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From 'classical' antipsychotics to 'multidimensional stabilizers': do we need a new classification for novel drugs used in schizophrenia?

机译:从“经典”抗精神病药到“多维稳定剂”:对于精神分裂症中使用的新药,我们是否需要进行新的分类?

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This article revisits the roots of the clinical categorical concept of schizophrenia and Its biopathogenetic model ('dopaminergic model'), based on dopaminergic dysfunctioning in CNS, as conceived in the 1960s and 1970s. These clinical/biopathogenic concepts have been challenged by the dimensional approach and by a more complex neurochemical model of schizophrenia, arising mainly from the use of novel compounds, which involves activity on different neurotransmitters in the CNS, Moreover, new compounds used in the treatment of schizophrenia are effective not only on the psychotic dimension, but also on other dimensions, such as negative, depressive and cognitive ones. Therefore, the term 'antipsychotic', which refers to a class of drugs acting mainly on acute psychotic symptoms, seems obsolete, and schizophrenia should not be conceived as an acute disorder, but rather as a chronic multidimensional dysfunction. Consequently, novel compounds acting on different dimensions can better stabilize patients, avoiding the shift from positive to negative symptoms due to the D_2 antagonism. Thus, a new denomination is needed considering all of the peculiarities of new compounds compared with neuroleptics for stabilizing not just psychotic symptoms in the acute phase, but also affective, negative and anergic symptoms (which are integral parts of the disorder), even in the medium-long term; more appropriately, they should be considered as 'multidimensional stabilizers' instead of antipsychotics. Moreover, this denomination also refers to their efficacy in bipolar disorders, since their use is being increasingly proven to be effective in the treatment of this disorder as well. Finally, a change in the name of this pharmacological class may contribute to reducing the stigma that is now closely linked to antipsychotic drugs, such as chronicity, unfavorable prognosis and 'craziness'.
机译:本文回顾了1960年代和1970年代构思的基于CNS多巴胺能功能障碍的精神分裂症的临床分类概念及其生物病理模型(“多巴胺能模型”)的根源。这些临床/生物致病性概念已受到维度方法和更复杂的精神分裂症神经化学模型的挑战,这主要是由于使用新化合物引起的,该化合物涉及中枢神经系统中不同神经递质的活性。此外,用于治疗精神分裂症的新化合物精神分裂症不仅在精神病方面有效,而且在其他方​​面也有效,例如消极,抑郁和认知方面。因此,术语“抗精神病药”是指主要作用于急性精神病性症状的一类药物,似乎已经过时了,精神分裂症不应被视为一种急性疾病,而应被视为一种慢性多维性功能障碍。因此,作用于不同维度的新型化合物可以更好地稳定患者,避免由于D_2拮抗作用而从阳性症状转变为阴性症状。因此,考虑到新化合物与抗精神病药相比的所有特性,需要一种新的面额,以便不仅在急性期稳定精神病症状,而且还稳定情绪,阴性和无痛症状(这是疾病的组成部分),甚至在稳定期也是如此。中长期更合适的是,它们应被视为“多维稳定剂”而不是抗精神病药。此外,该名称也指其在双相情感障碍中的功效,因为越来越多地证明它们的使用也可有效治疗这种疾病。最后,更改此药理学类别的名称可能有助于减少现在与抗精神病药密切相关的耻辱感,例如慢性,预后不良和“疯狂”。

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