GGz Centraal Psychiatric Center, Innova, Amersfoort, The Netherlands.
Int Rev Neurobiol. 2011;98:211-30. doi: 10.1016/B978-0-12-381328-2.00009-2.
Dyskinesia can develop in patients with schizophrenia in the course of the disease with or without the use of antipsychotics.In patients with psychiatric disorders other than schizophrenia Tardive Dyskinesia (TD) can develop in patients treated with antipsychotics or other drugs with dopamine D2 blocking properties. Spontaneous Dyskinesia in antipsychotic naive patients with schizophrenia ranges from 4 to 40%, depending on the age and duration of the illness. Moreover, siblings of patients with schizophrenia have higher prevalence rates of dyskinesia than matched controls. Incidence rates of TD due to dopamine blocking properties vary due to the sample population and the affinity for the dopamine blocker to the D2 dopamine receptor. Once developed, TD seems very persistent, the course of TD might be mediated by the affinity for the dopamine D2 receptor. Risk factors for TD in the literature are numerous, in this chapter only replicated and risk factors from longitudinal studies will be reported limiting the amount of risk factors. Furthermore only meta-analyses on genetic factors related to TD will be discussed due to inconsistency of genetic effects because of sample heterogeneity, small effects of multiple genes, (epi)genetic interactions,pleiotropy and small sample size. Finally the concept "Tardive Dyskinesia" will be discussed and the influence hereof on the above mentioned factors.
运动障碍可在精神分裂症患者的疾病过程中发生,无论是否使用抗精神病药物。在非精神分裂症的精神障碍患者中,使用抗精神病药物或其他具有多巴胺 D2 阻断特性的药物治疗可能会导致迟发性运动障碍(TD)。在未经抗精神病药物治疗的精神分裂症患者中,自发性运动障碍的发生率为 4%至 40%,具体取决于年龄和病程。此外,精神分裂症患者的兄弟姐妹比匹配的对照组更容易出现运动障碍。由于样本人群和多巴胺阻断剂与 D2 多巴胺受体的亲和力不同,多巴胺阻断特性引起的 TD 的发生率也有所不同。一旦发生 TD,似乎就非常持久,TD 的病程可能受多巴胺 D2 受体亲和力的影响。文献中迟发性运动障碍的危险因素很多,在这一章中,仅报告了经过复制的和来自纵向研究的危险因素,以限制危险因素的数量。此外,由于样本异质性、多个基因的小效应、(表观)遗传相互作用、多效性和样本量小,与 TD 相关的遗传因素的荟萃分析结果不一致,因此仅讨论与 TD 相关的遗传因素的荟萃分析。最后,将讨论“迟发性运动障碍”的概念及其对上述因素的影响。