Airway ion transport impacts on disease presentation and severity in cystic fibrosis

被引:14
作者
Leal, Teresinha [1 ]
Fajac, Isabelle [2 ]
Wallace, Helen L. [3 ]
Lebecque, Patrick [1 ]
Lebacq, Jean [1 ]
Hubert, Dominique [2 ]
Dall'Ava, Josette [2 ]
Dusser, Daniel [2 ]
Ganesan, Anusha P. [3 ]
Knoop, Christiane [4 ]
Cumps, Jean [1 ]
Wallemacq, Pierre [1 ]
Southern, Kevin W. [3 ]
机构
[1] Catholic Univ Louvain, B-1200 Brussels, Belgium
[2] Univ Paris 05, Cochin Hosp, AP HP, Paris, France
[3] Univ Liverpool, Inst Child Hlth, Liverpool L69 3BX, Merseyside, England
[4] Univ Libre Bruxelles, Brussels, Belgium
关键词
cystic fibrosis; CFTR; membrane potentials; ion transport;
D O I
10.1016/j.clinbiochem.2008.03.013
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Abnormal airway ion transport is a feature of cystic fibrosis. The aim of this study was to investigate whether distinct components of ion transport are associated with the clinical expression and severity of the disease. Design and methods: Univariate and multivariate analyses were used to study interaction effects between nasal potential difference parameters and clinical status, recorded at stable conditions, in 75 F508del homozygous young adults. Results: All patients demonstrated increased sodium and reduced chloride conductances. Less sodium transport abnormalities were related to better respiratory function and nutrition. Presentation with digestive symptoms at diagnosis was associated with lower chloride conductance. With an accuracy of 85% good nutritional status was linked to more preserved lung function, increasing age and more preserved chloride conductance. Conclusions: Ion transport abnormalities have distinct clinical outcomes. Sodium conductance relates to respiratory function and nutrition; chloride conductance to nutrition and presentation with digestive symptoms at diagnosis. (C) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:764 / 772
页数:9
相关论文
共 46 条
[1]   Use of nasal potential difference and sweat chloride as outcome measures in multicenter clinical trials in subjects with cystic fibrosis [J].
Ahrens, RC ;
Standaert, TA ;
Launspach, J ;
Han, SH ;
Teresi, ME ;
Aitken, ML ;
Kelley, TJ ;
Hilliard, KA ;
Milgram, LJH ;
Konstan, MW ;
Weatherly, MR ;
McCarty, NA .
PEDIATRIC PULMONOLOGY, 2002, 33 (02) :142-150
[2]  
ALTON EWFW, 1990, EUR RESPIR J, V3, P922
[3]   Airway surface dehydration in cystic fibrosis: Pathogenesis and therapy [J].
Boucher, Richard C. .
ANNUAL REVIEW OF MEDICINE, 2007, 58 :157-170
[4]  
Bronsveld I, 2001, J CLIN INVEST, V108, P1705
[5]   Neutrophil elastase activates near-silent epithelial Na+ channels and increases airway epithelial Na+ transport [J].
Caldwell, RA ;
Boucher, RC ;
Stutts, MJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2005, 288 (05) :L813-L819
[6]  
CLANCY JP, 2006, PEDIATR PULM, V29, P301
[7]   RELATIONSHIP OF A NON-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR-MEDIATED CHLORIDE CONDUCTANCE TO ORGAN-LEVEL DISEASE IN CFTR(-/-) MICE [J].
CLARKE, LL ;
GRUBB, BR ;
YANKASKAS, JR ;
COTTON, CU ;
MCKENZIE, A ;
BOUCHER, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :479-483
[8]   Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis:: a European consensus [J].
Döring, G ;
Conway, SP ;
Heijerman, HGM ;
Hodson, ME ;
Hoiby, N ;
Smyth, A ;
Touw, DJ .
EUROPEAN RESPIRATORY JOURNAL, 2000, 16 (04) :749-767
[9]   Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients [J].
Dray-Charier, N ;
Paul, A ;
Scoazec, JY ;
Veissière, D ;
Mergey, M ;
Capeau, J ;
Soubrane, O ;
Housset, C .
HEPATOLOGY, 1999, 29 (06) :1624-1634
[10]   Relationships between nasal potential difference and respiratory function in adults with cystic fibrosis [J].
Fajac, I ;
Hubert, D ;
Bienvenu, T ;
Richaud-Thiriez, B ;
Matran, R ;
Kaplan, JC ;
Dall'Ava-Santucci, J ;
Dusser, DJ .
EUROPEAN RESPIRATORY JOURNAL, 1998, 12 (06) :1295-1300