MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Norwegian Centre for Mental Disorders Research, Division of Mental Health and Addiction, University of Oslo and Oslo University Hospital, Oslo, Norway.
Biol Psychiatry. 2023 Jan 15;93(2):149-156. doi: 10.1016/j.biopsych.2022.07.014. Epub 2022 Aug 5.
Treatment-resistant schizophrenia affects approximately 30% of individuals with the disorder. Clozapine is the medication of choice in treatment-resistant schizophrenia, but optimizing administration and dose titration is complex. The identification of factors influencing clozapine prescription and response, including genetics, is of interest in a precision psychiatry framework.
We used linear regression models accounting for demographic, pharmacological, and clinical covariates to determine whether a polygenic risk score (PRS) for schizophrenia would be associated with the highest dose recorded during clozapine treatment. Analyses were performed across 2 independent multiancestry samples of individuals from a UK patient monitoring system, CLOZUK2 (n = 3133) and CLOZUK3 (n = 909), and a European sample from a Norwegian therapeutic drug monitoring service (n = 417). In a secondary analysis merging both UK cohorts, logistic regression models were used to estimate the relationship between schizophrenia PRSs and clozapine doses classified as low, standard, or high.
After controlling for relevant covariates, the schizophrenia PRS was correlated with the highest clozapine dose on record for each individual across all samples: CLOZUK2 (β = 12.22, SE = 3.78, p = .001), CLOZUK3 (β = 12.73, SE = 5.99, p = .034), and the Norwegian cohort (β = 46.45, SE = 18.83, p = .014). In a secondary analysis, the schizophrenia PRS was associated with taking clozapine doses >600 mg/day (odds ratio = 1.279, p = .006).
The schizophrenia PRS was associated with the highest clozapine dose prescribed for an individual in records from 3 independent samples, suggesting that the genetic liability for schizophrenia might index factors associated with therapeutic decisions in cohorts of patients with treatment-resistant schizophrenia.
约 30%的精神分裂症患者存在治疗抵抗。氯氮平是治疗抵抗性精神分裂症的首选药物,但优化管理和剂量滴定较为复杂。在精准精神病学框架下,确定影响氯氮平处方和疗效的因素(包括遗传因素)很有意义。
我们使用线性回归模型,考虑了人口统计学、药理学和临床协变量,以确定精神分裂症的多基因风险评分(PRS)是否与氯氮平治疗期间记录的最高剂量相关。在来自英国患者监测系统的 2 个独立的多民族样本(CLOZUK2 [n=3133]和 CLOZUK3 [n=909])和来自挪威治疗药物监测服务的欧洲样本(n=417)中进行了分析。在合并英国队列的二次分析中,使用逻辑回归模型来估计精神分裂症 PRS 与分类为低、标准或高的氯氮平剂量之间的关系。
在控制了相关协变量后,精神分裂症 PRS 与所有样本中每个个体记录的最高氯氮平剂量相关:CLOZUK2(β=12.22,SE=3.78,p=.001)、CLOZUK3(β=12.73,SE=5.99,p=.034)和挪威队列(β=46.45,SE=18.83,p=.014)。在二次分析中,精神分裂症 PRS 与服用氯氮平剂量>600 mg/d 相关(比值比=1.279,p=.006)。
精神分裂症 PRS 与 3 个独立样本中记录的个体服用的最高氯氮平剂量相关,这表明精神分裂症的遗传易感性可能反映了治疗抵抗性精神分裂症患者队列中与治疗决策相关的因素。