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Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome
Background. Obesity and asthma are associated. There is a relationship between lung function impairment and the metabolic syndrome. Whether this relationship also exists in the morbidly obese patients is still unknown. Hypothesis. Low-grade systemic inflammation associated with the metabolic syndrom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595660/ https://www.ncbi.nlm.nih.gov/pubmed/23509614 http://dx.doi.org/10.1155/2013/131349 |
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author | van Huisstede, Astrid Cabezas, Manuel Castro Birnie, Erwin van de Geijn, Gert-Jan M. Rudolphus, Arjan Mannaerts, Guido Njo, Tjin L. Hiemstra, Pieter S. Braunstahl, Gert-Jan |
author_facet | van Huisstede, Astrid Cabezas, Manuel Castro Birnie, Erwin van de Geijn, Gert-Jan M. Rudolphus, Arjan Mannaerts, Guido Njo, Tjin L. Hiemstra, Pieter S. Braunstahl, Gert-Jan |
author_sort | van Huisstede, Astrid |
collection | PubMed |
description | Background. Obesity and asthma are associated. There is a relationship between lung function impairment and the metabolic syndrome. Whether this relationship also exists in the morbidly obese patients is still unknown. Hypothesis. Low-grade systemic inflammation associated with the metabolic syndrome causes inflammation in the lungs and, hence, lung function impairment. Methods. This is cross-sectional study of morbidly obese patients undergoing preoperative screening for bariatric surgery. Metabolic syndrome was assessed according to the revised NCEP-ATP III criteria. Results. A total of 452 patients were included. Patients with the metabolic syndrome (n = 293) had significantly higher blood monocyte (mean 5.3 versus 4.9, P = 0.044) and eosinophil percentages (median 1.0 versus 0.8, P = 0.002), while the total leukocyte count did not differ between the groups. The FEV(1)/FVC ratio was significantly lower in patients with the metabolic syndrome (76.7% versus 78.2%, P = 0.032). Blood eosinophils were associated with FEV(1)/FVC ratio (adj. B −0.113, P = 0.018). Conclusion. Although the difference in FEV(1)/FVC ratio between the groups is relatively small, in this cross-sectional study, and its clinical relevance may be limited, these data indicate that the presence of the metabolic syndrome may influence lung function impairment, through the induction of relative eosinophilia. |
format | Online Article Text |
id | pubmed-3595660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35956602013-03-18 Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome van Huisstede, Astrid Cabezas, Manuel Castro Birnie, Erwin van de Geijn, Gert-Jan M. Rudolphus, Arjan Mannaerts, Guido Njo, Tjin L. Hiemstra, Pieter S. Braunstahl, Gert-Jan J Obes Clinical Study Background. Obesity and asthma are associated. There is a relationship between lung function impairment and the metabolic syndrome. Whether this relationship also exists in the morbidly obese patients is still unknown. Hypothesis. Low-grade systemic inflammation associated with the metabolic syndrome causes inflammation in the lungs and, hence, lung function impairment. Methods. This is cross-sectional study of morbidly obese patients undergoing preoperative screening for bariatric surgery. Metabolic syndrome was assessed according to the revised NCEP-ATP III criteria. Results. A total of 452 patients were included. Patients with the metabolic syndrome (n = 293) had significantly higher blood monocyte (mean 5.3 versus 4.9, P = 0.044) and eosinophil percentages (median 1.0 versus 0.8, P = 0.002), while the total leukocyte count did not differ between the groups. The FEV(1)/FVC ratio was significantly lower in patients with the metabolic syndrome (76.7% versus 78.2%, P = 0.032). Blood eosinophils were associated with FEV(1)/FVC ratio (adj. B −0.113, P = 0.018). Conclusion. Although the difference in FEV(1)/FVC ratio between the groups is relatively small, in this cross-sectional study, and its clinical relevance may be limited, these data indicate that the presence of the metabolic syndrome may influence lung function impairment, through the induction of relative eosinophilia. Hindawi Publishing Corporation 2013 2013-02-24 /pmc/articles/PMC3595660/ /pubmed/23509614 http://dx.doi.org/10.1155/2013/131349 Text en Copyright © 2013 Astrid van Huisstede 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 | Clinical Study van Huisstede, Astrid Cabezas, Manuel Castro Birnie, Erwin van de Geijn, Gert-Jan M. Rudolphus, Arjan Mannaerts, Guido Njo, Tjin L. Hiemstra, Pieter S. Braunstahl, Gert-Jan Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title | Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title_full | Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title_fullStr | Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title_full_unstemmed | Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title_short | Systemic Inflammation and Lung Function Impairment in Morbidly Obese Subjects with the Metabolic Syndrome |
title_sort | systemic inflammation and lung function impairment in morbidly obese subjects with the metabolic syndrome |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595660/ https://www.ncbi.nlm.nih.gov/pubmed/23509614 http://dx.doi.org/10.1155/2013/131349 |
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