Laboratory of Experimental Psychiatry, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico2Neuropsychiatry Department, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico.
JAMA Psychiatry. 2013 Oct;70(10):1057-66. doi: 10.1001/jamapsychiatry.2013.289.
Increased glutamate levels in the right associative striatum have been described in patients during a first episode of psychosis. Whether this increase would persist after effective antipsychotic treatment is unknown.
To compare the glutamate levels in antipsychotic-naive patients with first-episode psychosis in the right associative striatum and right cerebellar cortex using proton magnetic resonance spectroscopy before and 4 weeks after antipsychotic treatment and to compare these results with normative data from sex-matched healthy control subjects.
DESIGN, SETTING, AND PARTICIPANTS: Before-after trial in an inpatient psychiatric research unit among 24 antipsychotic-naive patients with first-episode psychosis and 18 healthy controls matched for age, sex, handedness, and cigarette smoking.
Participants underwent 2 proton magnetic resonance spectroscopy studies: patients were imaged at baseline and after 4 weeks of antipsychotic treatment, while controls were imaged at baseline and at 4 weeks after the baseline measurement. Patients were treated with oral risperidone (open label) for 4 weeks with dosages that were titrated on the basis of clinical judgment.
Glutamate levels were estimated using LCModel (version 6.2-1T) and were corrected for the cerebrospinal fluid proportion within the voxel.
Patients with first-episode psychosis had higher levels of glutamate in the associative striatum and the cerebellum during the antipsychotic-naive condition compared with controls. After clinically effective antipsychotic treatment, glutamate levels significantly decreased in the associative striatum, with no significant change in the cerebellum. No differences in glutamate levels were observed between groups at 4 weeks.
Increased glutamate levels observed at baseline in patients with first-episode psychosis normalized after 4 weeks of clinically effective antipsychotic treatment. These results provide support for the hypothesis that improvement in clinical symptoms might be related to a decrease in glutamate levels.
在首次精神病发作期间,已在患者的右联合纹状体中描述了谷氨酸水平升高。在有效的抗精神病治疗后,这种增加是否会持续存在尚不清楚。
使用质子磁共振波谱比较抗精神病药初发精神病患者右联合纹状体和右小脑皮质的谷氨酸水平,这些患者在抗精神病药物治疗前和治疗后 4 周进行,并将这些结果与性别匹配的健康对照者的正常数据进行比较。
设计、地点和参与者:在精神病住院研究单位进行的前后试验,包括 24 名抗精神病药初发精神病患者和 18 名年龄、性别、利手和吸烟情况相匹配的健康对照者。
参与者进行了 2 次质子磁共振波谱研究:患者在基线和抗精神病药物治疗 4 周后进行成像,而对照组在基线和基线测量后 4 周进行成像。患者接受口服利培酮(开放标签)治疗 4 周,剂量根据临床判断滴定。
使用 LCModel(版本 6.2-1T)估计谷氨酸水平,并对体素内脑脊液比例进行校正。
在抗精神病药物初发的情况下,精神病患者的联合纹状体和小脑的谷氨酸水平高于对照组。在临床有效的抗精神病治疗后,联合纹状体的谷氨酸水平显著降低,小脑无显著变化。治疗 4 周后,两组之间的谷氨酸水平无差异。
在首次精神病发作的患者中,在基线时观察到的谷氨酸水平升高在 4 周的临床有效抗精神病治疗后恢复正常。这些结果支持这样的假设,即临床症状的改善可能与谷氨酸水平的降低有关。