Central Institute of Mental Health, Department of Psychiatry and Psychotherapy, P.O. Box 12 21 20, D-68072 Mannheim, Germany.
Curr Neuropharmacol. 2012 Mar;10(1):88-95. doi: 10.2174/157015912799362724.
Obsessive-compulsive disorder (OCD) is rarely associated with schizophrenia, whereas 20 to 30% of schizophrenic patients, suffer from comorbid obsessive-compulsive symptoms (OCS). So far no single pathogenetic theory convincingly explained this fact suggesting heterogeneous subgroups. Based on long-term case observations, one hypothesis assumes that second-onset OCS in the course of schizophrenia might be a side effect of second generation antipsychotics (SGA), most importantly clozapine (CLZ). This review summarizes the supporting epidemiological and pharmacological evidence: Estimations on prevalence of OCS increase in more recent cross-sectional studies and in later disease stages. Longitudinal observations report the de novo-onset of OCS under clozapine treatment. This association has not been reported with first generation antipsychotics (FGA) or SGAs with mainly dopaminergic mode of action. Finally, significant correlations of OCS-severity with duration of treatment, dose and serum levels suggest clozapine-induced OCS. However, supposed causal interactions need further verifications. It is also unclear, which neurobiological mechanisms might underlie the pathogenetic process. Detailed genotypic and phenotypic characterizations of schizophrenics with comorbid OCS regarding neurocognitive functioning and activation in sensitive tasks of functional magnetic imaging are needed. Multimodal large-scaled prospective studies are necessary to define patients at risk for second-onset OCS and to improve early detection and therapeutic interventions.
强迫症(OCD)与精神分裂症很少同时发生,而 20%到 30%的精神分裂症患者则伴有共病性强迫症状(OCS)。到目前为止,还没有一个单一的发病机制理论能够令人信服地解释这一事实,这表明存在异质亚组。基于长期的病例观察,有一个假设认为,精神分裂症过程中继发的 OCS 可能是第二代抗精神病药物(SGA),尤其是氯氮平(CLZ)的副作用。本综述总结了支持这一假说的流行病学和药理学证据:横断面研究和疾病后期的最新研究结果表明,OCS 的患病率增加。纵向观察报告了氯氮平治疗下 OCS 的新发。这一关联尚未在第一代抗精神病药物(FGA)或主要作用于多巴胺能的 SGA 中报道。最后,OCS 严重程度与治疗持续时间、剂量和血清水平的显著相关性提示氯氮平诱导的 OCS。然而,假设的因果相互作用仍需要进一步验证。氯氮平引发 OCS 的潜在神经生物学机制也尚不清楚。需要对伴有共病 OCS 的精神分裂症患者进行详细的基因型和表型特征分析,包括神经认知功能和敏感任务的功能磁共振成像激活。需要进行多模态、大规模的前瞻性研究,以确定具有继发 OCS 风险的患者,并提高早期检测和治疗干预的效果。