Kleymann Phillip, Morgenroth Carla, Gutwinski Stefan, Bermpohl Felix, Schulze Daniel, Wagner Elias, Hasan Alkomiet, Okhuijsen-Pfeifer Cynthia, Luykx Jurjen J, van der Horst Marte Z, Oviedo-Salcedo Tatiana, Schreiter Stefanie
Department of Psychiatry and Neurosciences, Charité Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.
Department of Psychiatry and Psychotherapy, St. Hedwig-Krankenhaus, Charité-Universitätsmedizin, Berlin, Germany.
Eur Arch Psychiatry Clin Neurosci. 2025 May 16. doi: 10.1007/s00406-025-02021-z.
Obsessive-compulsive symptoms (OCS) frequently manifest in individuals with schizophrenia, affecting their prognosis and quality of life. The etiology of OCS in schizophrenia is complex, with theories ranging from subtype-specific manifestations to pharmacological influences. Notably, clozapine has been associated with a higher prevalence of OCS. However, the clinical factors influencing clozapine-induced OCS remain unclear. This cross-sectional study recruited individuals diagnosed with schizophrenia who were using clozapine, as well as a comparison group of individuals diagnosed with schizophrenia who were using other second-generation antipsychotics (SGA). Clinical assessments included OCS which were quantified using the Obsessive-Compulsive Inventory-Revised (OCI-R). 189 Participants were recruited, of whom 129 were taking clozapine and 60 other atypical antipsychotics. Statistical analyses, including moderated regression modeling, identified clinical factors influencing OCS occurrence. Clozapine users exhibited significantly higher OCI-R scores compared to non-clozapine users (p = 0.001). Moderated regression analysis revealed a moderating effect of negative symptom severity, indicating that when negative symptoms increased, the difference in OCI-R scores between clozapine and non-clozapine groups decreased. Other factors like duration of illness, medication duration, and psychopathology severity did not significantly moderate the group differences in OCI-R scores. As negative symptoms worsened, the impact of clozapine on OCS lessened, a pattern not seen with other antipsychotics. This suggests that clozapine's effect on OCS is specific and influenced by different mechanisms. The study recommends screening for OCS in patients with mild negative symptoms and further research into biological markers to better understand clozapine-induced OCS.
强迫症状(OCS)在精神分裂症患者中经常出现,影响其预后和生活质量。精神分裂症中OCS的病因复杂,理论范围从亚型特异性表现到药理学影响。值得注意的是,氯氮平与较高的OCS患病率相关。然而,影响氯氮平诱发OCS的临床因素仍不清楚。这项横断面研究招募了正在使用氯氮平的精神分裂症患者,以及使用其他第二代抗精神病药物(SGA)的精神分裂症患者作为对照组。临床评估包括使用强迫观念与强迫行为量表修订版(OCI-R)进行量化的OCS。共招募了189名参与者,其中129人服用氯氮平,60人服用其他非典型抗精神病药物。统计分析,包括调节回归建模,确定了影响OCS发生的临床因素。与未使用氯氮平的患者相比,使用氯氮平的患者OCI-R评分显著更高(p = 0.001)。调节回归分析显示阴性症状严重程度具有调节作用,表明当阴性症状增加时,氯氮平组和非氯氮平组之间OCI-R评分的差异减小。疾病持续时间、用药持续时间和精神病理学严重程度等其他因素并未显著调节OCI-R评分的组间差异。随着阴性症状恶化,氯氮平对OCS 的影响减弱,这一模式在其他抗精神病药物中未出现。这表明氯氮平对OCS的影响是特异性的,且受不同机制影响。该研究建议对轻度阴性症状患者进行OCS筛查,并进一步研究生物标志物以更好地理解氯氮平诱发的OCS。