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Survival in COPD: Impact of Lung Dysfunction and Comorbidities

Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality in industrialized countries. Recent studies investigated the impact of comorbidities on the survival in COPD, but most of them lacked a referent group of comorbidity-matched, nonobstructed individuals. We examin...

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Autores principales: Miniati, Massimo, Monti, Simonetta, Pavlickova, Ivana, Bottai, Matteo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616266/
https://www.ncbi.nlm.nih.gov/pubmed/25211048
http://dx.doi.org/10.1097/MD.0000000000000076
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author Miniati, Massimo
Monti, Simonetta
Pavlickova, Ivana
Bottai, Matteo
author_facet Miniati, Massimo
Monti, Simonetta
Pavlickova, Ivana
Bottai, Matteo
author_sort Miniati, Massimo
collection PubMed
description Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality in industrialized countries. Recent studies investigated the impact of comorbidities on the survival in COPD, but most of them lacked a referent group of comorbidity-matched, nonobstructed individuals. We examined the 10-year mortality in a sample of 200 COPD patients and 201 nonobstructed controls. They were part of a larger cohort enrolled in a European case–control study aimed at assessing genetic susceptibility to COPD. By design, the COPD group included patients with a forced expiratory volume in 1 second (FEV(1)) ≤70% predicted. Cases and controls were matched on age, sex, and cumulative smoking history, and shared a nearly identical prevalence of cardiovascular and metabolic disorders. We estimated the hazard of death with Cox regression and percentiles of survival with Laplace regression. COPD was the main exposure variable of interest. Five comorbidities (hypertension, coronary artery disease, prior myocardial infarction, chronic heart failure, and diabetes) were included as covariates in multiple regression models. The all-cause mortality rate was significantly higher in cases than in controls (43% vs 16%, P < 0.001). The unadjusted hazard of death for COPD was 3-fold higher than the referent category (P < 0.001), and remained nearly unchanged after introducing the 5 comorbidities in multiple regression. Patients with COPD had significantly shorter survival percentiles than comorbidity-matched controls (P < 0.001). Notably, 15% of the nonobstructed controls died by 10.3 years into the study; the same proportion of COPD patients had died some 6 years earlier, at 4.6 years. In a separate analysis, we split the whole sample into 2 groups based on the lower tertile of FEV(1) and carbon monoxide lung diffusing capacity (DL(CO)). The hazard of death for COPD patients with low FEV(1) and DL(CO) was nearly 3.5-fold higher than in all the others (P < 0.001), and decreased only slightly after introducing age and chronic heart failure as relevant covariates. COPD is a strong predictor of reduced survival independently of coexisting cardiovascular and metabolic disorders. Efforts should be made to identify patients at risk and to ensure adherence to prescribed therapeutic regimens.
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spelling pubmed-46162662015-10-27 Survival in COPD: Impact of Lung Dysfunction and Comorbidities Miniati, Massimo Monti, Simonetta Pavlickova, Ivana Bottai, Matteo Medicine (Baltimore) 6700 Chronic obstructive pulmonary disease (COPD) is a major cause of morbidity and mortality in industrialized countries. Recent studies investigated the impact of comorbidities on the survival in COPD, but most of them lacked a referent group of comorbidity-matched, nonobstructed individuals. We examined the 10-year mortality in a sample of 200 COPD patients and 201 nonobstructed controls. They were part of a larger cohort enrolled in a European case–control study aimed at assessing genetic susceptibility to COPD. By design, the COPD group included patients with a forced expiratory volume in 1 second (FEV(1)) ≤70% predicted. Cases and controls were matched on age, sex, and cumulative smoking history, and shared a nearly identical prevalence of cardiovascular and metabolic disorders. We estimated the hazard of death with Cox regression and percentiles of survival with Laplace regression. COPD was the main exposure variable of interest. Five comorbidities (hypertension, coronary artery disease, prior myocardial infarction, chronic heart failure, and diabetes) were included as covariates in multiple regression models. The all-cause mortality rate was significantly higher in cases than in controls (43% vs 16%, P < 0.001). The unadjusted hazard of death for COPD was 3-fold higher than the referent category (P < 0.001), and remained nearly unchanged after introducing the 5 comorbidities in multiple regression. Patients with COPD had significantly shorter survival percentiles than comorbidity-matched controls (P < 0.001). Notably, 15% of the nonobstructed controls died by 10.3 years into the study; the same proportion of COPD patients had died some 6 years earlier, at 4.6 years. In a separate analysis, we split the whole sample into 2 groups based on the lower tertile of FEV(1) and carbon monoxide lung diffusing capacity (DL(CO)). The hazard of death for COPD patients with low FEV(1) and DL(CO) was nearly 3.5-fold higher than in all the others (P < 0.001), and decreased only slightly after introducing age and chronic heart failure as relevant covariates. COPD is a strong predictor of reduced survival independently of coexisting cardiovascular and metabolic disorders. Efforts should be made to identify patients at risk and to ensure adherence to prescribed therapeutic regimens. Wolters Kluwer Health 2014-09-05 /pmc/articles/PMC4616266/ /pubmed/25211048 http://dx.doi.org/10.1097/MD.0000000000000076 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0
spellingShingle 6700
Miniati, Massimo
Monti, Simonetta
Pavlickova, Ivana
Bottai, Matteo
Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title_full Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title_fullStr Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title_full_unstemmed Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title_short Survival in COPD: Impact of Lung Dysfunction and Comorbidities
title_sort survival in copd: impact of lung dysfunction and comorbidities
topic 6700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616266/
https://www.ncbi.nlm.nih.gov/pubmed/25211048
http://dx.doi.org/10.1097/MD.0000000000000076
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