4.6 Article

Autonomic dysfunction and white matter microstructural changes in drug-naive patients with Parkinson's disease

期刊

PEERJ
卷 6, 期 -, 页码 -

出版社

PEERJ INC
DOI: 10.7717/peerj.5539

关键词

SCOPA-AUT; Parkinson Disease; Autonomic Dysfunction; Connectometry; Hoehn & Yahr stage; Diffusion MRI

资金

  1. Michael J. Fox Foundation for Parkinson's Research
  2. W Garfield Weston Foundation
  3. Alzheimer's Association
  4. Canadian Institutes for Health Research
  5. Natural Sciences and Engineering Research Council of Canada
  6. AbbVie
  7. Avid Radiopharmaceuticals
  8. Biogen
  9. Bristol-Myers Squibb
  10. Covance
  11. GE Healthcare
  12. Genentech
  13. GlaxoSmithKline (GSK)
  14. Eli Lilly and Company
  15. Lundbeck
  16. Merck
  17. Meso Scale Discovery (MSD)
  18. Pfizer
  19. Piramal Imaging
  20. Roche
  21. Servier
  22. UCB

向作者/读者索取更多资源

Background. Autonomic dysfunction (AD) is one of the non-motor features of Parkinson's disease (PD). Some symptoms tend to occur in the early stages of PD. AD also has a great impact on patient's quality of life. In this study, we aimed to discover the association between AD (Scales for Outcomes in Parkinson's disease-Autonomic, SCOPA-AUT) and microstructural changes in white matter tracts in drug-naive early PD patients to elucidate the central effects of autonomic nervous system impairments. Method. In total, this study included 85 subjects with PD recruited from the Parkinson's Progression Markers Initiative (PPMI) database. Among the 85 PD patients, 38 were in Hoehn & Yahr stage 1 (HY1PD) and 47 were in stage 2 (HY2PD). Diffusion magnetic resonance imaging (DMRI) data were reconstructed in the MNI space using q-space diffeomorphic reconstruction to obtain the spin distribution function. The spin distribution function (SDF) values were used in DMRI connectometry analysis. We investigated through diffusion MRI connectometry the structural correlates of white matter tracts with SCOPA-AUT subscores and total score. Results. Connectometry analysis also revealed positive association with white matter density in bilateral corticospinal tract in HY1PD patients and negative association in genu of corpus callosum (CC) and, bilateral cingulum in both groups. In addition, there were associations between gastrointestinal, sexual, thermoregulatory and urinary items and structural brain connectivity in PD. Conclusion. Our study reveals positive correlation, suggesting neural compensations in early PD. Cingulum and CC tracts have well-known roles in PD pathology, compatible with our findings that bring new insights to specific areas of AD and its role in central nervous system (CNS) neurodegeneration, paving the way for using prodromal makers in the diagnosis and treatment of PD.

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