Department of Psychiatry, Charité-Universitaetsmedizin Berlin, Campus Mitte, Germany.
Schizophr Res. 2010 May;118(1-3):189-200. doi: 10.1016/j.schres.2010.01.022. Epub 2010 Feb 26.
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.
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).
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.
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.
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。
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。
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。
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。