Papageorgiou Charalabos, Oulis Panayiotis, Vasios Christos, Kontopantelis Evagelos, Uzunoglu Nikolaos, Rabavilas Andreas, Christodoulou George N
Psychophysiology Laboratory, Department of Psychiatry, Eginition Hospital, University of Athens, 74 Vas. Sophias Ave., Athens, 11528, Greece.
Eur Neuropsychopharmacol. 2004 May;14(3):227-36. doi: 10.1016/S0924-977X(03)00147-0.
Attentional deficits have been implicated in the pathophysiology of auditory hallucinations in schizophrenia. Since the latency of the P300 component of event-related potentials (ERPs) is considered to be a sensitive measure of stimulus classification speed, while its amplitude-a measure of attentional resource allocation when memory updating is engaged, the present study focuses on the comparison of P300 between healthy subjects and schizophrenic patients experiencing auditory hallucinations and treated with clozapine and olanzapine.
The auditory P300 was assessed during the anticipatory period of a short memory test, in 16 male hallucinated schizophrenic patients and 13 male normal subjects matched for age and educational level. The patients were reexamined under identical conditions when their hallucinations had resolved following treatment with clozapine (8 patients) and olanzapine (8 patients).
The patients with hallucinations exhibited significantly reduced P300 amplitude at leads Fp1, F3, (C3-T5)/2, F4, Cz and Fz, when compared to the normal controls and at leads Fp1, F3, F4, (C4-T6)/2, C4, P4, Cz and Fz when compared to themselves during the remission phase. However logistic regression models revealed that the most important leads, differentiating the patient group before treatment either with the healthy controls, or with itself after treatment, were that at the left temporoparietal and at the left prefrontal area. Memory performance of the patient group, even after treatment and in spite of its significant improvement, remained significantly less than that of healthy controls. both antipsychotic agents had similar effects on the p300 amplitude and memory performance.
These findings indicate that auditory hallucinations in schizophrenia manifest abnormal aspects of attention, mediated by a distributed network involving or affecting the left temporoparietal and left prefrontal area. Additionally, the present study points to an improvement of attentional function in schizophrenic patients experiencing auditory hallucinations, both in the clozapine group but also in the olanzapine group.
注意力缺陷与精神分裂症幻听的病理生理学有关。由于事件相关电位(ERP)的P300成分的潜伏期被认为是刺激分类速度的敏感指标,而其波幅是记忆更新时注意力资源分配的指标,因此本研究重点比较健康受试者与经历幻听并接受氯氮平和奥氮平治疗的精神分裂症患者之间的P300。
在一项短记忆测试的预期期内,对16名有幻觉的男性精神分裂症患者和13名年龄及教育水平匹配的男性正常受试者进行听觉P300评估。在用氯氮平(8例患者)和奥氮平(8例患者)治疗幻觉消失后,在相同条件下对患者进行复查。
与正常对照组相比,有幻觉的患者在Fp1、F3、(C3-T5)/2、F4、Cz和Fz导联处的P300波幅显著降低;与缓解期的自身相比,在Fp1、F3、F4、(C4-T6)/2、C4、P4、Cz和Fz导联处的P300波幅也显著降低。然而,逻辑回归模型显示,区分治疗前患者组与健康对照组或治疗后自身的最重要导联是左颞顶叶和左前额叶区域。患者组的记忆表现,即使在治疗后且有显著改善,仍显著低于健康对照组。两种抗精神病药物对P300波幅和记忆表现有相似的影响。
这些发现表明,精神分裂症的幻听表现出注意力的异常方面,由涉及或影响左颞顶叶和左前额叶区域的分布式网络介导。此外,本研究表明,氯氮平组和奥氮平组中经历幻听的精神分裂症患者的注意力功能均有改善。