首发精神病患者大脑生物能异常。

Schizophrenia Bulletin Open Pub Date : 2021-01-30 eCollection Date: 2021-01-01 DOI:10.1093/schizbullopen/sgaa073
Cagri Yuksel, Xi Chen, Virginie-Anne Chouinard, Lisa D Nickerson, Margaret Gardner, Talia Cohen, Dost Öngür, Fei Du
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摘要

背景:越来越多的证据表明,精神分裂症和其他精神疾病患者的大脑能量代谢功能受损。肌酸激酶(CK)在为细胞提供三磷酸腺苷并在能量需求增加时维持其水平方面起着关键作用。然而,尚未对首发精神分裂症谱系障碍患者体内肌酸激酶的活性进行研究:方法:我们使用体内磷磁化转移光谱法测量了首发精神分裂症患者(FEP;n = 16)和健康对照组(n = 34)静息时额叶中 CK 的一阶前向速度常数(k f):结果:与健康对照组相比,FEP 患者的 CK k f 明显降低。其他能量代谢相关指标(包括磷酸肌酸(PCr)或 ATP)在组间没有差异。我们还发现患者体内甘油-3-磷酸胆碱(一种假定的膜分解产物)含量增加:本研究结果表明,脑生物能异常在精神分裂症谱系障碍的早期就已经存在。未来的研究需要确定 CK k f 减少与精神症状之间的关系,并测试针对这一途径的替代治疗方法。甘油-3-磷酸胆碱的增加与早期对药物治疗无效患者的研究以及后来对首发精神分裂症患者的研究一致,并表明突触修剪功能增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Abnormal Brain Bioenergetics in First-Episode Psychosis.

Background: Converging evidence indicates impaired brain energy metabolism in schizophrenia and other psychotic disorders. Creatine kinase (CK) is pivotal in providing adenosine triphosphate in the cell and maintaining its levels when energy demand is increased. However, the activity of CK has not been investigated in patients with first-episode schizophrenia spectrum disorders.

Methods: Using in vivo phosphorus magnetization transfer spectroscopy, we measured CK first-order forward rate constant (k f ) in the frontal lobe, in patients with first-episode psychosis (FEP; n = 16) and healthy controls (n = 34), at rest.

Results: CK k f was significantly reduced in FEP compared to healthy controls. There were no differences in other energy metabolism-related measures, including phosphocreatine (PCr) or ATP, between groups. We also found increase in glycerol-3-phosphorylcholine, a putative membrane breakdown product, in patients.

Conclusions: The results of this study indicate that brain bioenergetic abnormalities are already present early in the course of schizophrenia spectrum disorders. Future research is needed to identify the relationship of reduced CK k f with psychotic symptoms and to test treatment alternatives targeting this pathway. Increased glycerol-3-phosphorylcholine is consistent with earlier studies in medication-naïve patients and later studies in first-episode schizophrenia, and suggest enhanced synaptic pruning.

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