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阿立哌唑与利培酮对精神分裂症计划和社会情感评估期间大脑激活的影响:一项单盲随机探索性研究。

Effects of aripiprazole versus risperidone on brain activation during planning and social-emotional evaluation in schizophrenia: A single-blind randomized exploratory study.

机构信息

BCN Neuroimaging Center, Department of Neuroscience, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; Rob Giel Research Center, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Rob Giel Research Center, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands; University Center Psychiatry, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2017 Oct 3;79(Pt B):112-119. doi: 10.1016/j.pnpbp.2017.05.022. Epub 2017 May 27.

Abstract

Impaired function of prefrontal brain networks may be the source of both negative symptoms and neurocognitive problems in psychotic disorders. Whereas most antipsychotics may decrease prefrontal activation, the partial dopamine D2-receptor agonist aripiprazole is hypothesized to improve prefrontal function. This study investigated whether patients with a psychotic disorder would show stronger activation of prefrontal areas and associated regions after treatment with aripiprazole compared to risperidone treatment. In this exploratory pharmacological neuroimaging study, 24 patients were randomly assigned to either aripiprazole or risperidone. At baseline and after nine weeks treatment they underwent an interview and MRI session. Here we report on brain activation (measured with arterial spin labeling) during performance of two tasks, the Tower of London and the Wall of Faces. Aripiprazole treatment decreased activation of the middle frontal, superior frontal and occipital gyrus (ToL) and medial temporal and inferior frontal gyrus, putamen and cuneus (WoF), while activation increased after risperidone. Activation increased in the ventral anterior cingulate and posterior insula (ToL), and superior frontal, superior temporal and precentral gyrus (WoF) after aripiprazole treatment and decreased after risperidone. Both treatment groups had increased ventral insula activation (ToL) and middle temporal gyrus (WoF), and decreased occipital cortex, precuneus and caudate head activation (ToL) activation. In conclusion, patients treated with aripiprazole may need less frontal resources for planning performance and may show increased frontotemporal and frontostriatal reactivity to emotional stimuli. More research is needed to corroborate and extend these preliminary findings.

摘要

前额叶大脑网络功能障碍可能是精神病性障碍中阴性症状和神经认知问题的根源。虽然大多数抗精神病药物可能会降低前额叶的激活,但部分多巴胺 D2 受体激动剂阿立哌唑被假设可以改善前额叶功能。这项研究调查了与利培酮治疗相比,患有精神病性障碍的患者在接受阿立哌唑治疗后,前额叶区域和相关区域是否会表现出更强的激活。在这项探索性的药物神经影像学研究中,24 名患者被随机分配到阿立哌唑或利培酮组。在基线和 9 周治疗后,他们接受了访谈和 MRI 检查。在这里,我们报告了在执行两项任务(伦敦塔和面孔墙)期间大脑的激活(通过动脉自旋标记测量)。阿立哌唑治疗降低了前额叶、额上回和枕叶(伦敦塔)以及内侧颞叶和额下回、壳核和楔前叶(面孔墙)的激活,而利培酮治疗后激活增加。阿立哌唑治疗后,腹侧前扣带回和后岛叶(伦敦塔)以及额上回、额上回和中央前回(面孔墙)的激活增加,而利培酮治疗后则减少。两组治疗后都增加了腹侧岛叶(伦敦塔)和颞上回(面孔墙)的激活,减少了枕叶皮质、楔前叶和尾状核头部(伦敦塔)的激活。总之,接受阿立哌唑治疗的患者可能需要较少的前额叶资源来进行规划表现,并且可能表现出对情绪刺激的额颞叶和额纹状体反应性增加。需要进一步的研究来证实和扩展这些初步发现。

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