Altered glymphatic enhancement of cerebrospinal fluid tracer in individuals with chronic poor sleep quality. Issue 9 (September 2022)

• Record Type: Journal Article
• Authors: Eide, Per Kristian; Pripp, Are Hugo; Berge, Benedikte; Hrubos-Strøm, Harald; Ringstad, Geir; Valnes, Lars Magnus
• Is Part Of: Journal of cerebral blood flow & metabolism. Volume 42:Issue 9(2022)
• Page Start: 1676
• Page End: 1692
• Publication Date: 2022-09
• Subjects: Sleep quality -- brain metabolism -- molecular clearance -- magnetic resonance imaging -- cerebrospinal fluid tracer; Cerebral circulation -- Periodicals; Brain -- Metabolism -- Periodicals; Brain -- Blood-vessels -- Periodicals; Cerebrovascular disease -- Periodicals; 612.824
• DOI: 10.1177/0271678X221090747
• Languages: English
• ISSNs: 0271-678X

Abstract

Chronic sleep disturbance is a risk factor for dementia disease, possibly due to impaired sleep-dependent clearance of toxic metabolic by-products. We compared enrichment of a cerebrospinal fluid (CSF) tracer within brain of patients reporting good or poor sleep quality, assessed by the Pittsburgh Sleep Quality Index (PSQI) questionnaire. Tracer enrichment in a selection of brain regions was assessed using multiphase magnetic resonance imaging up to 48 hours after intrathecal administration of the contrast agent gadobutrol (0.5 ml of 1 mmol/ml) serving as tracer. Tracer enrichment differed between patients with good (PSQI ≤5) and poor (PSQI >5) sleep quality in a cohort of non-dementia individuals (n = 44; age 42.3 ± 14.5 years), and in patients with the dementia subtype idiopathic normal pressure hydrocephalus (n = 24; age 71.0 ± 4.9 years). Sleep impairment was associated with increased CSF tracer enrichment in several brain regions. Cortical brain volume as well as entorhinal cortex thickness was reduced in the oldest cohort and was correlated with the severity of sleep disturbance and the degree of cortical tracer enrichment. We suggest chronic sleep disturbance is accompanied by altered glymphatic function along enlarged perivascular spaces.