Linden David E J
School of Psychology and North Wales Clinical School, Bangor University, Brigantia Building, Bangor, Wales, UK.
Eur Arch Psychiatry Clin Neurosci. 2008 Nov;258 Suppl 5:71-5. doi: 10.1007/s00406-008-5023-1.
The development of psychotherapy has been based on psychological theories and clinical effects. However, an investigation of the neurobiological mechanisms of psychological interventions is also needed in order to improve indication and prognosis, inform the choice of parallel pharmacotherapy, provide outcome measures and potentially even aid the development of new treatment protocols. This neurobiological investigation can be informed by animal models, for example of learning and conditioning, but will essentially need the non-invasive techniques of functional neuroimaging in order to assess psychotherapy effects on patients' brains, which will be reviewed here. Most research so far has been conducted in obsessive compulsive disorder (OCD), anxiety disorders and depression. Effects in OCD were particularly exciting in that both cognitive behavioural therapy and medication with a selective serotonin inhibitor led to a reduction in blood flow in the caudate nucleus. In phobia, brief courses of behavioural therapy produced marked reductions of paralimbic responses to offensive stimuli in line with the clinical improvement. Findings in depression are less consistent, with both increases and decreases in prefrontal metabolism being reported. However, they are important in pointing to different mechanisms for the clinical effects of pharmacotherapy (more "bottom up") and psychotherapy (more "top down"). For the future it would be desirable if the findings of psychotherapy changes to brain activation patterns were confirmed in larger groups with homogenous imaging protocols. Functional imaging has already made great contributions to the understanding of the neural correlates of psychopathology. For example, evidence converges to suggest that the subgenual cingulate is crucial for mood regulation. One current clinical application of these findings is deep brain stimulation in areas highlighted by such imaging studies. I will discuss their initial application in depression and OCD, and suggest potential alternative options based on recent developments in neurofeedback technology.
心理治疗的发展一直基于心理学理论和临床疗效。然而,为了改善适应症和预后、指导并行药物治疗的选择、提供疗效评估指标,甚至可能有助于新治疗方案的开发,还需要对心理干预的神经生物学机制进行研究。这种神经生物学研究可以借助动物模型,比如学习与条件反射模型,但本质上需要功能性神经成像的非侵入性技术来评估心理治疗对患者大脑的影响,本文将对此进行综述。到目前为止,大多数研究是在强迫症、焦虑症和抑郁症患者中开展的。强迫症方面的研究结果尤其令人兴奋,因为认知行为疗法和使用选择性5-羟色胺再摄取抑制剂的药物治疗均导致尾状核血流量减少。在恐惧症方面,短期行为疗法显著降低了对冒犯性刺激的边缘旁反应,与临床改善情况相符。抑郁症方面的研究结果不太一致,有报告称前额叶代谢既有增加也有减少。然而,这些结果对于指出药物治疗(更多“自下而上”)和心理治疗(更多“自上而下”)临床疗效的不同机制很重要。未来,如果能在采用统一成像方案的更大样本群体中证实心理治疗对大脑激活模式的改变,那将是很理想的。功能成像已经为理解精神病理学的神经关联做出了巨大贡献。例如,越来越多的证据表明膝下扣带回对情绪调节至关重要。这些研究结果目前在临床上的一个应用是对这类成像研究突出显示的区域进行深部脑刺激。我将讨论其在抑郁症和强迫症中的初步应用,并根据神经反馈技术的最新进展提出潜在的替代方案。