Your browser doesn't support javascript.
loading
Structural Predictors of Lung Function Decline in Young Smokers with Normal Spirometry.
Ritchie, Andrew I; Donaldson, Gavin C; Hoffman, Eric A; Allinson, James P; Bloom, Chloe I; Bolton, Charlotte E; Choudhury, Gourab; Gerard, Sarah E; Guo, Junfeng; Alves-Moreira, Luana; McGarvey, Lorcan; Sapey, Elizabeth; Stockley, Robert A; Yip, K P; Singh, Dave; Wilkinson, Tom; Fageras, Malin; Ostridge, Kristoffer; Jöns, Olaf; Bucchioni, Enrica; Compton, Chris H; Jones, Paul; Mezzi, Karen; Vestbo, Jørgen; Calverley, Peter M A; Wedzicha, Jadwiga A.
Afiliação
  • Ritchie AI; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Donaldson GC; AstraZeneca, Cambridge, United Kingdom.
  • Hoffman EA; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Allinson JP; Department of Radiology and.
  • Bloom CI; Roy J. Carver Department of Biomedical Engineering, Medicine and Biomedical Engineering, University of Iowa, Iowa City, Iowa.
  • Bolton CE; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Choudhury G; Royal Brompton Hospital, London, United Kingdom.
  • Gerard SE; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Guo J; NIHR Nottingham Biomedical Research Centre.
  • Alves-Moreira L; Centre for Respiratory Research, NIHR Nottingham, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.
  • McGarvey L; ELEGI and COLT Laboratories, Queen's Medical Research Institute, Edinburgh, United Kingdom.
  • Sapey E; Roy J. Carver Department of Biomedical Engineering, Medicine and Biomedical Engineering, University of Iowa, Iowa City, Iowa.
  • Stockley RA; Department of Radiology and.
  • Yip KP; National Heart and Lung Institute, Imperial College London, London, United Kingdom.
  • Singh D; Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, United Kingdom.
  • Wilkinson T; Belfast Health and Social Care Trust, Belfast, United Kingdom.
  • Fageras M; Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.
  • Ostridge K; Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.
  • Jöns O; Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom.
  • Bucchioni E; Division of Infection, Immunity and Respiratory Medicine, University of Manchester, Manchester, United Kingdom.
  • Compton CH; Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
  • Jones P; National Institute for Health and Care Research Southampton Biomedical Research Centre, University Hospital Southampton, Southampton, United Kingdom.
  • Mezzi K; AstraZeneca, Gothenburg, Sweden.
  • Vestbo J; Faculty of Medicine, University of Southampton, Southampton, United Kingdom.
  • Calverley PMA; AstraZeneca, Gothenburg, Sweden.
  • Wedzicha JA; Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.
Am J Respir Crit Care Med ; 209(10): 1208-1218, 2024 05 15.
Article em En | MEDLINE | ID: mdl-38175920
ABSTRACT
Rationale Chronic obstructive pulmonary disease (COPD) due to tobacco smoking commonly presents when extensive lung damage has occurred.

Objectives:

We hypothesized that structural change would be detected early in the natural history of COPD and would relate to loss of lung function with time.

Methods:

We recruited 431 current smokers (median age, 39 yr; 16 pack-years smoked) and recorded symptoms using the COPD Assessment Test (CAT), spirometry, and quantitative thoracic computed tomography (QCT) scans at study entry. These scan results were compared with those from 67 never-smoking control subjects. Three hundred sixty-eight participants were followed every six months with measurement of postbronchodilator spirometry for a median of 32 months. The rate of FEV1 decline, adjusted for current smoking status, age, and sex, was related to the initial QCT appearances and symptoms, measured using the CAT. Measurements and Main

Results:

There were no material differences in demography or subjective CT appearances between the young smokers and control subjects, but 55.7% of the former had CAT scores greater than 10, and 24.2% reported chronic bronchitis. QCT assessments of disease probability-defined functional small airway disease, ground-glass opacification, bronchovascular prominence, and ratio of small blood vessel volume to total pulmonary vessel volume were increased compared with control subjects and were all associated with a faster FEV1 decline, as was a higher CAT score.

Conclusions:

Radiological abnormalities on CT are already established in young smokers with normal lung function and are associated with FEV1 loss independently of the impact of symptoms. Structural abnormalities are present early in the natural history of COPD and are markers of disease progression. Clinical trial registered with www.clinicaltrials.gov (NCT03480347).
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espirometria / Tomografia Computadorizada por Raios X / Doença Pulmonar Obstrutiva Crônica / Pulmão Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espirometria / Tomografia Computadorizada por Raios X / Doença Pulmonar Obstrutiva Crônica / Pulmão Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article