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Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study
Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study
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Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study
Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study

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Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study
Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study
Journal Article

Sleep apnea, hypoxia, and late-onset epilepsy: the Atherosclerosis Risk in Communities study

2024
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Overview
Abstract Study Objective Sleep apnea is associated with unexplained epilepsy in older adults in small studies. We sought to determine the relationship between sleep apnea and additional sleep characteristics and late-onset epilepsy (LOE), adjusting for comorbidities, using data from the large, prospective Atherosclerosis Risk in Communities (ARIC) Study cohort. Methods We used Medicare claims to identify cases of LOE in ARIC participants. We used polysomnography data from 1309 ARIC participants who also participated in the Sleep Heart Health Study in 1995–1998, and demographic and comorbidity data from ARIC. Later risk of LOE was evaluated using survival analysis with a competing risk of death. We also used survival analysis in 2672 ARIC participants to identify the association between self-reported obstructive sleep apnea (2011–2013), and the risk of subsequent LOE. Results Late-midlife oxygen desaturation to less than 80% during sleep was associated with subsequent development of LOE, adjusted subhazard ratio 3.28 (1.18–9.08), but the apnea–hypopnea index was not related. Participant report of diagnosis of sleep apnea in 2011–2013 was also associated with subsequent LOE, adjusted subhazard ratio 2.59 (1.24–5.39). Conclusions Sleep apnea and oxygen saturation nadir during sleep are associated with LOE, independently of hypertension and other comorbidities. These potentially modifiable risk factors could have large clinical implications for LOE. Graphical Abstract Graphical Abstract