Older age and obesity are associated with increased airway closure in response to methacholine in patients with asthma.


Journal

Respirology (Carlton, Vic.)
ISSN: 1440-1843
Titre abrégé: Respirology
Pays: Australia
ID NLM: 9616368

Informations de publication

Date de publication:
07 2019
Historique:
received: 13 02 2018
revised: 29 11 2018
accepted: 02 01 2019
pubmed: 7 3 2019
medline: 28 4 2020
entrez: 7 3 2019
Statut: ppublish

Résumé

The reduction of forced expiratory volume in 1 s (FEV We used the methacholine challenge data from participants in five studies of the ALA-ACRC to determine the closing index, defined as the contribution of airway closure to the decrease in FEV There were a total of 936 participants with asthma, among whom the median closing index was 0.67 relative to that of a published healthy population of 0.54. A higher closing index was associated with increased age (10-year increments) (0.04, 95% CI = 0.02, 0.05, P < 0.005) and obesity (0.07, 95% CI = 0.03, 0.10, P < 0.001). There was no association between the closing index and asthma control. Our findings confirm that airway closure in response to methacholine occurs in a large, diverse population of asthmatic participants, and that increased airway closure is associated with older age and obesity. These findings suggest that therapies targeting airway closure may be important in patients with a high closing index.

Sections du résumé

BACKGROUND AND OBJECTIVE
The reduction of forced expiratory volume in 1 s (FEV
METHODS
We used the methacholine challenge data from participants in five studies of the ALA-ACRC to determine the closing index, defined as the contribution of airway closure to the decrease in FEV
RESULTS
There were a total of 936 participants with asthma, among whom the median closing index was 0.67 relative to that of a published healthy population of 0.54. A higher closing index was associated with increased age (10-year increments) (0.04, 95% CI = 0.02, 0.05, P < 0.005) and obesity (0.07, 95% CI = 0.03, 0.10, P < 0.001). There was no association between the closing index and asthma control.
CONCLUSION
Our findings confirm that airway closure in response to methacholine occurs in a large, diverse population of asthmatic participants, and that increased airway closure is associated with older age and obesity. These findings suggest that therapies targeting airway closure may be important in patients with a high closing index.

Identifiants

pubmed: 30838750
doi: 10.1111/resp.13496
pmc: PMC9511501
mid: NIHMS1824138
doi:

Substances chimiques

Bronchoconstrictor Agents 0
Methacholine Chloride 0W5ETF9M2K

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

638-645

Subventions

Organisme : NHLBI NIH HHS
ID : U01 HL108730
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL080450
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL089464
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL089510
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL072968
Pays : United States
Organisme : NEI NIH HHS
ID : UG1 EY028091
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL080433
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Asian Pacific Society of Respirology.

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Auteurs

David A Kaminsky (DA)

Pulmonary and Critical Care, University of Vermont Larner College of Medicine, Burlington, VT, USA.

David G Chapman (DG)

Pulmonary and Critical Care, University of Vermont Larner College of Medicine, Burlington, VT, USA.
Translational Airways Group, School of Life Sciences, University of Technology Sydney, Sydney, NSW, Australia.
Airway Physiology and Imaging Group, Woolcock Institute of Medical Research, Sydney, NSW, Australia.

Janet T Holbrook (JT)

Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.

Robert J Henderson (RJ)

Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.

Elizabeth A Sugar (EA)

Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.

John Mastronarde (J)

Division of Pulmonary Medicine, Providence Portland Medical Center, Portland, OR, USA.

William G Teague (WG)

Division of Pediatric Respiratory Medicine and Allergy, University of Virginia, Charlottesville, VA, USA.

Michael Busk (M)

Division of Pulmonary Medicine, St. Vincent Hospital and Health Care Center, Inc., Indianapolis, IN, USA.

Kaharu Sumino (K)

Division of Pulmonary and Critical Care Medicine, Washington University, St. Louis, MO, USA.

Anne E Dixon (AE)

Pulmonary and Critical Care, University of Vermont Larner College of Medicine, Burlington, VT, USA.

Robert A Wise (RA)

Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Charles G Irvin (CG)

Pulmonary and Critical Care, University of Vermont Larner College of Medicine, Burlington, VT, USA.

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