环氧乙烷暴露与成年人心血管疾病之间的关系:基于NHANES 2013~2018

毛金花, 程序, 魏琼, 张冬梅

中国环境科学 ›› 2025, Vol. 45 ›› Issue (11) : 6423-6432.

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中国环境科学 ›› 2025, Vol. 45 ›› Issue (11) : 6423-6432.
环境毒理与健康

环氧乙烷暴露与成年人心血管疾病之间的关系:基于NHANES 2013~2018

  • 毛金花, 程序, 魏琼, 张冬梅
作者信息 +

Relationship between adult’s cardiovascular diseases and ethylene oxide exposure: Based on NHANES 2013~2018

  • MAO Jin-hua, CHENG Xu, WEI Qiong, ZHANG Dong-mei
Author information +
文章历史 +

摘要

为探讨环氧乙烷(EO)与心血管疾病风险之间的关系,纳入2013~2018年美国国家健康与营养检查调查(NHANES)数据库中的5041名成年人,采用血红蛋白-环氧乙烷结合物(HbEO)测定血清中的环氧乙烷水平.通过加权logistic回归模型和限制性三次样条图探讨HbEO与心血管疾病风险之间的剂量-反应关系,并进行亚组分析以评估研究的异质性.通过多因素回归分析发现,血清HbEO水平与心血管疾病风险呈正相关,且在调整混杂因素后具有统计学显著性(OR:1.15,[95%CI:1.02~1.30],P=0.021).对于大多数心血管疾病,随着环氧乙烷暴露量的增加,OR值也有所增加,但这种增加并不总是具有统计学显著性.此外,HbEO与心绞痛、心脏病发作患病率呈正相关,且在调整混杂因素后OR值最高(OR:1.36,[95%CI:1.11~1.68],OR:1.35[95%CI:1.14~1.60]),其中对心绞痛的影响更为显著.HbEO与心血管疾病风险之间存在显著的非线性关系(P-overall=0.002, P-nonlinear=0.006).剂量-反应相关性提示,血清HbEO水平升高与心绞痛风险相关,血清HbEO水平与心绞痛风险之间可能存在线性关系(p-overall=0.012,p-nonlinear= 0.748).HbEO与心脏病发作风险之间存在显著的非线性关系(p-overall<0.001, p-nonlinear=0.011).综上,血液中环氧乙烷代谢产物与心血管疾病患病率的升高有关,尤其是心绞痛和心脏病发作两种心血管疾病,但仍需进一步研究证实.

Abstract

The relationship between ethylene oxide (EO) and cardiovascular disease risk was investigated in this article. A total of 5041 adults were enrolled, and ethylene oxide levels were measured in serum using hemoglobin ethylene oxide conjugate (HbEO) as a biomarker. Data were obtained from the National Health and and Nutrition Examination Survey (NHANES) database in the United States between 2013 and 2018. Weighted logistic regression models and restricted cubic spline plots were used to examine the dose-response relationship between HbEO and cardiovascular disease risk. Subgroup analyses were conducted to evaluate heterogeneity in the study. Through multiple regression analysis, it was found that serum HbEO levels were positively associated with cardiovascular disease risk, and statistical significance was maintained after adjustment for multiple confounders (OR: 1.15, [95% CI: 1.02~1.30], P=0.021). For most cardiovascular diseases, increased exposure to ethylene oxide was associated with elevated OR values, although this increase was not always statistically significant. Additionally, HbEO was positively correlated with the incidence of angina pectoris and heart attack, with the highest OR values observed after full adjustment (OR=1.36 [95% CI: 1.11~1.68] and OR=1.35 [95% CI: 1.14~1.60], respectively). Angina pectoris was the most affected outcome.A significant non-linear relationship was identified between HbEO and overall cardiovascular disease risk (P-overall=0.002, P-non-linear=0.006). Dose-response analysis indicated that elevated serum HbEO levels were associated with an increased risk of angina, with evidence supporting a linear relationship (p-overall=0.012, p-non-linear=0.748). A significant non-linear association was also observed between HbEO and heart attack risk (p-overall<0.001, p-non-linear=0.011).In summary, ethylene oxide metabolites in the blood were associated with an increased incidence of cardiovascular diseases, particularly angina pectoris and heart attack. Further research is needed to confirm these findings.

关键词

心血管疾病 / 环氧乙烷 / 横断面研究 / NHANES

Key words

cardiovascular disease / ethylene oxide / cross-sectional study / NHANES

引用本文

导出引用
毛金花, 程序, 魏琼, 张冬梅. 环氧乙烷暴露与成年人心血管疾病之间的关系:基于NHANES 2013~2018[J]. 中国环境科学. 2025, 45(11): 6423-6432
MAO Jin-hua, CHENG Xu, WEI Qiong, ZHANG Dong-mei. Relationship between adult’s cardiovascular diseases and ethylene oxide exposure: Based on NHANES 2013~2018[J]. China Environmental Science. 2025, 45(11): 6423-6432
中图分类号: X503.1   

参考文献

[1] Ma Y, Zheng Z, Zhuang L, et al. Dietary macronutrient intake and cardiovascular disease risk and mortality: A systematic review and dose-response meta-analysis of prospective cohort studies [J]. Nutrients, 2024,16(1):41.
[2] 刘 昊,李 响.冠状动脉疾病发病机制及治疗策略研究进展 [J]. 生物技术进展, 2025,15(2):254-262. Liu H, Li X. Research progress on the pathogenesis and treatment strategies of coronary artery disease [J]. Advances in Biotechnology, 2025,15(2):254-262.
[3] Roth G A, Mensah G A, Johnson C O, et al. Global burden of cardiovascular diseases and risk factors, 1990~2019: Update from the GBD 2019 study [J]. J Am Coll Cardiol, 2020,76(25):2982-3021.
[4] 张贵涛,李淑娟.心脑血管疾病研究前沿进展与热点 [J]. 基础医学与临床, 2025,45(2):141. Zhang G T, Li S J. Frontiers and hotspots in research on cardiovascular and cerebrovascular diseases [J]. Basic Medicine and Clinical Medicine, 2025,45(2):141.
[5] Wong N D, Sattar N. Cardiovascular risk in diabetes mellitus: epidemiology, assessment and prevention [J]. Nat. Rev. Cardiol., 2023, 20(10):685-695.
[6] Münzel T, Miller M R, Sørensen M, et al. Reduction of environmental pollutants for prevention of cardiovascular disease: It's time to act [J]. Eur. Heart. J., 2020,41(41):3989-3997.
[7] 邢光伟,陆荣柱,顾祖维.环境毒理学中的营养学问题 [J]. 环境与职业医学, 2005,(3):211. Xing G W, Lu R Z, Gu Z W. Nutritional issues in environmental toxicology [J]. Environmental and Occupational Medicine, 2005, (3):211.
[8] Kirman C R, Li A A, Sheehan P J, et al. Ethylene oxide review: Characterization of total exposure via endogenous and exogenous pathways and their implications to risk assessment and risk management [J]. J. Toxicol. Environ. Health B Crit. Rev., 2021,24(1): 1-29.
[9] O'Kelley L, Swanson B, Bishop-Royse J C. Integrative literature review: Ethylene oxide exposure signs and symptoms [J]. Public Health Nurs., 2023,40(5):790-809.
[10] Kirman C R, Hays S M. Derivation of endogenous equivalent values to support risk assessment and risk management decisions for an endogenous carcinogen: Ethylene oxide [J]. Regul. Toxicol. Pharmacol., 2017,91:165-172.
[11] Bolognesi C, Bruzzone M, Ceppi M, et al. The lymphocyte cytokinesis block micronucleus test in human populations occupationally exposed to vinyl chloride: A systematic review and meta-analysis [J]. Mutat. Res. Rev. Mutat. Res., 2017,774:1-11.
[12] Guo J, Wan Z, Cui G, et al. Association of exposure to ethylene oxide with risk of diabetes mellitus: results from NHANES 2013~2016 [J]. Environ. Sci. Pollut. Res. Int., 2021,28(48):68551-68559.
[13] Jinot J, Fritz J M, Vulimiri S V, et al. Carcinogenicity of ethylene oxide: key findings and scientific issues [J]. Toxicol Mech Methods, 2018,28(5):386-396.
[14] Ghosh M, Godderis L. Genotoxicity of ethylene oxide: A review of micronucleus assay results in human population [J]. Mutat. Res. Rev. Mutat Res, 2016,770(Pt A):84-91.
[15] Ogawa M, Oyama T, Isse T, et al. Hemoglobin adducts as a marker of exposure to chemical substances, especially PRTR class I designated chemical substances [J]. J. Occup. Health, 2006,48(5):314-328.
[16] Ranasinghe P, Mathangasinghe Y, Jayawardena R, et al. Prevalence and trends of metabolic syndrome among adults in the asia-pacific region: a systematic review [J]. BMC Public Health, 2017,17(1):101.
[17] Shahab L, Goniewicz M L, Blount B C, et al. Nicotine, carcinogen, and toxin exposure in long-term e-cigarette and nicotine replacement therapy users: A cross-sectional Study [J]. Ann. Intern. Med., 2017,166(6):390-400.
[18] Sahakyan K R, Somers V K, Rodriguez-Escudero J P, et al. Normal-weight central obesity: Implications for total and cardiovascular mortality [J]. Ann. Intern. Med., 2015,163(11):827- 835.
[19] Du D, Yuan Y, Guan X, et al. Ethylene oxide exposure, inflammatory indicators, and depressive symptoms: a cross-sectional study and mediation analysis based on a non-institutionalized American population [J]. Front Public Health, 2024,12:1445257.
[20] Scimeca M, Palumbo V, Giacobbi E, et al. Impact of the environmental pollution on cardiovascular diseases: From epidemiological to molecular evidence [J]. Heliyon, 2024,10(18): e38047.
[21] Zhang H, Zhang Z. Association between ethylene oxide exposure and Klotho levels in US adults [J]. Sci. Rep., 2025,15(1):12528.
[22] 齐 丽,韩 莉,吴 笛.急性环氧乙烷中毒致脑电、心电改变3例报告 [J]. 职业与健康, 2006,(10):741-742. Qi L, Han L, Wu D. Three case reports of EEG and ECG changes caused by acute ethylene oxide poisoning [J]. Occupational and Health, 2006,(10):741-742.
[23] Han S, Xie M, Cheng S, et al. Associations between specific volatile organic chemical exposures and cardiovascular disease risks: insights from NHANES [J]. Front Public Health, 2024,12:1378444.
[24] Liu B, Lehmler H, Ye Z, et al. Exposure to polybrominated diphenyl ethers and risk of all-cause and cause-specific mortality [J]. JAMA Netw Open, 2024,7(4):e243127.
[25] Feng X, Qiu F, Zheng L, et al. Exposure to volatile organic compounds and mortality in US adults: A population-based prospective cohort study [J]. Sci. Total. Environ., 2024,928:172512.
[26] Vecchio D, Sasco A J, Cann C I. Occupational risk in health care and research [J]. Am J Ind Med, 2003,43(4):369-397.
[27] Kiran S, Cocco P, Mannetje A, et al. Occupational exposure to ethylene oxide and risk of lymphoma [J]. Epidemiology, 2010,21(6): 905-910.
[28] Rubinstein M L, Delucchi K, Benowitz N L, et al. Adolescent exposure to toxic volatile organic chemicals from e-cigarettes [J]. Pediatrics, 2018,141(4).
[29] Gardner M J, Coggon D, Pannett B, et al. Workers exposed to ethylene oxide: a follow up study [J]. Br. J. Ind. Med., 1989,46(12):860-865.
[30] Swaen G M H, Burns C, Teta J M, et al. Mortality study update of ethylene oxide workers in chemical manufacturing: A 15 year update [J]. J. Occup. Environ. Med., 2009,51(6):714-723.
[31] Hagmar L, Bellander T, Englander V, et al. Mortality and cancer morbidity among workers in a chemical factory [J]. Scand. J. Work Environ. Health, 1986,12(6):545-551.
[32] Hogstedt C, Rohlén O, Berndtsson B S, et al. A cohort study of mortality and cancer incidence in ethylene oxide production workers [J]. Br. J. Ind. Med., 1979,36(4):276-280.
[33] Hong F, Liang X, Liu W, et al. Roles of eNOS in atherosclerosis treatment [J]. Inflamm Res., 2019,68(6):429-441.
[34] Xin G, Ming Y, Ji C, et al. Novel potent antiplatelet thrombotic agent derived from biguanide for ischemic stroke [J]. Eur. J. Med. Chem., 2020,200:112462.
[35] Zheng J, Zhuo Y, Zhang C, et al. LncRNA TTTY15 regulates hypoxia-induced vascular endothelial cell injury via targeting miR-186-5p in cardiovascular disease [J]. Eur. Rev. Med. Pharmacol. Sci., 2020,24(6):3293-3301.
[36] Keiran S, Bhimani B, Dixit A. Ethylene glycol toxicity [J]. Am. J. Kidney Dis., 2005,46(3):e31-e33.
[37] Cox R D, Phillips W J. Ethylene glycol toxicity [J]. Mil. Med., 2004,169(8):660-663.
[38] Andrews J E, Courtney K D, Donaldson W E. The effects of ethylene chlorohydrin on fatty acid synthesis [J]. J. Environ. Sci. Health B, 1983,18(3):351-367.
[39] Rutledge J C, Generoso W M. Fetal pathology produced by ethylene oxide treatment of the murine zygote [J]. Teratology, 1989,39(6): 563-572.
[40] Polifka J E, Rutledge J C, Kimmel G L, et al. Exposure to ethylene oxide during the early zygotic period induces skeletal anomalies in mouse fetuses [J]. Teratology, 1996,53(1):1-9.
[41] Hamad A, Iweala O I, Henderson C, et al. Recurrent anaphylaxis during cardiac catheterization due to ethylene oxide [J]. J. Allergy Clin. Immunol. Pract., 2018,6(6):2148-2150.

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