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他汀类药物联用非诺贝特的安全性荟萃分析 被引量:8

A meta-analysis on the safety of combination therapy with fenofibrate and statins
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摘要 目的系统评价他汀类药物联用非诺贝特的安全性。方法检索1981至2013年Medline、Cochrane Library、Web of Knowledge和中国知网数据库中的随机对照临床试验,采用RevMan5.0软件对所纳入的数据进行荟萃分析。共检索2184篇相关文献,有26篇文献入选,26项随机对照临床研究共纳入9494例患者。结果他汀类药物联合非诺贝特组转氨酶升高的风险明显高于单药他汀组(OR1.67,95%CI1.22—2.30,P〈0.05)。肌酸激酶升高(OR0.86,95%CI0.62—1.20,P〉0.05)、肌肉不良反应(OR 0.98,95%CI0.88—1.09,P〉0.05)、肝功异常和肌肉不良反应导致退出的发生率两组问差异无统计学意义。常规剂量他汀类药物联合非诺贝特的安全性与总剂量他汀类药物联合非诺贝特相似。结论他汀类药物联用非诺贝特具有良好的安全性和耐受性,不增加肌肉不良反应的风险。联合用药时要定期检测转氨酶,防止发生肝功能异常。 Objective The aim of this study was to assess the safety of fenofibrate-statin combination therapy. Methods Medline, Coehrane Library, Web of Knowledge and CNKI were searched for 2184 randomized controlled trims. Finally, twenty-six studies with a total of 9494 participants were included in this analysis. Results Compared with statins group, the fenofibrate-statin group had significantly higher incidence of aminotransferase elevations ( OR 1.67,95% CI 1.22 - 2. 30 ,P 〈 0. 05 ). The two groups had identical incidence of creatin kinase elevations ( OR 0. 86,95% CI 0. 62 - 1.20, P 〉 0. 05 ) , muscle- associated adverse events ( OR 0. 98,95% CI0. 88 - 1.09 ,P 〉 0. 05 ) and withdrawals due to hepatotoxicity or muscle toxicity. The safety of fenofibrate + standard-dose statin regimens were similar to those in fenofibrate-statin group. Conclusion Combined fenofibrate-statin treatment is generally safe and well tolerated, liver function should be monitored before and during and after therapy.
出处 《中华心血管病杂志》 CAS CSCD 北大核心 2013年第12期1063-1068,共6页 Chinese Journal of Cardiology
基金 国家自然科学基金(NSFC81070179,30570712)
关键词 降血脂药 可重复性 结果 META分析 Antilipemie agents Reprodueility of results Meta-analysis
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  • 1Farnier M. Combination therapy with an HMG-CoA reductase inhibitor and a fibric acid derivative. Am J Cardiovasc Drugs, 2003, 3 : 169-178.
  • 2Fruchart JC, Sacks FM, Hermans MP, et al. The residual risk reduction initiative : a call to action to reduce residual vascular risk indyslipidaemic patients. Diabetes Vasc Dis Res, 2008, 5: 319- 335.
  • 3Grundy SM, Vega GL, Yuan Z, et al. Effectiveness and tolerability of simvastatin plus fenofibrate for combined hyperlipidemia ( the SAFARI triM). Am J Cardiol, 2005, 5 : 462- 468.
  • 4Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med, 2009, 6: e1000097.
  • 5Higgins JPT, Green S. Cochrane handbook for systematic reviews of interventions[ M/OL]. USA : John Wiley & Sons, 2011 [ 2013- 03-21 ]. http://www, cochrane- handbook, org.
  • 6Muhlestein JB, May HT, Jensen JR, et al. The reduction of inflammatory binmarkers by statin, fibrate, and combination therapy among diabetic patients with mixed dyslipidaemia. The DIACOR (diabetes and combined lipid therapy regimen) study. J Am Coil Cardiol, 2006, 48:396-401.
  • 7Krysiak R, Gdula-Dymek A, Okopien B. Effect of simvastatin and fenofibrate on cytokine release and systemic inflammation in type 2 diabetes mellitus with mixed dyslipidemia. Am J Cardiol, 2011, 107 : 1010-1018.
  • 8Derosa G, Maffioli P, Salvadeoa SA, et al. Fenofibrate, simvastatin and their combination in the management of dyslipidaemia in type 2 diabetic patients. Curr Med Res Opin, 2009, 25 : 1973-1983.
  • 9Derosa G, Cicero AE, Bertone G, et al. Comparison of fluvastatin + fenofibrate combination therapy and fluvastatin monotherapy in the treatment of combined byperhpidemia, type 2 diabetes mellitus, and coronary heart disease : a 12-month, randomized, double-blind, controlled trial. Clin Ther, 2004, 26 : 1599-1607.
  • 10Agouridis AP, Tsimihodimos V, Filippatos TD, et al. High doses of rosuvastatin are superior to low doses of rosuvastatin plus fenofibrate or n-3 fatty acids in mixed dyslipidemia. Lipids, 2011, 46 : 521-528.

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