Individual Alpha Peak Frequency, an Important Biomarker for Live Z-Score Training Neurofeedback in Adolescents with Learning Disabilities

• Main Authors: Rubén Pérez-Elvira, Javier Oltra-Cucarella, José Antonio Carrobles, Minodora Teodoru, Ciprian Bacila, Bogdan Neamtu
• Format: Article
• Language: English
• Published: MDPI AG 2021-01-01
• Series: Brain Sciences
• Subjects: neurofeedback; Z-score training; learning disabilities; endophenotypes; alpha peak frequency; QEEG
• Online Access: https://www.mdpi.com/2076-3425/11/2/167

Learning disabilities (LDs) have an estimated prevalence between 5% and 9% in the pediatric population and are associated with difficulties in reading, arithmetic, and writing. Previous electroencephalography (EEG) research has reported a lag in alpha-band development in specific LD phenotypes, which seems to offer a possible explanation for differences in EEG maturation. In this study, 40 adolescents aged 10–15 years with LDs underwent 10 sessions of Live Z-Score Training Neurofeedback (LZT-NF) Training to improve their cognition and behavior. Based on the individual alpha peak frequency (i-APF) values from the spectrogram, a group with normal i-APF (ni-APF) and a group with low i-APF (li-APF) were compared in a pre-and-post-LZT-NF intervention. There were no statistical differences in age, gender, or the distribution of LDs between the groups. The li-APF group showed a higher theta absolute power in P4 (<i>p</i> = 0.016) at baseline and higher Hi-Beta absolute power in F3 (<i>p</i> = 0.007) post-treatment compared with the ni-APF group. In both groups, extreme waves (absolute Z-score of ≥1.5) were more likely to move toward the normative values, with better results in the ni-APF group. Conversely, the waves within the normal range at baseline were more likely to move out of the range after treatment in the li-APF group. Our results provide evidence of a viable biomarker for identifying optimal responders for the LZT-NF technique based on the i-APF metric reflecting the patient’s neurophysiological individuality.