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Early detection of COPD patients in GOLD 0 population: an observational non-interventional cohort study - MARKO study

机译:GOLD 0人群中COPD患者的早期发现:一项观察性非干预队列研究-MARKO研究

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Background Main risk factor for the development of chronic obstructive pulmonary disease (COPD) is smoking, although only less than 1/3 of smokers develop clinically manifest COPD. COPD’s progressive nature with high disability and mortality makes it plausible to detect it as early as possible thus allowing for an early intervention. The only tool for an early diagnosis that could be used on the global scale is spirometry, even though symptoms and deprivation of health related quality of life (HRQoL) precede relevant spirometric changes. Existing HRQoL questionnaires are too complicated or not developed for an early detection of COPD. The aim of our study was to develop a new simple HRQoL tool that will allow (alone or in combination with other markers) early detection of patients with COPD. Methods A multicenter prospective cohort study recruiting 500 subjects at risk for COPD (smokers/ex-smokers ≥20 pack-years, 40–65 years, both sexes, with no prior diagnosis of COPD) will be carried out in two phases: (1) cross-sectional - development and validation of a new questionnaire; and (2) prospective - follow-up of a cohort of patients at risk for COPD. Subjects were recruited by 25 GPs and assessed for COPD by dedicated pulmonologists in 7 hospital centers using a predefined protocol: HRQoL, history, physical, blood sampling, exhaled breath temperature (EBT), lung function, 6-min walk test (6MWT). Patients without COPD and those in GOLD stage 1 at initial assessment will be reassessed for disease progression by the same pulmonologist after 2 and 5?years. Discussion This is one of the first cohort studies attempting to establish the incidence of COPD in the pre-symptomatic stage before significant end organ damage. We intend to assess the validity, predictability and discriminative power (‘healthy’ smokers vs. pre-symptomatic phase in newly developed COPD) of newly developed HRQoL tool alone or in combination with other markers; EBT, lung function, 6MWT, genomics, transcriptomics, proteomics). We expect that the results of this study can improve our understanding of the development of COPD, identify some new underlying pathophysiological pathways, and offer to sensitive smokers/ex-smokers new preventive and early intervention measures thus improving the management of COPD. Trial registration Clinicaltrial.gov NCT01550679 retrospectively registered February 28, 2012.
机译:背景技术慢性阻塞性肺疾病(COPD)发生的主要危险因素是吸烟,尽管只有不到1/3的吸烟者发展出临床表现为COPD。 COPD具有高度的残障和高死亡率,因此具有进步性,因此可以尽早发现它,从而可以及早进行干预。肺活量测定法是可在全球范围内使用的唯一早期诊断工具,即使症状和健康相关生活质量(HRQoL)丧失也先于相关的肺活量测定法改变。现有的HRQoL问卷太复杂或无法开发,无法及早发现COPD。我们研究的目的是开发一种新的简单HRQoL工具,该工具可以(单独或与其他标志物结合使用)早期检测COPD患者。方法:一项多中心的前瞻性队列研究将分两个阶段进行,该研究招募了500名有COPD风险的受试者(吸烟者/前吸烟者≥20包年,40-65岁,男女,均未事先诊断为COPD): )横断面-开发和验证新的问卷; (2)前瞻性-跟踪有COPD风险的患者队列。由25名GP招募受试者,并由7个医院中心的专职肺科医师按照以下预定规程评估COPD:HRQoL,病史,身体,血液采样,呼气温度(EBT),肺功能,6分钟步行测试(6MWT)。最初评估时无COPD的患者和处于GOLD 1期的患者将在2年和5年后由同一位肺科医师重新评估疾病进展。讨论这是第一批试图确定症状严重之前终末器官损害之前的COPD发病率的队列研究之一。我们打算单独评估新开发的HRQoL工具或与其他标记结合使用的有效性,可预测性和判别力(“健康的吸烟者与新开发的COPD中的症状前期”)。 EBT,肺功能,6MWT,基因组学,转录组学,蛋白质组学)。我们希望这项研究的结果可以增进我们对COPD发生发展的了解,确定一些新的潜在病理生理途径,并为敏感的吸烟者/吸烟者提供新的预防和早期干预措施,从而改善COPD的管理。试用注册Clinicaltrial.gov NCT01550679追溯注册于2012年2月28日。

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