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首页> 外文期刊>The pharmacogenomics journal >BDNF Val66Met polymorphism and clinical response to antipsychotic treatment in schizophrenia and schizoaffective disorder patients: a meta-analysis
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BDNF Val66Met polymorphism and clinical response to antipsychotic treatment in schizophrenia and schizoaffective disorder patients: a meta-analysis

机译:BDNF Val66met多态性和对精神分裂症和SchizoAfferical疾病患者的抗精神病治疗的临床反应:META分析

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摘要

Brain-derived neurotrophic factor (BDNF) plays an important role in dopaminergic and serotonergic neurotransmission by modulating dopaminergic neuron differentiation and establishment. Multiple studies have analyzed the functional BDNF Val66Met variant in relation to antipsychotic response in schizophrenia (SCZ) patients, yielding mixed results. A meta-analysis was thus performed to examine the relationship between this variant and symptom improvement during antipsychotic treatment. Searches using PubMed, Web of Science, and Psyclnfo until October 2017 yielded 11 studies that met inclusion criteria (total n = 3774). These studies investigated the BDNF Val66Met variant and antipsychotic response in patients with SCZ or schizoaffective disorder. Responders to antipsychotics were defined using the original criteria applied in each study. Effect sizes were computed using odds ratios, which were pooled according to the Mantel-Haenszel method. The BDNF Val66Met variant was not associated with the total number of responders and non-responders (p > 0.05) under dominant, recessive, or allelic models. Secondary analyses stratifying for individuals of each ethnicity and drug type also revealed no significant associations. Our findings suggest that the BDNF Val66Met variant is not associated with response to antipsychotics in individuals with SCZ. However, considering the current sample size, small effects cannot be ruled out. Moreover, recent studies have suggested that Val66Met forms haplotypes with other BDNF variants. Future studies should examine the Val66Met variant in conjunction with these other variants in relation to antipsychotic response. Moreover, since illness duration appears to influence BDNF levels in SCZ patients, future studies should aim to control for this potential confounding factor in response analyses.
机译:脑衍生的神经营养因子(BDNF)通过调节多巴胺能神经元分化和建立,在多巴胺能和血清奈良加神经递血中起着重要作用。多项研究已经分析了有关精神分裂症(SCZ)患者的抗精神病药反应的功能性BDNF Val66met变体,产生了混合结果。因此进行了META分析以检查抗精神病药治疗过程中这种变体和症状改善之间的关系。在2017年10月,使用PubMed,Science和PSYCLNFO的搜索产生了11项研究,符合纳入标准(总N = 3774)。这些研究研究了SCZ或SchizoAfferive疾病患者的BDNF Val66met变异和抗精神病药反应。使用每项研究中应用的原始标准定义抗精神病药物的响应者。使用根据Mantel-Haenszel方法汇集的odds比率来计算效果大小。 BDNF Val66met变体与主导,隐性或等位基因模型的响应者和非响应者的总数无关。对每个种族和药物类型的个体分层的二次分析也没有显着的协会。我们的研究结果表明,BDNF Val66met变体与SCZ中个体的抗精神病药物无关。但是,考虑到当前的样本大小,不能排除小效果。此外,最近的研究表明Val66met与其他BDNF变体形成单倍型。未来的研究应与与抗精神病药反应相关的这些其他变体一起检查Val66met变体。此外,由于疾病持续时间似乎影响了SCZ患者的BDNF水平,因此未来的研究应旨在控制这种潜在的混淆因素在反应分析中。

著录项

  • 来源
    《The pharmacogenomics journal》 |2019年第3期|共8页
  • 作者单位

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Rudjer Boskovic Inst Div Mol Med Lab Mol Neuropsychiat Zagreb Croatia;

    Rudjer Boskovic Inst Div Mol Med Lab Mol Neuropsychiat Zagreb Croatia;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

    Univ Toronto Campbell Family Res Inst Ctr Addict &

    Mental Hlth Psychiat Neurogenet Sect Toronto;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

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