血液环氧乙烷水平与骨关节炎和类风湿性关节炎的关系:来自NHANES的证据(2013-2020)

IF 3.9
Zhaoyi Fang , Qingxiang Hu , Wenxin Liu
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引用次数: 0

摘要

目的骨关节炎(OA)和类风湿关节炎(RA)是具有重要公共卫生意义的常见疾病。环境毒素在其发病机制中的作用日益得到认识;然而,环氧乙烷(EO)暴露对OA和RA的影响尚不清楚。本研究使用2013-2020年国家健康与营养检查调查(NHANES)的数据,调查了美国人群中血液EO水平与OA和RA患病率之间的关系。方法纳入在NHANES访谈中报告病情的≥40岁OA或RA的snhanes 2013-2020参与者。采用血红蛋白加合物定量法直接测定血EO水平。单变量和多变量logistic回归模型用于评估EO暴露与OA和RA之间的关系,并对潜在的混杂因素进行调整。采用限制性三次样条(RCS)分析来评估潜在的非线性关系。结果共3476例受试者,平均年龄60.0岁;52.0%女性)被纳入研究。在未调整的模型中,EO最高五分位数的参与者患OA的可能性并没有显著提高(比值比[OR] = 1.23;95%置信区间[CI]: 0.86-1.74)或RA (or = 1.58;95% CI: 0.97-2.58)与最低五分位数的人相比。然而,调整后,EO最高五分位数的参与者患OA的可能性显著增加(aOR = 2.00;95% CI: 1.30-3.07)和RA (aOR = 1.81;95% CI: 1.08-3.03)与最低五分位数的人相比。RCS分析显示EO暴露与OA或RA之间没有显著的非线性关联。结论:本研究确定了EO暴露与OA和RA患病率增加之间的独立关联。这些发现强调需要采取监管措施以尽量减少EO暴露,并进一步调查以确认因果关系。
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 blood ethylene oxide levels with osteoarthritis and rheumatoid arthritis: Evidence from NHANES (2013–2020)

Objectives

Osteoarthritis (OA) and rheumatoid arthritis (RA) are common conditions with important public health implications. The role of environmental toxins in their pathogenesis is increasingly recognized; however, the impact of ethylene oxide (EO) exposure on OA and RA remains unexplored. This study investigated the association between blood EO levels and the prevalence of OA and RA in the US population, using data from the National Health and Nutrition Examination Survey (NHANES) 2013–2020.

Methods

NHANES 2013–2020 participants ≥40 years old with OA or RA who reported the condition during the NHANES interview were included. Blood EO levels were directly measured using hemoglobin adduct quantification. Univariate and multivariable logistic regression models were used to evaluate the association between EO exposure and OA and RA, adjusting for potential confounders. Restricted cubic spline (RCS) analysis was performed to assess potential non-linear relations.

Results

A total of 3476 participants (mean age: 60.0 years; 52.0 % female) were included in the study. In the unadjusted model, participants in the highest EO quintile did not have a significantly higher likelihood of OA (odds ratio [OR] = 1.23; 95 % confidence interval [CI]: 0.86–1.74) or RA (OR = 1.58; 95 % CI: 0.97–2.58) compared to those in the lowest quintile. However, after adjustment, participants in the highest EO quintile had significantly greater likelihood of having OA (aOR = 2.00; 95 % CI: 1.30–3.07) and RA (aOR = 1.81; 95 % CI: 1.08–3.03) compared to those in the lowest quintile. RCS analyses suggested no significant non-linear associations between EO exposure and OA or RA.

Conclusion

This study identified independent associations between EO exposures and an increased prevalence of OA and RA. These findings highlight the need for regulatory measures to minimize EO exposure and further investigations to confirm causal relationships.
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来源期刊
Experimental gerontology
Experimental gerontology Ageing, Biochemistry, Geriatrics and Gerontology
CiteScore
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