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Bruzzone, S. E. P.

Publications and source records attributed to Bruzzone, S. E. P..

2 recordsLinked to original sources

Applying SCA for high-accuracy cortical auditory ERPs in children

Overlapping neurophysiological signals are the main obstacle preventing from using cortical event-related potentials (ERPs) in clinical settings. Children ERPs are particularly affected by this problem, as their cerebral cortex is still maturing. To overcome this problem, we applied a new version of Spike-density Component Analysis (SCA), an analysis method recently introduced, to isolate with high accuracy the neural components of auditory ERP responses (AEPs) in 8-year-old children. Electroencephalography was used with 33 children to record AEPs to auditory stimuli varying in spectrotemporal features. Three different analysis approaches were adopted: the standard ERP analysis procedure, SCA with template-match (SCA-TM), and SCA with half-split average consistency (SCA-HSAC). SCA-HSAC most successfully allowed the extraction of AEPs for each child, revealing that the most consistent components were P1 and N2. An immature N1 component was also detected. Superior accuracy in isolating neural components at the individual level even in children was demonstrated for SCA-HSAC over other SCA approaches. Reliable methods of extraction of neurophysiological signals at the individual level are crucial for the application of cortical AEPs for routine diagnostic exams in clinical settings both in children and adults. HighlightsO_LISpike-density component analysis (SCA) was validated on children ERPs C_LIO_LISCA extracted overlapping neural components from auditory ERPs (AEPs) C_LIO_LIChild AEPs were modelled at the individual level C_LI

neuroscience

Association between COMT gene Val158Met heterozygote polymorphism and enhanced brain predicting processes

Predicting events in the ever-changing environment is a fundamental survival function intrinsic to the physiology of sensory systems, whose efficiency varies among the population. Even though it is established that a major source of such variations is genetic heritage, there are no studies tracking down auditory predicting processes to genetic mutations. Thus, we examined the neurophysiological responses to deviant stimuli recorded with magnetoencephalography (MEG) in 108 healthy participants carrying different variants of the Val158Met single-nucleotide polymorphism (SNP) within the catechol-O-methyltransferase (COMT) gene, which is responsible for the majority of catecholamines degradation in the prefrontal cortex. Our results showed significant amplitude enhancement of neural responses localized within inferior frontal gyrus, superior and middle temporal cortices to deviant auditory stimuli in heterozygote genotype carriers (Val/Met) vs homozygote (Val/Val and Met/Met) carriers. Integrating neurophysiology and genetics, this study provided new and broader insights into the brain mechanisms underlying optimal deviant detection.

neuroscience