骨蛋白酶和 NGAL 在慢性阻塞性肺病急性加重和肺炎鉴别诊断中的作用

Selda Günaydın, T. Özlü, S. Özsu, Asım Örem
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摘要

目的:慢性阻塞性肺疾病(COPD)是一种炎症性肺病,会随着病情发作而恶化。肺炎是一种传染性肺部疾病,随着肺部浸润而发展。Osteopontin(OP)是一种参与炎症的细胞因子。中性粒细胞明胶酶相关脂质体(NGAL)是一种抗菌肽,具有激活中性粒细胞和抗菌特性。本研究对慢性阻塞性肺疾病加重期、慢性阻塞性肺疾病稳定期和肺炎患者的血清 OP 和 NGAL 水平进行了检测。我们研究的目的是评估 NGAL 和 OP 水平作为生物标志物在 COPD 和肺炎鉴别诊断中的重要性:研究对象包括 2011 年 5 月至 2013 年 8 月期间在我科住院的 120 名连续患者。在确诊后 24 小时内用 ELISA 方法测量血清 OP 和 NGAL 水平。慢性阻塞性肺疾病急性加重(AE-COPD)组有 95 名患者(87 名男性,平均年龄(69.0±10.6)岁),肺炎组有 25 名患者(16 名男性,平均年龄(57.5±22.9)岁)。AE-COPD组患者的血清OP和NGAL水平在急性加重后30-45天的稳定期内重新测定:肺炎组的血清 OP 水平高于 AE-COPD 组(93.47 ng/ml vs 53.10 ng/ml;p84 ng/ml 是一个独立的预测因子,可使肺炎风险增加 8 倍多(95% CI,2.43-26.59)。经测定,OP 在区分肺炎和 AE-COPD 方面的敏感性和特异性分别为 80% 和 92%。随着慢性阻塞性肺病严重程度的增加,血清 NGAL 水平也会升高,且具有统计学意义(P:0.032):结论:研究表明,血清骨蛋白酶水平是区分慢性阻塞性肺病恶化和肺炎的独立预测指标。此外,随着慢性阻塞性肺病严重程度(阶段)的增加,血清 NGAL 水平也会增加,这可能有助于评估慢性阻塞性肺病的严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Osteopontin and NGAL in Differential Diagnosis of Acute Exacerbations of COPD and Pneumonia
Objective: Chronic Obstructive Pulmonary Diesase (COPD) is an inflammatory lung disease that progresses with attacks. Pneumonia is an infectious lung disease that progresses with lung infiltrations. Osteopontin (OP) is a cytokine which participates in inflammation. Neutrophil Gelatinase Associated Lipocalin (NGAL) is an antimicrobial peptide with neutrophil activation and antibacterial properties. In this study, serum OP and NGAL levels were assayed in COPD exacerbation, stabile COPD and pneumonia. The aim of our study is to assess the importance of NGAL and OP levels as biomarkers in the differential diagnosis of COPD and pneumonia. Material and Methods: One hundred twenty consecutive patients who were admitted to our department between May 2011 and August 2013 were included in the study. Serum OP and NGAL levels were measured with ELISA method within 24 hours following the determination of diagnosis. COPD acute exacerbation (AE-COPD) group was comprised of 95 patients (87 male and mean age 69.0±10.6), and the pneumonia group was comprised of 25 patients (16 male and mean age 57.5±22.9). Serum OP and NGAL levels of the patients in the AE-COPD group were re-measured within 30-45 days following acute exacerbation in stabile period. Results: Serum OP levels were higher in the pneumonia group compared to the AE-COPD group (93.47 ng/ml vs 53.10 ng/ml; p<0.001). Multivariate regression analyses indicated that OP levels to be >84 ng/ml is an independent predictor that increases risk for pneumonia more than 8-fold (95% CI, 2.43-26.59). Sensitivity and specificity of OP in the differentiation of pneumonias from AE-COPD were determined to 80% and 92%, respectively. Serum NGAL levels also increased as COPD severity increased and was found to be statistically significant (p: 0.032). Conclusion: It has been indicated that serum osteopontin level can be an independent predictor in differentiating COPD exacerbation from pneumonia. Additionally, as COPD severity (stage) increases, serum NGAL levels also increase, which may be helpful in assessing the severity of COPD.
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