Serum biomarkers and outcomes in patients with moderate COPD: a substudy of the randomised SUMMIT trial.


Journal

BMJ open respiratory research
ISSN: 2052-4439
Titre abrégé: BMJ Open Respir Res
Pays: England
ID NLM: 101638061

Informations de publication

Date de publication:
2019
Historique:
received: 20 03 2019
revised: 29 03 2019
entrez: 2 7 2019
pubmed: 2 7 2019
medline: 2 7 2019
Statut: epublish

Résumé

Systemic levels of C reactive protein (CRP), surfactant protein D (SPD), fibrinogen, soluble receptor of activated glycogen end-product (sRAGE) and club cell protein 16 (CC-16) have been associated with chronic obstructive pulmonary disease (COPD) outcomes. However, they require validation in different cohorts. Relate systemic levels of those proteins to forced expiratory volume in 1 s (FEV Participants were randomised to daily inhalations of placebo, vilanterol 25 µg (VI), fluticasone furoate 100 µg (FF) or their combination (VI 25/FF 100) and followed quarterly until 1000 deaths in the overall 16 485 participants occurred. Biomarker blood samples were available from 1673 patients. The FEV Systemic levels of CC-16, CRP, sRAGE, SPD and fibrinogen did not relate to baseline FEV In COPD, systemic levels of CC-16, CRP, sRAGE, SPD and fibrinogen were not associated with FEV NCT01313676.

Identifiants

pubmed: 31258919
doi: 10.1136/bmjresp-2019-000431
pii: bmjresp-2019-000431
pmc: PMC6561388
doi:

Substances chimiques

AGER protein, human 0
Androstadienes 0
Benzyl Alcohols 0
Biomarkers 0
Bronchodilator Agents 0
Chlorobenzenes 0
Pulmonary Surfactant-Associated Protein D 0
Receptor for Advanced Glycation End Products 0
SCGB1A1 protein, human 0
vilanterol 028LZY775B
Fibrinogen 9001-32-5
C-Reactive Protein 9007-41-4
Uteroglobin 9060-09-7
fluticasone furoate JS86977WNV

Banques de données

ClinicalTrials.gov
['NCT01313676']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Pagination

e000431

Subventions

Organisme : British Heart Foundation
ID : CH/09/002/26360
Pays : United Kingdom

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Bartolome R Celli (BR)

Pulmonary and Critical Care Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Julie A Anderson (JA)

Research & Development, GlaxoSmithKline Plc Stockley Park, Uxbridge, Middlesex, UK.

Robert Brook (R)

Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Peter Calverley (P)

Department of Medicine, Clinical Sciences Centre, University of Liverpool, University Hospital Aintree, Liverpool, Liverpool, UK.

Nicholas J Cowans (NJ)

GlaxoSmithKline Plc Stockley Park, Uxbridge, Middlesex, UK.
Veramed Ltd, Twickenham, UK.

Courtney Crim (C)

GlaxoSmithKline Research Triangle Park, Research Triangle Park, North Carolina, USA.

Ian Dixon (I)

GlaxoSmithKline Plc Stockley Park, Uxbridge, Middlesex, UK.
Veramed Ltd, Twickenham, UK.

Victor Kim (V)

Department of Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania, USA.

Fernando J Martinez (FJ)

Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medicine Samuel J Wood Library, New York City, New York, USA.

Andrea Morris (A)

GlaxoSmithKline Research Triangle Park, Research Triangle Park, North Carolina, USA.

David E Newby (DE)

British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, Edinburgh, UK.

Julie Yates (J)

GlaxoSmithKline Research Triangle Park, Research Triangle Park, North Carolina, USA.

Joergen Vestbo (J)

Division of Infection, Immunity and Respiratory Medicine and Allergy, Manchester Academic Health Science Centre, The University of Manchester, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

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Classifications MeSH