首页> 外文期刊>Schizophrenia Bulletin >Gene-Environment Interactions in Schizophrenia: Review of Epidemiological Findings and Future Directions
【24h】

Gene-Environment Interactions in Schizophrenia: Review of Epidemiological Findings and Future Directions

机译:精神分裂症中的基因-环境相互作用:流行病学发现和未来方向的回顾。

获取原文
获取原文并翻译 | 示例
           

摘要

Concern is building about high rates of schizophrenia in large cities, and among immigrants, cannabis users, and traumatized individuals, some of which likely reflects the causal influence of environmental exposures. This, in combination with very slow progress in the area of molecular genetics, has generated interest in more complicated models of schizophrenia etiology that explicitly posit gene-environment interactions (EU-GEI. European Network of Schizophrenia Networks for the Study of Gene Environment Interactions. Schizophrenia aetiology: do gene-environment interactions hold the key? [published online ahead of print April 25, 2008] Schizophr Res; S0920-9964(08) 00170–9). Although findings of epidemiological gene-environment interaction (G × E) studies are suggestive of widespread gene-environment interactions in the etiology of schizophrenia, numerous challenges remain. For example, attempts to identify gene-environment interactions cannot be equated with molecular genetic studies with a few putative environmental variables “thrown in”: G × E is a multidisciplinary exercise involving epidemiology, psychology, psychiatry, neuroscience, neuroimaging, pharmacology, biostatistics, and genetics. Epidemiological G × E studies using indirect measures of genetic risk in genetically sensitive designs have the advantage that they are able to model the net, albeit nonspecific, genetic load. In studies using direct molecular measures of genetic variation, a hypothesis-driven approach postulating synergistic effects between genes and environment impacting on a final common pathway, such as “sensitization” of mesolimbic dopamine neurotransmission, while simplistic, may provide initial focus and protection against the numerous false-positive and false-negative results that these investigations engender. Experimental ecogenetic approaches with randomized assignment may help to overcome some of the limitations of observational studies and allow for the additional elucidation of underlying mechanisms using a combination of functional enviromics and functional genomics.
机译:在大城市以及移民,大麻使用者和受创伤的个人中,精神分裂症的发病率正在上升,这引起了人们的关注,其中一些可能反映了环境暴露的因果关系。这与分子遗传学领域的进展非常缓慢相结合,引起了人们对更复杂的精神分裂症病因学模型的兴趣,这些模型明确提出了基因与环境之间的相互作用(EU-GEI。欧洲精神分裂症网络对基因环境相互作用的研究。精神分裂症的病因:基因与环境的相互作用是否是关键?[2008年4月25日,在线提前出版] Schizophr Res; S0920-9964(08)00170-9)。尽管流行病学的基因-环境相互作用(G×E)研究表明精神分裂症的病因学中存在广泛的基因-环境相互作用,但仍然存在许多挑战。例如,鉴定基因与环境相互作用的尝试不能等同于分子遗传学研究,该分子遗传学研究带有“推论”的一些假定环境变量:G×E是一种多学科研究,涉及流行病学,心理学,精神病学,神经科学,神经影像学,药理学,生物统计学,和遗传学。在遗传敏感设计中使用遗传风险间接测量方法进行的流行病学G×E研究的优势在于,它们能够对净的,非特异性的遗传负荷进行建模。在使用直接分子手段测量遗传变异的研究中,假设驱动的方法假设基因与环境之间的协同效应会影响最终的共同途径,例如中脑边缘多巴胺神经传递的“致敏性”,尽管这很简单,但可能会提供最初的关注点并保护其免受这些调查产生了大量的假阳性和假阴性结果。具有随机分配的实验性生态遗传学方法可能有助于克服观察性研究的某些局限性,并可以结合使用功能环境学和功能基因组学来进一步阐明潜在机制。

著录项

  • 来源
    《Schizophrenia Bulletin》 |2008年第6期|1066-1082|共17页
  • 作者单位

    Department of Psychiatry and Neuropsychology School of Mental Health and Neuroscience Maastricht University Medical Centre EURON SEARCH PO Box 616 (location DOT 10) Maastricht 6200 MD The Netherlands;

    Division of Psychological Medicine Institute of Psychiatry London SE5 8AF UK;

    Dunedin Multidisciplinary Health and Development Research Unit Department of Preventive and Social Medicine Dunedin School of Medicine University of Otago PO Box 913 Dunedin New Zealand;

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

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号