Chronic respiratory disease, inhaled corticosteroids and risk of non-tuberculous mycobacteriosis

被引:240
作者
Andrejak, Claire [1 ,2 ,3 ,4 ]
Nielsen, Rikke [1 ]
Thomsen, Vibeke O. [5 ]
Duhaut, Pierre [3 ,6 ]
Sorensen, Henrik Toft [1 ]
Thomsen, Reimar Wernich [1 ]
机构
[1] Aarhus Univ Hosp, Inst Clin Med, Dept Clin Epidemiol, DK-8000 Aarhus, Denmark
[2] Picardie Jules Verne Univ, Teaching Hosp Amiens, Dept Resp Dis, Amiens, France
[3] Reseau Epidemiol Int Francophone Unit, Amiens, France
[4] Picardie Jules Verne Univ, INSERM, U1088, Amiens, France
[5] Statens Serum Inst, Int Reference Lab Mycobacteriol, DK-2300 Copenhagen, Denmark
[6] Picardie Jules Verne Univ, Teaching Hosp Amiens, Dept Internal Med, Amiens, France
关键词
OBSTRUCTIVE PULMONARY-DISEASE; AFRICAN GOLD MINERS; BUDESONIDE; PREVALENCE; BRONCHIECTASIS; INFECTIONS; PNEUMONIA; DIAGNOSIS;
D O I
10.1136/thoraxjnl-2012-201772
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Chronic respiratory disease and inhaled corticosteroid (ICS) therapy for chronic obstructive pulmonary disease (COPD) increase the risk of pneumonia. Few data are available on the association of these risk factors with non-tuberculous mycobacterial (NTM) pulmonary disease. Methods This study examined chronic respiratory diseases and ICS use as risk factors in a population-based case-control study encompassing all adults in Denmark with microbiologically confirmed NTM pulmonary disease between 1997 and 2008. The study included 10 matched population controls per case. Conditional logistic regression was used to compute adjusted ORs for NTM pulmonary disease with regard to chronic respiratory disease history. Results Overall, chronic respiratory disease was associated with a 16.5-fold (95% CI 12.2 to 22.2) increased risk of NTM pulmonary disease. The adjusted OR for NTM disease was 15.7 (95% CI 11.4 to 21.5) for COPD, 7.8 (95% CI 5.2 to 11.6) for asthma, 9.8 (95% CI 2.03 to 52.8) for pneumoconiosis, 187.5 (95% CI 24.8 to 1417.4) for bronchiectasis, and 178.3 (95% CI 55.4 to 574.3) for tuberculosis history. ORs were 29.1 (95% CI 13.3 to 63.8) for patients with COPD on current ICS therapy and 7.6 (95% CI 3.4 to 16.8) for patients with COPD who had never received ICS therapy. Among patients with COPD, ORs increased according to ICS dose, from 28.1 for low-dose intake to 47.5 for high-dose intake (more than 800 mu g/day). The OR was higher for fluticasone than for budesonide. Conclusion Chronic respiratory disease, particularly COPD treated with ICS therapy, is a strong risk factor for NTM pulmonary disease.
引用
收藏
页码:256 / 262
页数:7
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