Plasma amyloid levels within the Alzheimer's process and correlations with central biomarkers

Olivier Hanon(Délégation Paris 5), Jean‐Sébastien Vidal(Délégation Paris 5), Sylvain Lehmann(Inserm), Stéphanie Bombois(Inserm), Bernadette Allinquant(Délégation Paris 5), Jean‐Marc Tréluyer(Hôpital Necker-Enfants Malades), Patrick Gelé(Inserm), Christine Delmaire(Inserm), Frédéric Blanc(Centre National de la Recherche Scientifique), Jean‐François Mangin(Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Luc Buée(Inserm), Jacques Touchon(Université de Montpellier), Jacques Hugon(Délégation Paris 7), Bruno Vellas, Evelyne Galbrun(Centre hospitalier Emile Roux), Athanase Bénétos(Centre Hospitalier Régional et Universitaire de Nancy), Gilles Berrut(Centre Hospitalier Universitaire de Nantes), Éléna Paillaud(Hôpitaux Universitaires Henri-Mondor), David Wallon(Inserm), Giovanni Castelnovo(Centre Hospitalier Universitaire de Nîmes), Lisette Volpe‐Gillot, Marc Paccalin(Centre de Recherches Interdisciplinaires en Histoire, Histoire de l'Art et Musicologie), P.H. Robert(Centre Hospitalier Universitaire de Nice), Olivier Godefroy(Centre Hospitalier Universitaire Amiens-Picardie), Thierry Dantoine(Centre Hospitalier Universitaire de Limoges), Vincent Camus(Université de Tours), Joël Belmin(Université Paris Cité), Pierre Vandel(Centre Hospitalier Universitaire de Tours), Jean‐Luc Novella(Conseil Régional de Champagne-Ardenne), Emmanuelle Duron(Délégation Paris 5), Anne‐Sophie Rigaud(Délégation Paris 5), Susanna Schraen‐Maschke(Inserm), Audrey Gabelle(Université de Montpellier), on behalf of the BALTAZAR study group
Alzheimer s & Dementia
February 16, 2018
Cited by 130Open Access
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Abstract

Abstract Introduction Diagnostic relevance of plasma amyloid β (Aβ) for Alzheimer's disease (AD) process yields conflicting results. The objective of the study was to assess plasma levels of Aβ 42 and Aβ 40 in amnestic mild cognitive impairment (MCI), nonamnestic MCI, and AD patients and to investigate relationships between peripheral and central biomarkers. Methods One thousand forty participants (417 amnestic MCI, 122 nonamnestic MCI, and 501 AD) from the Biomarker of AmyLoïd pepTide and AlZheimer's diseAse Risk multicenter prospective study with cognition, plasma, cerebrospinal fluid (CSF), and magnetic resonance imaging assessments were included. Results Plasma Aβ 1–42 and Aβ 1–40 were lower in AD (36.9 [11.7] and 263 [80] pg/mL) than in amnestic MCI (38.2 [11.9] and 269 [68] pg/mL) than in nonamnestic MCI (39.7 [10.5] and 272 [52] pg/mL), respectively ( P = .01 for overall difference between groups for Aβ 1–42 and P = .04 for Aβ 1–40 ). Globally, plasma Aβ 1–42 correlated with age, Mini–Mental State Examination, and APOE ε4 allele. Plasma Aβ 1–42 correlated with all CSF biomarkers in MCI but only with CSF Aβ 42 in AD. Discussion Plasma Aβ was associated with cognitive status and CSF biomarkers, suggesting the interest of plasma amyloid biomarkers for diagnosis purpose.


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