Evidence map›Paper›PMID 26098755›Full record

Observational studyJAMA internal medicine2015

Clinical and Radiologic Disease in Smokers With Normal Spirometry.

Elizabeth A Regan, David A Lynch, Douglas Curran-Everett, Jeffrey L Curtis, John H M Austin, Philippe A Grenier, Hans-Ulrich Kauczor, William C Bailey, Dawn L DeMeo, Richard H Casaburi and 18 more

Erratum issued 2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JAMA internal medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 277 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
277citing papers in PubMed, 2 pooled it
33.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03026439 completednot on this map

The Boundaries of Mild Chronic Obstructive Pulmonary Disease: Searching Clinical COPD Onset

TypeobservationalSponsorPontificia Universidad Catolica de ChileRan2014 to 2018Enrolled240ConditionsCopd
NCT03263130 recruitingnot on this mapstarted 2017, after this paper: background citation

Site and Mechanism(s) of Expiratory Airflow Limitation in COPD, Emphysema and Asthma-COPD Overlap

Typeobservational_patient_registrySponsorGelb, Arthur F., M.D.Ran2017 to 2027Enrolled60ConditionsCOPD, Emphysema, Asthma COPD Overlap, EmphysemaArmsAs above: diagnosis: COPD, Emphysema, Asthma-COPD Overlap
3 · Its place in the literature

Who cites it

277 citing papers in PubMed, 2 syntheses or guidelines pooled it, 464 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Integrated Bioinformatics and Experimental Validation to Identify Shared Sialylation-Related Signatures in Emphysematous and Fibrotic Lung Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  8. Imaging Markers of Chronic Obstructive Pulmonary Disease on Computed Tomography of the Lungs: a Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Mosaic loss of Y chromosome associates with lung function, emphysema, and epigenetic aging.American journal of respiratory and critical care medicine · 2026
    Article
  13. Article
  14. Article
  15. Long isoforms of the COPD risk gene FAM13A orchestrate human lung epithelial development.American journal of respiratory cell and molecular biology · 2026
    Article
  16. Observational
  17. Article
  18. Article
  19. Article
  20. Observational

217 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 20 institutions in 6 countries.

Elizabeth A ReganNational Jewish Health, Denver, Colorado2Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Anschutz Medical Campus, Aurora.
David A LynchNational Jewish Health, Denver, Colorado.
Douglas Curran-EverettNational Jewish Health, Denver, Colorado.
Jeffrey L CurtisSection of Pulmonary and Critical Care Medicine, Medical Service, Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, Michigan4Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Health System, An.
John H M AustinDepartment of Radiology, Columbia University Medical Center, New York, New York.
Philippe A GrenierDepartment of Diagnostic Radiology, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Université Pierre et Marie Curie, Paris, France.
Hans-Ulrich KauczorDepartment of Diagnostic and Interventional Radiology, University of Heidelberg, Heidelberg, Germany.
William C BaileyTranslational Lung Research Center Heidelberg, German Center of Lung Research, University of Alabama, Birmingham.
Dawn L DeMeoPulmonary and Critical Care, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Richard H CasaburiDivision of Respiratory and Critical Care Physiology and Medicine, Los Angeles Biomedical Research Institute, Harbor-University of California, Los Angeles, Medical Center, Torrance.
Paul FriedmanDepartment of Radiology, University of California, San Diego.
Edwin J R Van BeekDepartment of Radiology, University of Edinburgh, Edinburgh, Scotland.
John E HokansonDepartment of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Anschutz Medical Campus, Aurora.
Russell P BowlerNational Jewish Health, Denver, Colorado.
Terri H BeatyDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
George R WashkoPulmonary and Critical Care, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
MeiLan K HanDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Health System, Ann Arbor.
Victor KimSection of Pulmonary and Critical Care Medicine, Department of Medicine, Temple University, Philadelphia, Pennsylvania.
Song Soo KimDepartment of Radiology, Chungnam National University Hospital, Chungnam National University School of Medicine, Daejeon, Korea.
Kunihiro YagihashiDepartment of Radiology, St Marianna University School of Medicine, Sugao, Miyamaeku, Kawasaki, Kanagawa, Japan.
Lacey WashingtonDepartment of Radiology, Duke University Medical Center, Durham, North Carolina.
Charlene E McEvoyPulmonary Medicine, HealthPartners, Minneapolis-St Paul, Minnesota.
Clint TannerNational Jewish Health, Denver, Colorado.
David M ManninoDivision of Pulmonary, Critical Care, and Sleep Medicine, Department of Preventive Medicine and Environmental Health, College of Public Health, University of Kentucky, Lexington.
Barry J MakeNational Jewish Health, Denver, Colorado.
Edwin K SilvermanPulmonary and Critical Care, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
James D CrapoNational Jewish Health, Denver, Colorado.
Genetic Epidemiology of COPD (COPDGene) Investigators
University of Colorado Denver · USBrigham and Women's Hospital · USNational Jewish Health · USAssistance Publique – Hôpitaux de Paris · FRChungnam National University Hospital · KRColorado School of Public Health · USColumbia University Irving Medical Center · USDuke Medical Center · USHarvard University · USHealthPartners · USHeidelberg University · DEJohns Hopkins University · USLos Angeles Medical Center · USMichigan Medicine · USSt. Marianna University School of Medicine · JPTemple University · USUniversity of California, San Diego · USUniversity of Edinburgh · GBUniversity of Kentucky · USVA Ann Arbor Healthcare System · US

Funding

Genetic Epidemiology of COPDU01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2007 to 2021
$56.9M
Metabolomic signatures of empysema and COPD progression in the COPDGene cohortR01HL089897 · NHLBI · NATIONAL JEWISH HEALTH · PI CRAPO, JAMES D · 2012 to 2016
$31.1M
Genetic Epidemiology of COPDU01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2007 to 2021
$20.7M
(2 of 2) Genetic Epidemiology of COPDR01HL089856 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SILVERMAN, EDWIN K · 2012 to 2016
$18.9M
Design and Testing of tools to Identify individuals at high risk for COPD^ 73R01HL114055 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEIDY, NANCY KLINE, MANNINO, DAVID · 2012 to 2014
$2.4M
NHLBI NIH HHS R01 HL089856NHLBI NIH HHS R01HL089856NHLBI NIH HHS R01 HL089897NHLBI NIH HHS R01HL089897NHLBI NIH HHS R01 HL114055NHLBI NIH HHS U01 HL089856NHLBI NIH HHS U01 HL089897
6 · The paper itself

Abstract

importanceAirflow obstruction on spirometry is universally used to define chronic obstructive pulmonary disease (COPD), and current or former smokers without airflow obstruction may assume that they are disease free.

objectiveTo identify clinical and radiologic evidence of smoking-related disease in a cohort of current and former smokers who did not meet spirometric criteria for COPD, for whom we adopted the discarded label of Global Initiative for Obstructive Lung Disease (GOLD) 0. DESIGN, SETTING, AND

participantsIndividuals from the Genetic Epidemiology of COPD (COPDGene) cross-sectional observational study completed spirometry, chest computed tomography (CT) scans, a 6-minute walk, and questionnaires. Participants were recruited from local communities at 21 sites across the United States. The GOLD 0 group (n = 4388) (ratio of forced expiratory volume in the first second of expiration [FEV1] to forced vital capacity >0.7 and FEV1 ≥80% predicted) from the COPDGene study was compared with a GOLD 1 group (n = 794), COPD groups (n = 3690), and a group of never smokers (n = 108). Recruitment began in January 2008 and ended in July 2011. MAIN OUTCOMES AND MEASURES: Physical function impairments, respiratory symptoms, CT abnormalities, use of respiratory medications, and reduced respiratory-specific quality of life.

resultsOne or more respiratory-related impairments were found in 54.1% (2375 of 4388) of the GOLD 0 group. The GOLD 0 group had worse quality of life (mean [SD] St George's Respiratory Questionnaire total score, 17.0 [18.0] vs 3.8 [6.8] for the never smokers; P < .001) and a lower 6-minute walk distance, and 42.3% (127 of 300) of the GOLD 0 group had CT evidence of emphysema or airway thickening. The FEV1 percent predicted distribution and mean for the GOLD 0 group were lower but still within the normal range for the population. Current smoking was associated with more respiratory symptoms, but former smokers had greater emphysema and gas trapping. Advancing age was associated with smoking cessation and with more CT findings of disease. Individuals with respiratory impairments were more likely to use respiratory medications, and the use of these medications was associated with worse disease. CONCLUSIONS AND RELEVANCE: Lung disease and impairments were common in smokers without spirometric COPD. Based on these results, we project that there are 35 million current and former smokers older than 55 years in the United States who may have unrecognized disease or impairment. The effect of chronic smoking on the lungs and the individual is substantially underestimated when using spirometry alone.

Indexed as

AgedCase-Control StudiesCross-Sectional StudiesExercise ToleranceFemaleHumansMaleMiddle AgedNutrition SurveysPulmonary Disease, Chronic ObstructiveQuality of LifeRadiography, ThoracicSmokingSpirometryTomography, X-Ray ComputedUnited States

Identifiers

PMID26098755
PMCPMC4564354
OpenAlexW2164999687

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.