4.6 Article

A New MRI Measure to Early Differentiate Progressive Supranuclear Palsy From De Novo Parkinson's Disease in Clinical Practice: An International Study

Journal

MOVEMENT DISORDERS
Volume 36, Issue 3, Pages 681-689

Publisher

WILEY
DOI: 10.1002/mds.28364

Keywords

third ventricle width; Parkinson' s disease; progressive supranuclear palsy; MRI biomarker; clinical practice

Funding

  1. Michael J. Fox Foundation for Parkinson's Research
  2. AbbVie
  3. Allergan
  4. Amathus Therapeutics
  5. Avid Radiopharmaceuticals
  6. Biogen
  7. BioLegend
  8. Bristol-Myers Squibb
  9. Celgene
  10. Denali
  11. GE Healthcare
  12. Genentech
  13. GlaxoSmithKline
  14. Handl Therapeutics
  15. Insitro
  16. Janssen Neuroscience
  17. Lilly
  18. Lundbeck
  19. Merck
  20. Meso Scale Discovery
  21. Pfizer
  22. Piramal
  23. Prevail Therapeutics
  24. Roche
  25. Sanofi Genzyme
  26. Servier
  27. Takeda
  28. Teva
  29. UCB
  30. Verily
  31. Voyager Therapeutics
  32. Golub Capital

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The measurement of third ventricle width can distinguish Parkinson's disease (PD) from progressive supranuclear palsy (PSP).
Background Enlargement of the third ventricle has been reported in atypical parkinsonism. We investigated whether the measurement of third ventricle width could distinguish Parkinson's disease (PD) from progressive supranuclear palsy (PSP). Methods We assessed a new MR T1-weighted measurement (third ventricle width/internal skull diameter) in a training cohort of 268 participants (98 PD, 73 PSP, 98 controls from our center) and in a testing cohort of 291 participants (82 de novo PD patients and 133 controls from the Parkinson's Progression Markers Initiative, 76 early-stage PSP from an international research group). PD diagnosis was confirmed after a 4-year follow-up. Diagnostic performance of the third ventricle/internal skull diameter was assessed using receiver operating characteristic curve with bootstrapping; the area under the curve of the training cohort was compared with the area under the curve of the testing cohort using the De Long test. Results In both cohorts, third ventricle/internal skull diameter values did not differ between PD and controls but were significantly lower in PD than in PSP patients (P < 0.0001). In PD, third ventricle/internal skull diameter values did not change significantly between baseline and follow-up evaluation. Receiver operating characteristic analysis accurately differentiated PD from PSP in the training cohort (area under the curve, 0.94; 95% CI, 91.1-97.6; cutoff, 5.72) and in the testing cohort (area under the curve, 0.91; 95% CI, 87.0-97.0; cutoff,: 5.88), validating the generalizability of the results. Conclusion Our study provides a new reliable and validated MRI measurement for the early differentiation of PD and PSP. The simplicity and generalizability of this biomarker make it suitable for routine clinical practice and for selection of patients in clinical trials worldwide. (c) 2020 International Parkinson and Movement Disorder Society

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