特应性哮喘患儿俱乐部(Clara)细胞蛋白(CC16)表达的研究

IF 0.2 Q4 ALLERGY
Rasha H. El-Owaidy, G. Shousha, Heba‐Tullah M. M. Hamza, N. Lotfy, Rana Zakaria, Slma Badr, E. Hossny
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引用次数: 0

摘要

背景:据报道,俱乐部细胞(Clara细胞)分泌的CC16蛋白在急性呼吸窘迫综合征和慢性阻塞性肺病中失调。我们试图研究哮喘儿童的血清和尿液CC16与哮喘发作和静止的关系,并将其与肺功能测试结果相关联。方法:这项前瞻性对照研究在艾因沙姆斯大学儿童医院儿科过敏、免疫学和风湿病科进行,研究对象为40名6-12岁的特应性哮喘患者和40名匹配的健康对照,研究时间为2020年3月至2021年8月。患者在哮喘发作期间连续入组,并在哮喘静止时进行随访以重新评估。对患者进行临床评估、常见空气过敏原皮肤点刺试验、肺功能试验,以及在哮喘发作和静止期间通过ELISA测量血清和尿液CC16。结果:哮喘发作期(中位数分别为243.5和137.5 ng/ml)和静止期(中位数为112.5和55 ng/ml)患者的血清和尿液CC16水平显著高于匹配对照组(中位数为15和13 ng/ml)。此外,急性发作期血清和尿CC16水平高于静止期(z分别为-5.214和4941,p值<0.001)。尿CC16与预测的最佳FVC%呈显著负相关(r=-0.408,p=0.009),但与年龄、BMI、哮喘发作年龄、病程无显著相关性。结论:哮喘患儿血清和尿CC16水平升高,尤其是在哮喘加重期。测量尿液中的CC16可能是一种非侵入性的选择,可以取代血液采样。需要进一步更大规模的研究,包括及时测量CC16,以有效评估CC16作为哮喘恶化生物标志物的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A study of club (Clara) cell protein (CC16) expression in a group of atopic asthmatic children
of the CC16 gene was suggested to increase the risk of developing Background : The dysregulation of CC16 protein secreted by club cells (Clara cells) was reported in acute respiratory distress syndrome and Chronic obstructive pulmonary disease. We sought to investigate serum and urinary CC16 in asthmatic children in relation to asthma exacerbation and quiescence and correlate it to pulmonary function test results. Methods: This prospective controlled study was conducted in the Pediatric Allergy, Immunology and Rheumatology Unit, Children’s Hospital, Ain Shams University on 40 atopic asthmatic patients, 6-12 years old, and 40 matched healthy controls, during the period from March 2020 to August 2021. Patients were enrolled consecutively during an asthma flare and were followed up to be re-evaluated at asthma quiescence. Patients were subjected to clinical assessment, skin prick testing to common aeroallergens, pulmonary function testing, and measurement of serum and urinary CC16 by ELISA during asthma exacerbation and quiescence . Results: Serum and urinary CC16 levels in patients during asthma exacerbation (median 243.5 and 137.5 ng/ml, respectively) and quiescence (median 112.5 and 55 ng/ml) were significantly higher than the levels in matched controls (median 15 and 13 ng/ml). Moreover, serum and urinary CC16 levels were higher during exacerbation than during quiescence (z=-5.214 and 4,941 respectively, p values < 0.001). Urinary CC16 showed significant inverse correlation with best FVC% of predicted (r=-0.408, p= 0.009), but no significant correlation was found with age, BMI, age of onset of asthma, disease duration . Conclusion: Serum and urinary CC16 levels seem to be elevated in asthmatic children especially during asthma exacerbation. Measurement of CC16 in urine might represent a non-invasive option that can replace blood sampling. Further wider scale studies involving timely measurements of CC16 are needed to efficiently assess the role of CC16 as a biomarker of asthma exacerbation .
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