Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum

Neurofilament light chain (NfL) is a potential diagnostic and prognostic plasma biomarker for numerous neurological diseases including Alzheimer’s disease (AD). In this study, we investigated the relationship between baseline plasma concentration of Nfl and Mild Cognitive Impairment in participants...

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Main Authors: Sylvain Lehmann, Susanna Schraen-Maschke, Jean-Sébastien Vidal, Frédéric Blanc, Claire Paquet, Bernadette Allinquant, Stéphanie Bombois, Audrey Gabelle, Constance Delaby, Olivier Hanon
Format: Article
Language:English
Published: MDPI AG 2023-12-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/24/24/17361
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author Sylvain Lehmann
Susanna Schraen-Maschke
Jean-Sébastien Vidal
Frédéric Blanc
Claire Paquet
Bernadette Allinquant
Stéphanie Bombois
Audrey Gabelle
Constance Delaby
Olivier Hanon
author_facet Sylvain Lehmann
Susanna Schraen-Maschke
Jean-Sébastien Vidal
Frédéric Blanc
Claire Paquet
Bernadette Allinquant
Stéphanie Bombois
Audrey Gabelle
Constance Delaby
Olivier Hanon
author_sort Sylvain Lehmann
collection DOAJ
description Neurofilament light chain (NfL) is a potential diagnostic and prognostic plasma biomarker for numerous neurological diseases including Alzheimer’s disease (AD). In this study, we investigated the relationship between baseline plasma concentration of Nfl and Mild Cognitive Impairment in participants who did and did not have a clinically determined diagnosis of dementia by the end of the three-year study. Additionally, we explored the connection between baseline plasma concentration of NfL and AD dementia patients, considering their demographics, clinical features, and cognitive profiles. A total of 350 participants from the Biomarker of AmyLoid pepTide and AlZheimer’s diseAse Risk (BALTAZAR) multicenter prospective study were investigated: 161 AD dementia participants and 189 MCI participants (of which 141 had amnestic MCI and 48 non-amnestic MCI). Plasma biomarkers were measured at baseline and the progression of clinical and cognitive profiles was followed over the three years of follow-up. Baseline plasma NfL concentration increased across the Alzheimer’s disease continuum with a mean NfL value of 17.1 ng/mL [SD = 6.1] in non-amnestic MCI, 20.7 ng/mL [SD = 12.0] in amnestic MCI, and 23.1 ng/mL [SD = 22.7] in AD dementia patients. Plasma NfL concentration correlated with age, body mass index (BMI), and global cognitive performance and decline, as measured by the Mini-Mental State Examination (MMSE). MMSE scores decreased in parallel with increasing plasma NfL concentration, independently of age and BMI. However, NfL concentration did not predict MCI participants’ conversion to dementia within three years. Discussion: Baseline plasma NfL concentration is associated with cognitive status along the AD continuum, suggesting its usefulness as a potential informative biomarker for cognitive decline follow-up in patients.
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spelling doaj.art-4ce3401c0d724e1cb1267cc43c99cc662023-12-22T14:14:11ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-12-0124241736110.3390/ijms242417361Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease ContinuumSylvain Lehmann0Susanna Schraen-Maschke1Jean-Sébastien Vidal2Frédéric Blanc3Claire Paquet4Bernadette Allinquant5Stéphanie Bombois6Audrey Gabelle7Constance Delaby8Olivier Hanon9Laboratoire et Plateforme de Protéomique Clinique, Université de Montpellier, INM INSERM, IRMB CHU de Montpellier, 80 av Fliche, F-34295 Montpellier, FranceUniv. Lille, Inserm, CHU Lille, UMR-S-U1172, LiCEND, Lille Neuroscience & Cognition, LabEx DISTALZ, F-59000 Lille, FranceUniversité Paris Cité, INSERM U1144, GHU APHP Centre, Hopital Broca, Memory Resource and Research Centre de Paris-Broca-Ile de France, F-75013 Paris, FranceUniversité de Strasbourg, Hôpitaux Universitaires de Strasbourg, Memory Resource and Research, French National Centre for Scientific Research (CNRS), ICube Laboratory UMR7357 and Fédération de Médecine Translationnelle de Strasbourg (FMTS), Team Imagerie Multimodale Intégrative en Santé (IMIS), F-67000 Strasbourg, FranceUniversité Paris Cité, INSERM U1144, GHU APHP Nord Lariboisière Fernand Widal, Centre de Neurologie Cognitive, F-75010 Paris, FranceUniversité Paris Cité, Institute of Psychiatry and Neurosciences, Inserm, UMR-S 1266, F-75014 Paris, FranceUniv. Lille, Inserm, CHU Lille, UMR-S-U1172, LiCEND, Lille Neuroscience & Cognition, LabEx DISTALZ, F-59000 Lille, FranceUniversité de Montpellier, CHU Montpellier, Memory Research and Resources Center, Department of Neurology, Inserm INM NeuroPEPs Team, Excellence Center of Neurodegenerative Disorders, F-34000 Montpellier, FranceLaboratoire et Plateforme de Protéomique Clinique, Université de Montpellier, INM INSERM, IRMB CHU de Montpellier, 80 av Fliche, F-34295 Montpellier, FranceUniversité Paris Cité, INSERM U1144, GHU APHP Centre, Hopital Broca, Memory Resource and Research Centre de Paris-Broca-Ile de France, F-75013 Paris, FranceNeurofilament light chain (NfL) is a potential diagnostic and prognostic plasma biomarker for numerous neurological diseases including Alzheimer’s disease (AD). In this study, we investigated the relationship between baseline plasma concentration of Nfl and Mild Cognitive Impairment in participants who did and did not have a clinically determined diagnosis of dementia by the end of the three-year study. Additionally, we explored the connection between baseline plasma concentration of NfL and AD dementia patients, considering their demographics, clinical features, and cognitive profiles. A total of 350 participants from the Biomarker of AmyLoid pepTide and AlZheimer’s diseAse Risk (BALTAZAR) multicenter prospective study were investigated: 161 AD dementia participants and 189 MCI participants (of which 141 had amnestic MCI and 48 non-amnestic MCI). Plasma biomarkers were measured at baseline and the progression of clinical and cognitive profiles was followed over the three years of follow-up. Baseline plasma NfL concentration increased across the Alzheimer’s disease continuum with a mean NfL value of 17.1 ng/mL [SD = 6.1] in non-amnestic MCI, 20.7 ng/mL [SD = 12.0] in amnestic MCI, and 23.1 ng/mL [SD = 22.7] in AD dementia patients. Plasma NfL concentration correlated with age, body mass index (BMI), and global cognitive performance and decline, as measured by the Mini-Mental State Examination (MMSE). MMSE scores decreased in parallel with increasing plasma NfL concentration, independently of age and BMI. However, NfL concentration did not predict MCI participants’ conversion to dementia within three years. Discussion: Baseline plasma NfL concentration is associated with cognitive status along the AD continuum, suggesting its usefulness as a potential informative biomarker for cognitive decline follow-up in patients.https://www.mdpi.com/1422-0067/24/24/17361Alzheimer’s diseaseneurofilament light chainbloodcognitive decline
spellingShingle Sylvain Lehmann
Susanna Schraen-Maschke
Jean-Sébastien Vidal
Frédéric Blanc
Claire Paquet
Bernadette Allinquant
Stéphanie Bombois
Audrey Gabelle
Constance Delaby
Olivier Hanon
Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
International Journal of Molecular Sciences
Alzheimer’s disease
neurofilament light chain
blood
cognitive decline
title Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
title_full Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
title_fullStr Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
title_full_unstemmed Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
title_short Blood Neurofilament Levels Predict Cognitive Decline across the Alzheimer’s Disease Continuum
title_sort blood neurofilament levels predict cognitive decline across the alzheimer s disease continuum
topic Alzheimer’s disease
neurofilament light chain
blood
cognitive decline
url https://www.mdpi.com/1422-0067/24/24/17361
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