Year: 2026
Type: preprint
Study designs: Systematic Review, Meta-Analysis
Abstract: Sleep disorders such as obstructive sleep apnea (OSA), sleep deprivation (SD), and narcolepsy type 1 (NT1), are associated with cognitive dysfunction and an increased risk of neurodegenerative disease. Glymphatic transport disruption has been suggested as one potential mechanistic link. However, evidence across sleep disorders and glymphatic-related metrics remains fragmented. We aimed to determine whether glymphatic-related metrics are altered in OSA, SD, and NT1. We performed a systematic review and meta-analysis of clinical and preclinical studies to determine whether glymphatic-related metrics are altered in OSA, SD, and NT1. Across studies of OSA, glymphatic-related metrics indicated significant impairment of glymphatic transport with a moderate negative association between apnea-hypopnea index (AHI) and diffusion tensor imaging along the perivascular space (DTI-ALPS) index (r=−0.53, 95% confidence interval (CI): −0.63 to −0.41; p <0.001). Available evidence did not demonstrate statistically significant alterations in glymphatic measures in SD or NT1. These findings suggest that impaired glymphatic transport may represent a potential pathway linking OSA to cognitive decline and neurodegenerative risk. However, current evidence is insufficient to determine whether comparable alterations occur in SD or NT1. Substantial heterogeneity across studies highlights the need for standardized reporting and harmonized methodologies to advance the field.
Source: medRxiv
Institutions: MRC Cognition and Brain Sciences Unit, University of Cambridge, University of Warwick, The Queen's Medical Research Institute, University of Edinburgh, Capital Medical University, Beijing Shijitan Hospital, Beijing Institute for Brain Disorders, Montreal Neurological Institute and Hospital, McGill University
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funder: University of Warwick
OpenAlex ID: W7223216443
