Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, Kings College London, London, SE5 8AF, UK.
Psychiatric Imaging Group, MRC London Institute of Medical Sciences, Hammersmith Hospital, London, W12 0NN, UK.
Transl Psychiatry. 2021 May 27;11(1):322. doi: 10.1038/s41398-021-01455-y.
Alterations in cortical inter-areal functional connectivity, and aberrant glutamatergic signalling are implicated in the pathophysiology of schizophrenia but the relationship between the two is unclear. We used multimodal imaging to identify areas of convergence between the two systems. Two separate cohorts were examined, comprising 195 participants in total. All participants received resting state functional MRI to characterise functional brain networks and proton magnetic resonance spectroscopy (1H-MRS) to measure glutamate concentrations in the frontal cortex. Study A investigated the relationship between frontal cortex glutamate concentrations and network connectivity in individuals with schizophrenia and healthy controls. Study B also used 1H-MRS, and scanned individuals with schizophrenia and healthy controls before and after a challenge with the glutamatergic modulator riluzole, to investigate the relationship between changes in glutamate concentrations and changes in network connectivity. In both studies the network based statistic was used to probe associations between glutamate and connectivity, and glutamate associated networks were then characterised in terms of their overlap with canonical functional networks. Study A involved 76 individuals with schizophrenia and 82 controls, and identified a functional network negatively associated with glutamate concentrations that was concentrated within the salience network (p < 0.05) and did not differ significantly between patients and controls (p > 0.85). Study B involved 19 individuals with schizophrenia and 17 controls and found that increases in glutamate concentrations induced by riluzole were linked to increases in connectivity localised to the salience network (p < 0.05), and the relationship did not differ between patients and controls (p > 0.4). Frontal cortex glutamate concentrations are associated with inter-areal functional connectivity of a network that localises to the salience network. Changes in network connectivity in response to glutamate modulation show an opposite effect compared to the relationship observed at baseline, which may complicate pharmacological attempts to simultaneously correct glutamatergic and connectivity aberrations.
皮质间功能连接的改变和谷氨酸能信号的异常与精神分裂症的病理生理学有关,但两者之间的关系尚不清楚。我们使用多模态成像来确定这两个系统的交汇点。共检查了两个独立的队列,总共包括 195 名参与者。所有参与者都接受了静息状态功能磁共振成像(rs-fMRI)以描述功能脑网络,和质子磁共振波谱(1H-MRS)以测量额叶皮质中的谷氨酸浓度。研究 A 调查了精神分裂症患者和健康对照组个体额叶皮质谷氨酸浓度与网络连接之间的关系。研究 B 还使用 1H-MRS,在谷氨酸调节剂利鲁唑作用前后扫描精神分裂症患者和健康对照组个体,以研究谷氨酸浓度变化与网络连接变化之间的关系。在这两项研究中,网络基统计被用来探测谷氨酸和连接之间的关联,然后根据谷氨酸相关网络与经典功能网络的重叠来描述这些网络。研究 A 涉及 76 名精神分裂症患者和 82 名对照者,确定了一个与谷氨酸浓度呈负相关的功能网络,该网络集中在突显网络内(p<0.05),并且在患者和对照组之间没有显著差异(p>0.85)。研究 B 涉及 19 名精神分裂症患者和 17 名对照者,发现利鲁唑诱导的谷氨酸浓度增加与突显网络内的连接增加有关(p<0.05),并且这种关系在患者和对照组之间没有差异(p>0.4)。额叶皮质谷氨酸浓度与定位于突显网络的网络的区域间功能连接有关。对谷氨酸调节的网络连接变化与基线观察到的关系相反,这可能使同时纠正谷氨酸能和连接异常的药物治疗复杂化。