Turkoz Ibrahim, Fu Dong-Jing, Bossie Cynthia A, Alphs Larry
Dr. Turkoz is with Janssen Research and Development LLC, Titusville, New Jersey, USA, and Drs. Fu, Bossie, and Alphs are with Janssen Scientific Affairs LLC, Titusville, New Jersey, USA.
Innov Clin Neurosci. 2015 Nov-Dec;12(11-12):10-7.
This analysis evaluates improvement in symptoms of depression in patients with schizoaffective disorder administered oral paliperidone extended-release by accounting for the magnitude of direct and indirect (changes in negative and positive symptoms and worsening of extrapyramidal symptoms) treatment effects on depressive symptoms.
Data for this post hoc analysis were drawn from two six-week, randomized, placebo-controlled studies of paliperidone extended-release versus placebo in adult subjects with schizoaffective disorder (N=614; NCT00412373, NCT00397033). Subjects with baseline 17-item Hamilton Rating Scale for Depression scores of 16 or greater were included. Structural equation models (path analyses) were used to separate total effects into direct and indirect effects on depressive symptoms. Change from baseline in 17-item Hamilton Rating Scale for Depression score at the Week 6 end point was the dependent variable; changes in Positive and Negative Syndrome Scale positive and negative factors and Simpson-Angus Scale (to evaluate extrapyramidal symptoms) scores were independent variables.
At baseline, 332 of 614 (54.1%) subjects had a 17-item Hamilton Rating Scale for Depression score of 16 or greater. Path analysis determined that up to 26.4 percent of the paliperidone extended-release versus placebo effect on depressive symptoms may be attributed to a direct treatment effect, and 45.8 percent and 28.4 percent were mediated indirectly through improvements on positive and negative symptoms, respectively. No effects were identified as mediated through extrapyramidal symptoms changes (-0.7%).
RESULTS of this analysis suggest that paliperidone's effect on depressive symptoms in subjects with schizoaffective disorder participating in two six-week, randomized, placebo-controlled studies is mediated through indirect effects (e.g., positive and negative symptom changes) and a direct treatment effect.
本分析通过考虑对抑郁症状的直接和间接治疗效果(阴性和阳性症状的变化以及锥体外系症状的恶化)的程度,评估了口服帕利哌酮缓释片治疗分裂情感性障碍患者时抑郁症状的改善情况。
本事后分析的数据来自两项为期六周的随机、安慰剂对照研究,比较了帕利哌酮缓释片与安慰剂在成年分裂情感性障碍患者中的疗效(N = 614;NCT00412373,NCT00397033)。纳入了基线17项汉密尔顿抑郁量表评分≥16分的患者。采用结构方程模型(路径分析)将总效应分为对抑郁症状的直接和间接效应。以第6周终点时17项汉密尔顿抑郁量表评分相对于基线的变化作为因变量;阳性和阴性症状量表的阳性和阴性因子变化以及辛普森-安格斯量表(用于评估锥体外系症状)评分作为自变量。
基线时,614名患者中有332名(54.1%)的17项汉密尔顿抑郁量表评分≥16分。路径分析确定,帕利哌酮缓释片相对于安慰剂对抑郁症状的治疗效果中,高达26.4%可能归因于直接治疗效应,分别有45.8%和28.4%通过阳性和阴性症状的改善间接介导。未发现通过锥体外系症状变化介导的效应(-0.7%)。
本分析结果表明,在两项为期六周的随机、安慰剂对照研究中,帕利哌酮对分裂情感性障碍患者抑郁症状的影响是通过间接效应(如阳性和阴性症状变化)和直接治疗效应介导的。