首页> 美国卫生研究院文献>Frontiers in Neuroscience >Closed Loop Deep Brain Stimulation for PTSD Addiction and Disorders of Affective Facial Interpretation: Review and Discussion of Potential Biomarkers and Stimulation Paradigms
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Closed Loop Deep Brain Stimulation for PTSD Addiction and Disorders of Affective Facial Interpretation: Review and Discussion of Potential Biomarkers and Stimulation Paradigms

机译:PTSD成瘾和情感面部解释障碍的闭环深部脑刺激:潜在的生物标志物和刺激范例的审查和讨论。

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摘要

The treatment of psychiatric diseases with Deep Brain Stimulation (DBS) is becoming more of a reality as studies proliferate the indications and targets for therapies. Opinions on the initial failures of DBS trials for some psychiatric diseases point to a certain lack of finesse in using an Open Loop DBS (OLDBS) system in these dynamic, cyclical pathologies. OLDBS delivers monomorphic input into dysfunctional brain circuits with modulation of that input via human interface at discrete time points with no interim modulation or adaptation to the changing circuit dynamics. Closed Loop DBS (CLDBS) promises dynamic, intrinsic circuit modulation based on individual physiologic biomarkers of dysfunction. Discussed here are several psychiatric diseases which may be amenable to CLDBS paradigms as the neurophysiologic dysfunction is stochastic and not static. Post-Traumatic Stress Disorder (PTSD) has several peripheral and central physiologic and neurologic changes preceding stereotyped hyper-activation behavioral responses. Biomarkers for CLDBS potentially include skin conductance changes indicating changes in the sympathetic nervous system, changes in serum and central neurotransmitter concentrations, and limbic circuit activation. Chemical dependency and addiction have been demonstrated to be improved with both ablation and DBS of the Nucleus Accumbens and as a serendipitous side effect of movement disorder treatment. Potential peripheral biomarkers are similar to those proposed for PTSD with possible use of environmental and geolocation based cues, peripheral signs of physiologic arousal, and individual changes in central circuit patterns. Non-substance addiction disorders have also been serendipitously treated in patients with OLDBS for movement disorders. As more is learned about these behavioral addictions, DBS targets and effectors will be identified. Finally, discussed is the use of facial recognition software to modulate activation of inappropriate responses for psychiatric diseases in which misinterpretation of social cues feature prominently. These include Autism Spectrum Disorder, PTSD, and Schizophrenia—all of which have a common feature of dysfunctional interpretation of facial affective clues. Technological advances and improvements in circuit-based, individual-specific, real-time adaptable modulation, forecast functional neurosurgery treatments for heretofore treatment-resistant behavioral diseases.
机译:随着研究激增了治疗的适应症和靶标,用深部脑刺激(DBS)治疗精神疾病变得越来越现实。关于某些精神疾病的DBS试验最初失败的观点表明,在这些动态,周期性的病理学中使用开环DBS(OLDBS)系统时,缺乏一定的技巧。 OLDBS将单态输入传递到功能失调的大脑电路,并通过人机界面在离散时间点对该输入进行调制,而无需进行临时调制或适应不断变化的电路动态。闭环DBS(CLDBS)承诺基于功能障碍的各个生理生物标记物进行动态的,固有的电路调制。这里讨论的是几种精神疾病,它们可能适合CLDBS范例,因为神经生理功能障碍是随机的而不是静态的。创伤后应激障碍(PTSD)在刻板的过度激活行为反应之前有一些外周和中枢的生理和神经变化。 CLDBS的生物标志物可能包括皮肤电导率变化,指示交感神经系统变化,血清和中枢神经递质浓度变化以及边缘回路激活。化学依赖性和成瘾性已被证明可通过伏隔核的消融和DBS以及运动障碍治疗的偶然副作用来改善。潜在的外周生物标志物与针对PTSD提出的那些相似,可能使用基于环境和地理位置的线索,生理唤醒的外周标志以及中央回路模式的个体变化。非物质成瘾症也已在OLDBS运动障碍患者中得到了偶然治疗。随着对这些行为成瘾的了解越来越多,将确定DBS目标和效应器。最后,讨论了使用面部识别软件来调节对精神疾病的不适当反应的激活,在这些疾病中,对社会暗示的误解非常突出。这些包括自闭症谱系障碍,创伤后应激障碍和精神分裂症-所有这些都具有面部情感线索功能失调的共同特征。基于电路的,针对特定个体的实时适应性调制,预测功能神经外科治疗的技术进步和改进,用于迄今为止对治疗有抵抗力的行为疾病。

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