Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Schizophr Res. 2011 Aug;130(1-3):11-9. doi: 10.1016/j.schres.2011.03.015. Epub 2011 Apr 13.
Research has identified distinct trajectories of antipsychotic response in patients with chronic schizophrenia in short-duration trials (~12 weeks). This post-hoc analysis identified trajectories in patients with chronic schizophrenia treated for ≤24 weeks. We pooled data from 1990 patients with chronic schizophrenia from 6 randomized, double-blind, olanzapine-comparator trials of atypical antipsychotics. Trajectory analysis identified homogeneous subpopulations within the larger heterogeneous population. Baseline demographics were compared between the identified latent classes. Five distinct response trajectories based on Positive and Negative Syndrome Scale (PANSS) Total score were identified: Dramatic Responders (n=47/1990, 2.4%), severely-ill patients (PANSS=124) with rapid and sustained improvement (51%) by Week 3; Partial Responders (n=1802/1990, 90.6%), moderately-ill (PANSS=90) with minimal improvement (21%) by Week 4, and little further improvement; Partial Responders-Unsustained (Late) (n=32/1990, 1.6%), markedly-ill (PANSS=95) with minimal initial improvement followed by worsening after Week 12; Partial Responders-Unsustained (Early) (n=28/1990, 1.4%), markedly-ill (PANSS=102) with minimal initial improvement followed by worsening after Week 8; and Delayed Responders (n=81/1990, 4.1%), markedly-to-severely-ill (PANSS=113) with minimal (11%) improvement at Week 8, but noticeable improvement thereafter (49%). Significant differences were noted for several baseline characteristics (p<.05) and discontinuation rates (46%-72%). Dramatic Responders were younger and more likely to be female and Hispanic with higher baseline illness severity. Analysis of antipsychotic response over 24 weeks in a large, pooled, heterogeneous population treated for schizophrenia revealed 5 distinct trajectories. Most patients had modest and sustained improvements during atypical antipsychotic treatment, regardless of their baseline illness severity, representing a partial response to currently available treatments.
研究已经在短期试验(~12 周)中确定了慢性精神分裂症患者抗精神病药物反应的不同轨迹。本事后分析确定了接受治疗时间不超过 24 周的慢性精神分裂症患者的轨迹。我们汇总了来自 6 项随机、双盲、奥氮平对照的非典型抗精神病药物临床试验的 1990 例慢性精神分裂症患者的数据。轨迹分析在较大的异质人群中确定了同质亚群。在确定的潜在类别之间比较了基线人口统计学特征。根据阳性和阴性症状量表(PANSS)总分确定了 5 种不同的反应轨迹:明显缓解者(47/1990,2.4%),严重患者(PANSS=124)在第 3 周时迅速且持续改善(51%);部分缓解者(1802/1990,90.6%),中度患者(PANSS=90)在第 4 周时改善最小(21%),且进一步改善较少;部分缓解者-持续缓解不良(迟发)(32/1990,1.6%),严重患者(PANSS=95)初始改善轻微,之后在第 12 周后恶化;部分缓解者-持续缓解不良(早发)(28/1990,1.4%),严重患者(PANSS=102)初始改善轻微,之后在第 8 周后恶化;延迟缓解者(81/1990,4.1%),严重至极严重患者(PANSS=113)在第 8 周时改善最小(11%),但此后有明显改善(49%)。几项基线特征(p<.05)和停药率(46%-72%)存在显著差异。明显缓解者年龄较小,更有可能是女性和西班牙裔,基线疾病严重程度较高。对接受精神分裂症治疗的大型、汇总、异质人群进行的 24 周抗精神病药物反应分析显示,有 5 种不同的轨迹。大多数患者在接受非典型抗精神病药物治疗期间有适度且持续的改善,无论其基线疾病严重程度如何,这代表了对现有治疗方法的部分反应。