Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.

The diagnostic of Amyotrophic lateral sclerosis (ALS) remains based on clinical and neurophysiological observations. The actual delay between the onset of the symptoms and diagnosis is about 1 year, preventing early inclusion of patients into clinical trials and early care of the disease. Therefore,...

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Autores principales: Laurence Conraux, Catherine Pech, Halim Guerraoui, Denis Loyaux, Pascual Ferrara, Jean-Claude Guillemot, Vincent Meininger, Pierre-François Pradat, François Salachas, Gaëlle Bruneteau, Nadine Le Forestier, Lucette Lacomblez
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:9a2d498492274d5393a990430a9c586a2021-11-18T08:48:16ZPlasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.1932-620310.1371/journal.pone.0079733https://doaj.org/article/9a2d498492274d5393a990430a9c586a2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24224000/?tool=EBIhttps://doaj.org/toc/1932-6203The diagnostic of Amyotrophic lateral sclerosis (ALS) remains based on clinical and neurophysiological observations. The actual delay between the onset of the symptoms and diagnosis is about 1 year, preventing early inclusion of patients into clinical trials and early care of the disease. Therefore, finding biomarkers with high sensitivity and specificity remains urgent. In our study, we looked for peptide biomarkers in plasma samples using reverse phase magnetic beads (C18 and C8) and MALDI-TOF mass spectrometry analysis. From a set of ALS patients (n=30) and healthy age-matched controls (n=30), C18- or C8-SVM-based models for ALS diagnostic were constructed on the base of the minimum of the most discriminant peaks. These two SVM-based models end up in excellent separations between the 2 groups of patients (recognition capability overall classes > 97%) and classify blinded samples (10 ALS and 10 healthy age-matched controls) with very high sensitivities and specificities (>90%). Some of these discriminant peaks have been identified by Mass Spectrometry (MS) analyses and correspond to (or are fragments of) major plasma proteins, partly linked to the blood coagulation.Laurence ConrauxCatherine PechHalim GuerraouiDenis LoyauxPascual FerraraJean-Claude GuillemotVincent MeiningerPierre-François PradatFrançois SalachasGaëlle BruneteauNadine Le ForestierLucette LacomblezPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 11, p e79733 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Laurence Conraux
Catherine Pech
Halim Guerraoui
Denis Loyaux
Pascual Ferrara
Jean-Claude Guillemot
Vincent Meininger
Pierre-François Pradat
François Salachas
Gaëlle Bruneteau
Nadine Le Forestier
Lucette Lacomblez
Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
description The diagnostic of Amyotrophic lateral sclerosis (ALS) remains based on clinical and neurophysiological observations. The actual delay between the onset of the symptoms and diagnosis is about 1 year, preventing early inclusion of patients into clinical trials and early care of the disease. Therefore, finding biomarkers with high sensitivity and specificity remains urgent. In our study, we looked for peptide biomarkers in plasma samples using reverse phase magnetic beads (C18 and C8) and MALDI-TOF mass spectrometry analysis. From a set of ALS patients (n=30) and healthy age-matched controls (n=30), C18- or C8-SVM-based models for ALS diagnostic were constructed on the base of the minimum of the most discriminant peaks. These two SVM-based models end up in excellent separations between the 2 groups of patients (recognition capability overall classes > 97%) and classify blinded samples (10 ALS and 10 healthy age-matched controls) with very high sensitivities and specificities (>90%). Some of these discriminant peaks have been identified by Mass Spectrometry (MS) analyses and correspond to (or are fragments of) major plasma proteins, partly linked to the blood coagulation.
format article
author Laurence Conraux
Catherine Pech
Halim Guerraoui
Denis Loyaux
Pascual Ferrara
Jean-Claude Guillemot
Vincent Meininger
Pierre-François Pradat
François Salachas
Gaëlle Bruneteau
Nadine Le Forestier
Lucette Lacomblez
author_facet Laurence Conraux
Catherine Pech
Halim Guerraoui
Denis Loyaux
Pascual Ferrara
Jean-Claude Guillemot
Vincent Meininger
Pierre-François Pradat
François Salachas
Gaëlle Bruneteau
Nadine Le Forestier
Lucette Lacomblez
author_sort Laurence Conraux
title Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
title_short Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
title_full Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
title_fullStr Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
title_full_unstemmed Plasma peptide biomarker discovery for amyotrophic lateral sclerosis by MALDI-TOF mass spectrometry profiling.
title_sort plasma peptide biomarker discovery for amyotrophic lateral sclerosis by maldi-tof mass spectrometry profiling.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/9a2d498492274d5393a990430a9c586a
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