Dementia Risk Prediction in a Longitudinal Geriatric Parkinson?s Disease Cohort: Evaluation and Application of the Montreal Parkinson Risk of Dementia Scale

被引:3
|
作者
Bohn, Linzy [1 ,2 ,5 ]
McFall, Peggy [1 ,2 ]
Gee, Myrlene [3 ]
Postuma, Ronald B. [4 ]
Dixon, Roger A. [1 ,2 ]
Camicioli, Richard [2 ,3 ]
机构
[1] Univ Alberta, Dept Psychol, Edmonton, AB, Canada
[2] Univ Alberta, Neurosci & Mental Hlth Inst, Edmonton, AB, Canada
[3] Univ Alberta, Dept Med Neurol, Edmonton, AB, Canada
[4] McGill Univ, Dept Neurol, Montreal, PQ, Canada
[5] Univ Alberta, P217 Biol Sci, Edmonton, AB T6G 2E9, Canada
基金
加拿大健康研究院;
关键词
Parkinson?s disease; incipient dementia; lon-gitudinal change; risk factors; Montreal Parkinson Risk of Dementia Scale (MoPaRDS); MILD COGNITIVE IMPAIRMENT; VENTRICULAR DILATATION; BRAIN ATROPHY; HOMOCYSTEINE; BIOMARKERS; CRITERIA; RESERVE; CURVE;
D O I
10.5770/cgj.26.617
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background Parkinson's disease (PD) increases risk for dementia and cascading adverse outcomes. The eight-item Montreal Parkin-son 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. Methods 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 diag-nosis 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 harmon-ized with the original report, plus education. Results 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. Conclusions 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.
引用
收藏
页码:176 / 186
页数:11
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