Assistance Publique Hôpitaux de Paris, Department of Neurology, INSERM, CIC-9503, Pitié-Salpêtrière Hospital, Paris, France.
J Neural Transm (Vienna). 2013 Apr;120(4):665-71. doi: 10.1007/s00702-012-0934-4. Epub 2012 Dec 12.
Impulse control disorders (ICD) have been recognised in Parkinson's disease (PD) as adverse effects of dopamine replacement therapy, particularly with dopamine agonists. Although virtually all PD patients are treated with dopaminergic drugs, only a minority will develop hyperdopaminergic states, suggesting predisposing and/or protecting factors. The age at onset, the sex and the dose or type of dopaminergic drugs have been identified as clinical predictive factors. Recent genetic studies have investigated associations between ICD and polymorphisms of genes involved in the dopamine metabolism pathway (COMT, DAT), dopamine receptors (DRD1, DRD2, DRD3, DRD4), serotonin receptors and its transporter (HTR2A, 5HTT), and glutamate receptors (GRIN2B). Although validation in larger and independent cohorts is needed, the results from these studies give us some insights into the pathophysiology of hyperdopaminergic states and may be useful, at term, in personalising antiparkinsonian treatment in clinical practice.
冲动控制障碍(ICD)已被认为是帕金森病(PD)中多巴胺替代疗法的不良反应,特别是与多巴胺激动剂有关。尽管几乎所有的 PD 患者都接受了多巴胺能药物治疗,但只有少数患者会出现高多巴胺能状态,这表明存在易患和/或保护因素。发病年龄、性别以及多巴胺能药物的剂量或类型已被确定为临床预测因素。最近的遗传研究探讨了 ICD 与多巴胺代谢途径(COMT、DAT)、多巴胺受体(DRD1、DRD2、DRD3、DRD4)、5-羟色胺受体及其转运体(HTR2A、5HTT)和谷氨酸受体(GRIN2B)相关基因多态性之间的关联。虽然需要在更大和独立的队列中进行验证,但这些研究的结果使我们对高多巴胺能状态的病理生理学有了一些了解,并可能有助于在临床实践中个性化抗帕金森病治疗。