首页> 外文期刊>Pediatric Pulmonology >Serial changes in levels of IL-6 and IL-1beta in premature infants at risk for bronchopulmonary dysplasia.
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Serial changes in levels of IL-6 and IL-1beta in premature infants at risk for bronchopulmonary dysplasia.

机译:处于支气管肺发育异常风险的早产儿中IL-6和IL-1beta水平的系列变化。

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The aim of this study was to define the inflammatory changes occurring in the lungs of infants at risk for bronchopulmonary dysplasia (BPD) over the first 28 days of life, and to define an optimal strategy for steroids therapy in the prevention of BPD. We measured levels of interleukin-6 (IL-6) and interleukin-1 beta (IL-1beta) in tracheal aspirate (TA) samples and blood of premature infants with severe respiratory distress syndrome RDS (n = 45) on the first day of life prior to initiation of surfactant therapy and on days 5-7, 12-14, 19-21, and 26-28. Levels of IL-6 and IL-1beta were determined with a commercially available enzyme-linked immunoassay. Logistic regression analyses were performed in order to examine differences in trends in levels of IL-6 and IL-1beta between groups of infants. Infants were divided into group I (n = 30, FiO(2) < or = 0.35 at 28 days) and group II (n = 15, FiO(2) > 0.35 based on their likelihood of developing BPD at 36 weeks postconceptional age (PCA). The infants were comparable with respect to mean ( +/- SEM) birth weight (895 +/- 33 g vs. 900 +/- 40 g), gestational age (27 +/- 0.38 weeks vs. 27 +/- 0.54 weeks), and severity of respiratory illness at entry into the study (mean airway pressure: 12 +/- 1 cmH(2)O vs. 12 +/- 1 cmH(2)O, and oxygen index: 15 +/- 2 vs. 19 +/- 4) (group I vs. group II, respectively). Logistic regression analyses failed to reveal any significant differences in linear trends of levels of IL-6 and IL-1beta in TA samples between both groups of infants. No particular pattern of change in levels of IL-6 or IL-1beta could be identified among groups of infants. Levels of IL-6 and IL-1beta in TA samples on the first day of life failed to predict the need for FiO(2) > 0.35 at 28 days of age. We could not identify an increasing trend or a specific pattern of changes in postnatal levels of IL-6 or IL-1beta in TA samples of infants who were at greater risk of developing BPD at 36 weeks PCA compared to infants who were not. Copyright 2001 Wiley-Liss, Inc.
机译:这项研究的目的是确定在生命的前28天中处于患支气管肺发育不良(BPD)风险的婴儿的肺部发生的炎症变化,并确定类固醇治疗预防BPD的最佳策略。在第一天的严重呼吸窘迫综合征RDS(n = 45)的早产儿气管抽吸物(TA)和血液中,我们测量了IL-6(IL-6)和IL-1β(IL-1beta)的水平。在开始表面活性剂治疗之前和第5-7、12-14、19-21和26-28天的生命。用可商购的酶联免疫测定法测定IL-6和IL-1β的水平。进行逻辑回归分析以检查婴儿组之间IL-6和IL-1beta水平趋势的差异。根据婴儿在受孕后36周出现BPD的可能性,将其分为I组(n = 30,FiO(2)<或= 0.35,28天)和II组(n = 15,FiO(2)> 0.35)(这些婴儿的平均出生体重(+/- SEM)(895 +/- 33 g vs. 900 +/- 40 g),胎龄(27 +/- 0.38周vs. 27 + /)相当。 -0.54周),以及进入研究时的呼吸系统疾病严重程度(平均气道压力:12 +/- 1 cmH(2)O与12 +/- 1 cmH(2)O,氧气指数:15 + / -2 vs. 19 +/- 4)(分别为I组和II组)。Logistic回归分析未能揭示两组TA样品中IL-6和IL-1beta水平线性趋势的任何显着差异。婴儿组中没有发现IL-6或IL-1beta水平变化的特殊模式,出生后第一天TA样品中的IL-6和IL-1beta水平无法预测是否需要FiO (2)在28天龄时> 0.35。相比于没有婴儿的婴儿,在36周PCA患BPD的风险更大的婴儿的TA样本中,IL或IL-6或IL-1beta水平的变化趋势或特定变化模式。版权所有2001 Wiley-Liss,Inc.

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