Hu M, Zong X, Zheng J, Mann J J, Li Z, Pantazatos S P, Li Y, Liao Y, He Y, Zhou J, Sang D, Zhao H, Tang J, Chen H, Lv L, Chen X
Mental Health Institute of the Second Xiangya Hospital,Central South University,139 Middle Renmin Road,Changsha,Hunan 410011,People's Republic of China.
Key Laboratory for NeuroInformation of the Ministry of Education,School of Life Science and Technology,University of Electronic Science and Technology of China,Chengdu 610054,People's Republic of China.
Psychol Med. 2016 Sep;46(12):2549-60. doi: 10.1017/S0033291716001380. Epub 2016 Jun 24.
It remains unclear whether the topological deficits of the white matter network documented in cross-sectional studies of chronic schizophrenia patients are due to chronic illness or to other factors such as antipsychotic treatment effects. To answer this question, we evaluated the white matter network in medication-naive first-episode schizophrenia patients (FESP) before and after a course of treatment.
We performed a longitudinal diffusion tensor imaging study in 42 drug-naive FESP at baseline and then after 8 weeks of risperidone monotherapy, and compared them with 38 healthy volunteers. Graph theory was utilized to calculate the topological characteristics of brain anatomical network. Patients' clinical state was evaluated using the Positive and Negative Syndrome Scale (PANSS) before and after treatment.
Pretreatment, patients had relatively intact overall topological organizations, and deficient nodal topological properties primarily in prefrontal gyrus and limbic system components such as the bilateral anterior and posterior cingulate. Treatment with risperidone normalized topological parameters in the limbic system, and the enhancement positively correlated with the reduction in PANSS-positive symptoms. Prefrontal topological impairments persisted following treatment and negative symptoms did not improve.
During the early phase of antipsychotic medication treatment there are region-specific alterations in white matter topological measures. Limbic white matter topological dysfunction improves with positive symptom reduction. Prefrontal deficits and negative symptoms are unresponsive to medication intervention, and prefrontal deficits are potential trait biomarkers and targets for negative symptom treatment development.
在慢性精神分裂症患者的横断面研究中记录的白质网络拓扑缺陷是由于慢性疾病还是其他因素(如抗精神病药物治疗效果)所致,目前尚不清楚。为了回答这个问题,我们评估了未用药的首发精神分裂症患者(FESP)在一个疗程治疗前后的白质网络。
我们对42名未用药的FESP患者在基线时以及接受8周利培酮单药治疗后进行了纵向扩散张量成像研究,并将他们与38名健康志愿者进行比较。利用图论计算脑解剖网络的拓扑特征。在治疗前后使用阳性和阴性症状量表(PANSS)评估患者的临床状态。
治疗前,患者总体拓扑结构相对完整,主要在额叶回和边缘系统成分(如双侧前扣带回和后扣带回)存在节点拓扑特性缺陷。利培酮治疗使边缘系统的拓扑参数正常化,且这种增强与PANSS阳性症状的减轻呈正相关。治疗后额叶拓扑损伤持续存在,阴性症状未改善。
在抗精神病药物治疗的早期阶段,白质拓扑测量存在区域特异性改变。边缘白质拓扑功能障碍随阳性症状减轻而改善。额叶缺陷和阴性症状对药物干预无反应,额叶缺陷是阴性症状治疗发展的潜在特质生物标志物和靶点。