Sarpal Deepak K, Argyelan Miklos, Robinson Delbert G, Szeszko Philip R, Karlsgodt Katherine H, John Majnu, Weissman Noah, Gallego Juan A, Kane John M, Lencz Todd, Malhotra Anil K
From the Department of Psychiatry, Zucker Hillside Hospital, North Shore-LIJ Health System, Glen Oaks, N.Y.; the Center for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, N.Y.; the Department of Psychiatry, Hofstra North Shore-LIJ School of Medicine, Hempstead, N.Y.; and the Department of Mathematics, Hofstra University, Hempstead, N.Y.
Am J Psychiatry. 2016 Jan;173(1):69-77. doi: 10.1176/appi.ajp.2015.14121571. Epub 2015 Aug 28.
Clinical response to antipsychotic drug treatment is highly variable, yet prognostic biomarkers are lacking. The authors recently demonstrated that successful antipsychotic drug treatment alters resting-state functional connectivity of the striatum. The goal of the present study was to test whether intrinsic striatal connectivity patterns provide prognostic information and can serve as a potential biomarker of treatment response to antipsychotic drugs.
The authors used resting-state functional MRI (fMRI) to develop a prognostic index in a discovery cohort of 41 first-episode schizophrenia patients, then tested this index in an independent cohort of 40 newly hospitalized chronic patients with acute psychosis. In the discovery cohort, patients underwent resting-state fMRI scanning at the initiation of randomized controlled treatment with a second-generation antipsychotic. Whole-brain functional connectivity maps were generated for each subject from striatal seed regions. A stringent measure of clinical response was calculated that required sustained improvement over two consecutive study visits. Clinical response was entered into a survival analysis, and Cox regression was applied to the functional connectivity data. A striatal connectivity index was created, comprising functional connections of the striatum that predicted treatment response. This striatal connectivity index was tested on a generalizability cohort of patients with psychotic disorders who were hospitalized for an acute psychotic episode.
A total of 91 regions functionally connected with the striatum provided significant prognostic information. Connectivity in these regions was used to create a baseline striatal connectivity index that predicted response to antipsychotic treatment with high sensitivity and specificity in both the discovery and generalizability cohorts.
These results provide evidence that individual differences in striatal functional connectivity predict response to antipsychotic drug treatment in acutely psychotic patients. With further development, this has the potential to serve as a prognostic biomarker with clinical utility and to reduce the overall burden associated with psychotic illnesses.
抗精神病药物治疗的临床反应差异很大,但缺乏预后生物标志物。作者最近证明,成功的抗精神病药物治疗会改变纹状体的静息态功能连接。本研究的目的是测试纹状体内在连接模式是否能提供预后信息,并能否作为抗精神病药物治疗反应的潜在生物标志物。
作者使用静息态功能磁共振成像(fMRI)在41例首发精神分裂症患者的发现队列中建立一个预后指数,然后在40例新住院的急性精神病慢性患者的独立队列中测试该指数。在发现队列中,患者在开始使用第二代抗精神病药物进行随机对照治疗时接受静息态fMRI扫描。从纹状体种子区域为每个受试者生成全脑功能连接图。计算了一种严格的临床反应测量方法,该方法要求在连续两次研究访视中持续改善。将临床反应纳入生存分析,并将Cox回归应用于功能连接数据。创建了一个纹状体连接指数,包括预测治疗反应的纹状体功能连接。在因急性精神病发作住院的精神病性障碍患者的可推广性队列中测试了该纹状体连接指数。
总共91个与纹状体功能连接的区域提供了显著的预后信息。利用这些区域的连接性创建了一个基线纹状体连接指数,该指数在发现队列和可推广性队列中均以高敏感性和特异性预测抗精神病治疗反应。
这些结果提供了证据,表明纹状体功能连接的个体差异可预测急性精神病患者对抗精神病药物治疗 的反应。随着进一步发展,这有可能作为一种具有临床效用的预后生物标志物,并减轻与精神病性疾病相关的总体负担。