Harrison John, Minassian Sonia L, Jenkins Lisa, Black Ronald S, Koller Martin, Grundman Michael
CPC Pharma Services, PO Box 3223, Warminster, Wiltshire BA12 8XA, England.
Arch Neurol. 2007 Sep;64(9):1323-9. doi: 10.1001/archneur.64.9.1323.
To report the psychometric properties of an alternative instrument to the cognitive subscale of the Alzheimer's Disease Assessment Scale, a neuropsychological test battery (NTB) for measuring drug efficacy in Alzheimer disease clinical trials.
The NTB was evaluated in a randomized, double-blind, placebo-controlled trial of AN1792(QS-21) (synthetic beta-amyloid plus an adjuvant) (300 patients) and isotonic sodium chloride solution (72 patients). The test-retest reliability of the NTB was examined, and the NTB was correlated with other cognitive (cognitive subscale of the Alzheimer's Disease Assessment Scale and Mini-Mental State Examination) and functional (Disability Assessment Scale for Dementia and Clinical Dementia Rating Sum of Boxes) measures. In addition, a factor analysis was performed on NTB components. Finally, the sensitivity of the NTB to change was assessed as a function of Mini-Mental State Examination performance.
The NTB had high test-retest reliability at 6 (Pearson product moment correlation [r] = 0.92) and 12 (r = 0.88) months. Internal consistency was high (Cronbach alpha = 0.84). The correlations between the NTB z score and scores on traditional measures of cognition and function were significantly different from 0 (P < .001). A factor analysis yielded "memory" and "executive function" factors. The NTB z score declined linearly over 1 year in patients receiving placebo and, in contrast to the Alzheimer's Disease Assessment Scale cognitive subscale, demonstrated similar declines in patients with high (21-26) and low (15-20) Mini-Mental State Examination scores at baseline.
The NTB exhibits excellent psychometric properties and seems to be a reliable and sensitive measure of cognitive change in patients with mild to moderate Alzheimer disease. The psychometric properties of the NTB suggest that it may have particular utility in evaluating drug efficacy in clinical trials in which patients with mild Alzheimer disease are included.
报告一种用于阿尔茨海默病临床试验中测量药物疗效的神经心理测试组合(NTB),作为阿尔茨海默病评估量表认知子量表的替代工具的心理测量特性。
在一项AN1792(QS - 21)(合成β - 淀粉样蛋白加佐剂)(300例患者)和等渗氯化钠溶液(72例患者)的随机、双盲、安慰剂对照试验中对NTB进行评估。检查了NTB的重测信度,并将NTB与其他认知(阿尔茨海默病评估量表认知子量表和简易精神状态检查表)和功能(痴呆残疾评估量表和临床痴呆评定框和总分)测量指标进行相关性分析。此外,对NTB各组成部分进行了因子分析。最后,根据简易精神状态检查表的表现评估NTB对变化的敏感性。
NTB在6个月(Pearson积差相关[r]=0.92)和12个月(r = 0.88)时具有较高的重测信度。内部一致性较高(Cronbachα = 0.84)。NTB的z分数与传统认知和功能测量指标得分之间的相关性显著不同于0(P <.001)。因子分析得出“记忆”和“执行功能”因子。接受安慰剂的患者在1年中NTB的z分数呈线性下降,与阿尔茨海默病评估量表认知子量表不同的是,基线时简易精神状态检查表得分高(21 - 26)和低(15 - 20)的患者NTB的z分数下降相似。
NTB具有优异的心理测量特性,似乎是轻度至中度阿尔茨海默病患者认知变化的可靠且敏感的测量指标。NTB的心理测量特性表明,在纳入轻度阿尔茨海默病患者的临床试验中,它在评估药物疗效方面可能具有特殊用途。