Kreuter Michael, Bonella Francesco, Maher Toby M, Costabel Ulrich, Spagnolo Paolo, Weycker Derek, Kirchgaessler Klaus-Uwe, Kolb Martin
Center for Interstitial and Rare Lung Diseases, Pneumology and Respiratory Critical Care Medicine, Thoraxklinik, University of Heidelberg, and Translational Lung Research Center Heidelberg (TLRCH), Heidelberg, Germany.
Member of the German Center for Lung Research (DZL), Heidelberg, Germany.
Thorax. 2017 Feb;72(2):148-153. doi: 10.1136/thoraxjnl-2016-208819. Epub 2016 Oct 5.
Data are conflicting regarding the possible effects of statins in patients with idiopathic pulmonary fibrosis (IPF). This post hoc analysis assessed the effects of statin therapy on disease-related outcomes in IPF.
Patients randomised to placebo (n=624) in three controlled trials of pirfenidone in IPF (CAPACITY 004 and 006, ASCEND) were categorised by baseline statin use. Outcomes assessed during the 1-year follow-up included disease progression, mortality, hospitalisation and composite outcomes of death or ≥10% absolute decline in FVC and death or ≥50 m decline in 6-minute walk distance (6MWD).
At baseline, 276 (44%) patients were statin users versus 348 (56%) non-users. Baseline characteristics were similar between groups, except statin users were older and had higher prevalence of cardiovascular disease and risk factors. In multivariate analyses adjusting for differences in baseline characteristics, statin users had lower risks of death or 6MWD decline (HR 0.69; 95% CI 0.48 to 0.99, p=0.0465), all-cause hospitalisation (HR 0.58; 95% CI 0.35 to 0.94, p=0.0289), respiratory-related hospitalisation (HR 0.44; 95% CI 0.25 to 0.80, p=0.0063) and IPF-related mortality (HR 0.36; 95% CI 0.14 to 0.95, p=0.0393) versus non-users. Non-significant treatment effects favouring statin use were observed for disease progression (HR 0.75; 95% CI 0.52 to 1.07, p=0.1135), all-cause mortality (HR 0.54; 95% CI 0.24 to 1.21, p=0.1369) and death or FVC decline (HR 0.71; 95% CI 0.48 to 1.07, p=0.1032).
This post hoc analysis supports the hypothesis that statins may have a beneficial effect on clinical outcomes in IPF. Prospective clinical trials are required to validate these observations.
NCT01366209, NCT00287729 and NCT00287716.
关于他汀类药物对特发性肺纤维化(IPF)患者可能产生的影响,数据存在冲突。这项事后分析评估了他汀类药物治疗对IPF患者疾病相关结局的影响。
在三项吡非尼酮治疗IPF的对照试验(CAPACITY 004和006、ASCEND)中被随机分配至安慰剂组(n = 624)的患者,根据基线他汀类药物使用情况进行分类。在1年随访期间评估的结局包括疾病进展、死亡率、住院率以及死亡或FVC绝对值下降≥10%和死亡或6分钟步行距离(6MWD)下降≥50米的复合结局。
基线时,276名(44%)患者使用他汀类药物,348名(56%)患者未使用。除了使用他汀类药物的患者年龄更大、心血管疾病及危险因素患病率更高外,两组间基线特征相似。在对基线特征差异进行校正的多变量分析中,与未使用者相比,使用他汀类药物的患者死亡或6MWD下降风险更低(HR 0.69;95% CI 0.48至0.99,p = 0.0465)、全因住院风险更低(HR 0.58;95% CI 0.35至0.94,p = 0.0289)、呼吸相关住院风险更低(HR 0.44;95% CI 0.25至0.80,p = 0.0063)以及IPF相关死亡率更低(HR 0.36;95% CI 0.14至0.95,p = 0.0393)。在疾病进展(HR 0.75;95% CI 0.52至1.07,p = 0.1135)、全因死亡率(HR 0.54;95% CI 0.24至1.21,p = 0.1369)和死亡或FVC下降(HR 0.71;95% CI 0.48至1.07,p = 0.1032)方面,观察到有利于使用他汀类药物的非显著治疗效果。
这项事后分析支持他汀类药物可能对IPF临床结局产生有益影响的假设。需要进行前瞻性临床试验来验证这些观察结果。
NCT01366209、NCT00287729和NCT00287716。