持久性有机污染物多氯联苯和二恶英与心血管-肾-代谢综合征及其预后的关系:一项全国代表性研究

IF 2.9 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Wen Chen, Debin Chen, Yining Li, Yizhou Zhuang, Yaojie Wang, Youlan Chen, Yongju Ye, Qijun Zhang, Jianhui Zhao
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引用次数: 0

摘要

背景:持久性有机污染物(POPs)可能是心血管-肾-代谢(CKM)综合征发生和进展的危险因素。本研究旨在评估多氯联苯(PCBs)和二恶英对CKM综合征的影响,以及炎症细胞在这些关联中的介导作用。方法:收集2005-2012年全国健康与营养检查调查中多氯联苯及二恶英样化合物暴露与慢性肾病综合征的数据。我们应用多变量逻辑回归、加权分位数和回归、分位数g计算和亚组分析来评估多氯联苯和二恶英样化合物对CKM综合征的个体和联合健康影响。中介分析评估了炎症细胞在这些污染物和CKM综合征之间的关系中的作用。采用Cox比例风险回归法探讨多氯联苯和二恶英暴露对不同CKM综合征分期患者死亡风险的影响。结果:PCB138、PCB153、PCB180、1,2,3,6,7,8-六氯二苯并-对二恶英(hexa- cdd)和1,2,3,4,6,7,8-七氯二苯并-对二恶英(hepa - cdd)暴露与晚期CKM综合征风险分别增加约4%、3%、3%、3%、3%和2%相关。在混合效应分析中,发现多氯联苯和二恶英的组合可协同增加晚期CKM综合征的风险。加权分位数和回归确定1,2,3,4,6,7,8-七氯二苯并呋喃(HXCDF)是导致这种风险增加的最重要因素。此外,白细胞、淋巴细胞和中性粒细胞介导多氯联苯、二恶英样化合物与晚期CKM综合征之间的关联,介导比例为1.77%至3.95%。暴露于多氯联苯(HXCDF除外)和二恶英与CKM 0-2期患者死亡风险增加相关,而暴露于六氯联苯与CKM 3-4期患者全因死亡风险增加相关。结论:暴露于多氯联苯和二恶英样化合物会增加晚期CKM综合征的风险和不同CKM综合征阶段的死亡率。炎症细胞在这些污染物与晚期CKM综合征之间的关系中起中介作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Persistent Organic Pollutants Polychlorinated Biphenyls and Dioxins with Cardiovascular-Kidney-Metabolic Syndrome and Its Prognosis: A Nationally Representative Study.

Background: Persistent organic pollutants (POPs) may be risk factors for the development and progression of cardiovascular-kidney-metabolic (CKM) syndrome. This study aimed to evaluate the effects of polychlorinated biphenyls (PCBs) and dioxins on CKM syndrome, as well as the mediating role of inflammatory cells in these associations.

Methods: Data on PCB and dioxin-like compound exposure and CKM syndrome were obtained from the National Health and Nutrition Examination Survey 2005-2012. We applied multivariable logistic regression, weighted quantile sum regression, quantile g-computation, and subgroup analyses to assess the individual and combined health effects of PCBs and dioxin-like compounds on CKM syndrome. Mediation analyses evaluated the role of inflammatory cells in the relationship between these pollutants and CKM syndrome. Cox proportional hazards regression was performed to explore the impact of PCB and dioxin exposure on mortality risk among patients at different CKM syndrome stages.

Results: Exposure to PCB138, PCB153, PCB180, 1,2,3,6,7,8-hexachlorodibenzo-p-dioxin (hexa-CDDs), and 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin (hepta-CDDs) was associated with increased risk of advanced CKM syndrome by approximately 4%, 3%, 3%, ,3% and 2%, respectively. In the mixture effect analysis, a combination of PCBs and dioxins was found to synergistically increase the risk of advanced CKM syndrome. Weighted quantile sum regression identified 1,2,3,4,6,7,8-heptachlorodibenzofuran (HXCDF) as the most significant contributor to this increased risk. Furthermore, white blood cells, lymphocytes and neutrophils mediated the associations between PCBs, dioxin-like compounds, and advanced CKM syndrome, with mediation proportions ranging from 1.77% to 3.95%. Exposure to PCBs (except HXCDF) and dioxins was associated with increased mortality risk in CKM stage 0-2 patients, while exposure to hexa-CDDs was associated with increased all-cause mortality risk in CKM stage 3-4 patients.

Conclusion: Exposure to PCBs and dioxin-like compounds increases the risk of advanced CKM syndrome and mortality across different CKM syndrome stages. Inflammatory cells play a mediating role in the relationship between these pollutants and advanced CKM syndrome.

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来源期刊
Cardiorenal Medicine
Cardiorenal Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-UROLOGY & NEPHROLOGY
CiteScore
5.40
自引率
2.60%
发文量
25
审稿时长
>12 weeks
期刊介绍: The journal ''Cardiorenal Medicine'' explores the mechanisms by which obesity and other metabolic abnormalities promote the pathogenesis and progression of heart and kidney disease (cardiorenal metabolic syndrome). It provides an interdisciplinary platform for the advancement of research and clinical practice, focussing on translational issues.
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