Previous tuberculosis disease as a risk factor for chronic obstructive pulmonary disease: a cross-sectional analysis of multicountry, population-based studies

医学 慢性阻塞性肺病 肺结核 优势比 横断面研究 内科学 人口 疾病 肺活量 风险因素 阻塞性肺病 环境卫生 肺功能 病理 扩散能力
作者
Katarina Kamenar,Shakir Hossen,Akshay Gupte,Trishul Siddharthan,Suzanne L. Pollard,Muhammad Chowdhury,Adolfo Rubinstein,Vilma Irazola,Laura Gutiérrez,J. Jaime Miranda,Antonio Bernabé-Ortíz,Dewan S Alam,Bruce Kirenga,Rupert Jones,Frederik van Gemert,Robert A. Wise,William Checkley
出处
期刊:Thorax [BMJ]
卷期号:77 (11): 1088-1097 被引量:21
标识
DOI:10.1136/thoraxjnl-2020-216500
摘要

Background Risk factors for COPD in high-income settings are well understood; however, less attention has been paid to contributors of COPD in low-income and middle-income countries (LMICs) such as pulmonary tuberculosis. We sought to study the association between previous tuberculosis disease and COPD by using pooled population-based cross-sectional data in 13 geographically diverse, low-resource settings. Methods We pooled six cohorts in 13 different LMIC settings, 6 countries and 3 continents to study the relationship between self-reported previous tuberculosis disease and lung function outcomes including COPD (defined as a postbronchodilator forced expiratory volume in one second (FEV 1 )/forced vital capacity (FVC) below the lower limit of normal). Multivariable regressions with random effects were used to examine the association between previous tuberculosis disease and lung function outcomes. Results We analysed data for 12 396 participants (median age 54.0 years, 51.5% male); 332 (2.7%) of the participants had previous tuberculosis disease. Overall prevalence of COPD was 8.8% (range 1.7%–15.5% across sites). COPD was four times more common among those with previous tuberculosis disease (25.7% vs 8.3% without previous tuberculosis disease, p<0.001). The adjusted odds of having COPD was 3.78 times higher (95% CI 2.87 to 4.98) for participants with previous tuberculosis disease than those without a history of tuberculosis disease. The attributable fraction of COPD due to previous tuberculosis disease in the study sample was 6.9% (95% CI 4.8% to 9.6%). Participants with previous tuberculosis disease also had lower prebronchodilator Z-scores for FEV 1 (−0.70, 95% CI −0.84 to −0.55), FVC (−0.44, 95% CI −0.59 to −0.29) and the FEV 1 :FVC ratio (−0.63, 95% CI −0.76 to −0.51) when compared with those without previous tuberculosis disease. Conclusions Previous tuberculosis disease is a significant and under-recognised risk factor for COPD and poor lung function in LMICs. Better tuberculosis control will also likely reduce the global burden of COPD.
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