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Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis

AIM: Differential expression maps of microRNAs (miRNAs) are connected to the autoimmune diseases. This study sought to elucidate the expression maps of exosomal miRNA in plasma of rheumatoid arthritis (RA) patients and their potential clinical significance. METHODS: In the screening phase, small RNA...

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Autores principales: Yang, Xiaoke, Wang, Zhixin, Zhang, Mingming, Shuai, Zongwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473432/
https://www.ncbi.nlm.nih.gov/pubmed/37663759
http://dx.doi.org/10.2147/JIR.S413994
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author Yang, Xiaoke
Wang, Zhixin
Zhang, Mingming
Shuai, Zongwen
author_facet Yang, Xiaoke
Wang, Zhixin
Zhang, Mingming
Shuai, Zongwen
author_sort Yang, Xiaoke
collection PubMed
description AIM: Differential expression maps of microRNAs (miRNAs) are connected to the autoimmune diseases. This study sought to elucidate the expression maps of exosomal miRNA in plasma of rheumatoid arthritis (RA) patients and their potential clinical significance. METHODS: In the screening phase, small RNA sequencing was performed to characterize dysregulated exosome-derived miRNAs in the plasma samples from six patients with RA and six healthy patients. At the independent verification stage, the candidate plasma exosomal miRNAs were verified in 40 patients with RA and 32 healthy patients by using qRT-PCR. The correlation of miRNA levels and clinical characteristics was tested in patients with RA. The value of these miRNAs in diagnosing RA was assessed with the receiver operating characteristic curve. RESULTS: During the screening phase, 177 and 129 miRNAs were increased and decreased in RA patients and healthy controls, respectively. There were 10 candidate plasma exosomal miRNAs selected for the next identification. Compared with the healthy controls, eight plasma exosomal miRNAs (let-7a-5p, let-7b-5p, let-7d-5p, let-7f-5p, let-7g-5p, let-7i-5p, miR-128-3p, and miR-25-3p) were significantly elevated in RA patients, but miR-144-3p and miR-15a-5p expression exhibited no significant changes. The let-7a-5p and miR-25-3p levels were linked to the rheumatoid factor-positive phenotype in RA patients. For the eight miRNAs, the area under the subject work characteristic curve (AUC) is 0.641 to 0.843, and their combination had a high diagnostic accuracy for RA (AUC = 0.916). CONCLUSION: Our study illustrates that novel exosomal miRNAs in the plasma may represent potential noninvasive biomarkers for RA.
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spelling pubmed-104734322023-09-02 Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis Yang, Xiaoke Wang, Zhixin Zhang, Mingming Shuai, Zongwen J Inflamm Res Original Research AIM: Differential expression maps of microRNAs (miRNAs) are connected to the autoimmune diseases. This study sought to elucidate the expression maps of exosomal miRNA in plasma of rheumatoid arthritis (RA) patients and their potential clinical significance. METHODS: In the screening phase, small RNA sequencing was performed to characterize dysregulated exosome-derived miRNAs in the plasma samples from six patients with RA and six healthy patients. At the independent verification stage, the candidate plasma exosomal miRNAs were verified in 40 patients with RA and 32 healthy patients by using qRT-PCR. The correlation of miRNA levels and clinical characteristics was tested in patients with RA. The value of these miRNAs in diagnosing RA was assessed with the receiver operating characteristic curve. RESULTS: During the screening phase, 177 and 129 miRNAs were increased and decreased in RA patients and healthy controls, respectively. There were 10 candidate plasma exosomal miRNAs selected for the next identification. Compared with the healthy controls, eight plasma exosomal miRNAs (let-7a-5p, let-7b-5p, let-7d-5p, let-7f-5p, let-7g-5p, let-7i-5p, miR-128-3p, and miR-25-3p) were significantly elevated in RA patients, but miR-144-3p and miR-15a-5p expression exhibited no significant changes. The let-7a-5p and miR-25-3p levels were linked to the rheumatoid factor-positive phenotype in RA patients. For the eight miRNAs, the area under the subject work characteristic curve (AUC) is 0.641 to 0.843, and their combination had a high diagnostic accuracy for RA (AUC = 0.916). CONCLUSION: Our study illustrates that novel exosomal miRNAs in the plasma may represent potential noninvasive biomarkers for RA. Dove 2023-08-28 /pmc/articles/PMC10473432/ /pubmed/37663759 http://dx.doi.org/10.2147/JIR.S413994 Text en © 2023 Yang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yang, Xiaoke
Wang, Zhixin
Zhang, Mingming
Shuai, Zongwen
Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title_full Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title_fullStr Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title_full_unstemmed Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title_short Differential Expression Profiles of Plasma Exosomal microRNAs in Rheumatoid Arthritis
title_sort differential expression profiles of plasma exosomal micrornas in rheumatoid arthritis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473432/
https://www.ncbi.nlm.nih.gov/pubmed/37663759
http://dx.doi.org/10.2147/JIR.S413994
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