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Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD

Hyperinflation contributes to dyspnea intensity in COPD. Little is known about the molecular mechanisms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of COPD pathophysiology. To investigate the effect of ICS/long-acting β$_{2}$-agonist (LABA) treatment...

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Autores principales: Faiz, Alen, Imkamp, Kai, van der Wiel, Erica, Boudewijn, Ilse M, Koppelman, Gerard H, Brandsma, Corry-Anke, Kerstjens, Huib A M, Timens, Wim, Vroegop, Sebastiaan, Pasma, Henk R, Boersma, Wim G, Wielders, Pascal, van den Elshout, Frank, Mansour, Khaled, Steiling, Katrina, Spira, Avrum, Lenburg, Marc E, Heijink, Irene H, Postma, Dirkje S, van den Berge, Maarten
Lenguaje:eng
Publicado: 2020
Acceso en línea:https://dx.doi.org/10.1038/s41598-020-72551-0
http://cds.cern.ch/record/2744727
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author Faiz, Alen
Imkamp, Kai
van der Wiel, Erica
Boudewijn, Ilse M
Koppelman, Gerard H
Brandsma, Corry-Anke
Kerstjens, Huib A M
Timens, Wim
Vroegop, Sebastiaan
Pasma, Henk R
Boersma, Wim G
Wielders, Pascal
van den Elshout, Frank
Mansour, Khaled
Steiling, Katrina
Spira, Avrum
Lenburg, Marc E
Heijink, Irene H
Postma, Dirkje S
van den Berge, Maarten
author_facet Faiz, Alen
Imkamp, Kai
van der Wiel, Erica
Boudewijn, Ilse M
Koppelman, Gerard H
Brandsma, Corry-Anke
Kerstjens, Huib A M
Timens, Wim
Vroegop, Sebastiaan
Pasma, Henk R
Boersma, Wim G
Wielders, Pascal
van den Elshout, Frank
Mansour, Khaled
Steiling, Katrina
Spira, Avrum
Lenburg, Marc E
Heijink, Irene H
Postma, Dirkje S
van den Berge, Maarten
author_sort Faiz, Alen
collection CERN
description Hyperinflation contributes to dyspnea intensity in COPD. Little is known about the molecular mechanisms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of COPD pathophysiology. To investigate the effect of ICS/long-acting β$_{2}$-agonist (LABA) treatment on both lung function measures of hyperinflation, and the nasal epithelial gene-expression profile in severe COPD. 117 patients were screened and 60 COPD patients entered a 1-month run-in period on low-dose ICS/LABA budesonide/formoterol (BUD/F) 200/6 one inhalation b.i.d. Patients were then randomly assigned to 3-month treatment with either a high dose BDP/F 100/6 two inhalations b.i.d. (n = 31) or BUD/F 200/6 two inhalations b.i.d. (n = 29). Lung function measurements and nasal epithelial gene-expression were assessed before and after 3-month treatment and validated in independent datasets. After 3-month ICS/LABA treatment, residual volume (RV)/total lung capacity (TLC)% predicted was reduced compared to baseline (p < 0.05). We identified a nasal gene-expression signature at screening that associated with higher RV/TLC% predicted values. This signature, decreased by ICS/LABA treatment was enriched for genes associated with increased p53 mediated apoptosis was replicated in bronchial biopsies of COPD patients. Finally, this signature was increased in COPD patients compared to controls in nasal, bronchial and small airways brushings. Short-term ICS/LABA treatment improves RV/TLC% predicted in severe COPD. Furthermore, it decreases the expression of genes involved in the signal transduction by the p53 class mediator, which is a replicable COPD gene expression signature in the upper and lower airways.Trial registration: ClinicalTrials.gov registration number NCT01351792 (registration date May 11, 2011), ClinicalTrials.gov registration number NCT00848406 (registration date February 20, 2009), ClinicalTrials.gov registration number NCT00158847 (registration date September 12, 2005).
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institution Organización Europea para la Investigación Nuclear
language eng
publishDate 2020
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spelling oai-inspirehep.net-18236502020-11-17T20:25:12Zdoi:10.1038/s41598-020-72551-0http://cds.cern.ch/record/2744727engFaiz, AlenImkamp, Kaivan der Wiel, EricaBoudewijn, Ilse MKoppelman, Gerard HBrandsma, Corry-AnkeKerstjens, Huib A MTimens, WimVroegop, SebastiaanPasma, Henk RBoersma, Wim GWielders, Pascalvan den Elshout, FrankMansour, KhaledSteiling, KatrinaSpira, AvrumLenburg, Marc EHeijink, Irene HPostma, Dirkje Svan den Berge, MaartenIdentifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPDHyperinflation contributes to dyspnea intensity in COPD. Little is known about the molecular mechanisms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of COPD pathophysiology. To investigate the effect of ICS/long-acting β$_{2}$-agonist (LABA) treatment on both lung function measures of hyperinflation, and the nasal epithelial gene-expression profile in severe COPD. 117 patients were screened and 60 COPD patients entered a 1-month run-in period on low-dose ICS/LABA budesonide/formoterol (BUD/F) 200/6 one inhalation b.i.d. Patients were then randomly assigned to 3-month treatment with either a high dose BDP/F 100/6 two inhalations b.i.d. (n = 31) or BUD/F 200/6 two inhalations b.i.d. (n = 29). Lung function measurements and nasal epithelial gene-expression were assessed before and after 3-month treatment and validated in independent datasets. After 3-month ICS/LABA treatment, residual volume (RV)/total lung capacity (TLC)% predicted was reduced compared to baseline (p < 0.05). We identified a nasal gene-expression signature at screening that associated with higher RV/TLC% predicted values. This signature, decreased by ICS/LABA treatment was enriched for genes associated with increased p53 mediated apoptosis was replicated in bronchial biopsies of COPD patients. Finally, this signature was increased in COPD patients compared to controls in nasal, bronchial and small airways brushings. Short-term ICS/LABA treatment improves RV/TLC% predicted in severe COPD. Furthermore, it decreases the expression of genes involved in the signal transduction by the p53 class mediator, which is a replicable COPD gene expression signature in the upper and lower airways.Trial registration: ClinicalTrials.gov registration number NCT01351792 (registration date May 11, 2011), ClinicalTrials.gov registration number NCT00848406 (registration date February 20, 2009), ClinicalTrials.gov registration number NCT00158847 (registration date September 12, 2005).oai:inspirehep.net:18236502020
spellingShingle Faiz, Alen
Imkamp, Kai
van der Wiel, Erica
Boudewijn, Ilse M
Koppelman, Gerard H
Brandsma, Corry-Anke
Kerstjens, Huib A M
Timens, Wim
Vroegop, Sebastiaan
Pasma, Henk R
Boersma, Wim G
Wielders, Pascal
van den Elshout, Frank
Mansour, Khaled
Steiling, Katrina
Spira, Avrum
Lenburg, Marc E
Heijink, Irene H
Postma, Dirkje S
van den Berge, Maarten
Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title_full Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title_fullStr Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title_full_unstemmed Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title_short Identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe COPD
title_sort identifying a nasal gene expression signature associated with hyperinflation and treatment response in severe copd
url https://dx.doi.org/10.1038/s41598-020-72551-0
http://cds.cern.ch/record/2744727
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