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Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease

COPD (chronic obstructive pulmonary disease) is a common lung disease characterized by airflow limitation and systemic inflammation. Recently, adipose tissue mediated inflammation has gathered increasing interest in the pathogenesis of the disease. In this study, we investigated the role of novel ad...

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Autores principales: Leivo-Korpela, Sirpa, Lehtimäki, Lauri, Hämälainen, Mari, Vuolteenaho, Katriina, Kööbi, Lea, Järvenpää, Ritva, Kankaanranta, Hannu, Saarelainen, Seppo, Moilanen, Eeva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033393/
https://www.ncbi.nlm.nih.gov/pubmed/24891763
http://dx.doi.org/10.1155/2014/232167
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author Leivo-Korpela, Sirpa
Lehtimäki, Lauri
Hämälainen, Mari
Vuolteenaho, Katriina
Kööbi, Lea
Järvenpää, Ritva
Kankaanranta, Hannu
Saarelainen, Seppo
Moilanen, Eeva
author_facet Leivo-Korpela, Sirpa
Lehtimäki, Lauri
Hämälainen, Mari
Vuolteenaho, Katriina
Kööbi, Lea
Järvenpää, Ritva
Kankaanranta, Hannu
Saarelainen, Seppo
Moilanen, Eeva
author_sort Leivo-Korpela, Sirpa
collection PubMed
description COPD (chronic obstructive pulmonary disease) is a common lung disease characterized by airflow limitation and systemic inflammation. Recently, adipose tissue mediated inflammation has gathered increasing interest in the pathogenesis of the disease. In this study, we investigated the role of novel adipocytokines nesfatin-1 and visfatin in COPD by measuring if they are associated with the inflammatory activity, lung function, or symptoms. Plasma levels of NUCB2/nesfatin-1 and visfatin were measured together with IL-6, IL-8, TNF-α, and MMP-9, lung function, exhaled nitric oxide, and symptoms in 43 male patients with emphysematous COPD. The measurements were repeated in a subgroup of the patients after four weeks' treatment with inhaled fluticasone. Both visfatin and NUCB2/nesfatin-1 correlated positively with plasma levels of IL-6 (r = 0.341, P = 0.027 and rho = 0.401, P = 0.008, resp.) and TNF-α (r = 0.305, P = 0.052 and rho = 0.329, P = 0.033, resp.) and NUCB2/nesfatin-1 also with IL-8 (rho = 0.321, P = 0.036) in patients with COPD. Further, the plasma levels of visfatin correlated negatively with pulmonary diffusing capacity (r = −0.369, P = 0.016). Neither of the adipokines was affected by fluticasone treatment and they were not related to steroid-responsiveness. The present results introduce adipocytokines NUCB2/nesfatin-1 and visfatin as novel factors associated with systemic inflammation in COPD and suggest that visfatin may mediate impaired pulmonary diffusing capacity.
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spelling pubmed-40333932014-06-02 Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease Leivo-Korpela, Sirpa Lehtimäki, Lauri Hämälainen, Mari Vuolteenaho, Katriina Kööbi, Lea Järvenpää, Ritva Kankaanranta, Hannu Saarelainen, Seppo Moilanen, Eeva Mediators Inflamm Research Article COPD (chronic obstructive pulmonary disease) is a common lung disease characterized by airflow limitation and systemic inflammation. Recently, adipose tissue mediated inflammation has gathered increasing interest in the pathogenesis of the disease. In this study, we investigated the role of novel adipocytokines nesfatin-1 and visfatin in COPD by measuring if they are associated with the inflammatory activity, lung function, or symptoms. Plasma levels of NUCB2/nesfatin-1 and visfatin were measured together with IL-6, IL-8, TNF-α, and MMP-9, lung function, exhaled nitric oxide, and symptoms in 43 male patients with emphysematous COPD. The measurements were repeated in a subgroup of the patients after four weeks' treatment with inhaled fluticasone. Both visfatin and NUCB2/nesfatin-1 correlated positively with plasma levels of IL-6 (r = 0.341, P = 0.027 and rho = 0.401, P = 0.008, resp.) and TNF-α (r = 0.305, P = 0.052 and rho = 0.329, P = 0.033, resp.) and NUCB2/nesfatin-1 also with IL-8 (rho = 0.321, P = 0.036) in patients with COPD. Further, the plasma levels of visfatin correlated negatively with pulmonary diffusing capacity (r = −0.369, P = 0.016). Neither of the adipokines was affected by fluticasone treatment and they were not related to steroid-responsiveness. The present results introduce adipocytokines NUCB2/nesfatin-1 and visfatin as novel factors associated with systemic inflammation in COPD and suggest that visfatin may mediate impaired pulmonary diffusing capacity. Hindawi Publishing Corporation 2014 2014-05-06 /pmc/articles/PMC4033393/ /pubmed/24891763 http://dx.doi.org/10.1155/2014/232167 Text en Copyright © 2014 Sirpa Leivo-Korpela et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Leivo-Korpela, Sirpa
Lehtimäki, Lauri
Hämälainen, Mari
Vuolteenaho, Katriina
Kööbi, Lea
Järvenpää, Ritva
Kankaanranta, Hannu
Saarelainen, Seppo
Moilanen, Eeva
Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title_full Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title_fullStr Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title_full_unstemmed Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title_short Adipokines NUCB2/Nesfatin-1 and Visfatin as Novel Inflammatory Factors in Chronic Obstructive Pulmonary Disease
title_sort adipokines nucb2/nesfatin-1 and visfatin as novel inflammatory factors in chronic obstructive pulmonary disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033393/
https://www.ncbi.nlm.nih.gov/pubmed/24891763
http://dx.doi.org/10.1155/2014/232167
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