Movement Disorders Unit, Neurology Department, Sant Pau Hospital, Barcelona, Spain; Movement Disorders Section, Biomedical Research Institute (IIB-Sant Pau), Barcelona, Spain; Departament de Medicina, Universitat Autònoma de Barcelona, Barcelona, Spain.
Mov Disord. 2013 Sep;28(10):1376-83. doi: 10.1002/mds.25568. Epub 2013 Jul 19.
Lack of validated data on cutoff scores for mild cognitive impairment (MCI) and sensitivity to change in predementia stages of Parkinson's disease (PD) limit the utility of instruments measuring global cognition as screening and outcome measures in therapeutic trials. Investigators who were blinded to PD-Cognitive Rating Scale (PD-CRS) scores classified a cohort of prospectively recruited, nondemented patients into a PD with normal cognition (PD-NC) group and a PD with MCI (PD-MCI) group using Clinical Dementia Rating (CDR) and the Mattis Dementia Rating Scale-2 (MDRS-2). The discriminative power of the PD-CRS for PD-MCI was examined in a representative sample of 234 patients (145 in the PD-NC group; 89 in the PD-MCI group) and in a control group of 98 healthy individuals. Sensitivity to change in the PD-CRS score (the minimal clinically important difference was examined with the Clinical Global Impression of Change scale and was calculated with a combination of distribution-based and anchor-based approaches) was explored in a 6-month observational multicenter trial involving a subset of 120 patients (PD-NC, 63; PD-MCI, 57). Regression analysis demonstrated that PD-CRS total scores (P < 0.001) and age (P = 0.01) independently differentiated PD-NC from PD-MCI. Area under the receiver operating characteristic curve (AUC) analysis (AUC, 0.85; 95% confidence interval, 0.80-0.90) indicated that a score ≤ 81 of 134 was the optimal cutoff point on the total score for the PD-CRS (sensitivity, 79%; specificity, 80%; positive predictive value, 59%; negative predictive value, 91%). A range of change from 10 to 13 points on the PD-CRS total score was indicative of clinically significant change. These findings suggest that the PD-CRS is a useful tool to identify PD-MCI and to track cognitive changes in nondemented patients with PD.
用于轻度认知障碍 (MCI) 的截断分数和在帕金森病 (PD) 前驱期的变化敏感性的验证数据的缺乏,限制了用于测量整体认知的工具作为治疗试验的筛查和结果测量的效用。在这项研究中,对 PD-认知评定量表 (PD-CRS) 评分不知情的研究人员使用临床痴呆评定量表 (CDR) 和 Mattis 痴呆评定量表-2 (MDRS-2) 将一组前瞻性招募的非痴呆患者分为 PD 认知正常 (PD-NC) 组和 PD 伴 MCI (PD-MCI) 组。在 234 名患者(PD-NC 组 145 名,PD-MCI 组 89 名)的代表性样本中以及在 98 名健康个体的对照组中,检查了 PD-CRS 对 PD-MCI 的区分能力。使用临床总体印象变化量表 (Clinical Global Impression of Change scale) 检查了 PD-CRS 评分的变化敏感性(最小临床重要差异),并使用基于分布和基于锚定的方法相结合的方法进行了计算)在一项涉及 120 名患者(PD-NC,63 名;PD-MCI,57 名)的 6 个月观察性多中心试验中进行了探索。回归分析表明,PD-CRS 总分 (P < 0.001) 和年龄 (P = 0.01) 独立区分了 PD-NC 和 PD-MCI。受试者工作特征曲线下面积分析 (AUC) (AUC,0.85;95%置信区间,0.80-0.90) 表明,PD-CRS 总分 ≤ 81 分的 134 分是 PD-CRS 的最佳截断点 (敏感性,79%;特异性,80%;阳性预测值,59%;阴性预测值,91%)。PD-CRS 总分从 10 到 13 分的变化范围表明有临床显著变化。这些发现表明,PD-CRS 是一种有用的工具,可以识别 PD-MCI,并跟踪非痴呆 PD 患者的认知变化。