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Cerebrospinal fluid amyloid-ß 42/40 ratio in clinical setting of memory centers: a multicentric study.
Dumurgier, Julien; Schraen, Susanna; Gabelle, Audrey; Vercruysse, Olivier; Bombois, Stéphanie; Laplanche, Jean-Louis; Peoc'h, Katell; Sablonnière, Bernard; Kastanenka, Ksenia V; Delaby, Constance; Pasquier, Florence; Touchon, Jacques; Hugon, Jacques; Paquet, Claire; Lehmann, Sylvain.
Affiliation
  • Dumurgier J; Centre Mémoire Ressources Recherche (CM2R), Paris Nord Ile-de-France, Saint Louis, Lariboisière, Fernand-Widal Hospital, AP-HP, 200 rue du Faubourg Saint-Denis, 75010 Paris, France ; INSERM U942, Biomarkers in CardioNeuroVascular diseases (Bio-CANVAS), University of Paris 7-Denis Diderot, Paris, Fra
  • Schraen S; Inserm, UMR 1172, JPArc, Faculté de Médecine, Université de Lille, 59045 Lille, France ; Centre de Biologie-Pathologie, Centre Hospitalier Régional Universitaire, 59037 Lille, France.
  • Gabelle A; Centre Mémoire Ressources Recherche de Montpellier, Université de Montpellier, Montpellier, France ; Biochimie-Protéomique Clinique - IRB - CCBHM, INSERM U1040, Université de Montpellier, Montpellier, France.
  • Vercruysse O; Centre Mémoire Ressources Recherche, EA 1046, Centre Hospitalier Régional Universitaire de Lille, Lille, France.
  • Bombois S; Centre Mémoire Ressources Recherche, EA 1046, Centre Hospitalier Régional Universitaire de Lille, Lille, France.
  • Laplanche JL; Service de Biochimie et Biologie Moléculaire, Hôpitaux universitaires Saint-Louis, Lariboisière, Fernand-Widal, Assistance Publique-Hôpitaux de Paris (AP-HP), PRES Sorbonne Paris Cité, Paris, France.
  • Peoc'h K; Service de Biochimie et Biologie Moléculaire, Hôpitaux universitaires Saint-Louis, Lariboisière, Fernand-Widal, Assistance Publique-Hôpitaux de Paris (AP-HP), PRES Sorbonne Paris Cité, Paris, France.
  • Sablonnière B; Inserm, UMR 1172, JPArc, Faculté de Médecine, Université de Lille, 59045 Lille, France ; Centre de Biologie-Pathologie, Centre Hospitalier Régional Universitaire, 59037 Lille, France.
  • Kastanenka KV; Department of Neurology, MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA 02129 USA.
  • Delaby C; Biochimie-Protéomique Clinique - IRB - CCBHM, INSERM U1040, Université de Montpellier, Montpellier, France.
  • Pasquier F; Centre Mémoire Ressources Recherche, EA 1046, Centre Hospitalier Régional Universitaire de Lille, Lille, France.
  • Touchon J; Centre Mémoire Ressources Recherche de Montpellier, Université de Montpellier, Montpellier, France.
  • Hugon J; Centre Mémoire Ressources Recherche (CM2R), Paris Nord Ile-de-France, Saint Louis, Lariboisière, Fernand-Widal Hospital, AP-HP, 200 rue du Faubourg Saint-Denis, 75010 Paris, France ; INSERM U942, Biomarkers in CardioNeuroVascular diseases (Bio-CANVAS), University of Paris 7-Denis Diderot, Paris, Fra
  • Paquet C; Centre Mémoire Ressources Recherche (CM2R), Paris Nord Ile-de-France, Saint Louis, Lariboisière, Fernand-Widal Hospital, AP-HP, 200 rue du Faubourg Saint-Denis, 75010 Paris, France ; INSERM U942, Biomarkers in CardioNeuroVascular diseases (Bio-CANVAS), University of Paris 7-Denis Diderot, Paris, Fra
  • Lehmann S; Biochimie-Protéomique Clinique - IRB - CCBHM, INSERM U1040, Université de Montpellier, Montpellier, France.
Alzheimers Res Ther ; 7(1): 30, 2015.
Article in En | MEDLINE | ID: mdl-26034513
ABSTRACT

INTRODUCTION:

The cerebrospinal fluid (CSF) biomarkers amyloid-ß (Aß), tau and phosphorylated tau (p-tau181) are now used for the diagnosis of Alzheimer's disease (AD). Aß40 is the most abundant Aß peptide isoform in the CSF, and the Aß 42/40 ratio has been proposed to better reflect brain amyloid production. However, its additional value in the clinical setting remains uncertain.

METHODS:

A total of 367 subjects with cognitive disorders who underwent a lumbar puncture were prospectively included at three French memory centers (Paris-North, Lille and Montpellier; the PLM Study). The frequency of positive, negative and indeterminate CSF profiles were assessed by various methods, and their adequacies with the diagnosis of clinicians were tested using net reclassification improvement (NRI) analyses.

RESULTS:

On the basis of local optimum cutoffs for Aß42 and p-tau181, 22% of the explored patients had indeterminate CSF profiles. The systematic use of Aß 42/40 ratio instead of Aß42 levels alone decreased the number of indeterminate profiles (17%; P = 0.03), but it failed to improve the classification of subjects (NRI = -2.1%; P = 0.64). In contrast, the use of Aß 42/40 ratio instead of Aß42 levels alone in patients with a discrepancy between p-tau181 and Aß42 led to a reduction by half of the number of indeterminate profiles (10%; P < 0.001) and was further in agreement with clinician diagnosis (NRI = 10.5%; P = 0.003).

CONCLUSIONS:

In patients with a discrepancy between CSF p-tau181 and CSF Aß42, the assessment of Aß 42/40 ratio led to a reliable biological conclusion in over 50% of cases that agreed with a clinician's diagnosis.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Alzheimers Res Ther Year: 2015 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: Alzheimers Res Ther Year: 2015 Document type: Article