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Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression

BACKGROUND: Data on the long-term motor outcomes of genome-wide association study (GWAS)-linked Parkinson disease (PD) carriers are useful for clinical management. OBJECTIVES: To characterise the association between GWAS-linked PARK16 gene variant and disease progression in PD over a 9-year time fra...

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Autores principales: Deng, Xiao, Xiao, Bin, Allen, John Carson, Ng, Ebonne, Foo, Jia Nee, Lo, Yew-Long, Tan, Louis C S, Tan, Eng-King
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6860401/
https://www.ncbi.nlm.nih.gov/pubmed/30814270
http://dx.doi.org/10.1136/jmedgenet-2018-105661
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author Deng, Xiao
Xiao, Bin
Allen, John Carson
Ng, Ebonne
Foo, Jia Nee
Lo, Yew-Long
Tan, Louis C S
Tan, Eng-King
author_facet Deng, Xiao
Xiao, Bin
Allen, John Carson
Ng, Ebonne
Foo, Jia Nee
Lo, Yew-Long
Tan, Louis C S
Tan, Eng-King
author_sort Deng, Xiao
collection PubMed
description BACKGROUND: Data on the long-term motor outcomes of genome-wide association study (GWAS)-linked Parkinson disease (PD) carriers are useful for clinical management. OBJECTIVES: To characterise the association between GWAS-linked PARK16 gene variant and disease progression in PD over a 9-year time frame. METHODS: Over a 9-year period, carriers of PARK16 rs11240572 variant and non-carriers were followed up and evaluated using the modified Hoehn and Yahr (H&Y) staging scale and Unified Parkinson’s Disease Rating Scale (UPDRS) part III. A longitudinal, linear mixed model was performed to compare the changes of H&Y staging scale, UPDRS motor score and UPDRS subscores between the two groups. RESULTS: A total of 156 patients (41 PARK16 carriers and 115 non-carriers) were evaluated and followed up for up to 9 years. Using longitudinal linear mixed model analysis, there was a greater rate of deterioration in the motor function as measured by the UPDRS scores compared with non-carriers after 5 years from the date of diagnosis (p=0.009). In addition, we demonstrated that PARK16 variant carriers had worse gait scores (p=0.043) and greater motor progression than non-carriers after 6 years based on the modified H&Y staging scale (p=0.040). CONCLUSIONS: In a 9-year longitudinal study, we demonstrated that PD PARK16 variant carriers exhibited greater motor progression after 5 years of disease compared with non-carriers, suggesting that GWAS-linked gene variants may influence disease progression over time. Closer monitoring and management of these higher risk patients can facilitate a better quality of life.
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spelling pubmed-68604012019-12-03 Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression Deng, Xiao Xiao, Bin Allen, John Carson Ng, Ebonne Foo, Jia Nee Lo, Yew-Long Tan, Louis C S Tan, Eng-King J Med Genet Neurogenetics BACKGROUND: Data on the long-term motor outcomes of genome-wide association study (GWAS)-linked Parkinson disease (PD) carriers are useful for clinical management. OBJECTIVES: To characterise the association between GWAS-linked PARK16 gene variant and disease progression in PD over a 9-year time frame. METHODS: Over a 9-year period, carriers of PARK16 rs11240572 variant and non-carriers were followed up and evaluated using the modified Hoehn and Yahr (H&Y) staging scale and Unified Parkinson’s Disease Rating Scale (UPDRS) part III. A longitudinal, linear mixed model was performed to compare the changes of H&Y staging scale, UPDRS motor score and UPDRS subscores between the two groups. RESULTS: A total of 156 patients (41 PARK16 carriers and 115 non-carriers) were evaluated and followed up for up to 9 years. Using longitudinal linear mixed model analysis, there was a greater rate of deterioration in the motor function as measured by the UPDRS scores compared with non-carriers after 5 years from the date of diagnosis (p=0.009). In addition, we demonstrated that PARK16 variant carriers had worse gait scores (p=0.043) and greater motor progression than non-carriers after 6 years based on the modified H&Y staging scale (p=0.040). CONCLUSIONS: In a 9-year longitudinal study, we demonstrated that PD PARK16 variant carriers exhibited greater motor progression after 5 years of disease compared with non-carriers, suggesting that GWAS-linked gene variants may influence disease progression over time. Closer monitoring and management of these higher risk patients can facilitate a better quality of life. BMJ Publishing Group 2019-11 2019-02-27 /pmc/articles/PMC6860401/ /pubmed/30814270 http://dx.doi.org/10.1136/jmedgenet-2018-105661 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Neurogenetics
Deng, Xiao
Xiao, Bin
Allen, John Carson
Ng, Ebonne
Foo, Jia Nee
Lo, Yew-Long
Tan, Louis C S
Tan, Eng-King
Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title_full Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title_fullStr Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title_full_unstemmed Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title_short Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
title_sort parkinson’s disease gwas-linked park16 carriers show greater motor progression
topic Neurogenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6860401/
https://www.ncbi.nlm.nih.gov/pubmed/30814270
http://dx.doi.org/10.1136/jmedgenet-2018-105661
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