Levine Stephen Z, Leucht Stefan
Department of Community Mental Health, University of Haifa, Israel.
Klinik und Poliklinik für Psychiatrie und Psychotherapie, Klinikum rechts der Isar, Technische Universität München, München, Germany.
Schizophr Res. 2014 Jun;156(1):107-14. doi: 10.1016/j.schres.2014.04.005. Epub 2014 Apr 29.
The extent of heterogeneity in response to the psychopharmacological treatment of negative symptoms is unknown.
To examine the extent of heterogeneity in response to the treatment of predominantly negative symptoms of schizophrenia.
Data were analyzed from three clinical trials that compared placebo or amisulpride for up to 60days. Trial participants had predominantly negative symptoms of schizophrenia (n=485). Heterogeneity of percentage reduction on the Scale for the Assessment of Negative Symptoms (SANS) was examined with trajectory-group based modeling followed by descriptive statistics and the prediction of trajectory group membership with logistic regression modeling. Analyses were repeated separately for the placebo and amisulpride groups.
Trajectory group-based modeling identified groups of non- (n=297, 61.2%), gradual-moderate (n=135, 27.8%) and rapid- (n=53, 10.9%) responders. At baseline compared to non-responders, rapid-responders had consistently significantly (p<.05) higher SANS total and subscale scores. Percent SANS improvement at endpoint was greatest for the rapid-responders group, a finding that replicated stratifying by placebo and amisulpride treatment groups. Similarly, in the total sample and stratifying by placebo and amisulpride groups, dropout was not significantly associated with trajectory group membership.
Trajectories of treatment response to the psychopharmacological medication of the negative symptoms of schizophrenia demonstrate substantial heterogeneity. Approximately half of the patients included in our analysis showed little improvement, and the most severely ill at baseline responded the most.
精神药理学治疗阴性症状的反应异质性程度尚不清楚。
研究精神分裂症主要阴性症状治疗反应的异质性程度。
对三项比较安慰剂或氨磺必利长达60天的临床试验数据进行分析。试验参与者主要为精神分裂症阴性症状患者(n = 485)。采用基于轨迹组的模型检查阴性症状评估量表(SANS)上减少百分比的异质性,随后进行描述性统计,并使用逻辑回归模型预测轨迹组成员身份。分别对安慰剂组和氨磺必利组重复进行分析。
基于轨迹组的模型确定了无反应者组(n = 297,61.2%)、逐渐中度反应者组(n = 135,27.8%)和快速反应者组(n = 53,10.9%)。与无反应者相比,快速反应者在基线时SANS总分和分量表得分始终显著更高(p <.05)。终点时SANS改善百分比在快速反应者组中最大,这一发现在按安慰剂和氨磺必利治疗组分层时得到重复。同样,在总样本中以及按安慰剂和氨磺必利组分层时,退出与轨迹组成员身份无显著关联。
精神分裂症阴性症状心理药物治疗的反应轨迹显示出显著的异质性。我们分析中的约一半患者改善甚微,且基线时病情最严重的患者反应最大。