Cited by 32Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research

Assessment of plasma and cerebrospinal fluid biomarkers in different stages of Alzheimer's disease and frontotemporal dementia

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Álvarez-Sánchez, Lourdes, Peña-Bautista, Carmen, Ferré-González, Laura, Balaguer, Angel, Baquero, Miguel, Casanova-Estruch, Bonaventura, Cháfer-Pericás, Consuelo·2023·International Journal of Molecular Sciences

Abstract

Alzheimer’s disease (AD) is the primary type of dementia, followed by frontotemporal lobar degeneration (FTLD). They share some clinical characteristics, mainly at the early stages. So, the identification of early, specific, and minimally invasive biomarkers is required. In this study, some plasma biomarkers (Amyloid β42, p-Tau181, t-Tau, neurofilament light (NfL), TAR DNA-binding protein 43 (TDP-43)) were determined by single molecule array technology (SIMOA®) in control subjects (n = 22), mild cognitive impairment due to AD (MCI-AD, n = 33), mild dementia due to AD (n = 12), and FTLD (n = 11) patients. The correlations between plasma and cerebrospinal fluid (CSF) levels and the accuracy of plasma biomarkers for AD early diagnosis and discriminating from FTLD were analyzed. As result, plasma p-Tau181 and NfL levels correlated with the corresponding CSF levels. Additionally, plasma p-Tau181 showed good accuracy for distinguishing between the controls and AD, as well as discriminating between AD and FTLD. Moreover, plasma NfL could discriminate dementia-AD vs. controls, FTLD vs. controls, and MCI-AD vs. dementia-AD. Therefore, the determination of these biomarkers in plasma is potentially helpful in AD spectrum diagnosis, but also discriminating from FTLD. In addition, the accessibility of these potential early and specific biomarkers may be useful for AD screening protocols in the future.

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  • Previous studies have evaluated protein correlations between plasma and CSF biomarkers of AD.

    “Previous studies have evaluated protein correlations between plasma and CSF biomarkers of AD. 37 , 38 , 39 , 40 , 41 , 42 , 43”
  • Previous studies found plasma NfL correlated relatively strongly with CSF NfL levels (r = 0.64-0.86; sample size 78-188).

    “including some that found plasma NfL correlated relatively strongly with CSF NfL levels (r = 0.64‐0.86; sample size 78‐188), 38 , 40 , 43”

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Cited by

Sorted by citations

Authors
Álvarez-Sánchez, L., Peña-Bautista, C., Ferré-González, L., Balaguer, A., Baquero, M., Casanova-Estruch, B., & Cháfer-Pericás, C.
Affiliations
  • Alzheimer Disease Research Group, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain
  • Faculty of Mathematical Sciences, University of Valencia, 46100 Burjassot-Valencia, Spain
  • Hospital Universitari i Politècnic La Fe (ES)
Venue
International Journal of Molecular Sciences
Publisher
MDPI AG
Published
2023-01-08
Volume
24
Issue
2
Pages
1226
ISSN
1422-0067 (ISSN-L)
OpenAlex
W4313895196
Cited by
32
References
9
Citations by year
2026: 8 · 2025: 6 · 2024: 15 · 2023: 3
FWCI
6.49
Type
journal article
Language
en
Open access
Locations
  • International Journal of Molecular Sciences (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • Instituto de Salud Carlos III (PI19/00570)
  • European Regional Development Fund (PI19/00570)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
Keywords
Alzheimer's disease, frontotemporal lobar degeneration, plasma biomarkers, cerebrospinal fluid biomarkers, phosphorylated tau 181, neurofilament light chain, amyloid-beta 42, total tau, TDP-43, mild cognitive impairment, early diagnosis, differential diagnosis, single molecule array
MeSH terms
Alzheimer Disease, Humans, Biomarkers, Amyloid beta-Peptides, tau Proteins, Pick Disease of the Brain, Frontotemporal Lobar Degeneration, Frontotemporal Dementia

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