A Risk Prediction Model for Mortality Among Smokers in the COPDGene® Study.

COPD Genetic Epidemiology study COPDGene PRISm copd preserved ratio-impaired spirometry risk score spirometry

Journal

Chronic obstructive pulmonary diseases (Miami, Fla.)
ISSN: 2372-952X
Titre abrégé: Chronic Obstr Pulm Dis
Pays: United States
ID NLM: 101635411

Informations de publication

Date de publication:
Oct 2020
Historique:
pubmed: 3 9 2020
medline: 3 9 2020
entrez: 3 9 2020
Statut: ppublish

Résumé

Risk factor identification is a proven strategy in advancing treatments and preventive therapy for many chronic conditions. Quantifying the impact of those risk factors on health outcomes can consolidate and focus efforts on individuals with specific high-risk profiles. Using multiple risk factors and longitudinal outcomes in 2 independent cohorts, we developed and validated a risk score model to predict mortality in current and former cigarette smokers. We obtained extensive data on current and former smokers from the COPD Genetic Epidemiology (COPDGene Of 9867 COPDGene participants with standard baseline data, 17.6% died over 10 years of follow-up, and 9074 of these participants had the full set of baseline predictors (standard plus 6-minute walk distance and computed tomography variables) available for full model fits. The average age of participants in the cohort was 60 for both men and women, and the average predicted 10-year mortality risk was 18% for women and 25% for men. Model time-integrated area under the receiver operating characteristic curve statistics demonstrated good predictive model accuracy (0.797 average), validated in the external cohort (0.756 average). Risk of mortality was impacted most by 6-minute walk distance, forced expiratory volume in 1 second and age, for both men and women. Current and former smokers exhibited a wide range of mortality risk over a 10- year period. Our models can identify higher risk individuals who can be targeted for interventions to reduce risk of mortality, for participants with or without chronic obstructive pulmonary disease (COPD) using current Global initiative for obstructive Lung Disease (GOLD) criteria.

Sections du résumé

BACKGROUND BACKGROUND
Risk factor identification is a proven strategy in advancing treatments and preventive therapy for many chronic conditions. Quantifying the impact of those risk factors on health outcomes can consolidate and focus efforts on individuals with specific high-risk profiles. Using multiple risk factors and longitudinal outcomes in 2 independent cohorts, we developed and validated a risk score model to predict mortality in current and former cigarette smokers.
METHODS METHODS
We obtained extensive data on current and former smokers from the COPD Genetic Epidemiology (COPDGene
RESULTS RESULTS
Of 9867 COPDGene participants with standard baseline data, 17.6% died over 10 years of follow-up, and 9074 of these participants had the full set of baseline predictors (standard plus 6-minute walk distance and computed tomography variables) available for full model fits. The average age of participants in the cohort was 60 for both men and women, and the average predicted 10-year mortality risk was 18% for women and 25% for men. Model time-integrated area under the receiver operating characteristic curve statistics demonstrated good predictive model accuracy (0.797 average), validated in the external cohort (0.756 average). Risk of mortality was impacted most by 6-minute walk distance, forced expiratory volume in 1 second and age, for both men and women.
CONCLUSIONS CONCLUSIONS
Current and former smokers exhibited a wide range of mortality risk over a 10- year period. Our models can identify higher risk individuals who can be targeted for interventions to reduce risk of mortality, for participants with or without chronic obstructive pulmonary disease (COPD) using current Global initiative for obstructive Lung Disease (GOLD) criteria.

Identifiants

pubmed: 32877963
doi: 10.15326/jcopdf.7.4.2020.0146
pmc: PMC7883903
doi:

Types de publication

Journal Article

Langues

eng

Pagination

346-361

Subventions

Organisme : NIEHS NIH HHS
ID : P30 ES005605
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL133137
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL089856
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL137880
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL149861
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151452
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL136851
Pays : United States

Informations de copyright

JCOPDF © 2020.

Déclaration de conflit d'intérêts

The COPDGene

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Auteurs

Matthew Strand (M)

National Jewish Health, Denver, Colorado.

Erin Austin (E)

University of Colorado at Denver.

Matthew Moll (M)

Brigham and Women's Hospital, Boston, Massachusetts.

Katherine A Pratte (KA)

National Jewish Health, Denver, Colorado.

Elizabeth A Regan (EA)

National Jewish Health, Denver, Colorado.

Lystra P Hayden (LP)

Brigham and Women's Hospital, Boston, Massachusetts.

Surya P Bhatt (SP)

University of Alabama at Birmingham.

Aladin M Boriek (AM)

Baylor College of Medicine, Houston, Texas.

Richard Casaburi (R)

The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, California.

Edwin K Silverman (EK)

Brigham and Women's Hospital, Boston, Massachusetts.

Spyridon Fortis (S)

University of Iowa, Iowa City.

Ingo Ruczinski (I)

Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.

Harald Koegler (H)

Boehringer-Ingelheim, Ingelheim, Germany.

Harry B Rossiter (HB)

The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, California.
University of Leeds, Leeds, United Kingdom.

Mariaelena Occhipinti (M)

University of Florence, Florence, Italy.

Nicola A Hanania (NA)

Baylor College of Medicine, Houston, Texas.

Hirut T Gebrekristos (HT)

Morehouse School of Medicine, Atlanta, Georgia.

David A Lynch (DA)

National Jewish Health, Denver, Colorado.

Ken M Kunisaki (KM)

Minneapolis Veterans Administration Health Care System, Minnesota.

Kendra A Young (KA)

University of Colorado Anschutz Medical Campus, Aurora.

Jessica C Sieren (JC)

University of Iowa, Iowa City.

Margaret Ragland (M)

University of Colorado Anschutz Medical Campus, Aurora.

John E Hokanson (JE)

University of Colorado Anschutz Medical Campus, Aurora.

Sharon M Lutz (SM)

Harvard Medical School, Harvard University, Boston, Massachusetts.

Barry J Make (BJ)

National Jewish Health, Denver, Colorado.

Gregory L Kinney (GL)

University of Colorado Anschutz Medical Campus, Aurora.

Michael H Cho (MH)

Brigham and Women's Hospital, Boston, Massachusetts.

Massimo Pistolesi (M)

University of Florence, Florence, Italy.

Dawn L DeMeo (DL)

Brigham and Women's Hospital, Boston, Massachusetts.
Harvard Medical School, Harvard University, Boston, Massachusetts.

Frank C Sciurba (FC)

University of Pittsburgh, Pittsburgh, Pennsylvania.

Alejandro P Comellas (AP)

University of Iowa, Iowa City.

Alejandro A Diaz (AA)

Brigham and Women's Hospital, Boston, Massachusetts.

Igor Barjaktarevic (I)

David Geffen School of Medicine, University of California-Los Angeles, Los Angeles.

Russell P Bowler (RP)

National Jewish Health, Denver, Colorado.

Richard E Kanner (RE)

School of Medicine, University of Utah, Salt Lake City.

Stephen P Peters (SP)

Wake Forest School of Medicine, Wake Forest University, Winston-Salem, North Carolina.

Victor E Ortega (VE)

Wake Forest School of Medicine, Wake Forest University, Winston-Salem, North Carolina.

Mark T Dransfield (MT)

University of Alabama at Birmingham.

James D Crapo (JD)

National Jewish Health, Denver, Colorado.

Classifications MeSH