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Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study

Sleep apnea has been related to brain changes such as atrophy. However, which component of sleep apnea, the apnea-hypopnea index (AHI), nocturnal oxygen desaturation or arousals, can explain this association is unclear. In this large population-based study (n=681, mean age 62.1 years), we investigat...

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Autores principales: Zuurbier, Lisette A., Vernooij, Meike W., Luik, Annemarie I., Kocevska, Desana, Hofman, Albert, Whitmore, Harry, Ikram, M. Arfan, Tiemeier, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580891/
https://www.ncbi.nlm.nih.gov/pubmed/31236490
http://dx.doi.org/10.1016/j.nbscr.2016.04.001
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author Zuurbier, Lisette A.
Vernooij, Meike W.
Luik, Annemarie I.
Kocevska, Desana
Hofman, Albert
Whitmore, Harry
Ikram, M. Arfan
Tiemeier, Henning
author_facet Zuurbier, Lisette A.
Vernooij, Meike W.
Luik, Annemarie I.
Kocevska, Desana
Hofman, Albert
Whitmore, Harry
Ikram, M. Arfan
Tiemeier, Henning
author_sort Zuurbier, Lisette A.
collection PubMed
description Sleep apnea has been related to brain changes such as atrophy. However, which component of sleep apnea, the apnea-hypopnea index (AHI), nocturnal oxygen desaturation or arousals, can explain this association is unclear. In this large population-based study (n=681, mean age 62.1 years), we investigated the associations of AHI, nocturnal oxygen desaturation and arousals with global and regional gray matter and white matter volumes and with white matter lesion volumes. All participants underwent one night of polysomnography and MRI scanning of their brain. Gray matter, white matter and white matter lesion volumes adjusted for intracranial volume were studied as markers of brain atrophy. Nocturnal oxygen desaturation was related to whole brain white matter atrophy independent of covariates (multivariable adjusted B=−8.3, 95% CI=−16.7; −0.02). This association was most prominently reflected in the association between more oxygen desaturation and a smaller white matter parietal volume (B=−3.95 ml, 95% CI=−6.02; −1.88). Furthermore, oxygen desaturation was related to a smaller hippocampus (B=−0.22 ml, 95% CI=−0.42; −0.01). Although a higher AHI was related to smaller parietal gray (B=−0.05, 95% CI=−0.09; −0.004) and white matter (B=−0.06, 95% CI=−0.12; −0.10) volumes, these associations disappeared when adding oxygen desaturation to the model. We did not find a relation between arousals and gray and white matter brain atrophy and white matter lesion volumes. This suggests that oxygen desaturation mainly explains the association between sleep apnea and brain damage.
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spelling pubmed-65808912019-06-24 Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study Zuurbier, Lisette A. Vernooij, Meike W. Luik, Annemarie I. Kocevska, Desana Hofman, Albert Whitmore, Harry Ikram, M. Arfan Tiemeier, Henning Neurobiol Sleep Circadian Rhythms Research Paper Sleep apnea has been related to brain changes such as atrophy. However, which component of sleep apnea, the apnea-hypopnea index (AHI), nocturnal oxygen desaturation or arousals, can explain this association is unclear. In this large population-based study (n=681, mean age 62.1 years), we investigated the associations of AHI, nocturnal oxygen desaturation and arousals with global and regional gray matter and white matter volumes and with white matter lesion volumes. All participants underwent one night of polysomnography and MRI scanning of their brain. Gray matter, white matter and white matter lesion volumes adjusted for intracranial volume were studied as markers of brain atrophy. Nocturnal oxygen desaturation was related to whole brain white matter atrophy independent of covariates (multivariable adjusted B=−8.3, 95% CI=−16.7; −0.02). This association was most prominently reflected in the association between more oxygen desaturation and a smaller white matter parietal volume (B=−3.95 ml, 95% CI=−6.02; −1.88). Furthermore, oxygen desaturation was related to a smaller hippocampus (B=−0.22 ml, 95% CI=−0.42; −0.01). Although a higher AHI was related to smaller parietal gray (B=−0.05, 95% CI=−0.09; −0.004) and white matter (B=−0.06, 95% CI=−0.12; −0.10) volumes, these associations disappeared when adding oxygen desaturation to the model. We did not find a relation between arousals and gray and white matter brain atrophy and white matter lesion volumes. This suggests that oxygen desaturation mainly explains the association between sleep apnea and brain damage. Elsevier 2016-04-19 /pmc/articles/PMC6580891/ /pubmed/31236490 http://dx.doi.org/10.1016/j.nbscr.2016.04.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Zuurbier, Lisette A.
Vernooij, Meike W.
Luik, Annemarie I.
Kocevska, Desana
Hofman, Albert
Whitmore, Harry
Ikram, M. Arfan
Tiemeier, Henning
Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title_full Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title_fullStr Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title_full_unstemmed Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title_short Apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: A population-based study
title_sort apnea-hypopnea index, nocturnal arousals, oxygen desaturation and structural brain changes: a population-based study
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580891/
https://www.ncbi.nlm.nih.gov/pubmed/31236490
http://dx.doi.org/10.1016/j.nbscr.2016.04.001
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