4.6 Article

Alzheimer's disease neuropathology in the hippocampus and brainstem of people with obstructive sleep apnea

Journal

SLEEP
Volume 44, Issue 3, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/sleep/zsaa195

Keywords

amyloid beta; continuous positive airway pressure; Alzheimer's disease; neurofibrillary tangles; tau

Funding

  1. RMIT University Higher Degree by Research Publication Grant

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The study found a link between obstructive sleep apnea and Alzheimer's disease, with OSA severity potentially negatively affecting the hippocampus, but the presence of NFTs and A beta plaques may not necessarily be related to OSA severity.
Obstructive sleep apnea (OSA) involves intermittent cessations of breathing during sleep. People with OSA can experience memory deficits and have reduced hippocampal volume; these features are also characteristic of Alzheimer's disease (AD), where they are accompanied by neurofibrillary tangles (NFTs) and amyloid beta (A beta) plaques in the hippocampus and brainstem. We have recently shown reduced hippocampal volume to be related to OSA severity, and although OSA may be a risk factor for AD, the hippocampus and brainstems of clinically verified OSA cases have not yet been examined for NFTs and A beta plaques. The present study used quantitative immunohistochemistry to investigate postmortem hippocampi of 34 people with OSA (18 females, 16 males; mean age 67 years) and brainstems of 24 people with OSA for the presence of NFTs and A beta plaques. OSA severity was a significant predictor of A beta plaque burden in the hippocampus after controlling for age, sex, body mass index (BMI), and continuous positive airway pressure (CPAP) use. OSA severity also predicted NFT burden in the hippocampus, but not after controlling for age. Although 71% of brainstems contained NFTs and 21% contained A beta plaques, their burdens were not correlated with OSA severity. These results indicate that OSA accounts for some of the cognitively normal individuals who have been found to have substantial A beta burdens, and are currently considered to be at a prodromal stage of AD.

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