Obstructive sleep apnea and Alzheimer’s disease-related cerebrospinal fluid biomarkers in mild cognitive impairment

Author:

Díaz-Román Mónica123ORCID,Pulopulos Matias M45ORCID,Baquero Miguel6,Salvador Alicia5,Cuevas Ana6,Ferrer Inés56,Ciopat Oana12,Gómez Enriqueta12

Affiliation:

1. Sleep Medicine Unit, La Fe University and Polytechnic Hospital, Valencia, Spain

2. Department of Clinical Neurophysiology, La Fe University and Polytechnic Hospital, Valencia, Spain

3. Department of Clinical Neurophysiology, Lluís Alcanyís Hospital, Xàtiva, Spain

4. Department of Experimental Clinical and Health Psychology, Faculty of Psychology and Educational Sciences, Ghent University, Gent, Belgium

5. Laboratory of Social Cognitive Neuroscience, Department of Psychobiology, University of Valencia, IDOCAL, Valencia, Spain

6. Cognitive Disorders Unit, Department of Neurology La Fe University and Polytechnic Hospital, Valencia, Spain

Abstract

Abstract Previous studies have demonstrated that sleep-breathing disorders, and especially obstructive sleep apnea (OSA), can be observed in patients with a higher risk of progression to Alzheimer’s disease (AD). Recent evidence indicates that cerebrospinal fluid (CSF) AD-biomarkers are associated with OSA. In this study, we investigated these associations in a sample of patients with mild cognitive impairment (MCI), a condition that is considered the first clinical phase of AD, when patients showed biomarkers consistent with AD pathology. A total of 57 patients (mean age = 66.19; SD = 7.13) with MCI were included in the study. An overnight polysomnography recording was used to assess objective sleep parameters (i.e. apnea/hypopnea index [AHI], total sleep time, sleep efficiency, sleep latency, arousal index, awakening, stage 1, 2, and slow-wave sleep and rapid eye movement sleep, periodic limb movement index, O2 saturation during sleep, and percentage of time O2 saturation <90%). Phosphorylated-tau (P-tau), total-tau (T-tau), and amyloid-beta 42 (Aβ42) were measured in CSF. Unadjusted correlation analyses showed that a higher AHI (reflecting higher OSA severity) was related to higher P-tau and T-tau (both results remained significant after Bonferroni correction, p = 0.001). Importantly, these associations were observed even after adjusting for potential confounders (i.e. age, sex, body mass index, sleep medication, smoking, hypertension, and heart disease). Although more research is needed to establish a causal link, our findings provide evidence that OSA could be related to the pathophysiological mechanisms involved in neurodegeneration in MCI patients.

Funder

Research Foundation Flanders

Spanish Ministry of Economy and Competitiveness

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Neurology (clinical)

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