义加性模型拟合、惩罚性样条法、二片线性回归、递归算法、中介分析和皮尔逊分析:结果:暴露于环氧乙烷与葡萄糖代谢指标的变化以及糖尿病前期和糖尿病患病率的增加有关,显示出年龄一致性,在肥胖和非吸烟人群中更为明显。log2-HbEO 每增加 1 pmol/g Hb、1 SD 或 2 倍 SD,糖尿病前期风险分别增加 12%、16% 和 33%,糖尿病风险分别增加 18%、26% 和 61%。剂量-反应曲线显示,这种正相关性与糖尿病前期呈近似线性关系,与糖尿病呈 "J "形关系。当 log2-HbEO > 8.03 pmol/g Hb 时,患糖尿病的风险会进一步增加。皮尔逊相关性显示,在糖尿病前期,接触环氧乙烷与空腹胰岛素降低和 HbA1c 升高有关。而在糖尿病阶段,暴露于环氧乙烷与空腹血糖、HbA1c 和 HOMA-IR 升高相关,表明暴露于环氧乙烷会加剧糖尿病的发展。糖代谢受损的早期阶段可能是由环氧乙烷相关的炎症和氧化应激损伤胰腺β细胞,导致胰岛素分泌减少而引发的。这些推测得到了中介分析和中介因子皮尔逊分析的部分支持:结论:环氧乙烷暴露增加了美国普通人群糖代谢受损的发病率,有效抑制炎症和氧化应激失衡可能是一种潜在的干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethylene oxide exposure increases impaired glucose metabolism in the US general population: a national cross-sectional study.

Background: Current experimental evidence supports that ethylene oxide (EO) exposure-related pathophysiologies may affect glucose metabolism, but few population-based studies have explored the potential links.

Methods: This study used cross-sectional data from 15560 participants in the National Health and Nutrition Examination Survey (NHANES) from 2017 to 2020. EO exposure levels were calculated by testing hemoglobin adducts of EO (HbEO) via a modified Edman reaction. We focused on the association of EO exposure with prediabetes and diabetes as well as indicators of impaired glucose metabolism and further analyzed the potential pathogenic mechanisms. Statistics included logistic regression, generalized additive model fitting, penalized spline method, two-piecewise linear regression, recursive algorithm, mediation analysis, and Pearson's analysis.

Results: EO exposure was associated with changes in glucose metabolic indicators and increased prevalence of prediabetes and diabetes, showing age-consistency and being more pronounced in obese and non-smoking populations. For each one pmol/g Hb, one SD, or two-fold SD increase in log2-HbEO, the risk of prediabetes increased by 12%, 16%, and 33%, with an increased risk of diabetes by 18%, 26%, and 61%, respectively. Dose-response curves revealed that this positive correlation was approximately linear with prediabetes and "J" shaped with diabetes. When log2-HbEO > 8.03 pmol/g Hb, the risk of diabetes would be further increased. Pearson's correlation revealed that EO exposure was associated with reduced fasting insulin and elevated HbA1c in the prediabetic stage. While in the diabetes stage, EO exposure was correlated with elevated fasting glucose, HbA1c, and HOMA-IR, suggesting an exacerbation of diabetes progression by EO exposure. A potential mechanism that the early stages of impaired glucose metabolism may be initiated by EO-related inflammation and oxidative stress damaging pancreatic β-cells, resulting in decreased insulin secretion. These speculations were partially supported by mediation analysis and mediators' Pearson analysis.

Conclusion: Elevated ethylene oxide exposure increases the incidence of impaired glucose metabolism in the general U.S. population and a potential intervention may be to effectively suppress inflammation and oxidative stress imbalances.

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来源期刊
Environmental Health and Preventive Medicine
Environmental Health and Preventive Medicine PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH -
CiteScore
7.90
自引率
2.10%
发文量
44
审稿时长
10 weeks
期刊介绍: The official journal of the Japanese Society for Hygiene, Environmental Health and Preventive Medicine (EHPM) brings a comprehensive approach to prevention and environmental health related to medical, biological, molecular biological, genetic, physical, psychosocial, chemical, and other environmental factors. Environmental Health and Preventive Medicine features definitive studies on human health sciences and provides comprehensive and unique information to a worldwide readership.
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