TY - JOUR
T1 - Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
AU - Deng, Xiao
AU - Xiao, Bin
AU - Allen, John Carson
AU - Ng, Ebonne
AU - Foo, Jia Nee
AU - Lo, Yew Long
AU - Tan, Louis C.S.
AU - Tan, Eng King
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2019.
PY - 2019/2/27
Y1 - 2019/2/27
N2 - 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.
AB - 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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U2 - 10.1136/jmedgenet-2018-105661
DO - 10.1136/jmedgenet-2018-105661
M3 - Article
C2 - 30814270
AN - SCOPUS:85062283314
SN - 0022-2593
VL - 56
SP - 765
EP - 768
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
IS - 11
ER -