Please use this identifier to cite or link to this item: https://doi.org/10.1111/ene.12950
Title: The impact of non-motor symptoms on the quality of life of Parkinson's disease patients: A longitudinal study
Authors: Prakash K.M. 
Nadkarni N.V. 
Lye W.-K. 
Yong M.-H.
Tan E.-K. 
Keywords: Longitudinal study
Non-motor symptoms
Parkinson's disease
Quality of life
Issue Date: 2016
Publisher: Blackwell Publishing Ltd
Citation: Prakash K.M., Nadkarni N.V., Lye W.-K., Yong M.-H., Tan E.-K. (2016). The impact of non-motor symptoms on the quality of life of Parkinson's disease patients: A longitudinal study. European Journal of Neurology 23 (5) : 854-860. ScholarBank@NUS Repository. https://doi.org/10.1111/ene.12950
Abstract: Background and purpose: Non-motor symptoms (NMSs) are common amongst patients with Parkinson's disease (PD); however, little is known about their influence on the health-related quality of life (QoL) over a defined follow-up period. The study was aimed to establish the impact of NMSs on the QoL of patients with PD over a 2-year follow-up period. Method: A total of 227 newly referred PD patients were prospectively recruited between 2013 and 2014. The Non-Motor Symptoms Scale was used to evaluate NMSs burden whilst QoL was assessed with the Parkinson's Disease Questionnaire-39 items. Motor disabilities were assessed using the Part III (motor) Unified Parkinson's Disease Rating Scale (UPDRSm). Results: The mean age was 64.37 (10.18) years; 59.9% were males and a majority (89.0%) were ethnic Chinese. Almost 65% were unemployed and 84.6% had attained no more than secondary level of education. In the univariate analysis, total NMSs burden, age, gender, subsequent visit, Hoehn and Yahr staging, disease duration and UPDRSm score were individually predictive of change in the Parkinson's Disease Questionnaire Summary Index score from baseline to follow-up visit. However, in the multivariate analysis, total NMSs burden significantly predicted the QoL scores whilst motor scores did not. Specifically, NMS domains 2 (sleep/fatigue), 3 (mood/apathy) and 5 (attention/memory) were most significantly predictive of QoL change. Conclusion: Unlike motor disabilities, NMSs burden, in particular sleep, mood and attention, have a significant impact on the QoL of PD patients over a 2-year follow-up period. � 2016 European Academy of Neurology.
Source Title: European Journal of Neurology
URI: http://scholarbank.nus.edu.sg/handle/10635/149010
ISSN: 13515101
DOI: 10.1111/ene.12950
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