温度和基因组变异对癫痫患者颅内脑电图测量的影响。

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2024-09-10 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae269
Olivia C McNicholas, Diego Jiménez-Jiménez, Joana F A Oliveira, Lauren Ferguson, Ravishankara Bellampalli, Charlotte McLaughlin, Fahmida Amin Chowdhury, Helena Martins Custodio, Patrick Moloney, Anna Mavrogianni, Beate Diehl, Sanjay M Sisodiya
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引用次数: 0

摘要

热浪对人类健康有严重影响,是人为气候变化引起的主要健康问题。人们对热浪或不适应的温度有不同的耐受性。癫痫患者可能尤其会受到温度的影响,因为癫痫患者大脑兴奋性的电临床特征(发作间期癫痫样放电和癫痫发作)受到一系列生理和非生理条件的影响。热浪越来越常见,可能会影响大脑兴奋性。2015 年 5 月至 22 年 8 月期间,我们在伦敦国立神经学和神经外科医院的非空调遥测病房对癫痫患者进行颅内脑电图记录时,利用了自发热浪,研究了热浪对大脑兴奋性的影响。在伦敦,热浪的定义是连续三天或三天以上日最高气温≥28°C。在颅内脑电图记录期间,我们利用热浪内和热浪外的四个 10 分钟片段对每位参与者的发作间期癫痫样放电进行了计数。此外,我们还统计了热浪内外的所有临床和亚临床癫痫发作。我们搜索了致病的罕见基因变异,并计算了癫痫 PRS。研究共纳入了九名参与者(六名男性,三名女性),中位年龄为 30 岁(24-39 岁不等)。在热浪期间,三名参与者发作间期癫痫样放电的次数明显增加。五名参与者在热浪期间的癫痫发作次数增加,作为一个群体,热浪期间的癫痫发作次数明显增加。八名参与者的基因数据显示,没有人患有已知的罕见、由基因决定的癫痫,而所有参与者的癫痫多基因风险得分都很高。对于某些癫痫患者,而不仅仅是已知的罕见温度敏感性癫痫患者,热浪与大脑兴奋性增加之间存在关联。这些初步数据需要进一步验证和探讨,因为它们引起了人们对热浪直接影响大脑健康的担忧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of temperature and genomic variation on intracranial EEG measures in people with epilepsy.

Heatwaves have serious impacts on human health and constitute a key health concern from anthropogenic climate change. People have different individual tolerance for heatwaves or unaccustomed temperatures. Those with epilepsy may be particularly affected by temperature as the electroclinical hallmarks of brain excitability in epilepsy (inter-ictal epileptiform discharges and seizures) are influenced by a range of physiological and non-physiological conditions. Heatwaves are becoming more common and may affect brain excitability. Leveraging spontaneous heatwaves during periods of intracranial EEG recording in participants with epilepsy in a non-air-conditioned telemetry unit at the National Hospital for Neurology and Neurosurgery in London from May to August 2015-22, we examined the impact of heatwaves on brain excitability. In London, a heatwave is defined as three or more consecutive days with daily maximum temperatures ≥28°C. For each participant, we counted inter-ictal epileptiform discharges using four 10-min segments within, and outside of, heatwaves during periods of intracranial EEG recording. Additionally, we counted all clinical and subclinical seizures within, and outside of, heatwaves. We searched for causal rare genetic variants and calculated the epilepsy PRS. Nine participants were included in the study (six men, three women), median age 30 years (range 24-39). During heatwaves, there was a significant increase in the number of inter-ictal epileptiform discharges in three participants. Five participants had more seizures during the heatwave period, and as a group, there were significantly more seizures during the heatwaves. Genetic data, available for eight participants, showed none had known rare, genetically-determined epilepsies, whilst all had high polygenic risk scores for epilepsy. For some people with epilepsy, and not just those with known, rare, temperature-sensitive epilepsies, there is an association between heatwaves and increased brain excitability. These preliminary data require further validation and exploration, as they raise concerns about the impact of heatwaves directly on brain health.

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