Alzheimer's disease and late-onset epilepsy of unknown origin: two faces of beta amyloid pathology

被引:91
作者
Costa, Cinzia [1 ]
Romoli, Michele [1 ]
Liguori, Claudio [2 ]
Farotti, Lucia [1 ]
Eusebi, Paolo [1 ]
Bedetti, Chiara [1 ]
Siliquini, Sabrina [1 ]
Cesarini, Elena Nardi [1 ]
Romigi, Andrea [3 ]
Mercuri, Nicola B. [2 ,3 ]
Parnetti, Lucilla [1 ]
Calabresi, Paolo [1 ,2 ]
机构
[1] Univ Hosp Perugia, Neurol Clin, Dept Med, Perugia, Italy
[2] IRCCS Santa Lucia, Rome, Italy
[3] Tor Vergata Univ & Hosp, Sleep & Epilepsy Med Ctr, Dept Syst Med, Neurophysiopathol Unit, Rome, Italy
关键词
Dementia; Alzheimer's disease; Epilepsy; Beta amyloid; CSF biomarkers; TEMPORAL-LOBE EPILEPSY; MILD COGNITIVE IMPAIRMENT; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; PRECURSOR PROTEIN; DEMENTIA; SEIZURES; DEFINITION; RECOMMENDATIONS;
D O I
10.1016/j.neurobiolaging.2018.09.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Although amyloid pathology plays a role in epilepsy, little is known about the relationship between beta amyloid and progression to Alzheimer's disease (AD) among patients with late-onset epilepsy of unknown origin (LOEU). This multicenter, observational, prospective study enrolled 40 consecutive non-demented adults diagnosed with LOEU, together with 43 age- and sex-matched healthy controls. All patients completed neuropsychological tests, core CSF AD biomarkers assessment (A beta(1-42), total tau, and phosphorylated tau), and follow-up for a mean of 3 years to verify cognitive decline. Despite age and baseline cognitive performance were similar to healthy controls, patients with LOEU had significant prevalence of CSF pathological A beta(1-42) (<500 pg/mL; 37.5%), 7.5% displaying an AD-like CSF pattern. Moreover,17.5% of patients with LOEU converted to AD dementia, versus none among healthy controls (p < 0.005). Patients with LOEU with pathological A beta(1-42) had a hazard ratio 3.4 (CI 0.665-17.73) for progression to AD dementia at follow-up. Patients with LOEU have a high prevalence of abnormal CSF A beta(1-42) and progression to AD dementia compared with healthy controls, and therefore should be monitored for cognitive decline. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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