Yoshida Kazunari, Roberts Rachel, Suzuki Takefumi, Lebowitz Barry, Reeves Suzanne, Howard Robert, Abe Takayuki, Mimura Masaru, Uchida Hiroyuki
Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Center for Clinical Research, Keio University School of Medicine, Tokyo, Japan.
Am J Geriatr Psychiatry. 2017 Jul;25(7):708-716. doi: 10.1016/j.jagp.2017.01.016. Epub 2017 Jan 30.
Prediction of response or nonresponse to antipsychotics is especially important in patients with behavioral and psychological symptoms of dementia (BPSD) in whom antipsychotic exposure increases risks of death. This study examined whether the presence or absence of early improvement of BPSD with antipsychotics is associated with subsequent response or nonresponse.
In a post-hoc analysis of the Clinical Antipsychotic Trials of Intervention Effectiveness-Alzheimer's Disease (CATIE-AD) study (2001-2004) (clinicaltrials.gov; NCT00015548) in 45 U.S. sites, 245 subjects (olanzapine, N = 90; quetiapine, N = 81; risperidone, N = 74) with a DSM-IV diagnosis of dementia of the Alzheimer type who presented with a score of 1 or more in the Brief Psychiatric Rating Scale (BPRS) at baseline (phase I of CATIE-AD) were randomly assigned to treatment with olanzapine, quetiapine, risperidone, or placebo in a double-blind manner. Associations were examined between response at week 8 and demographic and clinical characteristics, including BPRS total score reduction at week 2, using logistic regression analyses. Prediction performance of binary classification (presence or absence) of improvement or no improvement at week 2 for response at week 8 was examined.
BPRS total score reduction at week 2 (mean percentage score reduction: 12.6%) was significantly associated with response at week 8 (odds ratio: 1.18; 95% CI: 1.11-1.26). The 5% score reduction cut-off at week 2 showed the highest accuracy (0.71), with sensitivity, specificity, and positive and negative predictivevalues of 0.76, 0.65, 0.69, and 0.72, respectively.
Lack of even a very small early improvement with antipsychotic treatment may be a marker of subsequent nonresponse in BPSD.
在患有痴呆行为和心理症状(BPSD)的患者中,预测对抗精神病药物的反应或无反应尤为重要,因为在这些患者中使用抗精神病药物会增加死亡风险。本研究探讨了使用抗精神病药物后BPSD早期改善与否是否与随后的反应或无反应相关。
在对美国45个地点开展的干预有效性临床抗精神病药物试验 - 阿尔茨海默病(CATIE - AD)研究(2001 - 2004年)(clinicaltrials.gov;NCT00015548)进行的事后分析中,245名受试者(奥氮平组,N = 90;喹硫平组,N = 81;利培酮组,N = 74),这些受试者根据《精神疾病诊断与统计手册》第四版(DSM - IV)被诊断为阿尔茨海默型痴呆,在基线时(CATIE - AD的第一阶段)简明精神病评定量表(BPRS)得分≥1,他们被随机双盲分配接受奥氮平、喹硫平、利培酮或安慰剂治疗。使用逻辑回归分析,研究第8周时的反应与人口统计学和临床特征之间的关联,包括第2周时BPRS总分的降低情况。检验了第2周时改善或未改善的二元分类(存在或不存在)对第8周反应的预测性能。
第2周时BPRS总分降低(平均得分降低百分比:12.6%)与第8周时的反应显著相关(比值比:1.18;95%置信区间:1.11 - 1.26)。第2周时5%的得分降低临界值显示出最高的准确性(0.71),敏感性、特异性、阳性预测值和阴性预测值分别为0.76、0.65、0.69和0.72。
抗精神病药物治疗即使没有非常小的早期改善,也可能是BPSD随后无反应的一个标志。