Leiva-Santana C, Alvarez-Saúco M
Servico de Neurología, Hospital General Universitario de Alicante, 03010 Alicante, Espana.
Rev Neurol. 2006;43(2):95-100.
Most of the patients with Parkinson's disease evaluated in formal neuropsychological studies are found to have cognitive disorders similar to those of patients with lesions in the prefrontal cortex. A large number of anatomical, physiological, pharmacological and clinical data indicate that dopamine transmission plays an important role in frontal cortical functions. We review the main types of cognitive impairment in Parkinson's disease and their response to treatment with levodopa.
In studies involving the acute administration of levodopa, the results obtained with regard to the cognitive functions have been heterogeneous, since improvements, exacerbations and the absence of any changes have all been observed. This heterogeneity is affected by methodological problems deriving from the disease itself, the treatment administered and the way evaluation is carried out. Longitudinal studies show a pattern of initial improvement, followed by stability, or maintenance, over a period of 2 or 3 years and then renewed exacerbation with no response to levodopa. On occasions, patients may only respond after a certain period of continued treatment. Generally speaking, the more severe the cognitive impairment is, the poorer the response to levodopa will be.
Therapy with levodopa modifies, in one sense or another, the cognitive disorders in Parkinson's disease, which indicates that the dopaminergic deficit unquestionably plays a role in these disorders. The absence of response in some patients or in some cognitive functions or the fact that it 'wears off' in most patients suggests that the dopaminergic deficit is only one of the factors in the aetiopathogenesis of the cognitive dysfunction found in Parkinson's disease.
在正式的神经心理学研究中评估的大多数帕金森病患者被发现存在与前额叶皮质病变患者相似的认知障碍。大量的解剖学、生理学、药理学和临床数据表明,多巴胺传递在额叶皮质功能中起重要作用。我们综述了帕金森病认知障碍的主要类型及其对左旋多巴治疗的反应。
在涉及左旋多巴急性给药的研究中,关于认知功能获得的结果是异质性的,因为观察到了改善、恶化以及无任何变化的情况。这种异质性受到源自疾病本身、所给予的治疗以及评估方式的方法学问题的影响。纵向研究显示出一种模式,即最初改善,随后在2或3年的时间内保持稳定或维持,然后再次恶化且对左旋多巴无反应。有时,患者可能仅在持续治疗一段时间后才有反应。一般来说,认知障碍越严重,对左旋多巴的反应就越差。
左旋多巴治疗在某种意义上改变了帕金森病的认知障碍,这表明多巴胺能缺陷无疑在这些障碍中起作用。一些患者或某些认知功能无反应,或者大多数患者出现“疗效减退”,这一事实表明多巴胺能缺陷只是帕金森病中发现的认知功能障碍病因发病机制中的因素之一。