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Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing
The lack of accessible noninvasive tools to examine the molecular alterations occurring in the brain limits our understanding of the causes and progression of Alzheimer’s disease (AD), as well as the identification of effective therapeutic strategies. Here, we conducted a comprehensive profiling of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821903/ https://www.ncbi.nlm.nih.gov/pubmed/33298436 http://dx.doi.org/10.1126/sciadv.abb1654 |
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author | Toden, Shusuke Zhuang, Jiali Acosta, Alexander D. Karns, Amy P. Salathia, Neeraj S. Brewer, James B. Wilcock, Donna M. Aballi, Jonathan Nerenberg, Mike Quake, Stephen R. Ibarra, Arkaitz |
author_facet | Toden, Shusuke Zhuang, Jiali Acosta, Alexander D. Karns, Amy P. Salathia, Neeraj S. Brewer, James B. Wilcock, Donna M. Aballi, Jonathan Nerenberg, Mike Quake, Stephen R. Ibarra, Arkaitz |
author_sort | Toden, Shusuke |
collection | PubMed |
description | The lack of accessible noninvasive tools to examine the molecular alterations occurring in the brain limits our understanding of the causes and progression of Alzheimer’s disease (AD), as well as the identification of effective therapeutic strategies. Here, we conducted a comprehensive profiling of circulating, cell-free messenger RNA (cf-mRNA) in plasma of 126 patients with AD and 116 healthy controls of similar age. We identified 2591 dysregulated genes in the cf-mRNA of patients with AD, which are enriched in biological processes well known to be associated with AD. Dysregulated genes included brain-specific genes and resembled those identified to be dysregulated in postmortem AD brain tissue. Furthermore, we identified disease-relevant circulating gene transcripts that correlated with the severity of cognitive impairment. These data highlight the potential of high-throughput cf-mRNA sequencing to evaluate AD-related pathophysiological alterations in the brain, leading to precision healthcare solutions that could improve AD patient management. |
format | Online Article Text |
id | pubmed-7821903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78219032021-01-29 Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing Toden, Shusuke Zhuang, Jiali Acosta, Alexander D. Karns, Amy P. Salathia, Neeraj S. Brewer, James B. Wilcock, Donna M. Aballi, Jonathan Nerenberg, Mike Quake, Stephen R. Ibarra, Arkaitz Sci Adv Research Articles The lack of accessible noninvasive tools to examine the molecular alterations occurring in the brain limits our understanding of the causes and progression of Alzheimer’s disease (AD), as well as the identification of effective therapeutic strategies. Here, we conducted a comprehensive profiling of circulating, cell-free messenger RNA (cf-mRNA) in plasma of 126 patients with AD and 116 healthy controls of similar age. We identified 2591 dysregulated genes in the cf-mRNA of patients with AD, which are enriched in biological processes well known to be associated with AD. Dysregulated genes included brain-specific genes and resembled those identified to be dysregulated in postmortem AD brain tissue. Furthermore, we identified disease-relevant circulating gene transcripts that correlated with the severity of cognitive impairment. These data highlight the potential of high-throughput cf-mRNA sequencing to evaluate AD-related pathophysiological alterations in the brain, leading to precision healthcare solutions that could improve AD patient management. American Association for the Advancement of Science 2020-12-09 /pmc/articles/PMC7821903/ /pubmed/33298436 http://dx.doi.org/10.1126/sciadv.abb1654 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Toden, Shusuke Zhuang, Jiali Acosta, Alexander D. Karns, Amy P. Salathia, Neeraj S. Brewer, James B. Wilcock, Donna M. Aballi, Jonathan Nerenberg, Mike Quake, Stephen R. Ibarra, Arkaitz Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title | Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title_full | Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title_fullStr | Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title_full_unstemmed | Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title_short | Noninvasive characterization of Alzheimer’s disease by circulating, cell-free messenger RNA next-generation sequencing |
title_sort | noninvasive characterization of alzheimer’s disease by circulating, cell-free messenger rna next-generation sequencing |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821903/ https://www.ncbi.nlm.nih.gov/pubmed/33298436 http://dx.doi.org/10.1126/sciadv.abb1654 |
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