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Devera, A.

Publications and source records attributed to Devera, A..

2 recordsLinked to original sources

Maturation of Sleep EEG Complexity in Preterm Newborns: Insights from Lempel-Ziv and Joint Lempel-Ziv Analyses

The development of the sleep-wake cycle reflects the progressive structural and functional maturation of the brain. However, the organization of neural dynamics during prematurity remains incompletely understood. In this study, we analyzed the EEG from 54 polysomnographic recordings obtained from 39 preterm infants, grouped according to postmenstrual age (PMA) into three categories: 30-31, 32-33 and 34-35 weeks. Lempel-Ziv Complexity (LZC) and Joint Lempel-Ziv Complexity (JLZC) of the electroencephalogram (EEG) were analyzed during active sleep (AS), quiet sleep (QS), and indeterminate sleep (IS). LZC computed from the raw, unfiltered recordings were significantly higher during QS than during AS and increased with PMA during AS. To further refine the analysis, LZC was also evaluated separately in the low-frequency (1-15.5 Hz) and high-frequency (16-30 Hz) EEG bands. In the low-frequency band, LZC was consistently higher during QS than during AS, an effect that was most pronounced in more immature groups. Furthermore, LZC increased with maturation particularly during AS. Sleep-state comparisons of LZC in the high-frequency EEG band also revealed higher values during QS than during AS across all PMA groups. Moreover, in contrast to the low-frequency band, LZC progressively decreased with advancing PMA both in AS and QS, suggesting that the neural mechanisms underlying low- and high-frequency EEG activity follow distinct maturational trajectories. Interestingly, larger LZC in the temporal cortex and interhemispheric differences were detected in the 32-33 PMA group. On the other hand, JLZC analysis revealed greater joint spatiotemporal dynamics across EEG channels during QS than during AS, with consistently higher JLZC values in temporal regions and lower in occipital regions. Together, these findings show that these complexity metrics distinguishes sleep states and captures maturational changes in EEG activity in preterm infants. These results provide novel insights into early brain development and suggest potential quantitative biomarkers of neonatal brain maturation.

neuroscience↗

Dorsal and median raphe neuronal firing dynamics characterized by non-linear metrics

The dorsal (DRN) and median (MRN) raphe are the main serotonergic nuclei, being implicated in sleep and mood regulation. The DRN is mainly serotonergic, where neurons have regular spiking activity, slow firing rate (FR), and long action potential duration (APD). The MRN is divided in a median serotonergic region and a paramedian region, containing principally GABAergic neurons, resulting in more diverse neurochemical and electrophysiological features. In the present study, we aimed to enrich the characterization of the raphe nuclei neurons by using non-linear metrics. This was done by analyzing the neuronal basal firing profile in both nuclei of urethane-anesthetized rats using Ordinal Patterns (OP) Entropy, Bins Entropy, and Permutation Lempel-Ziv Complexity (PLZC). In a first step, we found that typical linear metrics - such as FR, coefficient of variation (CV), and APD - fail to distinguish between MRN and DRN neurons, while OP entropy is significantly different between these nuclei. We also found that the FR has a strong linear relationship with CV, Bins Entropy, and PLZC. Similarly, CV has a strong correlation with FR and Bins Entropy, whereas PLZC shows a strong linear fit with Bins Entropy. However, OP Entropy has either a weak or no linear relationship with the rest of the metrics tested, suggesting that OP Entropy is a good metric to differentiate neuronal firing profiles. In a second step, we studied how these metrics are affected by the oscillatory properties of the firing patterns. We found that all metrics are sensitive to rhythmicity - with the exception of OP Entropy. Again, this highlights OP Entropy as a powerful and useful quantity for the characterization of neuronal discharge patterns.

neuroscience↗