Epilepsy is associated with the accelerated aging of brain activity in sleep.

IF 3.2 3区 医学 Q2 PHYSIOLOGY Frontiers in Physiology Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI:10.3389/fphys.2024.1458592
Peter N Hadar, Mike Westmeijer, Haoqi Sun, Erik-Jan Meulenbrugge, Jin Jing, Luis Paixao, Ryan A Tesh, Madalena Da Silva Cardoso, Pierrick Arnal, Rhoda Au, Chol Shin, Soriul Kim, Robert J Thomas, Sydney S Cash, M Brandon Westover
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Abstract

Objective: Although seizures are the cardinal feature, epilepsy is associated with other forms of brain dysfunction including impaired cognition, abnormal sleep, and increased risk of developing dementia. We hypothesized that, given the widespread neurologic dysfunction caused by epilepsy, accelerated brain aging would be seen. We measured the sleep-based brain age index (BAI) in a diverse group of patients with epilepsy. The BAI is a machine learning-based biomarker that measures how much the brain activity of a person during overnight sleep deviates from chronological age-based norms.

Methods: This case-control study drew information of age-matched controls without epilepsy from home sleep monitoring volunteers and from non-epilepsy patients with Sleep Lab testing. Patients with epilepsy underwent in-patient monitoring and were classified by epilepsy type and seizure burden. The primary outcomes measured were BAI, processed from electroencephalograms, and epilepsy severity metrics (years with epilepsy, seizure frequency standardized by year, and seizure burden [number of seizures in life]). Subanalyses were conducted on a subset with NIH Toolbox cognitive testing for total, fluid, and crystallized composite cognition.

Results: 138 patients with epilepsy (32 exclusively focal and 106 generalizable [focal seizures with secondary generalization]) underwent in-patient monitoring, and age-matched, non-epilepsy controls were analyzed. The mean BAI was higher in epilepsy patients vs controls and differed by epilepsy type: -0.05 years (controls) versus 5.02 years (all epilepsy, p < 0.001), 5.53 years (generalizable, p < 0.001), and 3.34 years (focal, p = 0.03). Sleep architecture was disrupted in epilepsy, especially in generalizable epilepsy. A higher BAI was positively associated with increased lifetime seizure burden in focal and generalizable epilepsies and associated with lower crystallized cognition. Lifetime seizure burden was inversely correlated with fluid, crystallized, and composite cognition.

Significance: Epilepsy is associated with accelerated brain aging. Higher brain age indices are associated with poorer cognition and more severe epilepsy, specifically generalizability and higher seizure burden. These findings strengthen the use of the sleep-derived, electroencephalography-based BAI as a biomarker for cognitive dysfunction in epilepsy.

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癫痫与睡眠中大脑活动的加速老化有关。
目的:虽然癫痫发作是癫痫的主要特征,但癫痫还与其他形式的脑功能障碍相关,包括认知障碍、睡眠异常和痴呆风险增加。我们假设,鉴于癫痫引起的广泛的神经功能障碍,将会看到加速的大脑衰老。我们测量了一组不同癫痫患者的睡眠脑年龄指数(BAI)。BAI是一种基于机器学习的生物标志物,可以测量一个人在夜间睡眠期间的大脑活动与实际年龄标准的偏差程度。方法:本病例对照研究从家庭睡眠监测志愿者和睡眠实验室测试的非癫痫患者中抽取年龄匹配的无癫痫对照者的信息。对癫痫患者进行住院监测,并根据癫痫类型和发作负担进行分类。测量的主要结果是由脑电图处理的BAI和癫痫严重程度指标(癫痫发作年限、按年标准化的癫痫发作频率和癫痫负担[一生中癫痫发作次数])。对NIH工具箱认知测试的一个子集进行了亚分析,包括总认知、流体认知和结晶复合认知。结果:138例癫痫患者(32例局灶性癫痫发作,106例全身性癫痫发作伴继发性癫痫发作)接受了住院监测,并分析了年龄匹配的非癫痫对照组。癫痫患者的平均BAI高于对照组,并因癫痫类型而异:-0.05年(对照组)、5.02年(所有癫痫,p < 0.001)、5.53年(可概括,p < 0.001)和3.34年(局灶性,p = 0.03)。癫痫患者,尤其是广泛性癫痫患者的睡眠结构被打乱。在局灶性和全身性癫痫中,较高的BAI与终生癫痫发作负担增加呈正相关,并与较低的结晶认知相关。终生癫痫发作负担与液体认知、结晶认知和复合认知呈负相关。意义:癫痫与脑老化加速有关。较高的脑年龄指数与较差的认知能力和更严重的癫痫有关,特别是广泛性和较高的癫痫发作负担。这些发现加强了睡眠衍生的、基于脑电图的BAI作为癫痫患者认知功能障碍的生物标志物的使用。
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来源期刊
CiteScore
6.50
自引率
5.00%
发文量
2608
审稿时长
14 weeks
期刊介绍: Frontiers in Physiology is a leading journal in its field, publishing rigorously peer-reviewed research on the physiology of living systems, from the subcellular and molecular domains to the intact organism, and its interaction with the environment. Field Chief Editor George E. Billman at the Ohio State University Columbus is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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