| Literature DB >> 30957276 |
Unal Sakoglu1, Mutlu Mete2, John Esquivel2, Katya Rubia3, Richard Briggs4, Bryon Adinoff5,6,7.
Abstract
Static functional connectivity (FC) analyses based on functional magnetic resonance imaging (fMRI) data have been extensively explored for studying various psychiatric conditions in the brain, including cocaine addiction. A recently emerging, more powerful technique, dynamic functional connectivity (DFC), studies how the FC dynamics change during the course of the fMRI experiments. The aim in this paper was to develop a computational approach, using a machine learning framework, to determine if DFC features were more successful than FC features in the classification of cocaine-dependent patients and healthy controls. fMRI data were obtained from of 25 healthy and 58 cocaine-dependent participants while performing a motor response inhibition task, stop signal task. Group independent component analysis was carried out on all participant data to compute spatially independent components (ICs). Eight ICs were selected manually as relevant brain networks, which were used to classify healthy versus cocaine-dependent participants. FC and DFC measures of the chosen IC pairs were used as features for the classification algorithm. Support Vector Machines were used for both feature selection/reduction and participant classification. Based on DFC with only seven IC pairs, participants were successfully classified with 95% accuracy (and with 90% accuracy with three IC pairs), whereas static FC yielded only 81% accuracy. Visual, sensorimotor, default mode, and executive control networks, amygdala, and insula played the most significant role in the DFC-based classification. These findings support the use of DFC-based classification of fMRI data as a potential biomarker for the identification of cocaine dependence.Entities:
Keywords: classification; cocaine addiction; cocaine dependence; dynamic functional connectivity; functional magnetic resonance imaging; independent component analysis; support vector machines
Year: 2019 PMID: 30957276 PMCID: PMC6530930 DOI: 10.1002/jnr.24421
Source DB: PubMed Journal: J Neurosci Res ISSN: 0360-4012 Impact factor: 4.164