High prevalence of interstitial lung abnormalities in middle-aged never-smokers.
Journal
ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641
Informations de publication
Date de publication:
Sep 2023
Sep 2023
Historique:
received:
17
01
2023
accepted:
03
07
2023
medline:
27
9
2023
pubmed:
27
9
2023
entrez:
27
9
2023
Statut:
epublish
Résumé
Interstitial lung abnormalities (ILA) are incidental findings on chest computed tomography (CT). These patterns can present at an early stage of fibrotic lung disease. Our aim was to estimate the prevalence of ILA in the Swedish population, in particular in never-smokers, and find out its association with demographics, comorbidities and symptoms. Participants were recruited to the Swedish CArdioPulmonary BioImage Study (SCAPIS), a population-based survey including men and women aged 50-64 years performed at six university hospitals in Sweden. CT scan, spirometry and questionnaires were performed. ILA were defined as cysts, ground-glass opacities, reticular abnormality, bronchiectasis and honeycombing. Out of 29 521 participants, 14 487 were never-smokers and 14 380 were men. In the whole population, 2870 (9.7%) had ILA of which 134 (0.5%) were fibrotic. In never-smokers, the prevalence was 7.9% of which 0.3% were fibrotic. In the whole population, age, smoking history, chronic bronchitis, cancer, coronary artery calcium score and high-sensitive C-reactive protein were associated with ILA. Both ILA and fibrotic ILA were associated with restrictive spirometric pattern and impaired diffusing capacity of the lung for carbon monoxide. However, individuals with ILA did not report more symptoms compared with individuals without ILA. ILA are common in a middle-aged Swedish population including never-smokers. ILA may be at risk of being underdiagnosed among never-smokers since they are not a target for screening.
Sections du résumé
Background
UNASSIGNED
Interstitial lung abnormalities (ILA) are incidental findings on chest computed tomography (CT). These patterns can present at an early stage of fibrotic lung disease. Our aim was to estimate the prevalence of ILA in the Swedish population, in particular in never-smokers, and find out its association with demographics, comorbidities and symptoms.
Methods
UNASSIGNED
Participants were recruited to the Swedish CArdioPulmonary BioImage Study (SCAPIS), a population-based survey including men and women aged 50-64 years performed at six university hospitals in Sweden. CT scan, spirometry and questionnaires were performed. ILA were defined as cysts, ground-glass opacities, reticular abnormality, bronchiectasis and honeycombing.
Findings
UNASSIGNED
Out of 29 521 participants, 14 487 were never-smokers and 14 380 were men. In the whole population, 2870 (9.7%) had ILA of which 134 (0.5%) were fibrotic. In never-smokers, the prevalence was 7.9% of which 0.3% were fibrotic. In the whole population, age, smoking history, chronic bronchitis, cancer, coronary artery calcium score and high-sensitive C-reactive protein were associated with ILA. Both ILA and fibrotic ILA were associated with restrictive spirometric pattern and impaired diffusing capacity of the lung for carbon monoxide. However, individuals with ILA did not report more symptoms compared with individuals without ILA.
Interpretation
UNASSIGNED
ILA are common in a middle-aged Swedish population including never-smokers. ILA may be at risk of being underdiagnosed among never-smokers since they are not a target for screening.
Identifiants
pubmed: 37753274
doi: 10.1183/23120541.00035-2023
pii: 00035-2023
pmc: PMC10518870
pii:
doi:
Types de publication
Journal Article
Langues
eng
Informations de copyright
Copyright ©The authors 2023.
Déclaration de conflit d'intérêts
Conflict of interest: I. Pesonen reports fees from Boehringer Ingelheim for lectures and participation on advisory boards. Conflict of interest: A. Egeston reports consulting fees from BioCryst, payment/honoraria from AstraZeneca and an unrestricted research grant from CSL-Behring. Conflict of interest: Ö.I. Emilsson reports payment from study work from Boehringer Ingelheim, unrelated to this publication. Conflict of interest: E. Hagström reports payments to institution from Pfizer and Amgen, small personal fees from Amgen, NovoNordisk, Bayer and AstraZeneca, and a small personal fee from Amarin AB for participation on an advisory board. He is the co-chair of the Swedish secondary prevention registry and the national coordinator for the trials DalCore DAL301 DalGne, Regeneron R1500-CL-1643 and Aegis II/Perfuse. Conflict of interest: L.E.G.W. Vanfleteren reports grants paid to his institution from the Swedish Heart and Lung Foundation and the family Kamprad foundation, and payments/honoraria from AstraZeneca, GSK, Boehringer, Novartis, Chiesi, Pulmonx for lectures and presentations. He also reports personal payments for participation on a data safety monitoring board or advisory board for AstraZeneca. He was member of the board for the Swedish National Airway registry. He is as associate editor of this journal. Conflict of interest: P. Wollmer received fees for lectures from Chiesi Pharma outside the scope of the study. He also has a patent issued for a device and method for pulmonary function measurement outside the scope of the study. Conflict of interest: S. Zaigham reports a research project grant from Magnus Bergvalls Stiftelse, and support for meeting attendance from the Swedish Heart and Lung Foundation and Bror Hjerpstedts Stiftelse. Conflict of interest: C.M. Sköld reports research grants from Boehringer Ingelheim for pulmonary fibrosis research, payments for lectures and educational activities related to pulmonary fibrosis, and participation on advisory boards related to pulmonary fibrosis. Conflict of interest: All other authors declare no conflicts of interest.
Références
Am J Respir Crit Care Med. 2019 Jul 15;200(2):175-183
pubmed: 30673508
Lancet Respir Med. 2020 Jul;8(7):726-737
pubmed: 32649920
Eur J Radiol. 2020 Aug;129:109073
pubmed: 32480316
Eur Respir J. 2015 Oct;46(4):1113-30
pubmed: 26424523
Am J Respir Crit Care Med. 2007 Oct 1;176(7):698-705
pubmed: 17641157
Respir Med. 2018 Mar;136:77-82
pubmed: 29501250
Respir Med. 2016 Nov;120:116-123
pubmed: 27817808
J Thorac Imaging. 2017 Sep;32(5):W54-W66
pubmed: 28832417
BMC Pulm Med. 2018 Jan 17;18(1):9
pubmed: 29343236
Am J Respir Crit Care Med. 2023 Aug 15;208(4):461-471
pubmed: 37339507
Am J Respir Crit Care Med. 1999 Dec;160(6):2028-33
pubmed: 10588624
Thorax. 2018 Sep;73(9):884-886
pubmed: 29317545
Am J Respir Crit Care Med. 2017 Oct 15;196(8):1031-1039
pubmed: 28753039
JAMA. 2016 Feb 16;315(7):672-81
pubmed: 26881370
Am J Respir Crit Care Med. 2016 Dec 15;194(12):1514-1522
pubmed: 27314401
Lancet Respir Med. 2017 Feb;5(2):95-96
pubmed: 28145231
Curr Opin Pulm Med. 2018 Sep;24(5):432-439
pubmed: 29939864
Lancet Respir Med. 2021 Sep;9(9):1065-1076
pubmed: 34331867
Eur Respir J. 2005 Aug;26(2):319-38
pubmed: 16055882
N Engl J Med. 2013 Jun 6;368(23):2192-200
pubmed: 23692170
J Intern Med. 2015 Dec;278(6):645-59
pubmed: 26096600
Eur Respir J. 2017 Jan 3;49(1):
pubmed: 28049168
Respir Res. 2019 May 24;20(1):103
pubmed: 31126287
Am J Respir Crit Care Med. 2002 Jan 15;165(2):277-304
pubmed: 11790668
Radiology. 2013 Aug;268(2):563-71
pubmed: 23513242
Radiology. 2008 Mar;246(3):697-722
pubmed: 18195376
Eur Respir J. 2005 Jul;26(1):153-61
pubmed: 15994402
Chest. 2022 Feb;161(2):470-482
pubmed: 34197782
Eur Respir J. 2012 Dec;40(6):1324-43
pubmed: 22743675
Am J Respir Crit Care Med. 2022 Jul 15;206(2):178-185
pubmed: 35426779
Radiology. 2007 May;243(2):527-38
pubmed: 17456875