INTRODUCTION: Obstructive sleep apnea syndrome (OSAS) is a recognized risk fac-tor for neurodegenerative disorders. However, a causal link between OSAS and brain damage has yet to be established. METHODS: Thirty cognitively normal patients with moderate-to-severe OSAS, free from systemic or neurological comorbidities, were enrolled and underwent18F-fluorodeoxyglucose positron emission tomography imaging. Their scans were compared to those of cognitively normal, OSAS-free controls from the Alzheimer’s Disease Neuroimaging Initiative database. Additional analyses included commonality map-ping, correlations with polysomnographic parameters, and seed-based metabolic connectivity of major resting-state networks. RESULTS: Group-level analyses showed fronto-parietal glucose hypometabolism and cerebellar glucose hypermetabolism in patients with OSAS compared to con-trols. Cerebellar glucose hypermetabolism was associated with reduced rapid eye movement sleep latency and duration. Seed-based connectivity analysis revealed alterations in attentional and limbic networks. DISCUSSION: Moderate-to-severe OSAS may represent a cause of brain dysfunc-tion, highlighting the importance of its early diagnosis and appropriate treatment to prevent worsening brain damage and possible future neurodegenerative processes.
Altered brain glucose metabolism and connectivity in young adults with obstructive sleep apnea
Caminiti, Silvia P.;Malito, Rachele;Liguori, Claudio
2026-01-01
Abstract
INTRODUCTION: Obstructive sleep apnea syndrome (OSAS) is a recognized risk fac-tor for neurodegenerative disorders. However, a causal link between OSAS and brain damage has yet to be established. METHODS: Thirty cognitively normal patients with moderate-to-severe OSAS, free from systemic or neurological comorbidities, were enrolled and underwent18F-fluorodeoxyglucose positron emission tomography imaging. Their scans were compared to those of cognitively normal, OSAS-free controls from the Alzheimer’s Disease Neuroimaging Initiative database. Additional analyses included commonality map-ping, correlations with polysomnographic parameters, and seed-based metabolic connectivity of major resting-state networks. RESULTS: Group-level analyses showed fronto-parietal glucose hypometabolism and cerebellar glucose hypermetabolism in patients with OSAS compared to con-trols. Cerebellar glucose hypermetabolism was associated with reduced rapid eye movement sleep latency and duration. Seed-based connectivity analysis revealed alterations in attentional and limbic networks. DISCUSSION: Moderate-to-severe OSAS may represent a cause of brain dysfunc-tion, highlighting the importance of its early diagnosis and appropriate treatment to prevent worsening brain damage and possible future neurodegenerative processes.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


