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Clinical Course Neurobiology and Therapeutic Approaches to Treatment Resistant Schizophrenia. Toward an Integrated View

机译:抵抗精神分裂症的临床课程神经生物学和治疗方法。走向综合视野

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摘要

Despite considerable psychotherapeutic advancement since the discovery of chlorpromazine, almost one third of patients with schizophrenia remain resistant to dopamine-blocking antipsychotics, and continue to be exposed to unwanted and often disabling side effects, but little if any clinical benefit. Even clozapine, the superior antipsychotic treatment, is ineffective in approximately half of these patients. Thus treatment resistant schizophrenia (TRS), continues to present a major therapeutic challenge to psychiatry. The main impediment to finding novel treatments is the lack of understanding of precise molecular mechanisms leading to TRS. Not only has the neurobiology been enigmatic for decades, but accurate and early detection of patients who are at risk of not responding to dopaminergic blockade remains elusive. Fortunately, recent work has started to unravel some of the neurobiological mechanisms underlying treatment resistance, providing long awaited answers, at least to some extent. Here we focus on the scientific advances in the field, from the clinical course of TRS to neurobiology and available treatment options. We specifically emphasize emerging evidence from TRS imaging and genetic literature that implicates dysregulation in several neurotransmitters, particularly dopamine and glutamate, and in addition genetic and neural alterations that concertedly may lead to the formation of TRS. Finally, we integrate available findings into a putative model of TRS, which may provide a platform for future studies in a bid to open the avenues for subsequent development of effective therapeutics.
机译:尽管自发现氯丙嗪以来,精神疗法取得了长足的进步,但精神分裂症患者中近三分之一仍对多巴胺阻滞性抗精神病药产生抗药性,并继续暴露于不良且经常使之致死的副作用,但几乎没有任何临床益处。甚至氯氮平(一种出色的抗精神病药物治疗)对这些患者中的大约一半也无效。因此,抗精神分裂症(TRS)的治疗继续给精神病学带来重大的治疗挑战。寻找新疗法的主要障碍是对导致TRS的精确分子机制缺乏了解。神经生物学不仅数十年来一直是令人迷惑的,而且仍然难以准确,早期地发现对多巴胺能阻滞没有反应的患者。幸运的是,最近的工作已经开始揭示治疗抗性的某些神经生物学机制,至少在一定程度上提供了人们期待已久的答案。在这里,我们专注于该领域的科学进展,从TRS的临床历程到神经生物学以及可用的治疗选择。我们特别强调来自TRS成像和遗传文献的新兴证据,这些证据暗示几种神经递质(尤其是多巴胺和谷氨酸)的失调,以及共同导致TRS形成的遗传和神经改变。最后,我们将可用的发现整合到TRS的推定模型中,该模型可以为将来的研究提供平台,以期为后续开发有效的治疗方法开辟道路。

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