From the Department of Neurology (I.Z., J.K., C.M.A., C.M., M.Q.), and School of Nursing (M.K.M.), University of Virginia, Charlottesville.
Neurology. 2024 Sep 24;103(6):e209820. doi: 10.1212/WNL.0000000000209820. Epub 2024 Aug 22.
Seizures are common in dementia and associated with accelerated cognitive decline. However, the impact of active vs remote seizures on cognition remains understudied. This study aimed to investigate the impact of active vs remote seizures on cognition in people with normal cognition and mild cognitive impairment (MCI).
This longitudinal, multicenter cohort is based on National Alzheimer's Coordinating Center data of participants recruited from 39 Alzheimer's Disease Centers in the United States from September 2005 to December 2021. All participants with normal cognition and MCI and at least 2 visits were included. Primary outcome, that is, cognitive decline, was determined using Clinical Dementia Rating (CDR) from (1) normal-to-impaired (CDR ≥0.5) and (2) MCI-to-dementia (CDR ≥1) groups. The effect of active seizures (over the preceding 12 months), remote seizures (previous seizures but none over the preceding 12 months), and no seizures (controls) on cognition was assessed. Subgroups of chronic seizures at enrollment and new-onset seizures were further analyzed. Cox regression models assessed the risk of all-cause MCI and/or dementia. All models were adjusted for age, sex, education, race, hypertension, and diabetes.
Of the 13,726 participants with normal cognition at enrollment (9,002 [66%] female; median age 71 years), 118 had active seizures and 226 had remote seizures. Of the 11,372 participants with MCI at enrollment (5,605 [49%] female; median age 73 years), 197 had active seizures and 226 had remote seizures. Active seizures were associated with 2.1 times higher risk of cognitive impairment (adjusted hazard ratio [aHR] 2.13, 95% CI 1.60-2.84, < 0.001) in cognitively healthy adults (median years to decline: active seizures = ∼1, remote seizures = ∼3, no seizures = ∼3) and 1.6 times higher risk of dementia (aHR 1.58, 95% CI 1.24-2.01, < 0.001) in those with MCI (median years to decline: active seizures = ∼1, remote seizures = ∼2, controls = ∼2). This risk was not observed with remote seizures.
In this study, active seizures but not remote seizures were associated with earlier cognitive decline in both cognitively normal adults and those with MCI, independent of other dementia risk factors. Therefore, early identification and management of seizures may present a path to mitigation of cognitive decline in the aging epileptic population. A limitation is that causality cannot be confirmed in our observational longitudinal study.
癫痫在痴呆症中很常见,并且与认知能力加速下降有关。然而,活动性癫痫与远程癫痫对认知的影响仍研究不足。本研究旨在调查活动性癫痫与认知正常和轻度认知障碍(MCI)患者的远程癫痫对认知的影响。
这是一项基于美国 39 个阿尔茨海默病中心的国家阿尔茨海默病协调中心数据的纵向、多中心队列研究,于 2005 年 9 月至 2021 年 12 月期间招募参与者。所有认知正常和 MCI 且至少有 2 次就诊的患者均被纳入本研究。主要结局是认知下降,使用临床痴呆评定量表(CDR)从(1)正常到受损(CDR≥0.5)和(2)MCI 到痴呆(CDR≥1)组来确定。评估了活动性癫痫(在过去 12 个月内)、远程癫痫(以前有过癫痫发作,但在过去 12 个月内没有发作)和无癫痫发作(对照组)对认知的影响。进一步分析了入组时慢性癫痫发作和新发癫痫发作的亚组。Cox 回归模型评估了所有原因导致的 MCI 和/或痴呆的风险。所有模型均根据年龄、性别、教育程度、种族、高血压和糖尿病进行了调整。
在认知正常的 13726 名入组患者中(9002 名[66%]为女性;中位年龄 71 岁),118 名患者有活动性癫痫发作,226 名患者有远程癫痫发作。在认知正常的 11372 名入组患者中(5605 名[49%]为女性;中位年龄 73 岁),197 名患者有活动性癫痫发作,226 名患者有远程癫痫发作。活动性癫痫发作使认知正常成年人认知障碍的风险增加 2.1 倍(调整后的危险比[HR]2.13,95%置信区间 1.60-2.84,<0.001),并且使 MCI 患者的痴呆风险增加 1.6 倍(HR 1.58,95%置信区间 1.24-2.01,<0.001)(认知正常成年人的中位下降年限:活动性癫痫发作=约 1 年,远程癫痫发作=约 3 年,无癫痫发作=约 3 年;MCI 患者的中位下降年限:活动性癫痫发作=约 1 年,远程癫痫发作=约 2 年,对照组=约 2 年)。而远程癫痫发作与认知下降无关。
在这项研究中,活动性癫痫发作而非远程癫痫发作与认知正常的成年人和 MCI 患者的认知能力早期下降有关,这与其他痴呆风险因素无关。因此,早期识别和管理癫痫发作可能为减缓衰老癫痫人群的认知能力下降提供途径。本研究的局限性在于我们的观察性纵向研究无法确认因果关系。