Bohn Linzy, McFall G Peggy, Gee Myrlene, Postuma Ronald B, Dixon Roger A, Camicioli Richard
Department of Psychology, University of Alberta, Edmonton, AB.
Neuroscience and Mental Health Institute, University of Alberta, Edmonton, AB.
Can Geriatr J. 2023 Mar 1;26(1):176-186. doi: 10.5770/cgj.26.617. eCollection 2023 Mar.
Parkinson's disease (PD) increases risk for dementia and cascading adverse outcomes. The eight-item Montreal Parkinson Risk of Dementia Scale (MoPaRDS) is a rapid, in-office dementia screening tool. We examine predictive validity and other characteristics of the MoPaRDS in a geriatric PD cohort by testing a series of alternative versions and modelling risk score change trajectories.
Participants were 48 initially non-demented PD patients (Mage = 71.6 years, range = 65-84) from a three-year, three-wave prospective Canadian cohort study. A dementia diagnosis at Wave 3 was used to stratify two baseline groups: PD with Incipient Dementia (PDID) and PD with No Dementia (PDND). We aimed to predict dementia three years prior to diagnosis using baseline data for eight indicators that harmonized with the original report, plus education.
Three MoPaRDS items (age, orthostatic hypotension, mild cognitive impairment [MCI]) discriminated the groups both independently and as a composite three-item scale (area under the curve [AUC] = 0.88). The eight-item MoPaRDS reliably discriminated PDID from PDND (AUC = 0.81). Education did not improve predictive validity (AUC = 0.77). Performance of the eight-item MoPaRDS varied across sex (AUCfemales = 0.91; AUCmales = 0.74), whereas the three-item configuration did not (AUCfemales = 0.88; AUCmales = 0.91). Risk scores of both configurations increased over time.
We report new data on the application of the MoPaRDS as a dementia prediction tool for a geriatric PD cohort. Results support the viability of the full MoPaRDS, and indicate that an empirically determined brief version is a promising complement.
帕金森病(PD)会增加患痴呆症及一系列不良后果的风险。八项蒙特利尔帕金森痴呆风险量表(MoPaRDS)是一种快速的门诊痴呆筛查工具。我们通过测试一系列替代版本并对风险评分变化轨迹进行建模,来研究MoPaRDS在老年帕金森病队列中的预测效度及其他特征。
参与者为来自一项为期三年、分三波进行的前瞻性加拿大队列研究的48名最初无痴呆的帕金森病患者(年龄中位数=71.6岁,范围=65 - 84岁)。第三波时的痴呆诊断用于将两个基线组分层:早期痴呆帕金森病(PDID)和无痴呆帕金森病(PDND)。我们旨在使用与原始报告一致的八个指标的基线数据以及教育程度,预测诊断前三年的痴呆情况。
MoPaRDS的三个项目(年龄、体位性低血压、轻度认知障碍[MCI])单独及作为一个三项综合量表均能区分这两组(曲线下面积[AUC]=0.88)。八项MoPaRDS能可靠地区分PDID和PDND(AUC = 0.81)。教育程度并未提高预测效度(AUC = 0.77)。八项MoPaRDS的表现因性别而异(女性AUC = 0.91;男性AUC = 0.74),而三项配置则不然(女性AUC = 0.88;男性AUC = 0.91)。两种配置的风险评分均随时间增加。
我们报告了关于MoPaRDS作为老年帕金森病队列痴呆预测工具应用的新数据。结果支持完整MoPaRDS的可行性,并表明根据经验确定的简短版本是一个有前景的补充。