Rossi Andrea, Inciardi Riccardo M, Rossi Andrea, Temporelli Pier Luigi, Lucci Donata, Gonzini Lucio, Marchioli Roberto, Nicolosi Gian Luigi, Tavazzi Luigi
Department of Medicine, University of Verona, Verona, Italy; AIPO Study Center, Milano, Italy.
Cardiology Unit, Department of Medicine, University and General Hospital (AOUI) of Verona, Verona, Italy.
Pulm Pharmacol Ther. 2017 Jun;44:16-23. doi: 10.1016/j.pupt.2017.03.001. Epub 2017 Mar 3.
Rising evidences showed a possible protective role of statins in chronic obstructive pulmonary disease (COPD). We aimed to evaluate in a post-hoc analysis of the GISSI-HF trial the prognostic effect of the use of rosuvastatin in patients with co-existing COPD and HF, assuming that the anti-inflammatory properties of these drugs may imply a potential beneficial effect in these associated chronic inflammatory conditions.
We analyzed patients with chronic HF and history of COPD deriving from the GISSI-HF study. Of all 4574 patients eligible to statin, 1060 ambulatory patients with HF and concomitant COPD were enrolled and randomly assigned to rosuvastatin 10 mg daily (538 patients) or placebo (522 patients). The primary end-point was to compare all cause death rate in patients randomized to rosuvastatin or placebo. Further, we assessed the effects of rosuvastatin (10 mg daily) on cardiovascular (CV) death, non-CV death and hospital admissions. Median follow-up was 3.9 years with an interquartile range (IQR) of 3.0-4.4.
During the follow-up 438 (41.3%) patients died, 304 (28.6%) for CV death and 687 (64.8%) had at least one hospitalization. The two patient groups had similar outcome, irrespective of randomization, in terms of all-cause mortality (log-rank test p = 0.30) CV, non CV-death (p = 0.88 and 0.09 respectively) and all-cause hospitalization (p = 0.82). Cox regression analysis did not show a favorable association between the use of statin and the examined end-points both on unadjusted and adjusted models.
Statin use is not associated with a beneficial effects on all cause, CV, non CV mortality and hospitalization in patients with coexistent chronic HF and history of COPD. ClinicalTrials.gov Identifier: NCT00336336.
越来越多的证据表明他汀类药物在慢性阻塞性肺疾病(COPD)中可能具有保护作用。我们旨在对GISSI-HF试验进行事后分析,评估瑞舒伐他汀在合并COPD和心力衰竭(HF)患者中的预后效果,假设这些药物的抗炎特性可能对这些相关的慢性炎症性疾病具有潜在的有益作用。
我们分析了来自GISSI-HF研究的慢性HF且有COPD病史的患者。在所有符合使用他汀类药物条件的4574例患者中,1060例门诊HF合并COPD患者被纳入研究,并随机分为每日服用10mg瑞舒伐他汀组(538例患者)或安慰剂组(522例患者)。主要终点是比较随机分配至瑞舒伐他汀组或安慰剂组患者的全因死亡率。此外,我们评估了瑞舒伐他汀(每日10mg)对心血管(CV)死亡、非CV死亡和住院的影响。中位随访时间为3.9年,四分位间距(IQR)为3.0 - 4.4年。
在随访期间,438例(41.3%)患者死亡,304例(28.6%)死于CV死亡,687例(64.8%)至少有一次住院治疗。无论随机分组情况如何,两组患者在全因死亡率(对数秩检验p = 0.30)、CV死亡、非CV死亡(分别为p = 0.88和0.09)以及全因住院率(p = 0.82)方面的结局相似。Cox回归分析显示,在未调整和调整模型中,使用他汀类药物与所检查的终点之间均未显示出有利关联。
对于合并慢性HF和COPD病史的患者,使用他汀类药物与全因、CV、非CV死亡率及住院率的有益影响无关。ClinicalTrials.gov标识符:NCT00336336。