Bernard Jessica A, Orr Joseph M, Mittal Vijay A
Department of Psychology, Texas A&M University, United States; Texas A&M Institute for Neuroscience, Texas A&M University, United States; Department of Psychology & Neuroscience, University of Colorado Boulder, United States.
Department of Psychology, Texas A&M University, United States; Texas A&M Institute for Neuroscience, Texas A&M University, United States; Institute of Cognitive Science, University of Colorado Boulder, United States.
Neuroimage Clin. 2017 Mar 6;14:622-628. doi: 10.1016/j.nicl.2017.03.001. eCollection 2017.
Prospective longitudinal evaluation of adolescents at ultra-high-risk (UHR) for the development of psychosis enables an enriched neurodevelopmental perspective of disease progression in the absence of many of the factors that typically confound research with formally psychotic patients (antipsychotic medications, drug/alcohol dependence). The cerebellum has been linked to cognitive dysfunction and symptom severity in schizophrenia and recent work from our team suggests that it is a promising target for investigation in UHR individuals as well. However, the cerebellum and cerebello-thalamo-cortical networks have not been investigated developmentally or with respect to disease progression in this critical population. Further, to date, the types of longitudinal multimodal connectivity studies that would substantially inform our understanding of this area have not yet been conducted. In the present investigation 26 UHR and 24 healthy control adolescents were administered structured clinical interviews and scanned at baseline and then again at 12-month time points to investigate both functional and structural connectivity development of cerebello-thalamo-cortical networks in conjunction with symptom progression. Our results provide evidence of abnormal functional and structural cerebellar network development in the UHR group. Crucially, we also found that cerebello-thalamo-cortical network development and connectivity at baseline are associated with positive symptom course, suggesting that cerebellar networks may be a biomarker of disease progression. Together, these findings provide support for neurodevelopmental models of psychotic disorders and suggest that the cerebellum and respective networks with the cortex may be especially important for elucidating the pathophysiology of psychosis and highlighting novel treatment targets.
对处于精神病发作超高风险(UHR)的青少年进行前瞻性纵向评估,能够在没有许多通常会混淆对正式精神病患者研究的因素(抗精神病药物、药物/酒精依赖)的情况下,从丰富的神经发育角度了解疾病进展。小脑已被证明与精神分裂症的认知功能障碍和症状严重程度有关,我们团队最近的研究表明,它也是UHR个体研究的一个有前景的靶点。然而,尚未在这个关键人群中对小脑和小脑 - 丘脑 - 皮质网络进行发育方面或疾病进展方面的研究。此外,迄今为止,尚未进行能够极大地增进我们对该领域理解的纵向多模态连接性研究。在本研究中,对26名UHR青少年和24名健康对照青少年进行了结构化临床访谈,并在基线时进行扫描,然后在12个月的时间点再次扫描,以研究小脑 - 丘脑 - 皮质网络的功能和结构连接性发展以及症状进展情况。我们的结果提供了UHR组中小脑网络功能和结构发育异常的证据。至关重要的是,我们还发现基线时小脑 - 丘脑 - 皮质网络的发育和连接性与阳性症状进程相关,这表明小脑网络可能是疾病进展的一个生物标志物。这些发现共同为精神障碍的神经发育模型提供了支持,并表明小脑以及与皮质的相应网络对于阐明精神病的病理生理学和突出新的治疗靶点可能特别重要。