Li Jimmy, Shlobin Nathan A, Thijs Roland D, Sylvestre Marie-Pierre, Josephson Colin B, Deacon Charles, Keezer Mark R
Neurology Division, Centre Hospitalier de l'Université de Sherbrooke, Sherbrooke, Québec, Canada.
Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, Québec, Canada.
JAMA Neurol. 2024 Nov 1;81(11):1178-1186. doi: 10.1001/jamaneurol.2024.3210. Epub 2024 Sep 30.
How epilepsy may promote cardiovascular disease remains poorly understood.
To estimate the odds of new-onset cardiovascular events (CVEs) over 6 years in older people with vs without epilepsy, exploring how enzyme-inducing antiseizure medications (EIASMs) and traditional cardiovascular risk factors mediate these odds.
DESIGN, SETTING, AND PARTICIPANTS: This was a prospective cohort study using the comprehensive cohort of the Canadian Longitudinal Study on Aging (CLSA), with 6 years of follow-up (2015-2021, analysis performed in December 2023). The CLSA is an ongoing, national study of 51 338 adults aged 45 to 85 years at baseline who are recruited in Canada. The comprehensive cohort includes 30 097 individuals living near 1 of 11 data collection centers. Participation in the CLSA was voluntary; participation rate was 45%. Among those in the comprehensive cohort, individuals reporting no previous history of CVEs (ie, stroke, transient ischemic attack [TIA], or myocardial infarction [MI]) at baseline were excluded. No other exclusion criteria were applied. A total of 86% of participants completed follow-up.
Lifetime history of epilepsy.
The primary outcome was new-onset CVEs over 6 years. Secondary outcomes were new-onset strokes, TIAs, and MIs. Logistic models were fitted for these outcomes as a function of epilepsy, age, sex, household income, and education level. Mediation analyses were conducted for strong EIASM use, weak EIASM use, Framingham score, Physical Activity Scale for the Elderly (PASE) score, and waist to hip ratio.
Among the 30 097 individuals in the comprehensive cohort, a total of 27 230 individuals (mean [SD] age, 62.3 [10.1] years; 14 268 female [52.4%]) were included, 431 with a lifetime history of epilepsy. New-onset CVEs were more likely in epilepsy, with an adjusted odds ratio of 2.20 (95% CI, 1.48-3.27). The proportion of the effect of epilepsy on new-onset CVEs was mediated as follows by each of the following variables: strong EIASM use, 24.6% (95% CI, 6.5%-54.6%), weak EIASM use, 4.0% (95% CI, 0.8%-11.0%), Framingham score, 1.4% (95% CI, -1.6% to 4.5%), PASE score, 3.3% (95% CI, 1.4%-6.8%), and waist to hip ratio, 1.6% (95% CI, 0.4%-3.7%).
Results of this cohort study reveal that epilepsy was associated with new-onset CVEs. Nearly one-third of this association can be explained by EIASMs. These findings should be considered when choosing an antiseizure medication for a person at risk for cardiovascular disease.
癫痫如何促进心血管疾病仍知之甚少。
评估有癫痫和无癫痫的老年人在6年内发生新发心血管事件(CVE)的几率,探讨酶诱导抗癫痫药物(EIASM)和传统心血管危险因素如何介导这些几率。
设计、设置和参与者:这是一项前瞻性队列研究,使用加拿大老龄化纵向研究(CLSA)的综合队列,随访6年(2015 - 2021年,于2023年12月进行分析)。CLSA是一项正在进行的全国性研究,基线时招募了51338名年龄在45至85岁的成年人,他们来自加拿大。综合队列包括居住在11个数据收集中心之一附近的30097人。参与CLSA是自愿的;参与率为45%。在综合队列中,排除了那些在基线时报告无CVE病史(即中风、短暂性脑缺血发作[TIA]或心肌梗死[MI])的个体。未应用其他排除标准。共有86%的参与者完成了随访。
癫痫的终生病史。
主要结局是6年内新发CVE。次要结局是新发中风、TIA和MI。针对这些结局拟合逻辑模型,将其作为癫痫、年龄、性别、家庭收入和教育水平的函数。对强烈使用EIASM、轻度使用EIASM、弗雷明汉评分、老年人身体活动量表(PASE)评分以及腰臀比进行中介分析。
在综合队列的30097人中,共纳入27230人(平均[标准差]年龄,62.3[10.1]岁;14268名女性[52.4%]),其中431人有癫痫终生病史。癫痫患者发生新发CVE的可能性更大,调整后的优势比为2.20(95%置信区间,1.48 - 3.2