Abstract

Objectives: In a prospective 4-year study, we evaluated the progression of motor and non-motor symptoms in Parkinson's disease (PD) patients with Asian-specific LRRK2 risk variants and non-carriers.Methods: A total of 202 patients with PD, including 133 risk variant carriers and 69 non-carriers, were followed up and evaluated using the Modified Hoehn and Yahr staging scale, Unified Parkinson's Disease Rating Scale part III, Non-motor Symptom Scale, Parkinson's disease Questionnaire-39 item version. Means of generalized estimating equation model was performed to compare the differences from baseline between LRRK2 risk variant carriers and non-carriers.Results: Our longitudinal analysis revealed that risk variant carriers exhibited greater progression than non-carriers after 4 years based on the modified Hoehn and Yahr staging scale (risk variants carriers, 0.65; non-carriers, 0.06; P = 0.041). Meanwhile, Unified Parkinson's Disease Rating Scale gait and posture score in risk variant carriers also showed greater increase than that in non-carriers, although the difference was not statistically significant. Non-carriers experienced a transient improvement in non-motor symptoms at the early stage of PD, as scores at visit two significantly reduced compared to baseline in Non-motor Symptom Scale domain 3 (mood/apathy), Parkinson's disease Questionnaire-39 item version domain 3 (emotional well-being), and frequency of NMS in non-carriers but not in risk variants carriers.Conclusions: PD gene risk variant carriers were more likely to progress faster in their motor severity than non-carriers. There were transient differences in certain non-motor symptoms and quality of life in carriers. However, more studies are warranted to assess the association of PD risk variants and progression of non-motor symptoms.

Highlights

  • PD is a common neurodegenerative disease with clinical heterogeneity and diverse causative factors

  • A recent study showed that PD patients with the Asian LRRK2 variants experienced greater progression in motor symptoms (5)

  • To address this gap in knowledge, we conducted a longitudinal study to evaluate the progression of both motor and non-motor features in Asian LRRK2 PD carriers compared to non-carriers

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Summary

Introduction

PD is a common neurodegenerative disease with clinical heterogeneity and diverse causative factors. The common LRRK2 G2019S mutation is located in the kinase domain, possibly associated with an increase in kinase activity (2). The polymorphic variants G2385R, R1628P, and S1647T are associated with increased risk for PD in the Asian population (4). A recent study showed that PD patients with the Asian LRRK2 variants experienced greater progression in motor symptoms (5). Other aspects of the disease, including non-motor symptoms which greatly account for the decline of quality of life in PD, were not evaluated during the follow-up. To address this gap in knowledge, we conducted a longitudinal study to evaluate the progression of both motor and non-motor features in Asian LRRK2 PD carriers compared to non-carriers

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