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重组人脱氧核糖核酸酶对囊性纤维化患儿肺清除指数的影响:来自一组病例的经验教训

Effect of Dornase Alfa on the Lung Clearance Index in Children with Cystic Fibrosis: A Lesson from a Case Series.

作者信息

Terlizzi Vito, Parisi Giuseppe Fabio, Ferrari Beatrice, Castellani Chiara, Manti Sara, Leonardi Salvatore, Taccetti Giovanni

机构信息

Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Meyer Children's Hospital, 50139 Florence, Italy.

Pediatric Respiratory and Cystic Fibrosis Unit, Department of Clinical and Experimental Medicine, San Marco Hospital, University of Catania, 95121 Catania, Italy.

出版信息

Children (Basel). 2022 Oct 26;9(11):1625. doi: 10.3390/children9111625.

Abstract

BACKGROUND

Dornase alfa (DNase) is the only mucus-degrading agent that has proven efficacy in cystic fibrosis (CF). Few studies have evaluated the effects of DNase on the lung clearance index (LCI). We report the experience of two CF centers in which LCI monitoring was used to evaluate the efficacy of DNase therapy.

METHODS

This is a prospective and observational study, evaluating the effects of DNase therapy on LCI values in three CF children followed at CF centers in Florence and Catania, Italy. In both centers, LCI was performed routinely, every 3-6 months, based on the clinical picture and severity of the lung disease. In this study, we evaluated the LCI before and after long-term DNase therapy.

RESULTS

DNase improved LCI values in the absence of respiratory exacerbations: in case n. 1 LCI decreased by 39% in 16 months (from 11.1 to 6.8); in case n. 2 by 20% in 12 months (from 9.3 to 7.4); in case n. 3 by 24% in 16 months (from 9.3 to 7.0).

CONCLUSIONS

This case series confirms the efficacy of DNase therapy in CF children, as demonstrated by the LCI reduction in treated patients. Furthermore, our results suggest that LCI is a sensitive marker of disease and can be used for the evaluation of response to treatment.

摘要

背景

Dornase alfa(重组人脱氧核糖核酸酶)是唯一已被证实对囊性纤维化(CF)有效的黏液降解剂。很少有研究评估重组人脱氧核糖核酸酶对肺清除指数(LCI)的影响。我们报告了两个CF中心的经验,其中LCI监测用于评估重组人脱氧核糖核酸酶治疗的疗效。

方法

这是一项前瞻性观察性研究,评估重组人脱氧核糖核酸酶治疗对在意大利佛罗伦萨和卡塔尼亚的CF中心随访的3名CF儿童LCI值的影响。在两个中心,根据临床情况和肺部疾病的严重程度,每3 - 6个月定期进行LCI检测。在本研究中,我们评估了长期重组人脱氧核糖核酸酶治疗前后的LCI。

结果

在没有呼吸道加重的情况下,重组人脱氧核糖核酸酶改善了LCI值:病例1中,16个月内LCI下降了39%(从11.1降至6.8);病例2中,12个月内下降了20%(从9.3降至7.4);病例3中,16个月内下降了24%(从9.3降至7.0)。

结论

该病例系列证实了重组人脱氧核糖核酸酶治疗对CF儿童的疗效,治疗患者的LCI降低证明了这一点。此外,我们的结果表明LCI是疾病的敏感标志物,可用于评估治疗反应。

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本文引用的文献

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Cystic fibrosis.囊性纤维化。
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