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Cerebrospinal fluid Alzheimer biomarkers can be useful for discriminating dementia with Lewy bodies from Alzheimer's disease at the prodromal stage.
Bousiges, Olivier; Bombois, Stephanie; Schraen, Susanna; Wallon, David; Quillard, Muriel Muraine; Gabelle, Audrey; Lehmann, Sylvain; Paquet, Claire; Amar-Bouaziz, Elodie; Magnin, Eloi; Miguet-Alfonsi, Carole; Delbeuck, Xavier; Lavaux, Thomas; Anthony, Pierre; Philippi, Nathalie; Blanc, Frederic.
Afiliação
  • Bousiges O; Laboratory of Biochemistry and Molecular Biology, and CNRS, Laboratoire de Neurosciences Cognitives et Adaptatives (LNCA), University Hospital of Strasbourg, Strasbourg, Alsace, France.
  • Bombois S; Université Lille Nord de France, DISTALZ, Memory Center, Lille, France.
  • Schraen S; UMR-S 1172 - JPArc-Centre de recherches Jean-Pierre Aubert Neurosciences et Cancer and CHU Lille, UF Neurobiologie, Université Lille, Lille, France.
  • Wallon D; Department of Neurology, Rouen University Hospital, Rouen, France.
  • Quillard MM; Department of Biochemistry Laboratory, Rouen University Hospital, Rouen, France.
  • Gabelle A; CMRR (Memory Resources and Research Centre), Department of Neurology, CHU de Montpellier, Hôpital, Gui de Chauliac, Montpellier, France.
  • Lehmann S; Laboratoire de Biochimie et Protéomique Clinique, CHU de Montpellier and Université de Montpellier, IRMB, CRB, Montpellier, France.
  • Paquet C; CMRR (Memory Resources and Research Centre) Paris Nord Ile de France and Histologie et Biologie du Vieillissement, Groupe Hospitalier Saint-Louis Lariboisière Fernand-Widal APHP, INSERM U942, Université Paris Diderot, Paris, France.
  • Amar-Bouaziz E; Service de Biochimie et Biologie moléculaire, GH Saint-Louis-Lariboisière-Fernand Widal, APHP, Paris, France.
  • Magnin E; Department of Neurology, Centre Mémoire Ressources Recherche Besançon Franche-Comté, CHU de Besançon, Besançon, France.
  • Miguet-Alfonsi C; Laboratoire de pharmacologie clinique, CHU de Besançon, Besancon, France.
  • Delbeuck X; Université Lille Nord de France, DISTALZ, Memory Center, Lille, France.
  • Lavaux T; Laboratory of Biochemistry and Molecular Biology, University Hospital of Strasbourg, Strasbourg, France.
  • Anthony P; Neuropsychology Unit, Neurology Service, and CNRS, ICube Laboratory UMR 7357 and FMTS, Team IMIS/Neurocrypto, University Hospital of Strasbourg, CMRR (Memory Resources and Research Centre), Geriatrics Day Hospital, Geriatrics Service, Strasbourg, France.
  • Philippi N; Neuropsychology Unit, Neurology Service, and CNRS, ICube Laboratory UMR 7357 and FMTS, Team IMIS/Neurocrypto, University Hospital of Strasbourg, CMRR (Memory Resources and Research Centre), Geriatrics Day Hospital, Geriatrics Service, Strasbourg, France.
  • Blanc F; Neuropsychology Unit, Neurology Service, and CNRS, ICube Laboratory UMR 7357 and FMTS, Team IMIS/Neurocrypto, University Hospital of Strasbourg, CMRR (Memory Resources and Research Centre), Geriatrics Day Hospital, Geriatrics Service, Strasbourg, France.
J Neurol Neurosurg Psychiatry ; 89(5): 467-475, 2018 05.
Article em En | MEDLINE | ID: mdl-29321140
ABSTRACT

BACKGROUND:

Differential diagnosis between dementia with Lewy bodies (DLB) and Alzheimer's disease (AD) is not straightforward, especially in the early stages of disease. We compared AD biomarkers (phospho-Tau181, total-Tau, Aß42 and Aß40) in cerebrospinal fluid (CSF) of patients with DLB and AD, focusing especially on the prodromal stage.

METHODS:

A total of 1221 CSF were collected in different memory centres (ePLM network) in France and analysed retrospectively. Samples were obtained from patients with prodromal DLB (pro-DLB; n=57), DLB dementia (DLB-d; n=154), prodromal AD (pro-AD; n=132) and AD dementia (n=783), and control subjects (CS; n=95). These centres use the same diagnostic procedure and criteria to evaluate the patients.

RESULTS:

In patients with pro-DLB, CSF Aß42 levels appeared much less disrupted than in patients at the demented stage (DLB-d) (P<0.05 CS>pro-DLB; P<0.001 CS>DLB-d). On average, Aß40 levels in patients with DLB (pro-DLB and DLB-d) were much below those in patients with pro-AD (P<0.001 DLB groupspatients with pro-DLB remained close to that of CS. t-Tau and phospho-Tau181 levels were unaltered in patients with DLB (pro-DLB and DLB-d).

CONCLUSIONS:

Reduced levels of CSF Aß42 were found in patients with DLB but rather at a later stage, reaching those of patients with AD, in whom Aß42 levels were decreased even at the prodromal stage. At the prodromal stage of DLB, the majority of patients presented a normal CSF profile. CSF t-Tau and phospho-Tau181 were the best biomarkers to discriminate between AD and DLB, whatever the stage of disease.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença por Corpos de Lewy / Doença de Alzheimer / Sintomas Prodrômicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença por Corpos de Lewy / Doença de Alzheimer / Sintomas Prodrômicos Idioma: En Ano de publicação: 2018 Tipo de documento: Article País de afiliação: França