Clinical and spirometric variables are better predictors of COPD exacerbations than routine blood biomarkers.


Journal

Respiratory medicine
ISSN: 1532-3064
Titre abrégé: Respir Med
Pays: England
ID NLM: 8908438

Informations de publication

Date de publication:
09 2020
Historique:
received: 15 05 2020
revised: 14 07 2020
accepted: 20 07 2020
pubmed: 24 8 2020
medline: 18 5 2021
entrez: 24 8 2020
Statut: ppublish

Résumé

Understanding the risk factors for exacerbations of COPD may help provide a more personalised approach to exacerbation prevention. Observational, prospective, international, multicentre study aimed at identifying risk factors for exacerbations of COPD. Clinical variables, lung function and CAT scores were collected at baseline. In addition, routine blood biomarkers were also obtained, and patients were followed for 12 months. A total of 326 patients were included. Of these, 155 (47.5%) presented at least one exacerbation. The median time to the first exacerbation was 147 days. Exacerbators had more respiratory symptoms, more impairment in FEV1(%), FVC(%) and a worse CAT score. Regarding biomarkers, only C-reactive protein was significantly higher in exacerbators (2.8 (standard deviation (SD):3.8) mg/dL vs. 1.9 (SD:2.6) mg/dL; p = 0.037). In multivariate analysis, only CAT scores, FEV1(%) and previous exacerbations were significantly associated with having an exacerbation during follow-up. In the equation of risk, patients with a CAT score ≥15, FEV1(%) <55% and at least one exacerbation the previous year had a probability of 76% of having an exacerbation during the next year, compared with 17% in patients who had none of the previous variables. No biomarkers showed a significant association in multivariate analysis. Less than half of the patients presented an exacerbation during the one-year follow-up. CAT scores, FEV1(%) and previous exacerbations were the only variables associated with increased risk of exacerbations. Routine biomarkers did not provide additional information to evaluate the risk of exacerbations.

Sections du résumé

BACKGROUND
Understanding the risk factors for exacerbations of COPD may help provide a more personalised approach to exacerbation prevention.
METHOD
Observational, prospective, international, multicentre study aimed at identifying risk factors for exacerbations of COPD. Clinical variables, lung function and CAT scores were collected at baseline. In addition, routine blood biomarkers were also obtained, and patients were followed for 12 months.
RESULTS
A total of 326 patients were included. Of these, 155 (47.5%) presented at least one exacerbation. The median time to the first exacerbation was 147 days. Exacerbators had more respiratory symptoms, more impairment in FEV1(%), FVC(%) and a worse CAT score. Regarding biomarkers, only C-reactive protein was significantly higher in exacerbators (2.8 (standard deviation (SD):3.8) mg/dL vs. 1.9 (SD:2.6) mg/dL; p = 0.037). In multivariate analysis, only CAT scores, FEV1(%) and previous exacerbations were significantly associated with having an exacerbation during follow-up. In the equation of risk, patients with a CAT score ≥15, FEV1(%) <55% and at least one exacerbation the previous year had a probability of 76% of having an exacerbation during the next year, compared with 17% in patients who had none of the previous variables. No biomarkers showed a significant association in multivariate analysis.
CONCLUSIONS
Less than half of the patients presented an exacerbation during the one-year follow-up. CAT scores, FEV1(%) and previous exacerbations were the only variables associated with increased risk of exacerbations. Routine biomarkers did not provide additional information to evaluate the risk of exacerbations.

Identifiants

pubmed: 32829181
pii: S0954-6111(20)30231-6
doi: 10.1016/j.rmed.2020.106091
pii:
doi:

Substances chimiques

Biomarkers 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106091

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Alexa Nuñez (A)

Pneumology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

Viviana Marras (V)

Respiratory Unit, AOU Sassari, Sassari, Italy.

Matevz Harlander (M)

Department of Pulmonary diseases, University Medical Centre Ljubljana, Slovenia; Faculty of Medicine, University of Ljubljana, Slovenia.

Evgeni Mekov (E)

Department of Pulmonary Diseases, Medical Faculty, Medical University of Sofia, Bulgaria.

Matjaz Turel (M)

Department of Pulmonary diseases, University Medical Centre Ljubljana, Slovenia.

Rossen Petkov (R)

Department of Pulmonary Diseases, Medical Faculty, Medical University of Sofia, Bulgaria.

David Lestan (D)

Department of Pulmonary diseases, University Medical Centre Ljubljana, Slovenia.

Nikolay Yanev (N)

Department of Pulmonary Diseases, Medical Faculty, Medical University of Sofia, Bulgaria.

Silvia Negri (S)

Respiratory Unit, AOU Sassari, Sassari, Italy.

Miriam Barrecheguren (M)

Pneumology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

Pietro Pirina (P)

Respiratory Unit, AOU Sassari, Sassari, Italy.

Marc Miravitlles (M)

Pneumology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain; CIBER de Enfermedades Respiratorias (CIBERES), Barcelona, Spain. Electronic address: mmiravitlles@vhebron.net.

Cristina Esquinas (C)

Pneumology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.

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Classifications MeSH