Increased intracranial very low frequency pulsation power in central brain regions of high-functioning young adults with autism spectrum disorder

• Vasomotion-driven brain pulsation power is increased in young adults with ASD • Increased power was observed predominantly in subcortical grey matter nuclei and white matter • Increased pulsation power could serve as a potential clinical classifier • No alterations were found in the cardiorespiratory pulsation powers Autism spectrum disorder (ASD) is an increasingly diagnosed neurodevelopmental condition characterized by persistent difficulties in social communication and restricted, repetitive patterns of behavior and sensory processing that leads to functional impairment. The diagnosis of ASD relies on behavioral and clinical assessment as there are no currently available biomarkers. Recent brain imaging studies have suggested abnormalities in the brain fluid flow in individuals with ASD. Cardiorespiratory and vasomotion-induced very low frequency (VLF ≤ 0.1 Hz) brain pulsations are now considered to facilitate the cerebrospinal- and interstitial fluid exchange in the brain, thus contributing to maintaining cerebral homeostasis and fluid clearance. In this study, we utilized ultrafast resting-state functional magnetic resonance imaging (fMRI) to capture and compare the powers of each physiological pulsation in groups of 18 young adults diagnosed with ASD and 19 neurotypical controls (NTC). We further probed the clinical significance of findings by undertaking regression analyses examining the associations of both Autism Spectrum Quotient (AQ) and Autism Diagnostic Observation Schedule (ADOS) scores with pulsation powers, and by receiver operating characteristics (ROC) analysis. Compared to the NTC group, the ASD group showed significantly higher VLF pulsation power, which was located predominantly in subcortical grey matter nuclei and the white matter, indicating increased vasomotor power in ASD. In addition, the individual VLF power enabled good accuracy (ROC area under curve = 0.75-0.93) for discriminating ASD subjects from NTCs. In conclusion, present findings of increased VLF power are postulated as possible indication of altered driving force of cerebral neurofluid dynamics and could potentially serve as a useful clinical classifier.