Peters Bart D, Karlsgodt Katherine H
Division of Psychiatry Research, Zucker Hillside Hospital, NorthShore-LIJ Health System, Glen Oaks, NY, United States.
Division of Psychiatry Research, Zucker Hillside Hospital, NorthShore-LIJ Health System, Glen Oaks, NY, United States; Center for Psychiatric Neuroscience, The Feinstein Institute for Medical Research, Manhasset, NY, United States; Department of Psychiatry, Hofstra NorthShore-LIJ School of Medicine, Hempstead, NY, United States.
Schizophr Res. 2015 Jan;161(1):61-9. doi: 10.1016/j.schres.2014.05.021. Epub 2014 Jun 2.
Schizophrenia has been conceptualized as a disorder of both neurodevelopment and a disorder of connectivity. One important aspect of the neurodevelopmental hypothesis is that schizophrenia is no longer thought to have discrete illness time points, but rather a long trajectory of brain changes, spanning many years, across a series of stages of the disease including the prodrome, first episode, and chronic period. As the disease progresses, there is a complex relationship between age related changes and disease related changes. Therefore, neural changes, and specifically white matter based connectivity changes, in schizophrenia may be best conceptualized based on a lifespan trajectory. In this selective review, we discuss healthy changes in white matter integrity that occur with age, as well as changes that occur across illness stages. We further propose a set of models that might explain lifespan changes in white matter integrity in schizophrenia, with the conclusion that the evidence most strongly supports a pattern of disrupted maturation during adolescence, with the potential for later changes that may be a result of disease neurotoxicity, abnormal or excessive aging effects, as well as medication, cohort or other effects. Thus, when considering white matter integrity in psychosis, it is critical to consider age in addition to other contributing factors including disease specific effects. Discovery of the factors driving healthy white matter development across the lifespan and deviations from the normal developmental trajectory may provide insights relevant to the discovery of early treatment interventions.
精神分裂症已被概念化为一种神经发育障碍和一种连接性障碍。神经发育假说的一个重要方面是,精神分裂症不再被认为有离散的发病时间点,而是有一个跨越多年、涵盖疾病一系列阶段(包括前驱期、首发期和慢性期)的大脑变化的长期轨迹。随着疾病的进展,年龄相关变化和疾病相关变化之间存在复杂的关系。因此,精神分裂症中的神经变化,特别是基于白质的连接性变化,可能最好根据寿命轨迹来概念化。在这篇选择性综述中,我们讨论了随着年龄增长白质完整性发生的健康变化,以及在疾病各阶段发生的变化。我们进一步提出了一组模型,这些模型可能解释精神分裂症中白质完整性的寿命变化,得出的结论是,证据最有力地支持了青春期成熟中断的模式,后期可能会因疾病神经毒性、异常或过度衰老效应以及药物、队列或其他效应而发生变化。因此,在考虑精神病中的白质完整性时,除了包括疾病特异性效应在内的其他促成因素外,考虑年龄至关重要。发现驱动整个生命周期健康白质发育的因素以及与正常发育轨迹的偏差,可能为发现早期治疗干预措施提供相关见解。