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本文引用的文献

1
Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR.依伐卡托特对 G551D-CFTR 囊性纤维化患者黏液清除功能和临床结局的影响。
JCI Insight. 2018 Dec 20;3(24):122695. doi: 10.1172/jci.insight.122695.
2
Overnight delivery of hypertonic saline by nasal cannula aerosol for cystic fibrosis.经鼻导管雾化高渗盐水用于囊性纤维化的夜间给药
Pediatr Pulmonol. 2017 Sep;52(9):1142-1149. doi: 10.1002/ppul.23749. Epub 2017 Jul 24.
3
Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung.囊性纤维化肺部的铜绿假单胞菌感染以及黏液纤毛清除和吸收性清除
Eur Respir J. 2016 May;47(5):1392-401. doi: 10.1183/13993003.01880-2015. Epub 2016 Mar 23.
4
Effect of Posture on Regional Deposition of Coarse Particles in the Healthy Human Lung.姿势对健康人肺部粗颗粒区域沉积的影响。
J Aerosol Med Pulm Drug Deliv. 2015 Dec;28(6):423-31. doi: 10.1089/jamp.2014.1189. Epub 2015 Mar 31.
5
Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis.囊性纤维化跨膜传导调节因子增强剂依伐卡托在G551D介导的囊性纤维化中的临床机制
Am J Respir Crit Care Med. 2014 Jul 15;190(2):175-84. doi: 10.1164/rccm.201404-0703OC.
6
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Eur Respir J. 2014 Sep;44(3):675-84. doi: 10.1183/09031936.00220513. Epub 2014 Apr 17.
7
Sweat chloride as a biomarker of CFTR activity: proof of concept and ivacaftor clinical trial data.汗液氯化物作为囊性纤维化跨膜传导调节因子(CFTR)活性的生物标志物:概念验证及依伐卡托临床试验数据
J Cyst Fibros. 2014 Mar;13(2):139-47. doi: 10.1016/j.jcf.2013.09.007.
8
Mucus removal is impaired in children with cystic fibrosis who have been infected by Pseudomonas aeruginosa.黏液清除功能受损在感染铜绿假单胞菌的囊性纤维化患儿中较为常见。
J Pediatr. 2014 Apr;164(4):839-45. doi: 10.1016/j.jpeds.2013.11.031. Epub 2013 Dec 24.
9
Multisite comparison of mucociliary and cough clearance measures using standardized methods.使用标准化方法进行黏液纤毛清除和咳嗽清除措施的多中心比较。
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Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airway.液体超吸收导致囊性纤维化气道中 DTPA 清除率增加。
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囊性纤维化肺部的多探针核成像作为治疗效果的生物标志物。

Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

机构信息

1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.

2Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania.

出版信息

J Aerosol Med Pulm Drug Deliv. 2019 Aug;32(4):242-249. doi: 10.1089/jamp.2018.1491. Epub 2019 Apr 10.

DOI:10.1089/jamp.2018.1491
PMID:30969149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6685188/
Abstract

Nuclear imaging biomarkers illustrate unique aspects of lung physiology and are useful for assessing therapeutic effects in cystic fibrosis (CF) lung disease. We have developed a multiprobe method to simultaneously measure mucociliary clearance (MCC) and paracellular absorption (ABS). MCC is a direct measure of mucus clearance. ABS has been related to airway surface liquid (ASL) absorption through previous studies. We describe baseline factors affecting MCC and ABS using data from a retrospective group ( = 22) and the response of the measures to inhaled 7% hypertonic saline (HS) and dry powder mannitol using data from a prospective group ( = 7). A retrospective healthy group ( = 15) is also described. The and groups performed single measurements of MCC/ABS. The group performed baseline measurements of MCC/ABS and measurements after each intervention. ABS was correlated (Spearman's  = 0.51,  = 0.06) to sweat chloride, a systemic measure of cystic fibrosis transmembrane conductance regulator (CFTR) function, whereas MCC was not. Baseline MCC was depressed after infection as we have previously described. MCC provided a more sensitive indication of therapeutic effect and indicated improved clearance with mannitol compared with HS. MCC provides a useful and well-established means of testing therapies directed at improving mucus clearance in the lung. ABS may provide a means of detecting local changes in ASL absorption and CFTR function in the lung. Both are useful tools for studying the key aspects of CF lung pathophysiology (ASL hyperabsorption and MCC depression) that link the basic genetic defects of CF to disease manifestations in the lung.

摘要

核医学成像生物标志物可阐明肺部生理学的独特方面,有助于评估囊性纤维化 (CF) 肺部疾病的治疗效果。我们开发了一种多探针方法,可同时测量黏液清除率 (MCC) 和经细胞旁途径的吸收 (ABS)。MCC 是黏液清除的直接测量指标。先前的研究表明,ABS 与气道表面液体 (ASL) 吸收有关。我们使用回顾性队列 ( = 22) 的数据描述了影响 MCC 和 ABS 的基线因素,以及前瞻性队列 ( = 7) 的数据来描述这些指标对吸入 7%高渗盐水 (HS) 和干粉甘露醇的反应。还描述了一个回顾性的健康队列 ( = 15)。 和 队列分别进行了 MCC/ABS 的单次测量。 队列进行了 MCC/ABS 的基线测量和每次干预后的测量。 基线 MCC 在 感染后下降,正如我们之前所描述的那样。MCC 对治疗效果的指示更敏感,与 HS 相比,甘露醇可改善清除率。MCC 为测试旨在改善肺部黏液清除的治疗方法提供了一种有用且成熟的方法。ABS 可能提供一种检测肺部 ASL 吸收和 CFTR 功能局部变化的方法。两者都是研究 CF 肺部病理生理学关键方面 (ASL 过度吸收和 MCC 下降) 的有用工具,这些方面将 CF 的基本遗传缺陷与肺部疾病表现联系起来。