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Updated: Feb 5, 2026

Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
Published on: October 13, 2016
Brain functional networks become more connected as amyotrophic lateral sclerosis progresses: a source level
Pierpaolo Sorrentino1, Rosaria Rucco2, Francesca Jacini3
1Department of Engineering - University of Naples "Parthenope", Centro Direzionale Isola C4, 80133 Naples, Italy; Institute for High Performance Computing and Networking, CNR, via Pietro Castellino 111, 80131 Naples, Italy.
Amyotrophic lateral sclerosis (ALS) alters brain connectivity. This study found that as ALS progresses, brain networks become more interconnected, scale-free, and disassortative, indicating a sub-optimal topology compared to healthy controls.
Area of Science:
- Neuroscience
- Medical Physics
- Systems Biology
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease.
- Understanding alterations in brain network topology during ALS progression is crucial for developing therapeutic strategies.
Purpose of the Study:
- To investigate the hypothesis that brain networks exhibit increased hyper-connectivity as amyotrophic lateral sclerosis (ALS) progresses.
- To characterize changes in brain network topology and centrality in ALS patients at different disease stages.
Main Methods:
- Magnetoencephalography (MEG) and MRI recordings were performed on 54 ALS patients (early and advanced stages) and 25 controls.
- Brain activity reconstruction and synchronization estimation using the phase lag index in classical frequency bands.
- Calculation of brain topological metrics: leaf fraction, degree divergence, degree correlation, and betweenness centrality.
Main Results:
- Brain networks in ALS patients demonstrated increased connectivity, scale-freeness, and disassortativity across all frequency bands as the disease advanced.
- No significant differences were observed in specific brain areas, suggesting a global network alteration.
- The observed modified brain topology in ALS patients was found to be sub-optimal compared to healthy controls.
Conclusions:
- Brain network topology undergoes significant changes during the progression of amyotrophic lateral sclerosis (ALS).
- The findings indicate a progressive hyper-connectivity and altered network organization in ALS, which is sub-optimal for brain function.
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