REM睡眠時無呼吸と脳の変化・記憶障害の関連性を解明(Study links REM sleep apnea to brain changes, memory loss in older adults)

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2025-05-07 カリフォルニア大学アーバイン校 (UCI)

カリフォルニア大学アーバイン校(UC Irvine)の研究チームは、レム睡眠時の閉塞性睡眠時無呼吸(OSA)が高齢者の脳構造に変化をもたらし、記憶力低下と関連する可能性を明らかにしました。平均年齢73歳の認知機能正常な37人を対象に、睡眠ポリグラフ検査とMRIによる脳画像解析を実施。その結果、レム睡眠中の低酸素状態(低酸素血症)が、記憶形成に重要な内側側頭葉の構造変化や、白質高信号(ホワイトマター・ハイパーインテンシティ)と呼ばれる微小血管損傷と強く関連していることが判明しました。この研究は、軽度のOSAであっても認知症リスクを高める可能性があることを示唆しており、特にレム睡眠中の呼吸障害に対する早期の診断と治療の重要性を強調しています。

<関連情報>

閉塞性睡眠時無呼吸による低酸素血症と高齢者における白質高濃度および側頭葉の変化との関連性 Association of Hypoxemia Due to Obstructive Sleep Apnea With White Matter Hyperintensities and Temporal Lobe Changes in Older Adults

Destiny E. Berisha, Batool Rizvi, Miranda G. Chappel-Farley, Nicholas Tustison, Lisa Taylor, Abhishek Dave, Negin S. Sattari, … Show All … , and Bryce A. Mander
Neurology  Published:May 7, 2025
DOI:https://doi.org/10.1212/WNL.0000000000213639

Abstract

Background and Objectives

Cerebral small vessel disease (CSVD) is a leading cause of cognitive decline and functional loss in older adults. Obstructive sleep apnea (OSA) is common in older adults, can increase cerebrovascular disease risk, and is linked to medial temporal lobe (MTL) degeneration and cognitive impairment. However, the interaction between OSA features and CSVD burden and their combined effect on MTL structure and function are not well understood. This study tested the hypothesis that CSVD burden is a candidate mechanism linking OSA to MTL degeneration and impaired memory in older adults.

Methods

Cognitively unimpaired older adults from the Biomarker Exploration in Aging, Cognition, and Neurodegeneration cohort were recruited for an observational, in-lab overnight polysomnography (PSG) study with emotional mnemonic discrimination ability assessed before and after sleep. Participants had no neurologic or psychiatric disorders and were not on sleep-affecting medications. PSG-derived OSA variables included apnea-hypopnea index (AHI), total arousal index, and minimum SpO2. MRI was used to assess global and lobar white matter hyperintensity (WMH) volumes and MTL structure (hippocampal volume; entorhinal cortex [ERC] thickness) at an earlier time point. Regressions were implemented while adjusting for age, sex, and concurrent use of antihyperlipidemic and/or antihypertensive medication. Minimum SpO2 was transformed into a Hypoxemia Severity Index for normality, in which lower SpO2 values indicated more severe hypoxemia.

Results

Thirty-seven older adults were included in the study (age 72.5 ± 5.6 years, 23 women, AHI = 13.8 ± 18.0 [range 0–80]). Hypoxemia measures significantly predicted global WMH volume (bminSpO2 = 0.141 [0.001–0.282], bduration <90% = 0.008 [0.000–0.016]). This relationship was driven by hypoxemia severity during REM sleep (bREMminSpO2 = 0.143 [0.003–0.284]), which also predicted frontal (bREMminSpO2 = 0.101 [0.004–0.198]) and parietal (bREMminSpO2 = 0.121 [0.024–0.219]) WMH burden. Greater frontal WMH burden indirectly mediated the relationship between REM sleep hypoxemia and ERC thickness (indirect effect = -0.043, 95% CI -0.1174 to -0.00015). Reduced ERC thickness was, in turn, associated with worse overnight mnemonic discrimination ability (bleftERCthickness = 0.112 [0.014–0.211]).

Discussion

These findings identify CSVD as a candidate mechanism linking OSA-related hypoxemia to MTL degeneration and impaired sleep-dependent memory in older adults, specifically implicating hypoxic events during REM sleep.

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