Centre de Recherche, Institut universitaire de cardiologie et de pneumologie de Québec, 2725 Chemin Sainte Foy, Québec City, QC, G1V 4G5, Canada.
Klinische Forschung Berlin GbR, Berlin, Germany.
Ther Adv Respir Dis. 2020 Jan-Dec;14:1753466620965145. doi: 10.1177/1753466620965145.
The relationship between inhaled corticosteroids and bone mineral density (BMD) remains uncertain despite extensive research.
This was an international, multicenter, randomized, double-blind, parallel-group, 3-year noninferiority study. Patients with chronic obstructive pulmonary disease (COPD) (⩾40 years of age; smoking history ⩾10 pack years) and at least one native hip evaluable for BMD were enrolled and randomized 1:1, stratified by sex, to treatment with vilanterol (VI) 25 µg or fluticasone furoate/vilanterol (FF/VI) 100 µg/25 µg. BMD measurements were taken dual-energy X-ray absorptiometry every 6 months. The primary endpoint was assessment of the noninferiority of change from baseline in total hip BMD per year at the -1% noninferiority level. Change from baseline in BMD at the lumbar spine and BMD measurements by sex were secondary endpoints. Incidences of COPD exacerbations and bone fractures throughout the study were also recorded.
Of 283 randomized patients, 170 (60%) completed the study. Noninferiority was demonstrated for FF/VI VI with regards to change from baseline in total hip BMD per year, with changes of -0.27% and 0.18%, respectively, and a treatment difference of -0.46% per year [95% confidence interval (CI) -0.97 to 0.06]. The treatment difference for FF/VI VI regarding lumbar spine BMD was -0.51% per year (95% CI -1.11 to 0.10). COPD exacerbations and bone fracture rates were similar between treatment groups.
FF/VI showed noninferiority to VI for change from baseline in total hip BMD per year, when assessed at the -1% noninferiority margin in a combined sample of men and women with COPD.
尽管进行了广泛的研究,但吸入皮质类固醇与骨密度(BMD)之间的关系仍不确定。
这是一项国际、多中心、随机、双盲、平行组、3 年非劣效性研究。招募了年龄 ⩾40 岁、吸烟史 ⩾10 包年且至少有一个可评估 BMD 的原生髋骨的慢性阻塞性肺疾病(COPD)患者,并按性别 1:1 分层,随机分为维兰特罗(VI)25μg或氟替卡松富马酸/维兰特罗(FF/VI)100μg/25μg治疗组。每 6 个月使用双能 X 射线吸收法测量一次 BMD。主要终点是在 -1%非劣效性水平评估每年总髋部 BMD 从基线的变化。次要终点是腰椎 BMD 的变化和按性别测量的 BMD。整个研究过程中 COPD 加重和骨折的发生率也被记录下来。
在 283 名随机患者中,有 170 名(60%)完成了研究。FF/VI 在每年总髋部 BMD 从基线的变化方面表现出非劣效性,分别为 -0.27%和 0.18%,治疗差异为每年 -0.46%[95%置信区间(CI)-0.97 至 0.06]。FF/VI 每年腰椎 BMD 的治疗差异为 -0.51%(95%CI-1.11 至 0.10)。治疗组之间 COPD 加重和骨折的发生率相似。
在 COPD 男女混合样本中,以 -1%非劣效性边界评估时,FF/VI 在每年总髋部 BMD 从基线的变化方面显示出非劣效性,优于 VI。