We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement

New Technique Measures How Multiple Sclerosis Slows Brain Signals

Images of the brain's connections
Spatial structure tractography and temporal structure showing connection between edges. Image adapted from Sorrentino et al. 2022.

Want a FREE PDF version of This News Story?

Complete the form below and we will email you a PDF version of "New Technique Measures How Multiple Sclerosis Slows Brain Signals"

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

Read time:
 

Researchers of the Human Brain Project have developed a new methodology to calculate the delay of signal propagations in brains of patients suffering from multiple sclerosis, a chronic inflammatory disease that affects more than 2 million people worldwide. The results have been published in the Journal of Neuroscience by researchers at the Institut de Neurosciences des Systèmes, Marseille, France and of the University of Naples Parthenope and the University of Campania, Caserta in Italy.


In multiple sclerosis, the immune cells of the body attack the myelin, an insulating sheath that covers all the neurons. Myelin serves a similar purpose to the plastic that insulates electric cables, making electricity travel faster. A damage to the myelin layer in the brain causes the electrical signals to slow down, translating into delayed communications between brain areas and reduced or compromised abilities. Measuring the precise effect of the  myelinic damage can help doctors in providing a personalized approach to the patients.


This is harder than it looks for multiple sclerosis: “This illness is a diagnostic paradox,” explains Pierpaolo Sorrentino, lead author of the study. “There are patients whose MRI scans show extensive degradation of myelin but do not experience a corresponding impairment, and others that show little evident damage but still experience considerable issues. Often we are not able to tell by simply looking at the scans.” Stimulating the brain to measure real-time delay between areas is also not effective when attempting to estimate the delays of many brain connections and not just one: the signal ends up being too muddled up to be a reliable indicator of propagation. 

 

Instead, the researchers have developed a method to measure the delay that does not involve direct stimulation, but uses the neuronal avalanches (bursts of activity happening in cascades) that spontaneously travel across the brain. “These spontaneous bursts of activity can be used to measure the time it takes a signal to travel across the white-matter bundles connecting any two brain areas and then compare it with healthy controls without any myelinic damage,” says Sorrentino. “By not interfering directly with the signal, we can in a few minutes estimate the delay between most pairs of brain regions and then integrate it with what the MRI scans are showing us.”


In addition to informing the treatment, the method can also be used to refine virtual brain models of patients to further increase the level of personalization. Large-scale brain modelling typically assumes constant velocity of signal across the edges, but this isn’t exactly true even in a healthy brain. “We are now able to add the time delay factor to these simulations, improving the diagnostic and predictive tools available to doctors and their patients,” Sorrentino concludes.


Reference: Sorrentino P, Petkoski S, Sparaco M, et al. Whole-brain propagation delays in multiple sclerosis, a combined tractography - magnetoencephalography study. J Neurosci. Published online October 14, 2022. doi:10.1523/JNEUROSCI.0938-22.2022


This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

Advertisement