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Individualized prediction of lung-function decline in chronic obstructive pulmonary disease

Zafari, Zafar (author)
University of British Columbia
Sin, Don D. (author)
St. Paul’s Hospital,University of British Columbia
Postma, Dirkje S. (author)
University of Groningen
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Löfdahl, Claes Göran (author)
Lund University,Lunds universitet,Lungmedicin, allergologi och palliativ medicin,Sektion II,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Respiratory Medicine, Allergology, and Palliative Medicine,Section II,Department of Clinical Sciences, Lund,Faculty of Medicine
Vonk, Judith (author)
University of Groningen
Bryan, Stirling (author)
University of British Columbia
Lam, Stephen (author)
University of British Columbia
Tammemagi, C. Martin (author)
Brock University
Khakban, Rahman (author)
University of British Columbia
Man, S. F Paul (author)
St. Paul’s Hospital,University of British Columbia
Tashkin, Donald (author)
University of California, Los Angeles
Wise, Robert A. (author)
Johns Hopkins University School of Medicine
Connett, John E. (author)
University of Minnesota
McManus, Bruce (author)
PROOF Centre for Excellence,St. Paul’s Hospital,University of British Columbia
Ng, Raymond (author)
PROOF Centre for Excellence
Hollander, Zsuszanna (author)
PROOF Centre for Excellence,St. Paul’s Hospital,University of British Columbia
Sadatsafavi, Mohsen (author)
University of British Columbia
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University of British Columbia St Paul’s Hospital (creator_code:org_t)
2016-08-02
2016
English 7 s.
In: CMAJ. - : CMA Joule Inc.. - 0820-3946. ; 188:14, s. 1004-1010
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The rate of lung-function decline in chronic obstructive pulmonary disease (COPD) varies substantially among individuals. We sought to develop and validate an individualized prediction model for forced expiratory volume at 1 second (FEV1) in current smokers with mild-to-moderate COPD. Methods: Using data from a large long-term clinical trial (the Lung Health Study), we derived mixed-effects regression models to predict future FEV1 values over 11 years according to clinical traits. We modelled heterogeneity by allowing regression coefficients to vary across individuals. Two independent cohorts with COPD were used for validating the equations. Results: We used data from 5594 patients (mean age 48.4 yr, 63% men, mean baseline FEV1 2.75 L) to create the individualized prediction equations. There was significant between-individual variability in the rate of FEV1 decline, with the interval for the annual rate of decline that contained 95% of individuals being -124 to -15 mL/yr for smokers and -83 to 15 mL/yr for sustained quitters. Clinical variables in the final model explained 88% of variation around follow-up FEV1. The C statistic for predicting severity grades was 0.90. Prediction equations performed robustly in the 2 external data sets. Interpretation: A substantial part of individual variation in FEV1 decline can be explained by easily measured clinical variables. The model developed in this work can be used for prediction of future lung health in patients with mild-to-moderate COPD.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

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