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奎硫平对首发精神分裂症患者脑源性营养因子的影响 被引量:4

Effect of Quetiapine on Brain-derived Neurotrophic Factors in Patients with First-episode Schizophrenia
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摘要 目的观察奎硫平对首发精神分裂症患者血清脑源性营养因子(BDNF)的影响,探讨BDNF和精神症状、认知功能的关系。方法首发精神分裂症患者80例(治疗组),给予奎硫平初始剂量100 mg·d-1,平均剂量为(580±120)mg·d-1,po,qd,共4周。分别于治疗前后采用阳性和阴性症状量表(PANSS)、威斯康星卡片分类测验(WCST)评估精神症状和认知功能,采用酶联免疫吸附法检测血清BDNF水平。以健康体检者80例作为对照组。结果治疗组和对照组治疗前BDNF浓度分别为(13.72±8.79),(23.67±10.13)ng·mL-1(P<0.01),治疗组治疗后BDNF浓度(18.02±9.06)ng·mL-1,仍低于对照组(P<0.05)。治疗后患者PANSS量表总分及各分量表分下降,WCST分类数、正确应答数增加,错误应答数减少。血清BDNF浓度变化率和阴性症状(SANS)变化率呈正相关(r=0.54,P=0.032),和正确应答数呈正相关。结论奎硫平可提高精神分裂症患者BDNF水平,BDNF变化和阴性症状、认知功能相关。 Objective To investigate the effects of quetiapine on serum levels of brain-derived neurotrophic factors ( BDNF) and the correlation between BDNF and psychiatric symptoms and cognitive function in patients with first-episode schizophrenia. Methods Eighty patients with first-episode schizophrenia ( treatment group) were treated with quetiapine orally for 4 weeks,at initial dose of 100 mg·d^-1 and average dose of (580±120) mg·d^-1 . The psychiatric symptoms were evaluated by using the positive and negative syndrome scale ( PANSS) . The cognitive function was assessed by using Wisconsin cards sort test ( WCST) . The serum BDNF level was detected with enzyme-linked immunosorbent assay ( ELISA) . Results The serum level of BDNF was markedly lower in schizophrenic patients before[(13. 72±8. 79) ng·mL^-1,P〈0. 01] and after treatment[(18. 02±9.06) ng·mL^-1,P〈0.05]in comparison with normal controls(23. 67±10. 13) ng·mL^-1]. After treatment,the PANSS total scores and subscale scores decreased,WCST number of categories and the number of correct answers increased,and the number of wrong answers reduced. There was a positive correlation between the serum BDNF and negative symptoms ( SANS) ( r= 0. 54, P=0. 032),and the number of correct answers. Conclusion The quetiapine significantly increases serum level of BDNF in schizophrenia patients,which correlates positively with improvements in symptoms and cognitive function.
出处 《医药导报》 CAS 北大核心 2014年第9期1185-1187,共3页 Herald of Medicine
基金 浙江省医学会临床科研基金资助项目(20112YC-A74)
关键词 奎硫平 精神分裂症 营养因子 脑源性 认知功能 Quetiapine Schizophrenia Neurotrophic factors,brain-derived Cognitive function
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参考文献12

  • 1沈渔邨.精神病学[M].5版.北京:人民卫生出版社.2009:838.
  • 2陈大春,李艳丽,修梅红,王宁,杨可冰,聂鹰,卞清涛,张向阳.利培酮治疗首发精神分裂症患者血清脑源性神经营养因子的变化及其与临床疗效和认知功能的关系[J].中国神经精神疾病杂志,2010,36(9):529-532. 被引量:34
  • 3CHEN C C,HUANG T L. Effects of antipsychotics on theserum BDNF levels in schizophrenia[J]. Psychiatry Res,2011,189(3):327-330.
  • 4FRUNTES V,LIMOSIN F. Schizophrenia and viral infectionduring neurodevelopment:a pathogenesis model- [J]. MedSci Monit, 2008,14(6):71-77.
  • 5NUMAKAWA T,SUZUKI S,KUMAMARU E,et al. BDNFfunction and intracellular signaling in neurons[J]. HistolHistopathol, 2010,25(2):237-258.
  • 6陈大春,修梅红,李艳丽,王宁,杨可冰,卞清涛,谭云龙,张向阳.精神分裂症患者脑源性营养因子与临床特征的关系[J].临床精神医学杂志,2010,20(2):79-81. 被引量:5
  • 7ISSA G,WILSON C,TERRY A V,et al. An inverse rela-tionship between cortisol and BDNF levels in schizophrenia:data from human postmortem and animal studies [J].Neurobiol Dis, 2010,39(2):327-333.
  • 8FAVALLI G,LI J,BELMONTE-DE-ABREU P,et al. Therole of BDNF in the pathophysiology and treatment ofschizophrenia[J]. J Psychiatr Res,2012,46(1):1-11.
  • 9PARK S W,LEE S K,KIM J M,et al. Effects of quetiapineon the brain-derived neurotrophic factor expression in thehippocampus and neocortex of rats[J]. Neurosci Let,2006,402(1-2):25-29.
  • 10PARK S W,LEE C H,CHO H Y,et al. Effects of anti-psychotic drugs on the expression of synaptic proteins anddendritic outgrowth in hippocampal neuronal cultures[J].Synapse, 2013,67(5):224-234.

二级参考文献25

  • 1Lewin GR, Barde YA. Physiology of the neuortorphins[ J ], Annu Rev Neurosc, 1996,19:289-317.
  • 2Rizos EN, Rontos 1, l,askos E, et al. Investigation of serum BDNF levels in drug-naive patients with schizophrenia [ J ]. Progress in neuropsychopharmacology & Biological Psychiatry,2008,32 : 1308- 1311.
  • 3Peter FB, Anilkumar P, Denise E, et al. Brain derived neurotropite factor in first-episode psychosis[ J ]. Schizophrenia Research ,2007. 91:1-5.
  • 4Karege F, Schwahl M, Cisse M. Postnatal developmental profile of brain-derived neurotrophic factor in rat brain and platelets [ J ]. Neurosci. Lett ,2002,328:261-264.
  • 5Durany N,Miehel T,Zochling R,et al. Brain-derived neurotrophic factor and neurotrophin 3 in schizophrenic psychoses. Sehizophr Res [J].2001,52:79-86.
  • 6Toyooka K, Asama K,Watanabe Y,et al. Decreased level of brainderived neurotrophic factoring serum of ehronic schizophrenic patients[ J]. Psychiat~ Res ,2002,110:249-257.
  • 7Szeszko PR,Lipsky R, Mentschel C,et al. Brain-derived neurotrophic factor va166met polymorphism and volume of the hippocampal formation[ J]. Mol Psychiatry,2005,10:631-636.
  • 8Voge IM,Busse S,Freyberger HJ,et al. DopamineD3 receptor and schizophrenia: a widened scope for the immune hypothesis [ J ]. Medical hypotheses ,2006,67:354-355.
  • 9Shalev I, Lerer E, Israel S, et al. BDNF Va166Met polymorphism is associated with HPA axis reactivity to psychological stress characterized by genotype and gender interactions[ J ]. Psychoneuroendocrinology, 2009,34 : 382 -388.
  • 10Samira S, Valvassori, Laura S, et al. Lack of effect of antipsychotits on BNDF and NGF levels in hippocampus of Wistar rats[J]. Metab Brain Dis,2008,23:213-219.

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