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Cerebrospinal fluid ß-synuclein as a synaptic biomarker for preclinical Alzheimer's disease.
Barba, Lorenzo; Abu Rumeileh, Samir; Bellomo, Giovanni; Paolini Paoletti, Federico; Halbgebauer, Steffen; Oeckl, Patrick; Steinacker, Petra; Massa, Federico; Gaetani, Lorenzo; Parnetti, Lucilla; Otto, Markus.
Afiliação
  • Barba L; Department of Neurology, University Hospital Halle, Halle (Saale), Germany.
  • Abu Rumeileh S; Section of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
  • Bellomo G; Department of Neurology, University Hospital Halle, Halle (Saale), Germany.
  • Paolini Paoletti F; Section of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
  • Halbgebauer S; Section of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
  • Oeckl P; Department of Neurology, University of Ulm, Ulm, Germany.
  • Steinacker P; Department of Neurology, University of Ulm, Ulm, Germany.
  • Massa F; Department of Neurology, University Hospital Halle, Halle (Saale), Germany.
  • Gaetani L; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
  • Parnetti L; Section of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
  • Otto M; Section of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
J Neurol Neurosurg Psychiatry ; 94(1): 83-86, 2023 01.
Article em En | MEDLINE | ID: mdl-35944974
INTRODUCTION: ß-synuclein (ß-syn) is a presynaptic protein, whose cerebrospinal fluid (CSF) levels are increased in patients with Alzheimer's diseases (AD) showing mild cognitive impairment (MCI) and dementia (dem). Here, we aimed to investigate CSF ß-syn in subjects at different AD stages, including preclinical AD (pre-AD), and to compare its behaviour with another synaptic biomarker, α-synuclein (α-syn), and two biomarkers of neuro-axonal damage, namely neurofilament light chain protein (NfL) and total tau protein (t-tau). METHODS: We measured ß-syn, α-syn, t-tau and NfL in CSF of 75 patients with AD (pre-AD n=17, MCI-AD n=28, dem-AD n=30) and 35 controls (subjective memory complaints, SMC-Ctrl n=13, non-degenerative neurological disorders, Dis-Ctrl n=22). RESULTS: CSF ß-syn, α-syn, t-tau were significantly elevated in pre-AD patients compared with controls (p<0.0001, p=0.02 and p=0.0001, respectively), while NfL only increased in dem-AD (p=0.001). Pre-AD cases showed lower t-tau concentrations than MCI-AD (p=0.04) and dem-AD (p=0.01). CSF ß-syn had the best diagnostic performance for the discrimination of pre-AD subjects from all controls (area under the curve, AUC=0.97) and from SMC-Ctrl subjects (AUC=0.99). DISCUSSION: CSF ß-syn increases in the whole AD continuum since the preclinical stage and represents a promising biomarker of synaptic damage in AD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article