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Alzheimer's disease and late-onset epilepsy of unknown origin: two faces of beta amyloid pathology.
Costa, Cinzia; Romoli, Michele; Liguori, Claudio; Farotti, Lucia; Eusebi, Paolo; Bedetti, Chiara; Siliquini, Sabrina; Cesarini, Elena Nardi; Romigi, Andrea; Mercuri, Nicola B; Parnetti, Lucilla; Calabresi, Paolo.
Afiliação
  • Costa C; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy. Electronic address: cinzia.costa@unipg.it.
  • Romoli M; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Liguori C; IRCCS "Santa Lucia", Rome, Italy.
  • Farotti L; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Eusebi P; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Bedetti C; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Siliquini S; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Cesarini EN; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Romigi A; Neurophysiopathology Unit, Department of Systems Medicine, Sleep and Epilepsy Medicine Centre, Tor Vergata University and Hospital, Rome, Italy.
  • Mercuri NB; IRCCS "Santa Lucia", Rome, Italy; Neurophysiopathology Unit, Department of Systems Medicine, Sleep and Epilepsy Medicine Centre, Tor Vergata University and Hospital, Rome, Italy.
  • Parnetti L; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy.
  • Calabresi P; Department of Medicine, Neurology Clinic, University Hospital of Perugia, Italy; IRCCS "Santa Lucia", Rome, Italy.
Neurobiol Aging ; 73: 61-67, 2019 01.
Article em En | MEDLINE | ID: mdl-30317034
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 nondemented adults diagnosed with LOEU, together with 43 age- and sex-matched healthy controls. All patients completed neuropsychological tests, core CSF AD biomarkers assessment (Aß1-42, 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 Aß1-42 (<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 Aß1-42 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 Aß1-42 and progression to AD dementia compared with healthy controls, and therefore should be monitored for cognitive decline.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Peptídeos beta-Amiloides / Epilepsia / Doença de Alzheimer / Disfunção Cognitiva / Transtornos de Início Tardio Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Peptídeos beta-Amiloides / Epilepsia / Doença de Alzheimer / Disfunção Cognitiva / Transtornos de Início Tardio Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos