Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis

Background: Differential diagnosis of Alzheimer’s disease (AD) is a complex task due to the clinical similarity among neurodegenerative diseases. Previous studies showed the role of lipid peroxidation in early AD development. However, the clinical validation of potential specific biomarkers in minim...

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Main Authors: Carmen Peña-Bautista, Lourdes Álvarez, Thierry Durand, Claire Vigor, Ana Cuevas, Miguel Baquero, Máximo Vento, David Hervás, Consuelo Cháfer-Pericás
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Antioxidants
Subjects:
Online Access:https://www.mdpi.com/2076-3921/9/8/649
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author Carmen Peña-Bautista
Lourdes Álvarez
Thierry Durand
Claire Vigor
Ana Cuevas
Miguel Baquero
Máximo Vento
David Hervás
Consuelo Cháfer-Pericás
author_facet Carmen Peña-Bautista
Lourdes Álvarez
Thierry Durand
Claire Vigor
Ana Cuevas
Miguel Baquero
Máximo Vento
David Hervás
Consuelo Cháfer-Pericás
author_sort Carmen Peña-Bautista
collection DOAJ
description Background: Differential diagnosis of Alzheimer’s disease (AD) is a complex task due to the clinical similarity among neurodegenerative diseases. Previous studies showed the role of lipid peroxidation in early AD development. However, the clinical validation of potential specific biomarkers in minimally invasive samples constitutes a great challenge in early AD diagnosis. Methods: Plasma samples from participants classified into AD (<i>n</i> = 138), non-AD (including MCI and other dementias not due to AD) (<i>n</i> = 70) and healthy (<i>n</i> = 50) were analysed. Lipid peroxidation compounds (isoprostanes, isofurans, neuroprostanes, neurofurans) were determined by ultra-performance liquid chromatography coupled with tandem mass spectrometry. Statistical analysis for biomarkers’ clinical validation was based on Elastic Net. Results: A two-step diagnosis model was developed from plasma lipid peroxidation products to diagnose early AD specifically, and a bootstrap validated AUC of 0.74 was obtained. Conclusion: A promising AD differential diagnosis model was developed. It was clinically validated as a screening test. However, further external validation is required before clinical application.
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spelling doaj.art-1ad5dcae42c949e9a6801d9ead7455152023-11-20T07:35:10ZengMDPI AGAntioxidants2076-39212020-07-019864910.3390/antiox9080649Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential DiagnosisCarmen Peña-Bautista0Lourdes Álvarez1Thierry Durand2Claire Vigor3Ana Cuevas4Miguel Baquero5Máximo Vento6David Hervás7Consuelo Cháfer-Pericás8Neonatal Research Unit, Health Research Institute La Fe, 46026 Valencia, SpainNeurology Unit, University and Polytechnic Hospital La Fe, 46026 Valencia, SpainInstitut des Biomolécules Max Mousseron, IBMM, University of Montpellier, CNRS ENSCM, 34093 Montpellier, FranceInstitut des Biomolécules Max Mousseron, IBMM, University of Montpellier, CNRS ENSCM, 34093 Montpellier, FranceNeurology Unit, University and Polytechnic Hospital La Fe, 46026 Valencia, SpainNeurology Unit, University and Polytechnic Hospital La Fe, 46026 Valencia, SpainNeonatal Research Unit, Health Research Institute La Fe, 46026 Valencia, SpainBiostatistical Unit, Health Research Institute La Fe, 46026 Valencia, SpainNeonatal Research Unit, Health Research Institute La Fe, 46026 Valencia, SpainBackground: Differential diagnosis of Alzheimer’s disease (AD) is a complex task due to the clinical similarity among neurodegenerative diseases. Previous studies showed the role of lipid peroxidation in early AD development. However, the clinical validation of potential specific biomarkers in minimally invasive samples constitutes a great challenge in early AD diagnosis. Methods: Plasma samples from participants classified into AD (<i>n</i> = 138), non-AD (including MCI and other dementias not due to AD) (<i>n</i> = 70) and healthy (<i>n</i> = 50) were analysed. Lipid peroxidation compounds (isoprostanes, isofurans, neuroprostanes, neurofurans) were determined by ultra-performance liquid chromatography coupled with tandem mass spectrometry. Statistical analysis for biomarkers’ clinical validation was based on Elastic Net. Results: A two-step diagnosis model was developed from plasma lipid peroxidation products to diagnose early AD specifically, and a bootstrap validated AUC of 0.74 was obtained. Conclusion: A promising AD differential diagnosis model was developed. It was clinically validated as a screening test. However, further external validation is required before clinical application.https://www.mdpi.com/2076-3921/9/8/649plasmalipid peroxidationAlzheimer’s diseasedifferential diagnosisclinical validation
spellingShingle Carmen Peña-Bautista
Lourdes Álvarez
Thierry Durand
Claire Vigor
Ana Cuevas
Miguel Baquero
Máximo Vento
David Hervás
Consuelo Cháfer-Pericás
Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
Antioxidants
plasma
lipid peroxidation
Alzheimer’s disease
differential diagnosis
clinical validation
title Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
title_full Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
title_fullStr Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
title_full_unstemmed Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
title_short Clinical Utility of Plasma Lipid Peroxidation Biomarkers in Alzheimer’s Disease Differential Diagnosis
title_sort clinical utility of plasma lipid peroxidation biomarkers in alzheimer s disease differential diagnosis
topic plasma
lipid peroxidation
Alzheimer’s disease
differential diagnosis
clinical validation
url https://www.mdpi.com/2076-3921/9/8/649
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