Differences in systemic inflammation between cigarette and biomass smoke-induced COPD

被引:55
作者
Golpe, Rafael [1 ]
Martin-Robles, Irene [1 ]
Sanjuan-Lopez, Pilar [1 ]
Perez-de-Llano, Luis [1 ]
Gonzalez-Juanatey, Carlos [2 ]
Lopez-Campos, Jose L. [3 ,4 ]
Arellano-Orden, Elena [4 ]
机构
[1] Univ Hosp Lucus Augusti, Med Res Serv, Lugo, Spain
[2] Univ Hosp Lucus Augusti, Serv Cardiol, Lugo, Spain
[3] Univ Hosp Virgen del Rocio, Med Surg Unit Resp Dis, Seville, Spain
[4] Carlos III Hlth Inst, Ctr Biomed Res Resp Dis Network, Madrid, Spain
关键词
biomass smoke; COPD; cytokines; inflammation; smoking; OBSTRUCTIVE PULMONARY-DISEASE; CARDIOVASCULAR-DISEASE; TOBACCO-SMOKE; EXPOSURE; RISK; PHENOTYPES; COMORBIDITIES; PROTEIN; PROFILE;
D O I
10.2147/COPD.S141068
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
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-alpha, 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.
引用
收藏
页码:2639 / 2646
页数:8
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