Biology subjects

Shikauchi, Y.

Publications and source records attributed to Shikauchi, Y..

6 recordsLinked to original sources

bioRxiv2026

Cross-Modal Organization of Facial and Vocal Behavior Revealed by Coordination Metrics Derived from Temporal Alignment

Facial and vocal behaviors jointly convey affective and communicative information, yet their cross-modal organization remains difficult to characterize quantitatively. We propose a framework for characterizing facial-vocal organization by aligning facial and vocal dynamics using canonical time warping. Multivariate facial action unit trajectories and vocal prosodic trajectories were extracted from recordings of spontaneous speech and aligned in a shared latent space. From the alignment process, we derived three cross-modal coordination metrics: "scaling factor", reflecting the relative scaling between modalities; "time shift ratio", reflecting the frequency of temporal shifts; and "time shift magnitude", reflecting their size. We evaluated these metrics in verbally fluent adults with autism spectrum disorder (ASD; N = 35) and controls (N = 44). The proposed metrics did not differ significantly between diagnostic groups but showed associations with individual differences in communication and anxiety. Scaling factor was linked to trait anxiety in ASD, whereas time shift ratio was associated with communication characteristics across participants. The proposed metrics also showed little association with conventional vocal pitch variability, suggesting that they capture aspects of expressive organization not reflected by vocal variability alone. Our findings support alignment-derived metrics as a complementary approach for characterizing individual variability in facial-vocal expressive behavior.

neuroscience↗

bioRxiv2026

Reduced EEG Complexity and Its Association with Social Communication in Adults with Autism Spectrum Disorder: A Multiscale Entropy Study

Background: Brain functions emerge from temporally organized neural dynamics, and an appropriate level of neural complexity may support flexible information processing. Electroencephalographic (EEG) studies using multiscale entropy (MSE), which quantifies signal complexity across multiple temporal scales, have reported reduced MSE at longer scales in individuals with autism spectrum disorder (ASD). However, most evidence comes from studies of infant and child samples, leaving adult data scarce, and the associations between reduced MSE, clinical symptoms, and social information processing are insufficiently understood. Methods: We recorded and analyzed EEG data from adults with ASD (n = 47) and typically developing (TD) controls (n = 40) during eyes-closed rest and two movie viewing conditions: Inscapes, comprising dynamically changing abstract visual patterns, and Partly Cloudy, an emotionally engaging animated social narrative. Group and condition effects were assessed using cluster-based permutation tests, and associations between MSE and Social Affect (SA) scores from the Autism Diagnostic Observation Schedule, Second Edition (ADOS-2), as well as group differences in event-related MSE changes, were examined using linear mixed-effects models. Results: Across conditions, adults with ASD showed lower MSE at longer scales ({tau} = 16-30), corresponding to effective sampling rates of 12.50-6.67 Hz in the coarse-grained time series, than TD adults. Longer-scale MSE within the ASD-TD difference cluster was negatively associated with ADOS-2 SA scores across diagnostic groups. The difference in event-related MSE change between Social and Non-Social conditions, comparing empathic-pain and mentalizing events in Partly Cloudy with temporally matched non-social windows in Inscapes, was smaller in ASD participants than in TD participants. No significant difference between Social and Non-Social windows was observed among ASD participants, whereas TD participants showed significantly greater MSE change during Social than Non-Social windows. Limitations: This study used a modest sample without an independent replication cohort, and the short event windows limited the precision of the MSE estimation. Conclusions: Reduced longer-scale MSE extends to adults with ASD and is associated with higher ADOS-2 SA scores across diagnostic groups. Event-related findings further suggest attenuated differentiation of longer-scale MSE between socially relevant and matched non-social windows in ASD.

neuroscience↗

bioRxiv2026

Preserved Intrinsic Neural Timescale Organization with Hierarchical Variation in Autism Spectrum Disorder

Intrinsic neural timescales (INTs) index the temporal decay of neural activity and form a cortical hierarchy from fast sensorimotor to slow transmodal regions. Altered INTs have been reported in autism spectrum disorder (ASD), but it remains unclear whether the hierarchical organization is preserved and how individual variability along this hierarchy relates to sensory traits. Using resting-state fMRI from 182 participants (67 ASD, 115 typically developed controls (TDC)), we estimated INT at each cortical vertex from the autocorrelation half-life and averaged these values across four five-minute runs per participant. Vertex-wise INTs were then averaged within predefined cortical parcels and large-scale functional networks for subsequent analyses. The cortical INT hierarchy was preserved in ASD, showing comparable sensorimotor-to-transmodal hierarchy in both groups. However, regions operating at longer timescales showed prolonged INTs in ASD, and such tendency increased systematically along the hierarchy. No vertex, parcel, or network survived correction of multiple comparisons, indicating that observed alterations followed a distributed hierarchical trend rather than a focal pattern. To disentangle group-level differences from inter-individual variability, we next modeled each participants parcel-wise INT profile relative to a TDC-derived group-averaged template. At the individual level, decomposition of INT profiles revealed that global shifts and hierarchical scaling primarily reflected demographic variation (plimarily sex) rather than diagnostic group membership. After accounting for these components, residual deviations from theTDC-derived cortical INT hierarchy showed a modest association with sensory traits characterized by reduced sensory registration. Together, these findings indicate that while the large-scale hierarchical organization of cortical temporal dynamics is largely preserved in ASD, individual-specific deviations from this hierarchy may contribute to variability in sensory experience beyond group-level differences. HighlightsO_LIAcross both autism spectrum disorder (ASD) and typically developed controls (TDC), intrinsic neural timescales (INTs) followed the established sensory cortical hierarchy and showed a negative association with cortical microstructural markers (myelin content and neurite density index), with no group difference in hierarchical slope. C_LIO_LIAt the whole-brain level, the hierarchical organization of INTs was preserved across ASD and TDC, although regions operating at longer timescales exhibited relatively greater extension in ASD. C_LIO_LIGlobal shifts and hierarchical scaling, describing individual positioning within the INT-based cortical hierarchy, were more strongly associated with demographic variation (primarily sex) than with diagnosis. C_LIO_LIAfter accounting for these global and hierarchical components, residual deviations from the INT-based cortical hierarchy were modestly associated with sensory traits characterized by reduced sensory registration. C_LI

neuroscience↗

bioRxiv2025

Iron deposition and functional connectivity alterations in the right substantia nigra of adult males with autism

The substantia nigra (SN) is a midbrain nucleus implicated not only in motor control and reward processing but also in higher-order cognitive functions. Iron homeostasis in this region is essential for neurotransmitter synthesis, especially for dopamine, and thus, iron dysregulation may contribute to the symptomatology of autism spectrum disorder (ASD). However, iron deposition and functional circuits of the SN in the autistic brain remain underexplored. This study investigated iron deposition and functional connectivity (FC) of the SN in 53 adult males with ASD and 99 typically developing controls using quantitative susceptibility mapping and resting-state fMRI. Compared to controls, the ASD group exhibited higher magnetic susceptibility in the right SN, suggesting elevated iron deposition. Within the ASD group, higher iron deposition was associated with more severe socio-communicative deficits and reduced sensory-seeking behavior. Seed-based FC analyses further revealed that the ASD group exhibited stronger FC between the right SN and bilateral visual cortices and reduced FC with the right superior frontal gyrus. These results highlight the critical role of SN in the autistic brain and indicate that altered iron homeostasis in the SN may contribute to disruptions in the dopaminergic system that underlie the core symptoms of ASD.

neuroscience↗

bioRxiv2025

Quantifying state-dependent control properties of brain dynamics from perturbation responses

The brain can be conceptualized as a control system facilitating transitions between states, such as from rest to motor activity. Applying network control theory to measurements of brain signals enables characterization of brain dynamics through control properties. However, most prior studies that have applied network control theory have evaluated brain dynamics under unperturbed conditions, neglecting the critical role of external perturbations in accurate system identification. In this study, we combine a perturbation input paradigm with a network control theory framework and propose a novel method for estimating the controllability Gramian matrix in a simple, theoretically grounded manner. This method provides insights into brain dynamics, including overall controllability (quantified by the Gramians eigenvalues) and specific controllable directions (represented by its eigenvectors). As a proof of concept, we applied our method to transcranial magnetic stimulationinduced electroencephalographic responses across four motor-related states and two resting states. We found that states such as open-eye rest, closed-eye rest, and motor-related states were more effectively differentiated using controllable directions than overall controllability. However, certain states, like motor execution and motor imagery, remained indistinguishable using these measures. These findings indicate that some brain states differ in their intrinsic control properties as dynamical systems, while others share similarities that make them less distinguishable. This study underscores the value of control theory-based analyses in quantitatively how intrinsic brain states shape the brains responses to stimulation, providing deeper insights into the dynamic properties of these states. This methodology holds promise for diverse applications, including characterizing individual response variability and identifying conditions for optimal stimulation efficacy. Significant statementThe brain can be viewed as a control system transitioning between states, such as from rest to motor activity. Previous studies using network control theory mostly evaluated brain dynamics without external perturbations, neglecting their role in accurate system identification. This study integrates perturbation inputs with network control theory to propose a method for estimating the controllability Gramian, thereby providing insights into brain dynamics. We applied this approach to TMS-induced EEG responses in motor-related and resting states. Our findings show that controllable directions (eigenvectors) allow better discrimination between states than overall controllability. Our method can quantitatively assess brain state differences, and has potential applications in characterizing individual response variability and optimizing stimulation efficacy.

neuroscience↗

bioRxiv2025

Electroencephalographic responses before, during, and after upper limb paired associative stimulation

Paired associative stimulation (PAS) is a non-invasive protocol involving repeated stimulus pairs to activate two cortical areas alternately, inducing Hebbian-like plasticity. However, its neurophysiological impacts remain unclear. To determine the changes that occur in the brain during PAS, brain activity during PAS must be measured and distinguished from the electromagnetic artifacts produced by the stimulation. Here, we present a novel dataset of electroencephalography (EEG) measurements during PAS with an inter-stimulus-interval of 25 ms (PAS25, expected to induce long-term potentiation-like changes) or 35 ms (PAS35, no expected change). This dataset includes raw data and pre-processed data with electromagnetic artefacts removed. he right ulnar nerves electrical stimulation preceded transcranial magnetic stimulation to the left primary motor cortex in both cases. EEG was measured before and after the PAS sessions, with only electrical or magnetic stimulation. To demonstrate the quality of the data, we summarize the stability of the stimulation site and the event-related potentials before, during, and after PAS. This dataset will enable observing brain dynamics due to the accumulation of stimulations during PAS and differences in responsiveness to stimulations before and after PAS.

neuroscience↗