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A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types

BACKGROUND: Circular RNAs (circRNAs) have been demonstrated to be associated with Alzheimer’s disease (AD). Here, we conducted a study to explore whether circRNAs have the ability to differentiate AD from cognitively normal controls and other types of dementia, such as vascular dementia (VaD), Parki...

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Autores principales: Ren, Ziye, Chu, Changbiao, Pang, Yana, Cai, Huimin, Jia, Longfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389828/
https://www.ncbi.nlm.nih.gov/pubmed/35982472
http://dx.doi.org/10.1186/s40364-022-00405-0
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author Ren, Ziye
Chu, Changbiao
Pang, Yana
Cai, Huimin
Jia, Longfei
author_facet Ren, Ziye
Chu, Changbiao
Pang, Yana
Cai, Huimin
Jia, Longfei
author_sort Ren, Ziye
collection PubMed
description BACKGROUND: Circular RNAs (circRNAs) have been demonstrated to be associated with Alzheimer’s disease (AD). Here, we conducted a study to explore whether circRNAs have the ability to differentiate AD from cognitively normal controls and other types of dementia, such as vascular dementia (VaD), Parkinson’s disease dementia (PDD), behavioral variant frontotemporal dementia (bvFTD), and dementia with Lewy body (DLB). METHODS: Three datasets were included in this study to measure blood circRNAs. The pilot study (Dataset 1, n = 40; controls, 20; AD, 20) was used to screen differentially expressed circRNAs. Dataset 2 (n = 124; controls, 61; AD, 63) was recruited for the establishment of the diagnostic model using a circRNA panel. Further, the Dataset 3 (n = 321; control, 58; AD, 60; VaD, 50; PDD, 51; bvFTD, 52; DLB, 50) was used to verify the diagnostic model. RESULTS: In Dataset 1, 22 upregulated and 19 downregulated circRNAs were revealed. In Dataset 2, a six-circRNA panel was found to be able to distinguish patients with AD from controls. Then this panel was applied to Dataset 3 and successfully differentiated AD from other types of dementia. CONCLUSION: This study suggested that a six-circRNA panel is AD-specific and a promising biomarker of AD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-022-00405-0.
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spelling pubmed-93898282022-08-20 A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types Ren, Ziye Chu, Changbiao Pang, Yana Cai, Huimin Jia, Longfei Biomark Res Research BACKGROUND: Circular RNAs (circRNAs) have been demonstrated to be associated with Alzheimer’s disease (AD). Here, we conducted a study to explore whether circRNAs have the ability to differentiate AD from cognitively normal controls and other types of dementia, such as vascular dementia (VaD), Parkinson’s disease dementia (PDD), behavioral variant frontotemporal dementia (bvFTD), and dementia with Lewy body (DLB). METHODS: Three datasets were included in this study to measure blood circRNAs. The pilot study (Dataset 1, n = 40; controls, 20; AD, 20) was used to screen differentially expressed circRNAs. Dataset 2 (n = 124; controls, 61; AD, 63) was recruited for the establishment of the diagnostic model using a circRNA panel. Further, the Dataset 3 (n = 321; control, 58; AD, 60; VaD, 50; PDD, 51; bvFTD, 52; DLB, 50) was used to verify the diagnostic model. RESULTS: In Dataset 1, 22 upregulated and 19 downregulated circRNAs were revealed. In Dataset 2, a six-circRNA panel was found to be able to distinguish patients with AD from controls. Then this panel was applied to Dataset 3 and successfully differentiated AD from other types of dementia. CONCLUSION: This study suggested that a six-circRNA panel is AD-specific and a promising biomarker of AD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-022-00405-0. BioMed Central 2022-08-18 /pmc/articles/PMC9389828/ /pubmed/35982472 http://dx.doi.org/10.1186/s40364-022-00405-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ren, Ziye
Chu, Changbiao
Pang, Yana
Cai, Huimin
Jia, Longfei
A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title_full A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title_fullStr A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title_full_unstemmed A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title_short A circular RNA blood panel that differentiates Alzheimer’s disease from other dementia types
title_sort circular rna blood panel that differentiates alzheimer’s disease from other dementia types
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389828/
https://www.ncbi.nlm.nih.gov/pubmed/35982472
http://dx.doi.org/10.1186/s40364-022-00405-0
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