血浆和痰血栓调节蛋白在细菌性社区获得性肺炎中的诊断和预后潜力。

Helena Alpkvist, Simon Athlin, Anna Norrby-Teglund, Kristoffer Strålin
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引用次数: 0

摘要

背景:可溶性血栓调节蛋白是内皮细胞损伤的标志物,在内皮损伤过程中释放到血液循环中,并且在细菌感染中观察到其浓度升高。本研究旨在探讨细菌性社区获得性肺炎(CAP)患者血浆和痰中血栓调节蛋白浓度与疾病严重程度和病因的相关性。方法:对放射学证实的细菌性CAP住院的成人进行前瞻性研究。入院时收集血浆和痰样本,并使用酶联免疫吸附法定量血栓调节蛋白浓度。该研究包括一项多变量分析,以评估血栓调节素浓度是否与疾病严重程度和/或细菌病因相关。结果:在111例细菌性CAP患者中,包括15例重度CAP(根据美国胸科学会/美国传染病学会的标准定义)和63例肺炎球菌病因,所有患者的血浆和42例患者的痰中均检测到血栓调节蛋白。血浆血栓调节蛋白浓度升高与严重CAP独立相关。细菌性病因分层研究显示,血浆血栓调节蛋白浓度升高仅与肺炎球菌感染患者的严重肺炎相关。检测重症肺炎球菌CAP的受试者工作特征曲线下面积为0.87。相反,痰血栓调节蛋白浓度与疾病严重程度或细菌病因无关。结论:血浆凝血调节蛋白是鉴别严重肺炎球菌CAP的有希望的生物标志物。痰凝血调节蛋白与疾病严重程度或细菌病因无关。这些发现支持进一步研究血浆血栓调节蛋白在细菌感染中的诊断和预后作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic and prognostic potential of plasma and sputum thrombomodulin in bacterial community-acquired pneumonia.

Background: Soluble thrombomodulin, a marker of endothelial cell injury, is released into the circulation during endothelial damage and has been observed at elevated concentrations in bacterial infections. This study aimed to investigate the correlation of thrombomodulin concentrations in plasma and sputum with disease severity and etiology in bacterial community-acquired pneumonia (CAP).

Methods: A prospective study was conducted on adults hospitalized with radiologically confirmed bacterial CAP. Plasma and sputum samples were collected upon admission, and thrombomodulin concentrations were quantified using an enzyme-linked immunosorbent assay. The study included a multivariate analysis to assess whether thrombomodulin concentrations were associated with disease severity and/or bacterial etiology.

Results: Of 111 patients with bacterial CAP, including 15 with severe CAP (as defined by the American Thoracic Society/Infectious Diseases Society of America criteria) and 63 with pneumococcal etiology, thrombomodulin was measured in plasma in all patients and in sputum in 42 patients. Elevated plasma thrombomodulin concentrations were independently associated with severe CAP. Stratification by bacterial etiology showed that higher plasma thrombomodulin concentrations were linked to severe pneumonia only in patients with pneumococcal infection. The area under the receiver operating characteristic curve for detecting severe pneumococcal CAP was 0.87. Conversely, sputum thrombomodulin concentrations showed no association with disease severity or bacterial etiology.

Conclusions: Plasma thrombomodulin is a promising biomarker for identifying severe pneumococcal CAP. Sputum thrombomodulin did not correlate with disease severity or bacterial etiology. These findings support further investigation into the diagnostic and prognostic role of plasma thrombomodulin in bacterial infections.

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