Clinical Brain Disorders Branch, Genes, Cognition, and Psychosis Program, NIMH, NIH, Bethesda, MD, USA.
Curr Opin Genet Dev. 2011 Jun;21(3):340-8. doi: 10.1016/j.gde.2011.02.003. Epub 2011 Mar 4.
The small effect size of most individual risk factors for psychiatric disorders likely reflects biological heterogeneity and diagnostic imprecision, which has encouraged genetic studies of intermediate biological phenotypes that are closer to the molecular effects of risk genes than are the clinical symptoms. Neuroimaging-based intermediate phenotypes have emerged as particularly promising because they map risk associated gene effects onto physiological processes in brain that are altered in patients and in their healthy relatives. Recent evidence using this approach has elucidated discrete, dissociable biological mechanisms of risk genes at the level of neural circuitries, and their related cognitive functions. This approach may greatly contribute to our understanding of the genetics and pathophysiology of psychiatric disorders.
精神障碍大多数个体风险因素的小效应量可能反映了生物学异质性和诊断不精确性,这促使人们对更接近风险基因分子效应的中间生物学表型进行遗传研究,而不是对临床症状进行研究。基于神经影像学的中间表型已成为特别有前途的研究方法,因为它们将与风险相关的基因效应映射到患者及其健康亲属大脑中发生改变的生理过程上。最近使用这种方法的证据阐明了神经回路层面上风险基因的离散、可分离的生物学机制及其相关认知功能。这种方法可能极大地促进我们对精神障碍的遗传学和病理生理学的理解。