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Evaluation of von Willebrand factor in COPD patients

OBJECTIVE: To compare the absolute serum von Willebrand factor (vWF) levels and relative serum vWF activity in patients with clinically stable COPD, smokers without airway obstruction, and healthy never-smokers. METHODS: The study included 57 subjects, in three groups: COPD (n = 36); smoker (n = 12)...

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Autores principales: Bártholo, Thiago Prudente, da Costa, Cláudia Henrique, Rufino, Rogério
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Pneumologia e Tisiologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201167/
https://www.ncbi.nlm.nih.gov/pubmed/25210959
http://dx.doi.org/10.1590/S1806-37132014000400004
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author Bártholo, Thiago Prudente
da Costa, Cláudia Henrique
Rufino, Rogério
author_facet Bártholo, Thiago Prudente
da Costa, Cláudia Henrique
Rufino, Rogério
author_sort Bártholo, Thiago Prudente
collection PubMed
description OBJECTIVE: To compare the absolute serum von Willebrand factor (vWF) levels and relative serum vWF activity in patients with clinically stable COPD, smokers without airway obstruction, and healthy never-smokers. METHODS: The study included 57 subjects, in three groups: COPD (n = 36); smoker (n = 12); and control (n = 9). During the selection phase, all participants underwent chest X-rays, spirometry, and blood testing. Absolute serum vWF levels and relative serum vWF activity were obtained by turbidimetry and ELISA, respectively. The modified Medical Research Council scale (cut-off score = 2) was used in order to classify COPD patients as symptomatic or mildly symptomatic/asymptomatic. RESULTS: Absolute vWF levels were significantly lower in the control group than in the smoker and COPD groups: 989 ± 436 pg/mL vs. 2,220 ± 746 pg/mL (p < 0.001) and 1,865 ± 592 pg/mL (p < 0.01). Relative serum vWF activity was significantly higher in the COPD group than in the smoker group (136.7 ± 46.0% vs. 92.8 ± 34.0%; p < 0.05), as well as being significantly higher in the symptomatic COPD subgroup than in the mildly symptomatic/asymptomatic COPD subgroup (154 ± 48% vs. 119 ± 8%; p < 0.05). In all three groups, there was a negative correlation between FEV(1) (% of predicted) and relative serum vWF activity (r(2) = −0.13; p = 0.009). CONCLUSIONS: Our results suggest that increases in vWF levels and activity contribute to the persistence of systemic inflammation, as well as increasing cardiovascular risk, in COPD patients.
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spelling pubmed-42011672014-10-21 Evaluation of von Willebrand factor in COPD patients Bártholo, Thiago Prudente da Costa, Cláudia Henrique Rufino, Rogério J Bras Pneumol Original Articles OBJECTIVE: To compare the absolute serum von Willebrand factor (vWF) levels and relative serum vWF activity in patients with clinically stable COPD, smokers without airway obstruction, and healthy never-smokers. METHODS: The study included 57 subjects, in three groups: COPD (n = 36); smoker (n = 12); and control (n = 9). During the selection phase, all participants underwent chest X-rays, spirometry, and blood testing. Absolute serum vWF levels and relative serum vWF activity were obtained by turbidimetry and ELISA, respectively. The modified Medical Research Council scale (cut-off score = 2) was used in order to classify COPD patients as symptomatic or mildly symptomatic/asymptomatic. RESULTS: Absolute vWF levels were significantly lower in the control group than in the smoker and COPD groups: 989 ± 436 pg/mL vs. 2,220 ± 746 pg/mL (p < 0.001) and 1,865 ± 592 pg/mL (p < 0.01). Relative serum vWF activity was significantly higher in the COPD group than in the smoker group (136.7 ± 46.0% vs. 92.8 ± 34.0%; p < 0.05), as well as being significantly higher in the symptomatic COPD subgroup than in the mildly symptomatic/asymptomatic COPD subgroup (154 ± 48% vs. 119 ± 8%; p < 0.05). In all three groups, there was a negative correlation between FEV(1) (% of predicted) and relative serum vWF activity (r(2) = −0.13; p = 0.009). CONCLUSIONS: Our results suggest that increases in vWF levels and activity contribute to the persistence of systemic inflammation, as well as increasing cardiovascular risk, in COPD patients. Sociedade Brasileira de Pneumologia e Tisiologia 2014 /pmc/articles/PMC4201167/ /pubmed/25210959 http://dx.doi.org/10.1590/S1806-37132014000400004 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bártholo, Thiago Prudente
da Costa, Cláudia Henrique
Rufino, Rogério
Evaluation of von Willebrand factor in COPD patients
title Evaluation of von Willebrand factor in COPD patients
title_full Evaluation of von Willebrand factor in COPD patients
title_fullStr Evaluation of von Willebrand factor in COPD patients
title_full_unstemmed Evaluation of von Willebrand factor in COPD patients
title_short Evaluation of von Willebrand factor in COPD patients
title_sort evaluation of von willebrand factor in copd patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201167/
https://www.ncbi.nlm.nih.gov/pubmed/25210959
http://dx.doi.org/10.1590/S1806-37132014000400004
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