帕罗西汀治疗强迫症患者的定量脑电图。

Elsebet S Hansen, Leslie S Prichep, Tom G Bolwig, E Roy John
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引用次数: 49

摘要

对5 -羟色胺能神经递质系统的活性有特殊作用的药物的有效性已经改变了强迫症(OCD)患者的前景。这些化合物的应答率约为70%,在过去几十年里进行了大量的脑成像研究,对强迫症的生化性质和起源的理解开始展开。包括行为学和实验观察、临床病理结果和不同的成像方法在内的综合数据表明,基底神经节以及皮层和相关的丘脑结构参与了强迫症的病理生理。在之前的一项研究中,使用定量脑电图(QEEG)方法,即神经计量学,将强迫症患者的QEEG数据与年龄合适的正常人群的QEEG数据进行统计比较,在临床均质患者组中分为两种亚型。θ活动相对过度的患者,尤其是额叶区,对血清素再摄取抑制剂(SSRI)治疗无反应,而α活动相对增强的患者对药物治疗有反应。这些发现表明,患者群体中至少有两个亚组具有相似的症状,但对治疗的反应不同。在本研究中,我们使用神经测量QEEG对20例符合DSM-R-III标准的非抑郁强迫症患者进行了分型,并接受了帕罗西汀治疗,其中18例对治疗有反应。在治疗应答者中,94.4%的亚型成员预测为SSRI应答者。在这些受试者中有很强的相对基线活动;成功治疗至少3个月后,这种活动减少,看起来更正常。组平均地形图没有显示出无反应组的特征(θ没有多余的相对功率)。在之前的研究中,基线QEEG谱成员指向一个关于治疗反应的预测值。
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Quantitative electroencephalography in OCD patients treated with paroxetine.

The effectiveness of drugs that have a specific effect on the activity of the serotonergic neurotransmitter systemhas changed the outlook for patients suffering from obsessive-compulsive disorder (OCD). With a response rate of about 70% to such compounds and the great amount of brain imaging studies conducted over the past decades, an understanding of the biochemical nature and origins of OCD is beginning to unfold. Convergent data including ethological and experimental observations, clinico-pathological findings and different imaging methods have implicated the basal ganglia along with the cortical and related thalamic structures to be involved in the pathophysiology of OCD. In a previous study using the quantitative electroencephalographic (QEEG) method known as neurometrics, in which QEEG data from OCD patients were compared statistically with those from an age-appropriate normative population, two subtypes within a clinically homogeneous patient group were classified. Patients with relative excess theta activity, especially in the frontal regions, were nonresponders to treatment with serotonin reuptake inhibitors (SSRI), while those with increased relative power in alpha activity were responders to pharmacological treatment. These findings suggested at least two subgroups in a patient population with similar symptoms but differential responses to treatment. In the present study we used neurometric QEEG to subtype a group of 20 non-depressed OCD patients, fulfilling DSM-R-III criteria, treated with paroxetine, of whom 18 were responders to treatment. Of the treatment responders, 94.4% were predicted by subtype membership to be SSRI responsers. In these subjects there was a strong relative alpha baseline activity; after successful treatment through at least 3 months this activity decreased, looking more normal. The group average topographic maps showed none of the characteristics seen in the nonresponder cluster (no excess relative power in theta). As in the previous investigation, baseline QEEG profile membership points to a predictive value with regard to therapeutic response.

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