Cargando…

MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease

Clinical diagnosis of Alzheimer’s disease (AD) prior to the age of 65 years is classified as young-onset (YOAD), whereas diagnosis after the age of 65 years is considered late-onset (LOAD). Although rare autosomal mutations more commonly associate with YOAD, most YOAD and LOAD cases are sporadic. YO...

Descripción completa

Detalles Bibliográficos
Autores principales: McKeever, Paul M., Schneider, Raphael, Taghdiri, Foad, Weichert, Anna, Multani, Namita, Brown, Robert A., Boxer, Adam L., Karydas, Anna, Miller, Bruce, Robertson, Janice, Tartaglia, Maria Carmela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208843/
https://www.ncbi.nlm.nih.gov/pubmed/29603092
http://dx.doi.org/10.1007/s12035-018-1032-x
_version_ 1783366790387073024
author McKeever, Paul M.
Schneider, Raphael
Taghdiri, Foad
Weichert, Anna
Multani, Namita
Brown, Robert A.
Boxer, Adam L.
Karydas, Anna
Miller, Bruce
Robertson, Janice
Tartaglia, Maria Carmela
author_facet McKeever, Paul M.
Schneider, Raphael
Taghdiri, Foad
Weichert, Anna
Multani, Namita
Brown, Robert A.
Boxer, Adam L.
Karydas, Anna
Miller, Bruce
Robertson, Janice
Tartaglia, Maria Carmela
author_sort McKeever, Paul M.
collection PubMed
description Clinical diagnosis of Alzheimer’s disease (AD) prior to the age of 65 years is classified as young-onset (YOAD), whereas diagnosis after the age of 65 years is considered late-onset (LOAD). Although rare autosomal mutations more commonly associate with YOAD, most YOAD and LOAD cases are sporadic. YOAD and LOAD share amyloid and tau pathology, but many YOAD patients show increased disease severity and rate of progression. The current study examined the microRNA (miRNA) expression profile from exosomes isolated from the cerebrospinal fluid (CSF) of YOAD patients with biomarker-confirmed AD. Results uncovered miR-16-5p, miR-125b-5p, miR-451a, and miR-605-5p as differentially expressed in the CSF-derived exosomes of YOAD patients when compared with healthy controls (HC). In a cohort of LOAD patients, miR-125b-5p, miR-451a, and miR-605-5p were similarly altered in expression, but miR-16-5p showed similar expression to control. Analysis of the mRNA targets of these miRNAs revealed transcripts enriched in biological processes relevant to the post-mortem posterior cingulate cortex transcriptome in YOAD from a previously published microarray study, including those related to neuron projections, synaptic signaling, metabolism, apoptosis, and the immune system. Hence, these miRNAs represent novel targets for uncovering disease mechanisms and for biomarker development in both YOAD and LOAD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-018-1032-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6208843
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-62088432018-11-09 MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease McKeever, Paul M. Schneider, Raphael Taghdiri, Foad Weichert, Anna Multani, Namita Brown, Robert A. Boxer, Adam L. Karydas, Anna Miller, Bruce Robertson, Janice Tartaglia, Maria Carmela Mol Neurobiol Article Clinical diagnosis of Alzheimer’s disease (AD) prior to the age of 65 years is classified as young-onset (YOAD), whereas diagnosis after the age of 65 years is considered late-onset (LOAD). Although rare autosomal mutations more commonly associate with YOAD, most YOAD and LOAD cases are sporadic. YOAD and LOAD share amyloid and tau pathology, but many YOAD patients show increased disease severity and rate of progression. The current study examined the microRNA (miRNA) expression profile from exosomes isolated from the cerebrospinal fluid (CSF) of YOAD patients with biomarker-confirmed AD. Results uncovered miR-16-5p, miR-125b-5p, miR-451a, and miR-605-5p as differentially expressed in the CSF-derived exosomes of YOAD patients when compared with healthy controls (HC). In a cohort of LOAD patients, miR-125b-5p, miR-451a, and miR-605-5p were similarly altered in expression, but miR-16-5p showed similar expression to control. Analysis of the mRNA targets of these miRNAs revealed transcripts enriched in biological processes relevant to the post-mortem posterior cingulate cortex transcriptome in YOAD from a previously published microarray study, including those related to neuron projections, synaptic signaling, metabolism, apoptosis, and the immune system. Hence, these miRNAs represent novel targets for uncovering disease mechanisms and for biomarker development in both YOAD and LOAD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-018-1032-x) contains supplementary material, which is available to authorized users. Springer US 2018-03-30 2018 /pmc/articles/PMC6208843/ /pubmed/29603092 http://dx.doi.org/10.1007/s12035-018-1032-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
McKeever, Paul M.
Schneider, Raphael
Taghdiri, Foad
Weichert, Anna
Multani, Namita
Brown, Robert A.
Boxer, Adam L.
Karydas, Anna
Miller, Bruce
Robertson, Janice
Tartaglia, Maria Carmela
MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title_full MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title_fullStr MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title_full_unstemmed MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title_short MicroRNA Expression Levels Are Altered in the Cerebrospinal Fluid of Patients with Young-Onset Alzheimer’s Disease
title_sort microrna expression levels are altered in the cerebrospinal fluid of patients with young-onset alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6208843/
https://www.ncbi.nlm.nih.gov/pubmed/29603092
http://dx.doi.org/10.1007/s12035-018-1032-x
work_keys_str_mv AT mckeeverpaulm micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT schneiderraphael micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT taghdirifoad micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT weichertanna micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT multaninamita micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT brownroberta micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT boxeradaml micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT karydasanna micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT millerbruce micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT robertsonjanice micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease
AT tartagliamariacarmela micrornaexpressionlevelsarealteredinthecerebrospinalfluidofpatientswithyoungonsetalzheimersdisease