Identification of altered brain connectivity patterns for localizing the
epileptogenic tissue in patients with drug-resistant epilepsy
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Romanian Government UEFISCDI |
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Executive Summary
The outcome of the surgical treatment for epilepsy depends on the
accurate localization of the epileptogenic tissue. A significant number
of patients require long-term intracranial recordings during the
presurgical evaluation phase.
Our main objective is to provide an algorithm for identifying the
epileptogenic tissue based on altered directed functional connectivity
(effective connectivity) patterns and state-of-the-art machine learning
techniques. Altered connectivity associated with the epileptic tissue has
been recently reported, however no prior study systematically analyzes
the whole-brain effective connectivity patterns of healthy and
pathological brain structures. As effective connectivity is defined as "the
influence one neural system exerts over another", we will use
intracranial electrical stimulation to evoke iEEG potentials for assessing
the effective connectivity in a large patient cohort (n?75). We will be
using a proven methodology that we have recently introduced (Donos et
al., Neuroimage, 2016) and will benefit from ongoing collaboration on
the topic with centers from Neuroscience Institute - Grenoble and King's
College - London.
Secondary objectives include:
1. A differential analysis on the changes in effective connectivity
patterns induced by epilepsy. For each brain structure we will create two
subsets of patients, so that the structure will be considered
epileptogenic in the first subset, and healthy in the second. Using a
modulation index that quantifies the number and the strength of the
connections, we will compare the effective connectivity patterns of each
brain structure, in both conditions. These quantitative measures will be
used as features for the random forest classifier that will help us
accomplish our main objective.
2. A physiological effective connectivity map, presented as a whole
brain atlas, as well as individualized effective connectivity maps of both
healthy and pathological structures.