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Exploring the mechanisms of macrolides in cystic fibrosis.

Abstract:
Several studies have reported clinical improvements in cystic fibrosis (CF) patients on macrolide antibiotics although the mechanism of action remains unclear. We conducted an open-label study of azithromycin (500 mg daily for 2 weeks) in 9 adult CF patients to explore 3 possible mechanisms: up-regulation of the multi-drug resistance (MDR) or cystic fibrosis transmembrane regulator (CFTR) proteins, correction of epithelial ion transport and reduced bacterial adherence. End-points included nasal potential difference (PD) measurements, nasal epithelial MDR and CFTR mRNA levels and Pseudomonas aeruginosa adherence to nasal epithelium. Forced expiratory volume in the 1st second (FEV(1)) increased significantly after 2 weeks of azithromycin (pre- 41.1 [5.0]%; post- 44.6 [5.8]%; P<0.05), although improvements in forced vital capacity (FVC) did not reach significance (pre- 61.3 [4.0]%; post- 67.1 [5.4]%, NS). Before treatment all subjects had nasal PD measurements characteristic of CF. Treatment led to no significant group differences in any measures of either sodium absorption or chloride secretion. Neither CFTR nor MDR mRNA levels had altered significantly and the adherence of P. aeruginosa did not decrease. We conclude that these are unlikely to be significant contributing mechanisms accounting for the consistent beneficial results observed in clinical trials of macrolides in CF.
Publication status:
Published

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Publisher copy:
10.1016/j.rmed.2005.07.016

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Lab Sciences
Role:
Author


Journal:
Respiratory medicine More from this journal
Volume:
100
Issue:
4
Pages:
687-697
Publication date:
2006-04-01
DOI:
EISSN:
1532-3064
ISSN:
0954-6111


Language:
English
Keywords:
Pubs id:
pubs:246458
UUID:
uuid:b7a6b202-b5a5-49aa-a79d-1c1b846769bd
Local pid:
pubs:246458
Source identifiers:
246458
Deposit date:
2012-12-19

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