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Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
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Brain gray matter structural network in myotonic dystrophy type 1.
Atsuhiko Sugiyama1,2, Daichi Sone3, Noriko Sato1
1Department of Radiology, National Center of Neurology and Psychiatry, Tokyo, Japan.
Plos One
|November 3, 2017
Summary
This study explored brain network changes in myotonic dystrophy type 1 (DM1) patients. While global connectivity remained similar, specific regional alterations in DM1 may link to cognitive and personality differences.
Area of Science:
- Neuroscience
- Neurology
- Medical Imaging
Background:
- Myotonic dystrophy type 1 (DM1) is a multisystem disorder with central nervous system involvement.
- Understanding the neurobiological underpinnings of DM1 is crucial for managing its diverse symptoms.
Purpose of the Study:
- To investigate structural covariance network abnormalities in DM1 patients using graph theoretical analysis.
- To clarify the mechanisms of central nervous system involvement in DM1.
Main Methods:
- Included 28 DM1 patients and 28 healthy controls.
- Utilized voxel-based morphometry (VBM) and graph theoretical analysis on MRI-derived gray matter volume.
- Applied Graph Analysis Toolbox for network analysis.
Main Results:
- VBM showed widespread gray matter atrophy in DM1 patients.
- No significant differences in global network connectivity measures between DM1 and control groups.
- Increased betweenness centrality in the left fusiform gyrus and decreased centrality in the right striatum were observed in DM1 patients.
Conclusions:
- Preserved global cognitive function in DM1 aligns with stable global network measures.
- Altered connectivity in specific regions (left fusiform gyrus, right striatum) may underlie deficits in face perception, theory of mind, and personality traits in DM1.
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