4.6 Article

Parkinson's Disease,NOTCH3Genetic Variants, and White Matter Hyperintensities

期刊

MOVEMENT DISORDERS
卷 35, 期 11, 页码 2090-2095

出版社

WILEY
DOI: 10.1002/mds.28171

关键词

CADASIL; NOTCH3; ONDRI; Parkinson's disease; white matter hyperintensities

资金

  1. Ontario Brain Institute
  2. Ontario government
  3. Baycrest Foundation
  4. Bruyere Research Institute, Centre for Addiction and Mental Health Foundation
  5. London Health Sciences Foundation
  6. McMaster University Faculty of Health Sciences
  7. Ottawa Brain and Mind Research Institute
  8. Queen's University Faculty of Health Sciences
  9. Thunder Bay Regional Health Sciences Centre
  10. University of Ottawa Faculty of Medicine
  11. Windsor/Essex County ALS Association
  12. Temerty Family Foundation

向作者/读者索取更多资源

Background White matter hyperintensities (WMH) on magnetic resonance imaging may influence clinical presentation in patients with Parkinson's disease (PD), although their significance and pathophysiological origins remain unresolved. Studies examining WMH have identified pathogenic variants inNOTCH3as an underlying cause of inherited forms of cerebral small vessel disease. Methods We examinedNOTCH3variants, WMH volumes, and clinical correlates in 139 PD patients in the Ontario Neurodegenerative Disease Research Initiative cohort. Results We identified 13 PD patients (similar to 9%) with rare (<1% of general population), nonsynonymousNOTCH3variants. Bayesian linear modeling demonstrated a doubling of WMH between variant negative and positive patients (3.1 vs. 6.9 mL), with large effect sizes for periventricular WMH (d= 0.8) and lacunes (d= 1.2). Negative correlations were observed between WMH and global cognition (r= -0.2). Conclusion TheNOTCH3rare variants in PD may significantly contribute to increased WMH burden, which in turn may negatively influence cognition. (c) 2020 International Parkinson and Movement Disorder Society

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