Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan; Department of Neuropsychiatry, Kawasaki Municipal Kawasaki Hospital, Kanagawa, Japan.
Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Schizophr Res. 2020 Jan;215:173-180. doi: 10.1016/j.schres.2019.10.037. Epub 2019 Oct 28.
Little attention has been paid to the contribution of individual residual symptom to predict relapse in patients with schizophrenia receiving oral or long-acting injectable (LAI) antipsychotics.
We used the data from the Preventing Relapse on Oral Antipsychotics Compared to Injectables - Evaluating Efficacy (PROACTIVE) study, in which 305 outpatients with schizophrenia were randomly allocated to either biweekly LAI-risperidone (LAI-R) or daily oral second-generation antipsychotics (SGA) and assessed for up to 30 months. Baseline individual symptoms that could predict subsequent relapse were identified, using a Cox proportional hazards model. Moreover, among those who relapsed during the study (n = 73), individual symptoms were compared between baseline and biweekly ratings 8 to 2 weeks before relapse, using the linear mixed model.
A greater score in grandiosity at baseline was significantly associated with subsequent relapse (adjusted HR = 1.24, p = 0.006). When the two treatment groups were separately analyzed, more severe grandiosity (adjusted HR = 1.43, p = 0.003) and less severe hallucinatory behavior (adjusted HR = 0.70, p = 0.013) at baseline were significantly associated with relapse in the oral SGA group, but none was identified in the LAI-R group. Emotional withdrawal was significantly worse 8 and 2 weeks before relapse compared to the baseline (p = 0.032 and p = 0.043, respectively).
More severe grandiosity and less hallucination may have led to more frequent relapses in patients with schizophrenia receiving oral antipsychotics, which was not a case in those receiving LAI-R. The exploratory analysis indicates an increase in emotional withdrawal before relapse may be a useful marker for earlier interventions to possibly avert relapse.
在接受口服或长效注射(LAI)抗精神病药物的精神分裂症患者中,个体残留症状对预测复发的贡献很少受到关注。
我们使用了预防口服抗精神病药与注射剂相比复发的疗效评估(PROACTIVE)研究的数据,其中 305 名精神分裂症门诊患者被随机分配到每两周一次 LAI-利培酮(LAI-R)或每日口服第二代抗精神病药(SGA),并评估了长达 30 个月。使用 Cox 比例风险模型确定了基线时可以预测随后复发的个体症状。此外,在研究期间(n=73)复发的患者中,使用线性混合模型比较了复发前 8 至 2 周的基线和两周一次的评分之间的个体症状。
基线时自大得分较高与随后的复发显著相关(调整后的 HR=1.24,p=0.006)。当分别分析两个治疗组时,口服 SGA 组中基线时更严重的自大(调整后的 HR=1.43,p=0.003)和较轻的幻觉行为(调整后的 HR=0.70,p=0.013)与复发显著相关,但在 LAI-R 组中未发现。与基线相比,情感退缩在复发前 8 周和 2 周时明显恶化(p=0.032 和 p=0.043)。
在接受口服抗精神病药物治疗的精神分裂症患者中,更严重的自大和较轻的幻觉可能导致更频繁的复发,而接受 LAI-R 治疗的患者则不是这种情况。探索性分析表明,复发前情感退缩的增加可能是早期干预以避免复发的有用标志物。