Please use this identifier to cite or link to this item: https://doi.org/10.3389/fneur.2019.01379
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dc.titleFour-Year Longitudinal Study of Motor and Non-motor Symptoms in LRRK2-Related Parkinson's Disease
dc.contributor.authorDeng, X
dc.contributor.authorXiao, B
dc.contributor.authorLi, HH
dc.contributor.authorNg, E
dc.contributor.authorLo, YL
dc.contributor.authorTan, EK
dc.contributor.authorPrakash, KM
dc.date.accessioned2024-06-11T05:06:51Z
dc.date.available2024-06-11T05:06:51Z
dc.date.issued2020-01-17
dc.identifier.citationDeng, X, Xiao, B, Li, HH, Ng, E, Lo, YL, Tan, EK, Prakash, KM (2020-01-17). Four-Year Longitudinal Study of Motor and Non-motor Symptoms in LRRK2-Related Parkinson's Disease. Frontiers in Neurology 10 : 1379-. ScholarBank@NUS Repository. https://doi.org/10.3389/fneur.2019.01379
dc.identifier.issn1664-2295
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/248777
dc.description.abstractObjectives: 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.
dc.publisherFrontiers Media SA
dc.sourceElements
dc.subjectLRRK2
dc.subjectParkinson's disease
dc.subjectmotor
dc.subjectnon-motor
dc.subjectprogression
dc.typeArticle
dc.date.updated2024-06-11T00:19:49Z
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.description.doi10.3389/fneur.2019.01379
dc.description.sourcetitleFrontiers in Neurology
dc.description.volume10
dc.description.page1379-
dc.published.statePublished
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