Department of Medicine, University of Calgary, North Tower, 1403-29 St NW, Calgary, AB T2N 2T9, Canada; Department of Community Health Sciences, University of Calgary, 3D10 - 3280 Hospital Drive NW, Calgary, AB T2N 4Z6, Canada.
Department of Community Health Sciences, University of Calgary, 3D10 - 3280 Hospital Drive NW, Calgary, AB T2N 4Z6, Canada; Hotchkiss Brain Institute, University of Calgary, 1A10 - 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada; Department of Neurology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1137, New York, NY 10029, USA.
Epilepsy Behav. 2021 Jul;120:108006. doi: 10.1016/j.yebeh.2021.108006. Epub 2021 May 5.
Although the prevalence of comorbid epilepsy and dementia is expected to increase, the impact is not well understood. Our objectives were to examine risk factors associated with incident dementia and the impact of frailty and dementia on mortality in older adults with epilepsy.
The CALIBER scientific platform was used. People with incident epilepsy at or after age 65 were identified using Read codes and matched by age, sex, and general practitioner to a cohort without epilepsy (10:1). Baseline cohort characteristics were compared using conditional logistic regression models. Multivariate Cox proportional hazard regression models were used to examine the impact of frailty and dementia on mortality, and to assess risk factors for dementia development.
One thousand forty eight older adults with incident epilepsy were identified. The odds of having dementia at baseline were 7.39 [95% CI 5.21-10.50] times higher in older adults with epilepsy (n = 62, 5.92%) compared to older adults without epilepsy (n = 88, 0.86%). In the final multivariate Cox model (n = 326), age [HR: 1.20, 95% CI 1.09-1.32], Charlson comorbidity index score [HR: 1.26, 95% CI 1.10-1.44], and sleep disturbances [HR: 2.41, 95% CI 1.07-5.43] at baseline epilepsy diagnosis were significantly associated with an increased hazard of dementia development over the follow-up period. In a multivariate Cox model (n = 1047), age [HR: 1.07, 95% CI 1.03-1.11], baseline dementia [HR: 2.66, 95% CI 1.65-4.27] and baseline e-frailty index score [HR: 11.55, 95% CI 2.09-63.84] were significantly associated with a higher hazard of death among those with epilepsy. Female sex [HR: 0.77, 95% CI 0.59-0.99] was associated with a lower hazard of death.
The odds of having dementia were higher in older adults with incident epilepsy. A higher comorbidity burden acts as a risk factor for dementia, while prevalent dementia and increasing frailty were associated with mortality.
尽管合并癫痫和痴呆的患病率预计会增加,但影响尚未得到充分了解。我们的目标是研究与老年癫痫患者新发痴呆相关的危险因素,以及脆弱和痴呆对死亡率的影响。
使用 CALIBER 科学平台。使用 Read 代码确定 65 岁及以上新发癫痫的患者,并按年龄、性别和全科医生与无癫痫(10:1)的队列进行匹配。使用条件逻辑回归模型比较基线队列特征。使用多变量 Cox 比例风险回归模型来研究脆弱和痴呆对死亡率的影响,并评估痴呆发展的危险因素。
确定了 1048 名新发癫痫的老年患者。与无癫痫的老年患者(n=88,0.86%)相比,患有癫痫的老年患者(n=62,5.92%)在基线时患有痴呆的可能性高 7.39 倍[95%CI5.21-10.50]。在最终的多变量 Cox 模型(n=326)中,年龄[HR:1.20,95%CI1.09-1.32]、Charlson 合并症指数评分[HR:1.26,95%CI1.10-1.44]和睡眠障碍[HR:2.41,95%CI1.07-5.43]在基线癫痫诊断时与随访期间痴呆发展的风险增加显著相关。在多变量 Cox 模型(n=1047)中,年龄[HR:1.07,95%CI1.03-1.11]、基线痴呆[HR:2.66,95%CI1.65-4.27]和基线 e-脆弱指数评分[HR:11.55,95%CI2.09-63.84]与癫痫患者的死亡风险增加显著相关。女性[HR:0.77,95%CI0.59-0.99]与较低的死亡风险相关。
新发癫痫的老年患者发生痴呆的可能性更高。较高的合并症负担是痴呆的危险因素,而普遍存在的痴呆和脆弱程度增加与死亡率相关。