期刊文献+

普拉克索治疗帕金森病的系统评价 被引量:2

Systematic review on Parkinson's disease treated with pramipexole
原文传递
导出
摘要 目的系统评价普拉克索治疗帕金森病(Pakinson's disease,PD)的临床疗效。方法通过检索Pubmed、Embase、Cochrane Database及中国生物医学文献数据库,检索国内外2007年4月前已发表的普拉克索对照安慰剂治疗PD的临床研究。对所纳入的研究进行质量评价及meta分析。结果共纳入10项随机对照试验(RCT)研究(纳入患者1738例),meta分析结果显示:普拉克索可以降低PD患者统一PD评分量表(UPDRS)总分[加权均数差值(WMD)=-10.01,95%CI(-12.76~-7.26)]、UPDRS Ⅱ分值[WMD=-2.44,95%CI(-2.93~-1.95)]以及UPDRS Ⅲ分值[WMD=-6.61,95%CI(-8.38~-4.84)];普拉克索还可以降低晚期PD患者UPDRS Ⅳ分值[WMD=-0.73,95%CI(-1.16~-0.30)],以上结果皆有统计学意义(P〈0.05)。3项研究比较了普拉克索与安慰剂治疗震颤的疗效,研究间存在异质性,其中2项研究显示疗效差异有统计学意义。结论普拉克索可以缓解患者的运动症状,改善生活质量。普拉克索具有改善治疗震颤的趋势,还需要更多的RCT研究进一步证实。 Objective To systemically evaluate the therapeutic effect of pramipexole in treating Parkinson' s disease. Methods Pubmed, Embase, Cechrane Database were used to search for randomized control trials (RCTs) on Parkinson' s disease treated with pramipexole. Meticulous data wre extracted and meta-analysis was performed according to a preset protocol. Results Ten RCTs involving 1738 patients were included. The results of meta-analysis showed that pramipexole decreased the total scores of unified Parkinson' s disease rating scale [ UPDRS, WMD = - 10.01,95% CI ( - 12. 76, - 7.26) ], UPDRS part Ⅱ [WMD= -2.44, 95%CI ( -2.93, -1.95)], and UPDRS part Ⅲ [WMD = -6.61, 95%CI ( -8.38, -4. 84)]. Pramipexole also reduced the score of UPDRS part Ⅳ [ WMD = -0. 73, 95% CI ( - 1.16, - 0. 30) ] in advanced patients ( P 〈 0. 05 ). Three studies referred to the effect of pramipexole in treating parkinsonian tremor. However there was a clinical heterogeneity among the studies, and two of them revealed a significant difference. Conclusions Pramipexole might improve motor symptoms and the quality of life in advanced patients, as well as improve tremor, which needs more RCTs to be confirmed.
出处 《中华神经科杂志》 CAS CSCD 北大核心 2008年第3期147-151,共5页 Chinese Journal of Neurology
基金 国家教育部留学回国人员基金资助项目(2006-331) 上海市教委发展基金资助项目(06BZ048) 上海市浦江人才计划资助项目
关键词 帕金森病 噻唑类 多巴胺激动剂 药物评价 Parkinson disease Thiazoles Dopamine agonists Drug evaluation
  • 相关文献

参考文献20

  • 1Jadad AR, Moore RA, Carroll D, et al. Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control Clin Trial, 1996, 17: 1-12. 被引量:1
  • 2Pinter MM, Rutgers AW, Hebenstreit E. An open-label, multicentre clinical trial to determine the levodopa dose-sparing capacity of pramipexole in patients with idiopathic Parkinson' s disease. J Neural Transm, 2000, 107: 1307-1323. 被引量:1
  • 3Fabbrini G, Barbanti P, Aurilia C, et al. Pramipexole in Parkinson' s disease. A short-term study using the combined levodopa-dopamine agonist teat. Funet Neurol, 2002, 17 : 199-201. 被引量:1
  • 4Kunig G, Pogarell O, Moller JC, et al. Pramipexole, a nonergot dopamine agonist, is effective against rest tremor in intermediate to advanced Parkinson' s disease. Clin Neuropharmacol, 1999, 22 : 301-305. 被引量:1
  • 5Wang KS, Lu CS, Shah DE, et al. Efficacy, safety, and tolerability of pramipexole in untreated and levodopa-treated patients with Parkinson's disease. J Neurol Sci, 2003, 216: 81- 87. 被引量:1
  • 6Navan P, Findley LJ, Jeffs JA, et al. Double-blind, single-dose, cross-over study of the effects of pramipexole, pergolide, and placebo on rest tremor and UPDRS part Ⅲ in Parkinson' s disease. Mov Disord, 2003, 18: 176-180. 被引量:1
  • 7Safety and efficacy of pramipexole in early Parkinsen disease. A randomized dose-ranging study. Parkinson Study Group. JAMA, 1997, 278: 125-130. 被引量:1
  • 8Shannon KM, Bennett JP Jr, Friedman JH. Efficacy of pramipexole, a novel dopamine agonist, as monotherapy in mild to moderate Parkinson' s disease. The Pramipexole Study Group. Neurology, 1997, 49 : 724-728. 被引量:1
  • 9Molho ES, Factor SA, Weiner WJ, et al. The use of pramipexole, a novel dopamine (DA) agonist, in advanced Parkinson' s disease. J Neural Transm Suppl, 1995, 45 : 225-230. 被引量:1
  • 10Pinter MM, Pogarell O, Oertel WH. Efficacy, safety, and tolerance of the non-ergoline dopamine agonist pramipexole in the treatment of advanced Parkinson' s disease: a double blind, placebo controlled, randomised, multicentre study. J Neurol Neurosurg Psychiatry, 1999, 66 : 436-441. 被引量:1

同被引文献31

  • 1陈彪,刘焯霖,王枫.中国帕金森病遗传研究进展[J].中华神经科杂志,2005,38(3):160-164. 被引量:9
  • 2温洪波,张振馨,罗毅,陈生弟,蒋雨平,张小英,孙相如,王新德,姚晨.普拉克索治疗帕金森病的多中心、随机、双盲、溴隐亭对照临床疗效和安全性研究[J].中华神经科杂志,2006,39(9):604-608. 被引量:63
  • 3Hornykiewicz O. Dopamine miracle: from brain homogenate to dopamine replacement. Mov Disord, 2002, 17 : 501-508. 被引量:1
  • 4Goetz CG, Chmura TA, Lanska DJ. The history of Parkinson's disease: part 2 of the MDS-sponsored History of Movement Disorders Exhibit, Barcelona, June, 2000. Mov Disord, 2001, 16 : 156-161. 被引量:1
  • 5Hefti F, Melamed E, Wurtman RJ. Partial lesions of the dopaminergic nigrostriatal system in rat brain: biochemical characterization. Brain Res, 1980, 195: 123-137. 被引量:1
  • 6Glinka Y, Gassen M, Youdim MB. Mechanism of 6- hydroxydopamine neurotoxicity. J Neural Transm Suppl, 1997, 50 : 55-66. 被引量:1
  • 7Johannessen JN, Chiueh CC, Bums RS, et al. Differense in the metabolism of MPTP in the rodent and primate parallel differences in sensitivity to its neurotoxic effects. Life Sci, 1985, 36: 219- 224. 被引量:1
  • 8Arai N, Misugi K, Goshima Y, et al. Evaluation of a 1-methyl-4- phenyl-1,2,3,6- tetrahydropyridine ( MPTP)-treated C57 black mouse model for parkinsonism. Brain Res, 1990, 515 : 57-63. 被引量:1
  • 9Chen SD, Zhou XD, Xu DL, et al. Hemiparkinsonism in monkeys following unilateral common carotid artery infusion of MPTP. A study of behavior, biochemistry and histology. Chin Med J (Eng 1), 1991, 104: 758-763. 被引量:1
  • 10Xu DL, Yu WC, Pan GB, et al. Mechanism of action of L-leucylglycinamide and its effect on Parkinson's disease. Adv Neurol, 1987, 45:587-590. 被引量:1

引证文献2

二级引证文献17

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