期刊文献+

奥利司他对肥胖症治疗作用的Meta分析 被引量:3

A meta analysis of Orlistat on treatment of obesity
下载PDF
导出
摘要 目的 系统评价奥利司他对肥胖患者减重和改善心血管相关危险因素的作用。 方法 收集多个数据库的随机、对照、双盲研究15个 ,用RevMan4.1软件进行随机效应模型的统计处理 ,并进行异质性检验和敏感性分析 ,效应量为加权平均差异(WMD)和相对危险度(RR)。 结果 减重1年后奥利司他组体重下降百分比的WMD值(95 %可信区间 )为 -2.78%( -3.26%,-2.30%) ,<10 %减重比例的RR值为0.84(0.81,0.87) ,总胆固醇和低密度脂蛋白的WMD值为 -6.06%( -7.32%,-4.81 %)和 -7.29 %( -8.92%,-5.66%)。继续维持体重1年后,<10 %减重比例的RR值为0.86(0.82,0.91) ,总胆固醇、低密度脂蛋白的WMD值为 -5.89 %( -7.60%,-4.18 %)、-6.53 %( -9.00%,-4.05%) ,并腰围缩小和血糖、胰岛素、血压水平改善。 结论 奥利司他是一种安全、有效的减肥药物 ,结合行为调整治疗等更易达到临床治疗目的。 Objective To evaluate the effect of Orlistat in treatment of weight loss,weight maintenance and improvement of relative cardiovascular risk factors in obese patients.Methods Fifteen randomized placebo-con-trolled double-blinded trials were selected from different databases,analyzed by RevMan4.1software.Random Ef-fect Model was applied to analyze the pooled results and heterogeneity.Sensitivity analysis was done by calculating the fail-safe number.For continuous data,a pooled weighted mean difference(WMD)was generated and a summary relative risk(RR)was calculated for dichotomous variables.Results After1-year treatment of Orlistat,WMD of weight loss percentage was-2.78%(-3.26%,-2.30%).The RR of Orlistat-treated patients who lost<10% initial body weight were0.84(0.81,0.87).The WMD of total serum cholesterol and LDL-cholesterol were -6.06%(-7.32%,-4.81%)and-7.29%(-8.92%,-5.66%)respectively.At the end of second year,the RR of Orlistat-treated patients who lost<10%initial body weight were0.86(0.82,0.91).The WMD of to-tal serum cholesterol and LDL-cholesterol were-5.89%(-7.60%,-4.18%)and-6.53%(-9.00%,-4.05%).Orlistat was also associated with greater improvements than placebo in waist circumference,fasting plasma glucose,HbA 1C ,serum insulin and blood pressure.Conclusion Orlistat is an effective,safe new drug to treat obesity.With other methods,such as behavior adjustment,it will get more weight loss,weight maintenance and improvements of relative risk factors.
作者 张晋红 李红
出处 《浙江医学》 CAS 2003年第5期268-271,共4页 Zhejiang Medical Journal
关键词 奥利司他 肥胖症 治疗 META 危险因素 敏感性分析 Lipase-antagonists-and-inhibitors Obesity Meta analysis
  • 相关文献

参考文献19

  • 1Lindgarde F.The effect of Orlistat on body weight and coronary hert disease risk profile in obese patients:the Swedish Muhimorbidity Study.J Intern Med,2000,248(3) :245.
  • 2Hollander PA, Elbein SC, Hirsch IB, et al. Role of Orlistat in the treatment of obese patients with type 2 diabetes. A 1 - year randomized double - blind study. Disbetes Care, 1998,21(8) : 1288.
  • 3Reaven G, Segal K, Hauptman J, et al. Effect of Orlistat - assisted weight loss in decreasing coronary heart disease risk in patients with syndrome X. Am J Cardiol, 2001,87 (7) : 827.
  • 4Kelley DE, Bray GA, Pi - Sunyer FX, et al. Clinical efficacy of Orlistat therapy in overweight and obese patients with insulin- treated type 2 diabetes : a 1 - year randomized controlled trial . Diabetes Care,2002,25(6) : 1033.
  • 5Sjostrom L, Rissanen A, Andersen T, et al. Randomised placebocontrolled trial of Orlistat for weight loss and prevention of weight regain in obese patients. European Multicentre Orlistat Study Group.Lancet, 1998,352(9123) : 167.
  • 6Davidson MH, Hauptman J, DiGirolamo M, et al. Weight control and risk factor reduction in obese subjects treated for 2 years with Orlistat:a randomized controlled trial.JAMA, 1999,281(3) :235.
  • 7Hauptman J, Lucas C, Boldrin MN, et al. Orlistat in the long -term treatment of obesity in primary care settings.Arch Fam Med,2000,9(2) : 160.
  • 8Rossner S, Sjostrom L, Noack R, et al. Weight loss, weight maintenance, and improved cardiovascular risk factors after 2 years treatment with Orlistat for obesity. Obes Res, 2000, 8: 49.
  • 9Hill JO, Hauptman J, Anderson JW, et al. Orlistat, a lipase inhibitor,for weight maitenance after conventional dieting:a 1 -y study.Am J Clin Nutr, 1999, 69:1108.
  • 10Finer N, James WP, Kopelman PC., et al. One - year treatment of obesity : a randomized, double - blind, placebo - controlled, multicentre study of Orlistat, a gastrointestinal lipase inhibitor. Int J Obes Relat Metab Disord,2000,24:306.

二级参考文献4

  • 1Ge L,Asia Pacific J Clin Nutr,1997年,6卷,175页
  • 2方圻,中华心血管病杂志,1997年,25卷,169页
  • 3Chan J M,Diabetes Care,1994年,17卷,961页
  • 4方圻,王钟林,宁田海,邵耕,陈在嘉,陆宗良,李健斋,林传骧,周北凡,诸骏仁,诸永康,陶萍,陶寿淇,龚兰生,顾复生,游凯,戴玉华.血脂异常防治建议[J].中华心血管病杂志,1997,25(3):169-175. 被引量:3067

共引文献41

同被引文献44

  • 1Dooley M, Plosker GL. Levetiracetam. A review of its adjunctive use in the management of partial onset seizures[ J ]. Drugs, 2000,60(4) :871 - 893.
  • 2Temkin NR. Antiepileptogenesis and seizure prevention trials with antiepileptic drugs: meta-analysis of controlled trials [ J ].Epilepsia ,2001,42(4) :515 - 524.
  • 3Shorvon SD,Lowenthal A, Janz D, et al. Multicenter doubleblind, randomized, placebo-controlled trial of levetiracetam as add-on therapy in patients with refractory partial seizures [ J ]. Epilepsia ,2000,41 (9): 1179 - 1186.
  • 4Boon P, Chauvel P,Pohlmann-Eden B, et al. Dose-response ef fect of levetiracetam 1000 and 2000mg/day in partial epilepsy [J]. Epilepsy Res, 2002,48 ( 1 - 2): 77 - 89.
  • 5Betts T, Waegemans T, Crawford P. A multicentre, doubleblind, randomized, parallel group study to evaluate the tolerability and efficacy of two oral doses of levetiracetam,2000mg daily and 4000mg daily, without titration in patients with refractory epilepsy[J]. Seizure ,2000,9(2) :80 - 87.
  • 6Perucca E, Gidal BE, Baltes E. Effects of antiepileptic comedication on levetiracetam pharmacokinetics: a pooled analysis of data from randomized adjunctive therapy trials [ J ]. Epilepsy Res,2003,53(1-2) :47 - 56.
  • 7Cereghino J J, Biton V, Abou Khalil B, et al. Levetiracetam for partial seizures: results of a double-blind, randomized clinical trial [J]. Neurology ,2000,55(2) :236 - 242.
  • 8Ben-Menachem E, Edrich P, Vleymen B, et al. Evidence for sustained efficacy of levetiracetam as add-on epilepsy therapy [ J ].Epilepsy Res, 2003,53 ( 1 - 2): 57 - 64.
  • 9Welty TE,Gidal BE,Ficker DM, et al. Levetiracetam:a different approach to the pharmacotherapy of epilepsy[J]. Ann Pharmacother, 2002,36 (2): 296 - 304.
  • 10Lesaffre E,Boon P,Pledger GW. The value of the number-need ed-to treat method in antiepileptic drug trials [J ]. Epilepsy, 2000,41(4) :440 - 446.

引证文献3

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部