Inhaled corticosteroid normalizes some but not all airway vascular remodeling in COPD.
- Publisher:
- DOVE MEDICAL PRESS LTD
- Publication Type:
- Journal Article
- Citation:
- Int J Chron Obstruct Pulmon Dis, 2016, 11, (1), pp. 2359-2367
- Issue Date:
- 2016
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Full metadata record
| Field | Value | Language |
|---|---|---|
| dc.contributor.author | Soltani, A | |
| dc.contributor.author | Walters, EH | |
| dc.contributor.author | Reid, DW | |
| dc.contributor.author | Shukla, SD | |
| dc.contributor.author | Nowrin, K | |
| dc.contributor.author | Ward, C | |
| dc.contributor.author | Muller, HK | |
| dc.contributor.author | Sohal, SS | |
| dc.date.accessioned | 2022-08-16T22:20:02Z | |
| dc.date.available | 2022-08-16T22:20:02Z | |
| dc.date.issued | 2016 | |
| dc.identifier.citation | Int J Chron Obstruct Pulmon Dis, 2016, 11, (1), pp. 2359-2367 | |
| dc.identifier.issn | 1176-9106 | |
| dc.identifier.issn | 1178-2005 | |
| dc.identifier.uri | http://hdl.handle.net/10453/160392 | |
| dc.description.abstract | BACKGROUND: This study assessed the effects of inhaled corticosteroid (ICS) on airway vascular remodeling in chronic obstructive pulmonary disease (COPD). METHODS: Thirty-four subjects with mild-to-moderate COPD were randomly allocated 2:1 to ICS or placebo treatment in a double-blinded clinical trial over 6 months. Available tissue was compared before and after treatment for vessel density, and expression of VEGF, TGF-β1, and TGF-β1-related phosphorylated transcription factors p-SMAD 2/3. This clinical trial has been registered and allocated with the Australian New Zealand Clinical Trials Registry (ANZCTR) on 17/10/2012 with reference number ACTRN12612001111864. RESULTS: There were no significant baseline differences between treatment groups. With ICS, vessels and angiogenic factors did not change in hypervascular reticular basement membrane, but in the hypovascular lamina propria (LP), vessels increased and this had a proportionate effect on lung air trapping. There was modest evidence for a reduction in LP vessels staining for VEGF with ICS treatment, but a marked and significant reduction in p-SMAD 2/3 expression. CONCLUSION: Six-month high-dose ICS treatment had little effect on hypervascularity or angiogenic growth factors in the reticular basement membrane in COPD, but normalized hypovascularity in the LP, and this was physiologically relevant, though accompanied by a paradoxical reduction in growth factor expression. | |
| dc.format | Electronic-eCollection | |
| dc.language | eng | |
| dc.publisher | DOVE MEDICAL PRESS LTD | |
| dc.relation.ispartof | Int J Chron Obstruct Pulmon Dis | |
| dc.relation.isbasedon | 10.2147/COPD.S113176 | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | 1102 Cardiorespiratory Medicine and Haematology | |
| dc.subject.classification | Respiratory System | |
| dc.subject.mesh | Administration, Inhalation | |
| dc.subject.mesh | Adrenal Cortex Hormones | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Aged | |
| dc.subject.mesh | Anti-Inflammatory Agents | |
| dc.subject.mesh | Australia | |
| dc.subject.mesh | Bronchodilator Agents | |
| dc.subject.mesh | Double-Blind Method | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Fluticasone | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Lung | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Phosphorylation | |
| dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
| dc.subject.mesh | Smad2 Protein | |
| dc.subject.mesh | Smad3 Protein | |
| dc.subject.mesh | Time Factors | |
| dc.subject.mesh | Transforming Growth Factor beta1 | |
| dc.subject.mesh | Treatment Outcome | |
| dc.subject.mesh | Vascular Endothelial Growth Factor A | |
| dc.subject.mesh | Vascular Remodeling | |
| dc.subject.mesh | Lung | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
| dc.subject.mesh | Adrenal Cortex Hormones | |
| dc.subject.mesh | Vascular Endothelial Growth Factor A | |
| dc.subject.mesh | Bronchodilator Agents | |
| dc.subject.mesh | Anti-Inflammatory Agents | |
| dc.subject.mesh | Treatment Outcome | |
| dc.subject.mesh | Administration, Inhalation | |
| dc.subject.mesh | Double-Blind Method | |
| dc.subject.mesh | Phosphorylation | |
| dc.subject.mesh | Time Factors | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Aged | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Australia | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Smad2 Protein | |
| dc.subject.mesh | Smad3 Protein | |
| dc.subject.mesh | Transforming Growth Factor beta1 | |
| dc.subject.mesh | Vascular Remodeling | |
| dc.subject.mesh | Fluticasone | |
| dc.title | Inhaled corticosteroid normalizes some but not all airway vascular remodeling in COPD. | |
| dc.type | Journal Article | |
| utslib.citation.volume | 11 | |
| utslib.location.activity | New Zealand | |
| utslib.for | 1102 Cardiorespiratory Medicine and Haematology | |
| pubs.organisational-group | /University of Technology Sydney | |
| pubs.organisational-group | /University of Technology Sydney/Faculty of Health | |
| utslib.copyright.status | open_access | * |
| dc.date.updated | 2022-08-16T22:20:00Z | |
| pubs.issue | 1 | |
| pubs.publication-status | Published online | |
| pubs.volume | 11 | |
| utslib.citation.issue | 1 |
Abstract:
BACKGROUND: This study assessed the effects of inhaled corticosteroid (ICS) on airway vascular remodeling in chronic obstructive pulmonary disease (COPD). METHODS: Thirty-four subjects with mild-to-moderate COPD were randomly allocated 2:1 to ICS or placebo treatment in a double-blinded clinical trial over 6 months. Available tissue was compared before and after treatment for vessel density, and expression of VEGF, TGF-β1, and TGF-β1-related phosphorylated transcription factors p-SMAD 2/3. This clinical trial has been registered and allocated with the Australian New Zealand Clinical Trials Registry (ANZCTR) on 17/10/2012 with reference number ACTRN12612001111864. RESULTS: There were no significant baseline differences between treatment groups. With ICS, vessels and angiogenic factors did not change in hypervascular reticular basement membrane, but in the hypovascular lamina propria (LP), vessels increased and this had a proportionate effect on lung air trapping. There was modest evidence for a reduction in LP vessels staining for VEGF with ICS treatment, but a marked and significant reduction in p-SMAD 2/3 expression. CONCLUSION: Six-month high-dose ICS treatment had little effect on hypervascularity or angiogenic growth factors in the reticular basement membrane in COPD, but normalized hypovascularity in the LP, and this was physiologically relevant, though accompanied by a paradoxical reduction in growth factor expression.
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