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首页> 外文期刊>The international journal of neuropsychopharmacology >Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia
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Glutamatergic Neurometabolites in Clozapine-Responsive and -Resistant Schizophrenia

机译:氯氮平反应性和耐药性精神分裂症的谷氨酸能神经代谢物

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Background: According to the current schizophrenia treatment guidelines, 3 levels of responsiveness to antipsychotic medication exist: those who respond to first-line antipsychotics, those with treatment-resistant schizophrenia who respond to clozapine, and those with clozapine-resistant or ultra-treatment resistant schizophrenia. Proton magnetic resonance spectroscopy studies indicate that antipsychotic medication decreases glutamate or total glutamate + glutamine in the brains of patients with schizophrenia and may represent a biomarker of treatment response; however, the 3 levels of treatment responsiveness have not been evaluated. Methods: Proton magnetic resonance spectroscopy spectra were acquired at 3 Tesla from patients taking a second generation non-clozapine antipsychotic (first-line responders), patients with treatment-resistant schizophrenia taking clozapine, patients with ultra-treatment resistant schizophrenia taking a combination of antipsychotics, and healthy comparison subjects. Results: Group differences in cerebrospinal fluid-corrected total glutamate + glutamine levels scaled to creatine were detected in the dorsolateral prefrontal cortex [df(3,48); F = 3.07, P = .04, partial η2 = 0.16] and the putamen [df(3,32); F = 2.93, P = .05, partial η2 = 0.22]. The first-line responder group had higher dorsolateral prefrontal cortex total glutamate + glutamine levels scaled to creatine than those with ultra-treatment resistant schizophrenia [mean difference = 0.25, standard error = 0.09, P = .04, family-wise error-corrected]. Those with treatment-resistant schizophrenia had higher total glutamate + glutamine levels scaled to creatine in the putamen than the first-line responders (mean difference = 0.31, standard error = 0.12, P = .05, family-wise error-corrected) and those with ultra-treatment-resistant schizophrenia (mean difference = 0.39, standard error = 0.12, P = .02, family-wise error-corrected). Conclusions: Total glutamate + glutamine levels scaled to creatine in the putamen may represent a marker of response to clozapine. Future studies should investigate glutamatergic anomalies prior to clozapine initiation and following successful treatment.
机译:背景:根据当前的精神分裂症治疗指南,对抗精神病药物有3种反应水平:对一线抗精神病药物有反应的患者,对氯氮平有治疗抵抗力的精神分裂症患者以及对氯氮平耐药或对超治疗有抵抗力的患者精神分裂症。质子磁共振波谱研究表明,抗精神病药可减少精神分裂症患者大脑中的谷氨酸或总谷氨酸+谷氨酰胺,可能代表治疗反应的生物标志物。但是,尚未评估3种水平的治疗反应性。方法:质子磁共振波谱图是在3特斯拉处从服用第二代非氯氮平抗精神病药的患者(一线反应者),具有治疗难治性精神分裂症的患者服用氯氮平,对抗精神分裂症超治疗的患者服用了抗精神病药的组合获得的以及健康的比较对象。结果:在背外侧前额叶皮层中检测到脑脊液校正的总谷氨酸+谷氨酰胺水平成肌酸水平的组差异[df(3,48); F = 3.07,P = .04,部分η 2 = 0.16]和壳聚糖[df(3,32); F = 2.93,P = 0.05,部分η 2 = 0.22]。一线反应者组的背外侧前额叶皮层总谷氨酸+谷氨酰胺水平被定为肌酸水平高于那些具有高度治疗抵抗力的精神分裂症患者(平均差异= 0.25,标准误= 0.09,P = .04,按家庭方式校正过的误差) 。具有抗药性的精神分裂症患者的壳聚糖中的总谷氨酸+谷氨酰胺水平高于肌酸,与一线反应者相比(平均差异= 0.31,标准误= 0.12,P = 0.05,经家庭误差校正),以及患有高度抗药性的精神分裂症(平均差异= 0.39,标准误= 0.12,P = .02,已按家庭进行错误校正)。结论:壳聚糖中的总谷氨酸+谷氨酰胺水平按肌酸换算可能是对氯氮平反应的标志。未来的研究应在开始氯氮平之前和成功治疗后调查谷氨酸能异常。

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