Abstract
Background: The human striatum is a heterogeneous structure involved in diverse functional domains that related to distinct striatum subregions. Striatal dysfunction was thought to be a fundamental element in schizophrenia. However, the connectivity pattern of striatum solely based on functional or structural characteristics leads to inconsistent findings in healthy adult and also schizophrenia. This study aims to develop an integrated striatal model and reveal the altered functional connectivity pattern of the striatum in schizophrenia.Methods: Two data-driven approaches, task-dependent meta-analytic connectivity modeling (MACM) and task-independent resting-state functional connectivity (RSFC), were used for seven anatomical connectivity-based striatum subregions to provide an integrated striatal model. Then, RSFC analyses of seven striatal subregions were applied to 45 first-episode schizophrenia (FES) and 27 healthy controls to examine the difference, based on the integrated model, of functional connectivity pattern of striatal subregions.Results: MACM and RSFC results showed that striatum subregions were associated with discrete cortical regions and involved in distinct cognitive processes. Besides, RSFC results overlapped with MACM findings but showed broader distributions. Importantly, significantly reduced functional connectivity was identified between limbic subregion and thalamus, medial prefrontal cortex, anterior cingulate cortex, and insula and also between executive subregions and thalamus, supplementary motor area, and insula in FES.Conclusions: Combing functional and structural connectivity information, this study provides the integrated model of corticostriatal subcircuits and confirms the abnormal functional connectivity of limbic and executive striatum subregions with different networks and thalamus, supporting the important role of the corticostriatal-thalamic loop in the pathophysiology of schizophrenia.
Highlights
Recent evidence from nonhuman primates studies [1, 2] and human neuroimaging studies [3] suggests that the striatum, the main recipient of afferents projecting to the basal ganglia, is a complex brain structure with multiple and highly specific functions
Based on the integrated striatal model, we examine the dysfunctional connectivity of striatum in first-episode schizophrenia (FES) to explore the specific alternations of the striatum subregions and its related cortical pathways to provide new evidence for the pathophysiology and etiology of schizophrenia
The Str_limbic subregion was identified in 250 papers, 358 experiments, and 728 conditions in the Brainmap database, with data for 4,277 subjects and 4,915 locations being subjected to further activation likelihood estimation (ALE) analysis
Summary
Recent evidence from nonhuman primates studies [1, 2] and human neuroimaging studies [3] suggests that the striatum, the main recipient of afferents projecting to the basal ganglia, is a complex brain structure with multiple and highly specific functions It has well-documented roles in motor control and execution [4, 5] and being involved in a diverse array of other functional domains, such as emotion generation and regulation [6, 7] memory [8, 9], executive functions [10], and rewardrelated processes [11, 12]. This study aims to develop an integrated striatal model and reveal the altered functional connectivity pattern of the striatum in schizophrenia
Sign-in/Register to view highlights & summary Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
