Pulmonary Division, Heart Institute (InCor), University of São Paulo Medical School, Brazil; JundiaíMedical College, São Paulo, Brazil.
Pulmonary Division, Heart Institute (InCor), University of São Paulo Medical School, Brazil.
Chest. 2012 Jan;141(1):183-189. doi: 10.1378/chest.10-3181. Epub 2011 Jun 16.
This study aimed to evaluate a panel of proinflammatory and antiinflammatory cytokines in noncomplicated and complicated parapneumonic pleural effusions and to correlate their levels with pleural fluid biochemical parameters.
Serum and pleural effusion were collected from 60 patients with noncomplicated (n = 26) or complicated (n = 34) parapneumonic effusions and assayed for cytologic, biochemical, and proinflammatory and antiinflammatory cytokines. Student t test was used to compare serum and pleural fluid values, Spearman correlation to analyze the relationship between pleural fluid cytokines and biochemical parameters, and accuracy of pleural fluid cytokine levels to determine the optimal cutoff value for identification of complicated effusions. Corrections for multiple comparisons were applied and a P value < .05 was accepted as significant.
Serum and pleural fluid cytokine levels of IL-8, vascular endothelial growth factor (VEGF), IL-10, and tumor necrosis factor (TNF) soluble receptor (sR) II were similar between groups. In contrast, complicated effusions had higher levels of pleural fluid IL-1β, IL-1 receptor antagonist (ra), and TNF sRI. Negative correlations were found between pleural fluid glucose with IL-1β and TNF sRI and positive correlations between lactic dehydrogenate (LDH) with IL-1β, IL-8, and VEGF. Pleural fluid levels of IL-1β, IL-1ra, and TNF sRI were more accurate than IL-8, VEGF, IL-10, and TNF sRII in discriminating complicated effusions.
Both proinflammatory and antiinflammatory cytokine levels in pleural fluid are elevated in complicated in comparison with noncomplicated parapneumonic pleural effusions, and they correlate with both pleural fluid glucose and LDH levels. IL-1β, IL-1ra, and TNF sRI had higher sensitivity and specificity than IL-8, VEGF, IL-10, and TNF sRII in discriminating complicated effusions.
本研究旨在评估非复杂性和复杂性类肺炎性胸腔积液中的促炎和抗炎细胞因子,并将其水平与胸腔液生化参数相关联。
从 60 例非复杂性(n = 26)或复杂性(n = 34)类肺炎性胸腔积液患者中采集血清和胸腔液,并对其进行细胞学、生化和促炎及抗炎细胞因子检测。采用学生 t 检验比较血清和胸腔液值,采用 Spearman 相关分析评估胸腔液细胞因子与生化参数的关系,并采用胸腔液细胞因子水平的准确性确定用于鉴定复杂性胸腔积液的最佳截断值。应用多重比较校正,P 值 <.05 被认为有统计学意义。
血清和胸腔液细胞因子 IL-8、血管内皮生长因子(VEGF)、IL-10 和肿瘤坏死因子(TNF)可溶性受体(sR)II 在两组之间相似。相比之下,复杂性胸腔积液的胸腔液 IL-1β、IL-1 受体拮抗剂(ra)和 TNF sRI 水平较高。胸腔液葡萄糖与 IL-1β 和 TNF sRI 呈负相关,与乳酸脱氢酶(LDH)呈正相关。与 IL-8、VEGF、IL-10 和 TNF sRII 相比,胸腔液中 IL-1β、IL-1ra 和 TNF sRI 水平在鉴别复杂性胸腔积液方面更准确。
与非复杂性类肺炎性胸腔积液相比,复杂性胸腔积液中胸腔液的促炎和抗炎细胞因子水平均升高,且与胸腔液葡萄糖和 LDH 水平相关。与 IL-8、VEGF、IL-10 和 TNF sRII 相比,IL-1β、IL-1ra 和 TNF sRI 鉴别复杂性胸腔积液的敏感性和特异性更高。