期刊文献+

帕利哌酮治疗首发精神分裂症患者的疗效研究 被引量:7

Effect of Paliperidone on Patients with First-episode Schizophrenia
下载PDF
导出
摘要 目的:观察帕利哌酮治疗首发精神分裂症患者的疗效及对血清白介素-1β(IL-1β)、IL-2、IL-6和脑源性神经营养因子(BDNF)的水平的影响。方法:选择首发精神分裂症患者80例为精神分裂症组,采用帕利哌酮治疗8周,治疗前后采用酶联免疫吸附法检测血清IL-1β、IL-2、IL-6和BDNF水平。同期检测60名健康志愿者(正常对照组)上述指标。采用阳性与阴性症状量表(PANSS)评估精神症状,采用个人和社会功能量表(PSP)评估社会功能。结果:精神分裂症组治疗前的PANSS总分为(94.17±16.34)分,治疗第8周末为(46.09±12.52)分,痊愈68例,显著进步10例,好转2例;治疗前PSP评分为(47.94±10.88)分,治疗8周末PSP评分为(68.23±17.65)分,与治疗前比较,社会中有益的活动及扰乱及攻击行为评分有显著性差异(P<0.01)。治疗前精神分裂症组血清中IL-1β、IL-2、IL-6水平均显著高于正常对照组(P<0.01),血清BDNF水平低于正常对照组(P<0.05);治疗后血清IL-1β、IL-2水平与治疗前相比明显下降,有显著性差异(P<0.01);BDNF水平较治疗前有明显升高,差异有统计学意义(P<0.05)。治疗前IL-2水平与PANSS阳性症状评分呈正相关(r=0.551,P<0.05);治疗后BDNF水平与PSP评分呈正相关(r=0.692,P<0.05)结论:精神分裂症患者存在免疫紊乱,处于免疫激活状态。 Objective: To investigate the effects of Paliperidone on patients with first-episode schizophrenia, and to examine the effects in levels of serum interleukin-1β (IL-1β), IL-2, IL-6 and brain-derived neurotrophic factor (BDNF). Methods: Eighty patients with first-episode schizophrenia were enrolled in the schizophrenic group, and were treated with Paliperidone for eight weeks. The levels of Serum IL-1 β, IL-2, IL-6 and BDNF were measured with enzyme linked immunosorbent assay (ELISA) in 60 healthy volunteers (normal control group) and the schizophrenic group. The symptoms of patients were measured with positive and negative syndrome scale (PANSS), and the PSP scale was used to assess their social function. Results: The PANSS score of schizophrenic group was (94.17±16.34) before the treatment, and was (46.09±12.52) at the 8th week of the treatment. Sixty-eight cases were cured, 10 cases were significantly improved, and 2 cases were improved. Similarly, the PSP score of schizophrenic group was (47.94±10.88) before the treatment, and was (68.23 ±17.65) at the 8th week of the treatment. The scores of social beneficial activities and disrupt and aggression were significantly different after therapy (P〈 0.01). Before the treatment, the serum levels of IL-1 β, IL-2 and IL-6 in the schizophrenic group were significantly higher than those in the normal control group (P〈0.01), and the serum levels of BDNF in the schizophrenic group was lower than that in the normal control group (P〈0.05). The serum levels of IL-1 βand IL-2 in the schizophrenic group were significantly decreased after the treatment(P〈0.01), and the serum level of BDNF in the schizophrenic group was significantly increased after the treatment (P〈0.05). There was a positive correlation between the IL-2 level and the PANSS positive symptom scores before the treatment (r=0.551, P〈0.05), and a positive correlation between the BDNF level of and the PSP scores after the treatment (r=0.692,P 〈0.05). Conclusion: Schizophrenic patients present a state of immune activation.
作者 王颢 刘胜武
出处 《神经损伤与功能重建》 2014年第4期320-323,共4页 Neural Injury and Functional Reconstruction
关键词 精神分裂症 白介素-1Β 白介素-2 白介素-6 脑源性神经营养因子 schizophrenia interleukin- 1β interleukin-2 interleukin-6 brain-derived neurotrophic factor
  • 相关文献

参考文献27

  • 1Drzyzga L,Obuchowicz E,Marcinowska A,et al.Cytokines in schizophrenia and the effects ofantipsychotic drugs[J].Brain Be-hav Immun,2006,20:532-545.
  • 2Muller N.Role of the cytokine network in the CNS and psychiatric disorders[J].Nervenarzt,1997,68:11-20.
  • 3Kim YK,Lee MS,Suh KY.Dcereased interleukin-production in Korean schizophrenia patients[J].Biol Psychiatry,1998,43:701-704.
  • 4Arolt V,Rothermunth M,Wandinger KP,et al.Dcereased in vitro production of interferongamma and interleukin-2 in whole blood of par tients with schizophrenia during treatment[J].Mol Psychiatry,2000,5:150-158.
  • 5杜蘅,唐济生.精神分裂症细胞因子及细胞因子网络的研究进展[J].中国神经精神疾病杂志,2002,28(5). 被引量:14
  • 6中华医学会精神科分会.中国精神障碍分类与诊断标准(CCMD-Ⅲ)[M].第3版.济南:山东科学技术出版社,2001.
  • 7Fong WL,Grimley GW.Peripheral intravenous infusion of amino acids[J].Am J Hosp Pharm,1981,38:652-659.
  • 8Bums T,Patrick D.Social functioning as an outcome measure in schizophrenia studies[J].Acta Psychiatrica Scand,2007,116:403-418.
  • 9Juckel G,Schaub D,Fuchs N,et al.Validation of the personal and social performance(PSP) scale in a German sample of acutely ill patients with schizophrenia[J].Schizophr Res,2008,104:287-293.
  • 10于彩霞,冀德才,雷春燕.度洛西汀与帕罗西汀治疗社交焦虑症对照研究[J].中国实用医药,2011,6(13):21-22. 被引量:10

二级参考文献60

  • 1闵茗,刘燕,高哲石.抗抑郁药度洛西汀的临床应用[J].世界临床药物,2006,27(11):682-686. 被引量:13
  • 2汪辉,李胜利,钟杏圣,陈婉清,盘圣明,李敏伟,姚航平.精神分裂症免疫功能紊乱机理的研究[J].中国神经精神疾病杂志,1996,22(5):266-268. 被引量:11
  • 3[3]Ganguli R, Brar JS, Chengappa KN, et al. Autoimmunity in schizophrenia:a review of recent tindings. Psychiatry Res, 1992,44(2): 113.
  • 4[4]Licino L, Seiby JP, Altemus M, et al. Elevated CSF levels of interleukin-2 in neuroleptic-free schizophrenia patients. Am J Psychiatry, 1993, 150(9): 1408.
  • 5[5]O' Donnell MC, Carts SV, Ward PB, et al. Increased production of interleukin-2 (IL-2) in unmedicated patients with schizophrenia and schizophreniform disorders. Psychiatry Res, 1998 16,77(1 ) :63.
  • 6[7]Petitto J, McCarthy DB, Rinker GM, et al. Modulation of behavior and neurochemical measures of forebraln dopamine function in mice by speciesspecific interleukin-2. J Neuroimmune, 1997,73(1-2): 183.
  • 7[10]Cazzullo CL,Scarone S,Grassi B,et al. Cytokines production in chronic schizophrenia patients with or without paranoid behaviour. Prog Neuropsychopharmacol Biol Psychiatry, 1998, 22(6) :947.
  • 8[11]Sirota P, Schild K, Djaldetti M, et al. Increased interleukin- 1 and interleukin-3 like activity in schizophrenic patients. Prog Neuropsy-chopharmacol Biol Psychiatry, 1995, 19( 1 ) :75.
  • 9[13]Rothermundt M, Arolt V, Weitzsch, et al. Immunological dysfunction in schizophrenia: a systematic approach. Neuropsychobiology, 1998,37 (4):186.
  • 10[16]Gattaz WF,Dalgalarrondo P, Schroder HC,et al. Abnomalities in serum concentration of interleukin-2, interferon-alpha and interferon-gamma in schizophrenia not detected. Schizophr Res, 1992,6(3) :237.

共引文献24

同被引文献74

  • 1潘明.首发精神分裂症患者血清NSE和MBP的变化[J].中国热带医学,2006,6(4):648-648. 被引量:3
  • 2韩洁,高素强.乌灵胶囊的临床应用及不良反应[J].中国药房,2007,18(15):1184-1186. 被引量:33
  • 3Jeong BS, Kwon JS, KJm SY, et al. Function- al imaging evidence of the relationship between recurrent psychotic episodes and neurodegenera- five course in schizophrenia [J]. Neuroimaging, 2005, 139: 219-228.
  • 4Kinon BJ, Chen L, Ascher-Svanum H, et al. Predicting response to atypical antipsychotics based on early response in the treatment of schizophrenia [J]. Schizophr Res, 2008, 102: 230-240.
  • 5Emsley R, Berwaerts J, Eerdekens M, et al. Effcacy and safety of oral paliperidone extend- ed-release tablets in the treatment of acute schizophrenia: pooled data from three 52-week open-label studies [J]. Int Clin Psychopharmacol, 2008, 23: 343-356.
  • 6Mtiler HJ. Gradually improving treatment from the traditional oral neuroleptics to the fast atypical depot [J]. Eur Psychiatry, 2005, 20: 379-385.
  • 7Karlsson P, Dencker E, Nyberg S, et al. Phamacokinetic and dopamine D-2 and serotonin 5-HT2A receptor occupancy of paliperidone in health subjects: Two open-label, single-dose studies [J]. Pharmacopsychiatry, 2007,40: 386-396.
  • 8Kim DH, Maneen MJ, Stahl SM. Building a better antipsychotic: receptor targets for the treat- ment of multiple symptom dimensions of Schizophrenia [J]. Neurotherapeutics, 2009, 6: 78-85.
  • 9Schennach R, Meyer S, Seem:J ller F, et al. Response trajectories in "real-world" naturalisti- cally treated schizophrenia patients [J]. Schizophr Res, 2012, 139: 218-224.
  • 10Kinon B J, Chen L, Aseher-Svanum H, et al. Early response to antipsychotic drug therapy as clinical marker of subsequent response in the treatment of schizophrenia[J]. Neuropsychophar- macology, 2010, 35: 581-590.

引证文献7

二级引证文献65

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