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Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders
There is a lack of effective diagnostic biomarkers for neurodegenerative disorders (NDDs). Here, we established gene expression profiles for diagnosing Alzheimer’s disease (AD), Parkinson’s disease (PD), and vascular (VaD)/mixed dementia. Patients with AD had decreased APOE, PSEN1, and ABCA7 mRNA ex...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057696/ https://www.ncbi.nlm.nih.gov/pubmed/36982820 http://dx.doi.org/10.3390/ijms24065746 |
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author | Martínez-Iglesias, Olaia Naidoo, Vinogran Carril, Juan Carlos Seoane, Silvia Cacabelos, Natalia Cacabelos, Ramón |
author_facet | Martínez-Iglesias, Olaia Naidoo, Vinogran Carril, Juan Carlos Seoane, Silvia Cacabelos, Natalia Cacabelos, Ramón |
author_sort | Martínez-Iglesias, Olaia |
collection | PubMed |
description | There is a lack of effective diagnostic biomarkers for neurodegenerative disorders (NDDs). Here, we established gene expression profiles for diagnosing Alzheimer’s disease (AD), Parkinson’s disease (PD), and vascular (VaD)/mixed dementia. Patients with AD had decreased APOE, PSEN1, and ABCA7 mRNA expression. Subjects with VaD/mixed dementia had 98% higher PICALM mRNA levels, but 75% lower ABCA7 mRNA expression than healthy individuals. Patients with PD and PD-related disorders showed increased SNCA mRNA levels. There were no differences in mRNA expression for OPRK1, NTRK2, and LRRK2 between healthy subjects and NDD patients. APOE mRNA expression had high diagnostic accuracy for AD, and moderate accuracy for PD and VaD/mixed dementia. PSEN1 mRNA expression showed promising accuracy for AD. PICALM mRNA expression was less accurate as a biomarker for AD. ABCA7 and SNCA mRNA expression showed high-to-excellent diagnostic accuracy for AD and PD, and moderate-to-high accuracy for VaD/mixed dementia. The APOE E4 allele reduced APOE expression in patients with different APOE genotypes. There was no association between PSEN1, PICALM, ABCA7, and SNCA gene polymorphisms and expression. Our study suggests that gene expression analysis has diagnostic value for NDDs and provides a liquid biopsy alternative to current diagnostic methods. |
format | Online Article Text |
id | pubmed-10057696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100576962023-03-30 Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders Martínez-Iglesias, Olaia Naidoo, Vinogran Carril, Juan Carlos Seoane, Silvia Cacabelos, Natalia Cacabelos, Ramón Int J Mol Sci Article There is a lack of effective diagnostic biomarkers for neurodegenerative disorders (NDDs). Here, we established gene expression profiles for diagnosing Alzheimer’s disease (AD), Parkinson’s disease (PD), and vascular (VaD)/mixed dementia. Patients with AD had decreased APOE, PSEN1, and ABCA7 mRNA expression. Subjects with VaD/mixed dementia had 98% higher PICALM mRNA levels, but 75% lower ABCA7 mRNA expression than healthy individuals. Patients with PD and PD-related disorders showed increased SNCA mRNA levels. There were no differences in mRNA expression for OPRK1, NTRK2, and LRRK2 between healthy subjects and NDD patients. APOE mRNA expression had high diagnostic accuracy for AD, and moderate accuracy for PD and VaD/mixed dementia. PSEN1 mRNA expression showed promising accuracy for AD. PICALM mRNA expression was less accurate as a biomarker for AD. ABCA7 and SNCA mRNA expression showed high-to-excellent diagnostic accuracy for AD and PD, and moderate-to-high accuracy for VaD/mixed dementia. The APOE E4 allele reduced APOE expression in patients with different APOE genotypes. There was no association between PSEN1, PICALM, ABCA7, and SNCA gene polymorphisms and expression. Our study suggests that gene expression analysis has diagnostic value for NDDs and provides a liquid biopsy alternative to current diagnostic methods. MDPI 2023-03-17 /pmc/articles/PMC10057696/ /pubmed/36982820 http://dx.doi.org/10.3390/ijms24065746 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Martínez-Iglesias, Olaia Naidoo, Vinogran Carril, Juan Carlos Seoane, Silvia Cacabelos, Natalia Cacabelos, Ramón Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title | Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title_full | Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title_fullStr | Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title_full_unstemmed | Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title_short | Gene Expression Profiling as a Novel Diagnostic Tool for Neurodegenerative Disorders |
title_sort | gene expression profiling as a novel diagnostic tool for neurodegenerative disorders |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10057696/ https://www.ncbi.nlm.nih.gov/pubmed/36982820 http://dx.doi.org/10.3390/ijms24065746 |
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