Department of Psychology, University of Alabama at Birmingham, Birmingham, Alabama.
Department of Psychiatry and Behavioral Neurobiology, University of Alabama at Birmingham, Birmingham, Alabama.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2022 Jan;7(1):108-118. doi: 10.1016/j.bpsc.2020.04.014. Epub 2020 May 6.
Converging lines of evidence point to hippocampal dysfunction in schizophrenia. It is thought that hippocampal dysfunction spreads across hippocampal subfields and to cortical regions by way of long-range efferent projections. Importantly, abnormalities in the excitation/inhibition balance could impair the long-range modulation of neural networks. The goal of this project was twofold. First, we sought to identify replicable patterns of hippocampal dysconnectivity in patients with a psychosis spectrum disorder. Second, we aimed to investigate a putative link between glutamatergic metabolism and hippocampal connectivity alterations.
We evaluated resting-state hippocampal functional connectivity alterations in two cohorts of patients with a psychosis spectrum disorder. The first cohort consisted of 55 medication-naïve patients with first-episode psychosis and 41 matched healthy control subjects, and the second cohort consisted of 42 unmedicated patients with schizophrenia and 41 matched control subjects. We also acquired measurements of glutamate + glutamine in the left hippocampus using magnetic resonance spectroscopy for 42 patients with first-episode psychosis and 37 healthy control subjects from our first cohort.
We observed a pattern of hippocampal functional hypoconnectivity to regions of the default mode network and hyperconnectivity to the lateral occipital cortex in both cohorts. We also show that in healthy control subjects, greater hippocampal glutamate + glutamine levels predicted greater hippocampal functional connectivity to the anterior default mode network. Furthermore, this relationship was reversed in medication-naïve subjects with first-episode psychosis.
These results suggest that an alteration in the relationship between glutamate and functional connectivity may disrupt the dynamic of major neural networks.
越来越多的证据表明精神分裂症存在海马功能障碍。人们认为,海马功能障碍通过长程传出投射在海马亚区之间以及向皮质区域扩散。重要的是,兴奋性/抑制性平衡的异常可能会损害神经网络的长程调制。本项目的目标有两个。首先,我们试图确定精神分裂症谱系障碍患者中海马连接异常的可复制模式。其次,我们旨在研究谷氨酸能代谢与海马连接改变之间的潜在联系。
我们评估了两个精神分裂症谱系障碍患者队列的静息状态下海马功能连接改变。第一队列包括 55 名未经药物治疗的首发精神病患者和 41 名匹配的健康对照者,第二队列包括 42 名未经药物治疗的精神分裂症患者和 41 名匹配的对照者。我们还对来自我们第一队列的 42 名首发精神病患者和 37 名健康对照者的左侧海马区使用磁共振波谱技术获得了谷氨酸+谷氨酰胺的测量值。
我们观察到两个队列的海马功能连接都存在默认模式网络区域的连接不足和外侧枕叶皮质的连接过度的模式。我们还表明,在健康对照者中,海马区谷氨酸+谷氨酰胺水平越高,与前默认模式网络的海马功能连接就越强。此外,这种关系在未经药物治疗的首发精神病患者中是相反的。
这些结果表明,谷氨酸和功能连接之间关系的改变可能会破坏主要神经网络的动态。