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Clara Cell Protein CC16: A New Lung Epithelial Biomarker for Acute Lung Injury

机译:Clara细胞蛋白CC16:急性肺损伤的新的肺上皮生物标志物。

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摘要

There has been considerable interest in the contribution of lung epithelial injury to the pathogenesis of acute lung injury (ALI). Injury to the alveolar epithelium leads to alveolar edema, a decrease in surfactant activity, a reduction in alveolar fluid clearance, and more procoagulant and antifibrinolytic activity in the distal airspaces of the lung.1–3 One approach to estimating the degree of lung epithelial injury has been to measure plasma and airspace biomarkers of alveolar epithelial injury in patients with ALI. In addition to providing more insight into pathogenesis, biomarkers of lung epithelial injury may also have diagnostic value for differentiating cardiogenic edema from primary lung injury edema, particularly since the diagnostic criteria for ALI,4 bilateral chest radiographic infiltrates with arterial hypoxemia (PaO2/FiO2 ratio, < 300), are often present in patients with acute respiratory failure from cardiogenic edema as well as in patients with ALI.5 Also, elevated lung microvascular pressure often coexists in patients with ALI, as has been reported in the ARDS Network Fluid and Catheter Treatment Trial,6 in which 29% of patients in whom ALI had been diagnosed had a pulmonary artery wedge pressure of > 18 mm Hg. Thus, a biomarker that helps to make the diagnosis of ALI would be valuable to both guide clinical management as well as to define a more homogenous patient cohort for clinical trials of ALI.
机译:肺上皮损伤对急性肺损伤(ALI)发病机制的贡献引起了相当大的兴趣。肺泡上皮损伤导致肺泡水肿,表面活性剂活性降低,肺泡液清除率降低以及肺远端空域中更多的促凝血和抗纤维蛋白溶解活性。1-3一种评估肺上皮损伤程度的方法一直用于测量ALI患者肺泡上皮损伤的血浆和空域生物标志物。除了提供对发病机制的更多见解之外,肺上皮损伤的生物标志物还可能具有区分心源性水肿和原发性肺损伤水肿的诊断价值,尤其是因为ALI [4]的诊断标准是双侧胸部X线影像学浸润伴有动脉血氧不足(PaO2 / FiO2比,<300)经常存在于因心源性水肿引起的急性呼吸衰竭以及ALI患者中。5此外,如ARDS Network Fluid and Catheter所报道,ALI患者常常并存肺微血管压力升高治疗试验6,其中29%被诊断为ALI的患者的肺动脉楔压> 18 mm Hg。因此,有助于诊断ALI的生物标记物对于指导临床管理以及为ALI的临床试验定义更为同质的患者队列都是有价值的。

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  • 来源
    《Chest》 |2009年第6期|p.1408-1410|共3页
  • 作者单位

    Danny F. McAuley, MD Belfast, UKand Michael A. Matthay, MD, FCCP San Francisco, CA;

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  • 正文语种 eng
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