首页> 外文期刊>BMC Pulmonary Medicine >Can inhaled fluticasone alone or in combination with salmeterol reduce systemic inflammation in chronic obstructive pulmonary disease? – study protocol for a randomized controlled trial [NCT00120978]
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Can inhaled fluticasone alone or in combination with salmeterol reduce systemic inflammation in chronic obstructive pulmonary disease? – study protocol for a randomized controlled trial [NCT00120978]

机译:单独或与沙美特罗联合吸入氟替卡松是否可以减轻慢性阻塞性肺疾病的全身性炎症? –一项随机对照试验的研究方案[NCT00120978]

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Background Systemic inflammation is associated with various complications in chronic obstructive pulmonary disease including weight loss, cachexia, osteoporosis, cancer and cardiovascular diseases. Inhaled corticosteroids attenuate airway inflammation, reduce exacerbations, and improve mortality in chronic obstructive pulmonary disease. Whether inhaled corticosteroids by themselves or in combination with a long-acting β2-adrenoceptor agonist repress systemic inflammation in chronic obstructive pulmonary disease is unknown. The Advair Biomarkers in COPD (ABC) study will determine whether the effects of inhaled corticosteroids alone or in combination with a long-acting β2-adrenoceptor agonist reduce systemic inflammation and improve health status in patients with chronic obstructive pulmonary disease. Methods/Design After a 4-week run-in phase during which patients with stable chronic obstructive pulmonary disease will receive inhaled fluticasone (500 micrograms twice daily), followed by a 4-week withdrawal phase during which all inhaled corticosteroids and long acting β2-adrenoceptor agonists will be discontinued, patients will be randomized to receive fluticasone (500 micrograms twice daily), fluticasone/salmeterol combination (500/50 micrograms twice daily), or placebo for four weeks. The study will recruit 250 patients across 11 centers in western Canada. Patients must be 40 years of age or older with at least 10 pack-year smoking history and have chronic obstructive pulmonary disease defined as forced expiratory volume in one second to vital capacity ratio of 0.70 or less and forced expiratory volume in one second that is 80% of predicted or less. Patients will be excluded if they have any known chronic systemic infections, inflammatory conditions, history of previous solid organ transplantation, myocardial infarction, or cerebrovascular accident within the past 3 months prior to study enrolment. The primary end-point is serum C-reactive protein level. Secondary end-points include circulating inflammatory cytokines such as interleukin-6 and interleukin-8 as well as health-related quality of life and lung function. Discussion If inhaled corticosteroids by themselves or in combination with a long-acting β2-adrenoceptor agonist could repress systemic inflammation, they might greatly improve clinical prognosis by reducing various complications in chronic obstructive pulmonary disease.
机译:背景技术全身性炎症与慢性阻塞性肺疾病的各种并发症相关,包括体重减轻,恶病质,骨质疏松,癌症和心血管疾病。吸入皮质类固醇可减轻气道炎症,减轻病情恶化并提高慢性阻塞性肺疾病的死亡率。目前尚不清楚吸入皮质类固醇激素是单独服用还是与长效β 2 -肾上腺素能受体激动剂联用可抑制慢性阻塞性肺疾病的全身性炎症。 COPAIR中的Advair生物标志物(ABC)研究将确定吸入性糖皮质激素单独或与长效β 2 -肾上腺素受体激动剂联合使用是否能减轻慢性阻塞性肺疾病的系统性炎症并改善其健康状况肺病。方法/设计经过4周的磨合期,在此期间,稳定的慢性阻塞性肺疾病患者将接受吸入氟替卡松(每日两次,每次500微克),然后是4周戒断期,在此期间,所有吸入的糖皮质激素和长效β< sub> 2 -肾上腺素受体激动剂将停止使用,患者将被随机分配接受氟替卡松(每日两次,每次500微克),氟替卡松/沙美特罗组合(每天两次,每次500/50微克)或安慰剂治疗4周。该研究将在加拿大西部11个中心招募250名患者。患者必须年满40岁或以上,并且至少有10年的吸烟史,并且患有慢性阻塞性肺疾病,定义为一秒钟内的强制呼气量与肺活量之比等于或小于0.70,一秒钟内的强制呼气量为80预测的百分比或更少。如果患者在入组前三个月内有任何已知的慢性全身感染,炎性疾病,既往实体器官移植史,心肌梗塞或脑血管意外,则将其排除在外。主要终点是血清C反应蛋白水平。次要终点包括循环性炎性细胞因子,例如白介素6和白介素8,以及与健康相关的生活质量和肺功能。讨论如果吸入糖皮质激素本身或与长效β 2 -肾上腺素能受体激动剂联用可以抑制全身性炎症,则可以通过减少慢性阻塞性肺疾病的各种并发症来大大改善临床预后。

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