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Differences in systemic inflammation between cigarette and biomass smoke-induced COPD.
Golpe, Rafael; Martín-Robles, Irene; Sanjuán-López, Pilar; Pérez-de-Llano, Luis; González-Juanatey, Carlos; López-Campos, José L; Arellano-Orden, Elena.
Afiliação
  • Golpe R; Respiratory Medicine Service.
  • Martín-Robles I; Respiratory Medicine Service.
  • Sanjuán-López P; Respiratory Medicine Service.
  • Pérez-de-Llano L; Respiratory Medicine Service.
  • González-Juanatey C; Cardiology Service, University Hospital Lucus Augusti, Lugo.
  • López-Campos JL; Medical-Surgical Unit of Respiratory Diseases, University Hospital Virgen del Rocío, Sevilla.
  • Arellano-Orden E; Center for Biomedical Research in Respiratory Diseases Network, Carlos III Health Institute, Madrid, Spain.
Int J Chron Obstruct Pulmon Dis ; 12: 2639-2646, 2017.
Article em En | MEDLINE | ID: mdl-28979110
ABSTRACT
BACKGROUND AND

OBJECTIVE:

It is known that biomarkers of systemic inflammation are raised in COPD caused by tobacco (T-COPD) compared with healthy controls, but there is less information on the inflammatory status of subjects with COPD caused by biomass smoke (B-COPD). In addition, the possible (if any) differences in inflammation between both types of the disease are still not well known. The aim of this study was to assess the inflammatory profile in B-COPD and T-COPD.

METHODS:

A total of 20 subjects (15 men and five women) with T-COPD were matched one to one for sex, age and forced expiratory volume in 1 s (FEV1) to 20 B-COPD patients. In all, 20 sex-matched healthy subjects with normal lung function without smoking history or biomass exposure were included as controls. The following biomarkers were measured exhaled nitric oxide, serum IL-6, IL-8, IL-5, IL-13, periostin, surfactant protein-P, TNF-α, IgE, erythrocyte sedimentation rate, C-reactive protein and fibrinogen. Complete blood count was also obtained.

RESULTS:

The age of the subjects was 70.2±7.9 years and FEV1% was 56.2%±14.6%. Most inflammatory biomarkers were higher in both types of COPD than in healthy controls. IL-6, IL-8 and IL-5 were significantly higher in T-COPD than in B-COPD, without other significant differences.

CONCLUSION:

Both types of COPD are associated with high levels of systemic inflammation biomarkers. T-COPD patients have a higher systemic inflammatory status than the patients with B-COPD.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumaça / Fumar / Mediadores da Inflamação / Biomassa / Doença Pulmonar Obstrutiva Crônica Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumaça / Fumar / Mediadores da Inflamação / Biomassa / Doença Pulmonar Obstrutiva Crônica Idioma: En Ano de publicação: 2017 Tipo de documento: Article