Lind Penelope A, Parker Richard K, Northwood Korinne, Siskind Dan J, Medland Sarah E
Psychiatric Genetics, Mental Health and Neuroscience Research Program, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
School of Biomedical Sciences, Queensland University of Technology, Brisbane, Australia.
Schizophr Bull. 2025 Mar 14;51(2):458-469. doi: 10.1093/schbul/sbae065.
The ClozaGene Study is a nationwide cohort of adults who have been treated with clozapine. While clozapine is indicated in the management of treatment-resistant schizophrenia, it is associated with a considerable adverse drug reaction (ADR) burden, and not all patients achieve adequate symptomatic response. The current study focuses on self-reported experiences of clozapine use and response, clozapine-associated ADRs, and mental health comorbidity.
A total of 1021 participants (41.0% female; aged 46.2 ± 10.6 years [range 18-66]) were recruited via a mail-out based on prescriptions for clozapine. Participants completed a self-report questionnaire.
Most participants (90.1%, n = 912) were living with schizophrenia while 41.5% reported a lifetime diagnosis of depression, 15.6% bipolar disorder, and 8.1% schizoaffective disorder. Clozapine was currently prescribed to 944 (92.5%) participants and 37.8% of these participants self-reported currently taking additional antipsychotic medication. Nearly 3 quarters of participants living with schizophrenia reported that clozapine helped control their schizophrenia symptoms moderately to very well. The most commonly reported ADRs were sialorrhea (80.3%), weight gain (71.0%), constipation (56.9%), and sedation (52.8%). The prevalence of clozapine cessation due to clozapine-induced myocarditis and neutropenia was 1% and 0.4%, respectively.
Our findings highlight the high rate of psychotic and metabolic symptoms and ADRs among adults prescribed clozapine in the general Australian population. Future genomic analyses will focus on identifying genetic variants influencing clozapine treatment response and side effects.
ClozaGene研究是一项针对接受氯氮平治疗的成年人的全国性队列研究。虽然氯氮平被用于难治性精神分裂症的治疗,但其会带来相当大的药物不良反应负担,而且并非所有患者都能获得足够的症状缓解。当前的研究聚焦于氯氮平使用和反应的自我报告经历、氯氮平相关的药物不良反应以及心理健康合并症。
基于氯氮平处方通过邮件招募了1021名参与者(41.0%为女性;年龄46.2±10.6岁[范围18 - 66岁])。参与者完成了一份自我报告问卷。
大多数参与者(90.1%,n = 912)患有精神分裂症,41.5%报告有终生抑郁诊断,15.6%为双相情感障碍,8.1%为分裂情感性障碍。目前944名(92.5%)参与者正在服用氯氮平,其中37.8%的参与者自我报告目前还在服用其他抗精神病药物。近四分之三的精神分裂症患者报告氯氮平在一定程度上很好地帮助控制了他们的精神分裂症症状。最常报告的药物不良反应是流涎(80.3%)、体重增加(71.0%)、便秘(56.9%)和镇静(52.8%)。因氯氮平诱发的心肌炎和中性粒细胞减少而停用氯氮平的患病率分别为1%和0.
4%。
我们的研究结果凸显了澳大利亚普通人群中服用氯氮平的成年人出现精神病性和代谢症状及药物不良反应的高发生率。未来的基因组分析将聚焦于识别影响氯氮平治疗反应和副作用的基因变异。