{"title":"癫痫和阻塞性睡眠呼吸暂停患者的呼吸唤醒阈值。","authors":"Ting-Wei Liao, Chun-Wei Chang, Mei-Yun Cheng, Tony Wu, Ning-Hung Chen, Shih-Wei Lin, Li-Pang Chuang","doi":"10.2147/NSS.S535940","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Patients with epilepsy (PWE) have a higher likelihood of developing obstructive sleep apnea (OSA). However, limited literature investigates the phenotypes of OSA in this population. This study aimed to evaluate the respiratory arousal threshold (rAT) in PWE with concurrent OSA.</p><p><strong>Methods: </strong>Patients were recruited from the Sleep and Epilepsy Center at Chang Gung Memorial Hospital between January 2010 and June 2022. We included adult patients who underwent overnight in-laboratory polysomnography after the onset of epilepsy. Additionally, age-, sex-, and apnea-hypopnea index (AHI)-matched patients with OSA only were included as controls. Low rAT was defined using predictive models based on polysomnography criteria.</p><p><strong>Results: </strong>We enrolled 48 PWE, of whom 36 (75%) had concurrent OSA (PWE+OSA), and 108 patients with OSA only. PWE+OSA were older upon PSG examination and had a later epilepsy onset compared to PWE only. PWE had more concomitant antiseizure medications and hypnotics compared to patients with OSA only. Among those with OSA, 19 (52.8%) with PWE+OSA and 68 (63.0%) with OSA only were predicted to have a low rAT. Continuous positive airway pressure compliance was significantly lower in the low rAT subgroup compared to the high rAT subgroup (p = 0.021) within the OSA-only group, whereas no significant difference was observed between rAT subgroups in the PWE+OSA group.</p><p><strong>Conclusion: </strong>Our study provides insights into the presence of a low rAT in PWE+OSA, with no significant difference in its ratio compared to OSA controls. However, since rAT was estimated using a predictive model rather than direct measurement, this limitation may affect the interpretation of our findings. Further studies using gold-standard methods are needed to clarify the underlying mechanisms contributing to the higher OSA prevalence in PWE.</p>","PeriodicalId":18896,"journal":{"name":"Nature and Science of Sleep","volume":"17 ","pages":"1825-1836"},"PeriodicalIF":3.4000,"publicationDate":"2025-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12341830/pdf/","citationCount":"0","resultStr":"{\"title\":\"Respiratory Arousal Threshold in Patients with Epilepsy and Obstructive Sleep Apnea.\",\"authors\":\"Ting-Wei Liao, Chun-Wei Chang, Mei-Yun Cheng, Tony Wu, Ning-Hung Chen, Shih-Wei Lin, Li-Pang Chuang\",\"doi\":\"10.2147/NSS.S535940\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Patients with epilepsy (PWE) have a higher likelihood of developing obstructive sleep apnea (OSA). However, limited literature investigates the phenotypes of OSA in this population. This study aimed to evaluate the respiratory arousal threshold (rAT) in PWE with concurrent OSA.</p><p><strong>Methods: </strong>Patients were recruited from the Sleep and Epilepsy Center at Chang Gung Memorial Hospital between January 2010 and June 2022. We included adult patients who underwent overnight in-laboratory polysomnography after the onset of epilepsy. Additionally, age-, sex-, and apnea-hypopnea index (AHI)-matched patients with OSA only were included as controls. Low rAT was defined using predictive models based on polysomnography criteria.</p><p><strong>Results: </strong>We enrolled 48 PWE, of whom 36 (75%) had concurrent OSA (PWE+OSA), and 108 patients with OSA only. PWE+OSA were older upon PSG examination and had a later epilepsy onset compared to PWE only. PWE had more concomitant antiseizure medications and hypnotics compared to patients with OSA only. Among those with OSA, 19 (52.8%) with PWE+OSA and 68 (63.0%) with OSA only were predicted to have a low rAT. Continuous positive airway pressure compliance was significantly lower in the low rAT subgroup compared to the high rAT subgroup (p = 0.021) within the OSA-only group, whereas no significant difference was observed between rAT subgroups in the PWE+OSA group.</p><p><strong>Conclusion: </strong>Our study provides insights into the presence of a low rAT in PWE+OSA, with no significant difference in its ratio compared to OSA controls. However, since rAT was estimated using a predictive model rather than direct measurement, this limitation may affect the interpretation of our findings. Further studies using gold-standard methods are needed to clarify the underlying mechanisms contributing to the higher OSA prevalence in PWE.</p>\",\"PeriodicalId\":18896,\"journal\":{\"name\":\"Nature and Science of Sleep\",\"volume\":\"17 \",\"pages\":\"1825-1836\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-08-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12341830/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nature and Science of Sleep\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2147/NSS.S535940\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature and Science of Sleep","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/NSS.S535940","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Respiratory Arousal Threshold in Patients with Epilepsy and Obstructive Sleep Apnea.
Background: Patients with epilepsy (PWE) have a higher likelihood of developing obstructive sleep apnea (OSA). However, limited literature investigates the phenotypes of OSA in this population. This study aimed to evaluate the respiratory arousal threshold (rAT) in PWE with concurrent OSA.
Methods: Patients were recruited from the Sleep and Epilepsy Center at Chang Gung Memorial Hospital between January 2010 and June 2022. We included adult patients who underwent overnight in-laboratory polysomnography after the onset of epilepsy. Additionally, age-, sex-, and apnea-hypopnea index (AHI)-matched patients with OSA only were included as controls. Low rAT was defined using predictive models based on polysomnography criteria.
Results: We enrolled 48 PWE, of whom 36 (75%) had concurrent OSA (PWE+OSA), and 108 patients with OSA only. PWE+OSA were older upon PSG examination and had a later epilepsy onset compared to PWE only. PWE had more concomitant antiseizure medications and hypnotics compared to patients with OSA only. Among those with OSA, 19 (52.8%) with PWE+OSA and 68 (63.0%) with OSA only were predicted to have a low rAT. Continuous positive airway pressure compliance was significantly lower in the low rAT subgroup compared to the high rAT subgroup (p = 0.021) within the OSA-only group, whereas no significant difference was observed between rAT subgroups in the PWE+OSA group.
Conclusion: Our study provides insights into the presence of a low rAT in PWE+OSA, with no significant difference in its ratio compared to OSA controls. However, since rAT was estimated using a predictive model rather than direct measurement, this limitation may affect the interpretation of our findings. Further studies using gold-standard methods are needed to clarify the underlying mechanisms contributing to the higher OSA prevalence in PWE.
期刊介绍:
Nature and Science of Sleep is an international, peer-reviewed, open access journal covering all aspects of sleep science and sleep medicine, including the neurophysiology and functions of sleep, the genetics of sleep, sleep and society, biological rhythms, dreaming, sleep disorders and therapy, and strategies to optimize healthy sleep.
Specific topics covered in the journal include:
The functions of sleep in humans and other animals
Physiological and neurophysiological changes with sleep
The genetics of sleep and sleep differences
The neurotransmitters, receptors and pathways involved in controlling both sleep and wakefulness
Behavioral and pharmacological interventions aimed at improving sleep, and improving wakefulness
Sleep changes with development and with age
Sleep and reproduction (e.g., changes across the menstrual cycle, with pregnancy and menopause)
The science and nature of dreams
Sleep disorders
Impact of sleep and sleep disorders on health, daytime function and quality of life
Sleep problems secondary to clinical disorders
Interaction of society with sleep (e.g., consequences of shift work, occupational health, public health)
The microbiome and sleep
Chronotherapy
Impact of circadian rhythms on sleep, physiology, cognition and health
Mechanisms controlling circadian rhythms, centrally and peripherally
Impact of circadian rhythm disruptions (including night shift work, jet lag and social jet lag) on sleep, physiology, cognition and health
Behavioral and pharmacological interventions aimed at reducing adverse effects of circadian-related sleep disruption
Assessment of technologies and biomarkers for measuring sleep and/or circadian rhythms
Epigenetic markers of sleep or circadian disruption.