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Short report
Parkinson’s disease GWAS-linked Park16 carriers show greater motor progression
  1. Xiao Deng1,
  2. Bin Xiao1,
  3. John Carson Allen2,
  4. Ebonne Ng1,
  5. Jia Nee Foo3,
  6. Yew-Long Lo1,
  7. Louis C S Tan4,
  8. Eng-King Tan1
  1. 1 Department of Neurology, National Neuroscience Institute, Singapore general hospital campus, Singapore, Singapore
  2. 2 Centre for Quantitative Medicine, Duke-NUS Graduate Medical School, Singapore, Singapore
  3. 3 Department of Human Genetics, Genome Institute of Singapore, Singapore, Singapore
  4. 4 Department of Neurology, National Neuroscience Institute, Singapore, Singapore
  1. Correspondence to Dr Louis C S Tan, Department of Neurology, National Neuroscience Institute, Singapore ; louis_tan{at}nni.com.sg and Dr Eng-King Tan, Department of Neurology, National Neuroscience Institute, Singapore general hospital campus, Singapore ; gnrtek{at}sgh.com.sg

Abstract

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.

  • parkinson disease
  • motor progression
  • GWAS
  • Park 16

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Footnotes

  • XD and BX contributed equally.

  • Contributors XD and BX: analysis and interpretation of data, statistical analysis, drafting/revising the manuscript. JCA: statistical analysis, drafting/revising the manuscript. EN and JNF: acquisition of data. Y-LL: acquisition of data, interpretation of data, drafting/revising the manuscript. E-KT and LCST: study concept and design, acquisition of data, drafting/revising the manuscript, study supervision and coordination, obtaining funding.

  • Funding This research is supported by the Singapore National Research Foundation under its Translational and Clinical Research Flagship Programme.

  • Competing interests No competing interests.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Patient consent for publication Obtained.