Bonsu Kwadwo Osei, Reidpath Daniel Diamond, Kadirvelu Amudha
School of Medicine and Health Sciences, Monash University, Sunway Campus, Jalan Lagoon Selatan, Bandar Sunway, 46150, Selangor DE, Malaysia.
Pharmacy Department, Accident and Emergency Directorate, Komfo Anokye Teaching Hospital, P.O. Box 1934, Kumasi, Ghana.
Cardiovasc Drugs Ther. 2016 Apr;30(2):177-88. doi: 10.1007/s10557-015-6636-z.
This study aims to compare lipophilic and hydrophilic statin therapy on clinical outcomes of heart failure (HF) using a systematic review and an adjusted indirect comparison meta-analysis. Outcomes were all-cause mortality, cardiovascular mortality, cardiovascular hospitalization and hospitalization for worsening HF.
We conducted a search of PubMed, EMBASE and Cochrane databases until 31st December 2014 for randomized control trials (RCTs) in HF evaluating statins versus placebo. Identified RCTs and their respective abstracted information were grouped according to statin type evaluated and analyzed separately. Outcomes were initially pooled with the Peto's one-step method, producing odd ratios (OR) and 95 % confidence intervals (CI) for each statin type. Using these pooled estimates, we performed adjusted indirect comparisons of lipophilic versus hydrophilic statin for each outcome.
Thirteen studies involving 10,966 patients were identified and analyzed. Lipophilic statins were superior to hydrophilic rosuvastatin regarding all-cause mortality (OR 0 · 50; 95 % CI, 0 · 11-0 · 89; p = 0 · 01), cardiovascular mortality (OR 0 · 61; 0 · 25-0 · 97; p = 0 · 009), and hospitalization for worsening HF (OR 0 · 52; 0 · 21-0 · 83; p = 0 · 0005). However, both statins were comparable with regards to cardiovascular hospitalization [OR 0 · 80 (0 · 31, 1 · 28); p = 0 · 36].
Lipophilic statin treatment shows significant decreases in all-cause mortality, cardiovascular mortality and hospitalization for worsening HF compared with rosuvastatin treatment. This meta-analysis provides preliminary evidence that lipophilic statins offer better clinical outcomes in HF till data from head to head comparisons are available.
本研究旨在通过系统评价和校正间接比较荟萃分析,比较亲脂性他汀类药物和亲水性他汀类药物对心力衰竭(HF)临床结局的影响。结局指标包括全因死亡率、心血管死亡率、心血管住院率以及因HF恶化导致的住院率。
我们检索了截至2014年12月31日的PubMed、EMBASE和Cochrane数据库,以查找评估他汀类药物与安慰剂治疗HF的随机对照试验(RCT)。根据所评估的他汀类药物类型,将纳入的RCT及其各自提取的信息进行分组并分别分析。结局指标最初采用Peto一步法进行合并,得出每种他汀类药物的比值比(OR)和95%置信区间(CI)。利用这些合并估计值,我们对每种结局指标的亲脂性他汀类药物和亲水性他汀类药物进行了校正间接比较。
共识别并分析了13项研究,涉及10966例患者。在全因死亡率(OR 0.50;95%CI,0.11 - 0.89;p = 0.01)、心血管死亡率(OR 0.61;0.25 - 0.97;p = 0.009)以及因HF恶化导致的住院率(OR 0.52;0.21 - 0.83;p = 0.0005)方面,亲脂性他汀类药物优于亲水性瑞舒伐他汀。然而,在心血管住院率方面,两种他汀类药物相当[OR 0.80(0.31,1.28);p = 0.36]。
与瑞舒伐他汀治疗相比,亲脂性他汀类药物治疗在全因死亡率、心血管死亡率以及因HF恶化导致的住院率方面显著降低。这项荟萃分析提供了初步证据,表明在获得头对头比较的数据之前,亲脂性他汀类药物在HF中能提供更好的临床结局。