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A Genomic Investigation of Major Depressive Disorder and Antidepressant Response.

机译:主要抑郁症和抗抑郁反应的基因组研究。

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摘要

Major depressive disorder (MDD) is a common and complex disorder with consistent evidence of genetic influence on predisposition. The search for susceptibility genes has proved to be an arduous task with studies having ever increasing sample numbers still not leading to replicable findings. It is generally believed that the failure of common genetic studies to identify replicable genetic associations is a consequence of the multifactorial and heterogeneous nature of MDD. This etiological heterogeneity may also explain significant variability in treatment response. Accordingly, while effective treatments for MDD are available, approximately half of the patients fail to respond to conventional antidepressant treatment. We hypothesized that peripheral gene expression could help us better understand illness heterogeneity and mechanisms of antidepressant response, possibly helping to identify biomarkers. To test this hypothesis, we have prospectively followed, and treated with the antidepressant citalopram for eight weeks, a cohort of medication naive individuals with MDD. RNA and DNA from pre- and post-treatment blood samples of this cohort were used to perform high-throughput pharmacogenomic and genetic studies to identify genes involved in treatment response and in the pathophysiology of MDD. Significant gene expression alterations in immune related genes were observed after citalopram treatment, pointing to a possible mode of action of the treatment response, as well as possible biomarkers for future treatment response. Additionally, we identified copy number variable regions differentiating MDD and controls and having a significant impact on gene expression. These results provide important additional information which can be used to identify the genomic and molecular underpinnings of MDD and antidepressant response.
机译:重度抑郁症(MDD)是常见且复杂的疾病,具有遗传易感性的一致证据。事实证明,寻找易感基因是一项艰巨的任务,因为不断增加的样本数量的研究仍未导致可复制的发现。通常认为,通用遗传研究未能鉴定可复制的遗传关联是MDD具有多因素和异质性的结果。这种病因异质性也可以解释治疗反应的显着差异。因此,尽管可获得有效的MDD治疗方法,但是大约一半的患者对常规抗抑郁药治疗无效。我们假设外围基因表达可以帮助我们更好地了解疾病的异质性和抗抑郁反应的机制,可能有助于鉴定生物标志物。为了检验这一假设,我们前瞻性地追踪了抗抑郁药西酞普兰,并将其作为一组未经药物治疗的MDD个体接受了八周的治疗。使用该人群治疗前和治疗后血样的RNA和DNA进行高通量药物基因组学和基因研究,以鉴定参与治疗反应和MDD病理生理的基因。西酞普兰治疗后观察到免疫相关基因的显着基因表达改变,表明治疗反应的可能作用方式以及未来治疗反应的可能生物标志物。此外,我们确定了区分MDD和对照的拷贝数可变区,并且对基因表达有重大影响。这些结果提供了重要的附加信息,可用于鉴定MDD和抗抑郁反应的基因组和分子基础。

著录项

  • 作者

    Mamdani, Firoza.;

  • 作者单位

    McGill University (Canada).;

  • 授予单位 McGill University (Canada).;
  • 学科 Biology Genetics.;Biology Neuroscience.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 147 p.
  • 总页数 147
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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