将精神分裂症患者从典型的神经阻滞剂转换为阿立哌唑:对工作记忆相关功能激活的影响。

Switching schizophrenia patients from typical neuroleptics to aripiprazole: effects on working memory dependent functional activation.

机构信息

Department of Psychiatry, Charité-Universitaetsmedizin Berlin, Campus Mitte, Germany.

出版信息

Schizophr Res. 2010 May;118(1-3):189-200. doi: 10.1016/j.schres.2010.01.022. Epub 2010 Feb 26.

Abstract

BACKGROUND

Deficits in working memory (WM) are a core symptom of schizophrenia patients and have been linked to dysfunctional prefrontal activation, which might be caused by a mesocortical hypodopaminergic state. Aripiprazole--a partial dopamine antagonist--is a novel antipsychotic, which increases frontal dopamine concentrations in preclinical studies. However, little is known about specific medication effects on the modulation of frontal activation during WM performance.

METHODS

We measured BOLD-response during a WM task in a longitudinal fMRI-study in eleven schizophrenia patients first when they received conventional antipsychotics (T1) and a second time after they had been switched to aripiprazole (T2). A healthy control group matched for age, handedness and gender was investigated at two corresponding time points. Data was analyzed with SPM5 in a 2 x 2 x 2 design (groupxsessionxtask).

RESULTS

Schizophrenia patients showed fewer correct responses compared to healthy controls at T1 and a trend-wise normalization at T2. The task activated the fronto-parietal network during the contrast 2-back>0-back in all participants. At T1 patients revealed a hypoactivation in the dorsal anterior cingulate cortex (ACC), which normalized after switch to aripiprazole and correlated with improved task performance. This was due to a significant increase in the patients group while the control group did not change, as corroborated by a significant groupxtime interaction in this region.

CONCLUSIONS

This study showed for the first time that the partial dopamine antagonist aripiprazole increases BOLD-signal during a WM task in the cognitive part of the ACC in schizophrenia patients, which may reflect its beneficial effect on cognitive deficits.

摘要

背景

工作记忆(WM)缺陷是精神分裂症患者的核心症状,与前额叶激活功能障碍有关,而这种功能障碍可能是由中脑皮质多巴胺能低下状态引起的。阿立哌唑——一种部分多巴胺拮抗剂——是一种新型抗精神病药物,在临床前研究中可增加前额叶多巴胺浓度。然而,对于特定药物对 WM 表现期间前额叶激活的调节作用知之甚少。

方法

我们在一项精神分裂症患者的纵向 fMRI 研究中,在他们首次接受常规抗精神病药物(T1)和第二次换用阿立哌唑(T2)时,测量了 WM 任务期间的 BOLD 反应。一组年龄、利手和性别相匹配的健康对照组在两个相应的时间点进行了研究。数据采用 SPM5 在 2 x 2 x 2 设计(组 x 会话 x 任务)进行分析。

结果

与健康对照组相比,精神分裂症患者在 T1 时的正确反应较少,在 T2 时呈现出趋势性正常化。在所有参与者中,任务在对比 2 回>0 回时激活了额顶叶网络。在 T1 时,患者的背侧前扣带皮层(ACC)出现低激活,换用阿立哌唑后恢复正常,与任务表现的改善相关。这是由于患者组的信号显著增加,而对照组没有变化,这在该区域得到了显著的组间时间交互作用的证实。

结论

这项研究首次表明,部分多巴胺拮抗剂阿立哌唑可增加精神分裂症患者 WM 任务中认知性 ACC 区的 BOLD 信号,这可能反映了其对认知缺陷的有益作用。

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