Santosh Kumar Dash1, Albert Stezin2, Tejashree Takalkar3, Lija George1, Nitish L Kamble1, M Netravathi1, Ravi Yadav1, Keshav J Kumar4, Madhura Ingalhalikar3, Jitender Saini5, Pramod Kumar Pal6. 1. Department of Neurology, National Institute of Mental Health & Neurosciences, Hosur Road, Bangalore, Karnataka, 560029, India. 2. Department of Clinical Neuroscience and Department of Neurology, National Institute of Mental Health & Neurosciences, Hosur Road, Bangalore, Karnataka, 560029, India. 3. Symbiosis Institute of Technology, Symbiosis International University, Lavale, Pune, India. 4. Department of Clinical Psychology, National Institute of Mental Health and Neurosciences, Hosur Road, Bangalore, Karnataka, 560029, India. 5. Department of Neuroimaging & Interventional Radiology, National Institute of Mental Health & Neurosciences, Hosur Road, Bangalore, Karnataka, 560029, India. 6. Department of Neurology, National Institute of Mental Health & Neurosciences, Hosur Road, Bangalore, Karnataka, 560029, India. palpramod@hotmail.com.
Abstract
OBJECTIVE: Multiple system atrophy (MSA) is a neurodegenerative disorder with progressive motor and autonomic dysfunction. There is a paucity of information on the early neurostructural changes in MSA, especially its subtypes, MSA-P (patients with predominant parkinsonism) and MSA-C (patients with predominant cerebellar signs). This study investigates the abnormalities of grey matter (GM) and white matter (WM) in early MSA and its subtypes using multi-modal voxel-based analysis. MATERIALS AND METHODS: Twenty-six patients with MSA with duration of symptoms ≤ 2.5 years (mean duration: 1.6 ±0.9 years) were assessed clinically and with 3T MRI. Voxel-based morphometry (VBM) and diffusion tensor imaging (DTI) were performed to identify the structural changes in MSA and its subtypes. The GM changes and diffusion parameters of WM tracts were correlated with the clinical scores. The results were compared with MRI of 25 age- and gender-matched healthy controls. RESULTS: The early structural changes in MSA included GM loss of the cerebellum and subcallosal gyrus with widespread involvement of supratentorial and infratentorial WM fibres. In MSA-C, GM loss was limited to the cerebellum with WM changes predominantly affecting the infratentorial WM and association tracts. In contrast, MSA-P did not demonstrate any GM loss and the WM involvement was mainly supratentorial. There was no significant correlation between structural changes and clinical severity score. CONCLUSION: In early MSA, WM microstructure was more affected than GM. These changes were greater in MSA-C than in MSA-P, suggesting variable deterioration in the subtypes of MSA. KEY POINTS: • Structural changes in early multiple system atrophy were evaluated using multi-modal neuroimaging. • White matter was more affected than grey matter in early MSA. • Clinical variables did not correlate with early structural changes.
OBJECTIVE:Multiple system atrophy (MSA) is a neurodegenerative disorder with progressive motor and autonomic dysfunction. There is a paucity of information on the early neurostructural changes in MSA, especially its subtypes, MSA-P (patients with predominant parkinsonism) and MSA-C (patients with predominant cerebellar signs). This study investigates the abnormalities of grey matter (GM) and white matter (WM) in early MSA and its subtypes using multi-modal voxel-based analysis. MATERIALS AND METHODS: Twenty-six patients with MSA with duration of symptoms ≤ 2.5 years (mean duration: 1.6 ±0.9 years) were assessed clinically and with 3T MRI. Voxel-based morphometry (VBM) and diffusion tensor imaging (DTI) were performed to identify the structural changes in MSA and its subtypes. The GM changes and diffusion parameters of WM tracts were correlated with the clinical scores. The results were compared with MRI of 25 age- and gender-matched healthy controls. RESULTS: The early structural changes in MSA included GM loss of the cerebellum and subcallosal gyrus with widespread involvement of supratentorial and infratentorial WM fibres. In MSA-C, GM loss was limited to the cerebellum with WM changes predominantly affecting the infratentorial WM and association tracts. In contrast, MSA-P did not demonstrate any GM loss and the WM involvement was mainly supratentorial. There was no significant correlation between structural changes and clinical severity score. CONCLUSION: In early MSA, WM microstructure was more affected than GM. These changes were greater in MSA-C than in MSA-P, suggesting variable deterioration in the subtypes of MSA. KEY POINTS: • Structural changes in early multiple system atrophy were evaluated using multi-modal neuroimaging. • White matter was more affected than grey matter in early MSA. • Clinical variables did not correlate with early structural changes.
Entities:
Keywords:
Cerebellum; Diffusion tensor imaging; Multiple system atrophy; Neuroimaging
Authors: C R V Blain; G J Barker; J M Jarosz; N A Coyle; S Landau; R G Brown; K R Chaudhuri; A Simmons; D K Jones; S C R Williams; P N Leigh Journal: Neurology Date: 2006-12-26 Impact factor: 9.910
Authors: Till-Karsten Hauser; Andreas Luft; Martin Skalej; Thomas Nägele; Tilo T J Kircher; Dirk T Leube; Jörg B Schulz Journal: Mov Disord Date: 2006-10 Impact factor: 10.338
Authors: Christian Brenneis; Sylvia M Boesch; Karl E Egger; Klaus Seppi; Christoph Scherfler; Michael Schocke; Gregor K Wenning; Werner Poewe Journal: Mov Disord Date: 2006-02 Impact factor: 10.338
Authors: Christian Brenneis; Karl Egger; Christoph Scherfler; Klaus Seppi; Michael Schocke; Werner Poewe; Gregor K Wenning Journal: J Neurol Date: 2007-02 Impact factor: 4.849
Authors: M Minnerop; K Specht; J Ruhlmann; N Schimke; M Abele; A Weyer; U Wüllner; T Klockgether Journal: Neuroimage Date: 2007-04-25 Impact factor: 6.556
Authors: S Gilman; G K Wenning; P A Low; D J Brooks; C J Mathias; J Q Trojanowski; N W Wood; C Colosimo; A Dürr; C J Fowler; H Kaufmann; T Klockgether; A Lees; W Poewe; N Quinn; T Revesz; D Robertson; P Sandroni; K Seppi; M Vidailhet Journal: Neurology Date: 2008-08-26 Impact factor: 9.910
Authors: Ignazio S Piras; Christiane Bleul; Isabelle Schrauwen; Joshua Talboom; Lorida Llaci; Matthew D De Both; Marcus A Naymik; Glenda Halliday; Conceicao Bettencourt; Janice L Holton; Geidy E Serrano; Lucia I Sue; Thomas G Beach; Nadia Stefanova; Matthew J Huentelman Journal: Acta Neuropathol Commun Date: 2020-06-03 Impact factor: 7.801
Authors: Alexandra Abos; Hugo C Baggio; Barbara Segura; Anna Campabadal; Carme Uribe; Darly Milena Giraldo; Alexandra Perez-Soriano; Esteban Muñoz; Yaroslau Compta; Carme Junque; Maria Jose Marti Journal: Sci Rep Date: 2019-11-11 Impact factor: 4.379