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Breathing cessation events that compose the apnea-hypopnea index are distinctively associated with the adverse outcomes in Alzheimer's disease. | LitMetric

AI Article Synopsis

  • The study investigates how obstructive sleep apnea (OSA) affects Alzheimer's disease (AD) patients by analyzing the impact of different breathing events on sleep structure and cognitive decline.
  • Conducted with 116 mild-moderate AD patients, the study used polysomnography and cerebrospinal fluid analysis to identify links between apnea events and AD markers.
  • Results show that obstructive apneas and hypopneas disrupt sleep patterns, with hypopneas significantly contributing to cognitive decline over a year, emphasizing the need for tailored patient care in managing AD alongside sleep disorders.

Article Abstract

Background: Previous studies challenge the impact of obstructive sleep apnea (OSA) once patients are diagnosed with Alzheimer's disease (AD). Nevertheless, OSA recognizably disrupts sleep, and relevant associations between sleep, AD pathological markers, and cognition have been demonstrated. We aimed to further explore this, evaluating the associations between each breathing cessation event that compose the apnea-hypopnea index (AHI) and the sleep structure to finally investigate whether this was related to increased levels of AD markers and higher cognitive decline.

Methods: Observational, prospective study, including consecutive patients diagnosed with mild-moderate AD. The participants were submitted to overnight polysomnography followed by a cerebrospinal fluid collection for AD pathological markers levels determination. Neuropsychological assessment was performed at baseline and after 12 months of follow-up.

Results: The cohort was composed of 116 patients (55.2% females) with a median [p25;p75] age of 76.0 [72.0;80.0] years and an AHI of 25.9 [15.1;48.5], which was mainly defined by the presence of hypopneas and obstructive apneas. These were distinctively associated with the sleep structure, with obstructive apneas being related to arousals and sleep lightening and hypopneas being related to an increased number of arousals only. Despite having a lower frequency, mixed and central apneas also presented associations with the sleep structure, particularly increasing the time spent in the lighter sleep stages. In relation to AD pathological markers, obstructive and mixed apneas were related to an augment in neurofilament light levels while hypopneas were associated with a higher phosphorylated-tau/amyloid-beta protein ratio. Hypopneas were the most important event for an increased cognitive decline at the 12-month follow-up.

Conclusions: Our findings highlight the importance of a patient-centered approach, with a comprehensive and detailed analysis of the AHI to effectively predict the different outcomes and tailor the appropriate therapeutic strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347810PMC
http://dx.doi.org/10.1186/s13195-023-01266-xDOI Listing

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