eprintid: 20193
rev_number: 12
eprint_status: archive
userid: 1589
dir: disk0/00/02/01/93
datestamp: 2016-02-24 13:47:34
lastmod: 2024-05-17 16:41:07
status_changed: 2016-02-24 13:47:34
type: article
metadata_visibility: show
creators_name: Droste, Annette S.
creators_name: Rohde, David
creators_name: Völkers, Mirko
creators_name: Filusch, Arthur
creators_name: Bruckner, Thomas
creators_name: Borst, Mathias Maximilian
creators_name: Katus, Hugo A.
creators_name: Meyer, F. Joachim
title: Endothelin receptor antagonist and airway dysfunction in pulmonary arterial hypertension
subjects: ddc-610
divisions: i-910100
divisions: i-911800
abstract: Background: In idiopathic pulmonary arterial hypertension (IPAH), peripheral airway obstruction is frequent. This is partially attributed to the mediator dysbalance, particularly an excess of endothelin-1 (ET-1), to increased pulmonary vascular and airway tonus and to local inflammation. Bosentan (ET-1 receptor antagonist) improves pulmonary hemodynamics, exercise limitation, and disease severity in IPAH. We hypothesized that bosentan might affect airway obstruction.   Methods: In 32 IPAH-patients (19 female, WHO functional class II (n = 10), III (n = 22); (data presented as mean ± standard deviation) pulmonary vascular resistance (11 ± 5 Wood units), lung function, 6 minute walk test (6-MWT; 364 ± 363.7 (range 179.0-627.0) m), systolic pulmonary artery pressure, sPAP, 79 ± 19 mmHg), and NT-proBNP serum levels (1427 ± 2162.7 (range 59.3-10342.0) ng/L) were measured at baseline, after 3 and 12 months of oral bosentan (125 mg twice per day).   Results and Discussion: At baseline, maximal expiratory flow at 50 and 25% vital capacity were reduced to 65 ± 25 and 45 ± 24% predicted. Total lung capacity was 95.6 ± 12.5% predicted and residual volume was 109 ± 21.4% predicted. During 3 and 12 months of treatment, 6-MWT increased by 32 ± 19 and 53 ± 69 m, respectively; p < 0.01; whereas sPAP decreased by 7 ± 14 and 10 ± 19 mmHg, respectively; p < 0.05. NT-proBNP serum levels tended to be reduced by 123 ± 327 and by 529 ± 1942 ng/L; p = 0.11). There was no difference in expiratory flows or lung volumes during 3 and 12 months.   Conclusion: This study gives first evidence in IPAH, that during long-term bosentan, improvement of hemodynamics, functional parameters or serum biomarker occur independently from persisting peripheral airway obstruction.
date: 2009-12-30
publisher: BioMed Central
id_scheme: DOI
ppn_swb: 1655995804
own_urn: urn:nbn:de:bsz:16-heidok-201938
language: eng
bibsort: DROSTEANNEENDOTHELIN20091230
full_text_status: public
publication: Respiratory Research
volume: 10
number: 129
place_of_pub: London
pagerange: 1-7
issn: 1465-993X
citation:   Droste, Annette S. ; Rohde, David ; Völkers, Mirko ; Filusch, Arthur ; Bruckner, Thomas ; Borst, Mathias Maximilian ; Katus, Hugo A. ; Meyer, F. Joachim  (2009) Endothelin receptor antagonist and airway dysfunction in pulmonary arterial hypertension.  Respiratory Research, 10 (129).  pp. 1-7.  ISSN 1465-993X     
document_url: https://archiv.ub.uni-heidelberg.de/volltextserver/20193/1/12931_2009_Article_843.pdf