人工石英凝聚引起的慢性矽肺患者外周血生物标志物

A. Jiménez, Gema Jiménez Gómez, A. H. Molina, Antonio Córdoba Doña, Antonio Campos Caro
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引用次数: 1

摘要

背景:由人工石英凝聚体(AQA)引起的矽肺在矿工中比传统形式的矽肺发展得更积极。这一实体正在世界范围内出现,近年来在加的斯省(西班牙)发现了大量病例。矽肺病患者血液中的生物标志物是诊断、疾病预后和治疗反应的必要工具。目的:比较健康人群与单纯(SS)或复杂(CS)矽肺患者血浆中部分生物标志物(MP-1、MMP-2、MMP-7、MMP-9、MMP-10、tgf - β、IL-1β、tnf - α、IL-18和mmp -1α)的水平,以作为矽肺疾病的生物标志物。方法:对57例经AQA诊断为矽肺的患者和18例健康对照者进行研究。采用单酶联免疫吸附试验(ELISA)或多重酶联免疫吸附测定血液生物标志物。结果:与健康志愿者相比,矽肺患者的MMP-2和MMP-7升高,但当矽肺患者按照ILO分类分为SS和CS时,仅发现MMP-7(未发现MMP-2)显著升高。MMP-1、MMP-9、MMP-10、IL-18、tgf - β均无差异。与健康组相比,CS组IL-1β和TNFα显著升高,但与SS组相比无显著升高。MIP-1α水平在健康组、SS组和CS组间呈梯度升高。结论:结合一些生物标志物的研究结果可能有助于矽肺的诊断。此外,一些生物标志物,如MIP-1α,应该有助于改善疾病演变的预测
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomarkers in peripheral blood from patients with chronic silicosis caused by artificial quartz agglomerates
Background: Silicosis produced by Artificial Quartz Agglomerates (AQA) evolves more aggressively than the classical form in miners. This entity is emerging worldwide and a significant group of cases has been detected in the province of Cadiz (Spain) in recent years. Biomarkers in the blood of silicotic patients are needed as tools for diagnosis, prognosis of the disease and response to treatment. Objective: To evaluate the plasma levels of some biomarkers (MP-1, MMP-2, MMP-7, MMP-9 and MMP-10, TGFβ, IL-1β, TNFα, IL-18 and MIP-1α), in healthy subjects compared with patients with simple (SS) or complicated (CS) silicosis, in order to use them as biomarkers of the disease. Methods: Fifty-seven patients diagnosed with silicosis by AQA and 18 healthy controls were studied. The blood biomarkers were quantified by single or multiplex ELISA. Results: MMP-2 and MMP-7 were increased in patients with silicosis compared to healthy volunteers, but only MMP-7 (not MMP-2) was found significantly augmented when silicotic patients were split in SS and CS according to the ILO classification. No differences were found for MMP-1, MMP-9, MMP-10, IL-18 and TGFβ. However, IL-1β and TNFα were significantly increased in CS group compared to healthy patients, but not compared to SS group. MIP-1α, showed an increasing gradient when healthy, SS and CS groups were compared. Conclusions: Combining the results of some of the biomarkers studied may be useful in the diagnosis of silicosis. Moreover, several biomarkers, such as MIP-1α, should be helpful to improve predictions of the evolution of the disease
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