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Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis

Cell‐free circulating DNA (cfDNA), extracted by liquid biopsy, has been studied as a noninvasive biomarker for various diseases. The potential of cfDNA fragment size and level as a marker in lumbar canal stenosis (LCS) patients has never been studied. We investigated whether cfDNA is a biomarker of...

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Autores principales: Hiyama, Akihiko, Sakai, Daisuke, Nomura, Satoshi, Katoh, Hiroyuki, Watanabe, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238277/
https://www.ncbi.nlm.nih.gov/pubmed/35783906
http://dx.doi.org/10.1002/jsp2.1189
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author Hiyama, Akihiko
Sakai, Daisuke
Nomura, Satoshi
Katoh, Hiroyuki
Watanabe, Masahiko
author_facet Hiyama, Akihiko
Sakai, Daisuke
Nomura, Satoshi
Katoh, Hiroyuki
Watanabe, Masahiko
author_sort Hiyama, Akihiko
collection PubMed
description Cell‐free circulating DNA (cfDNA), extracted by liquid biopsy, has been studied as a noninvasive biomarker for various diseases. The potential of cfDNA fragment size and level as a marker in lumbar canal stenosis (LCS) patients has never been studied. We investigated whether cfDNA is a biomarker of low back pain, leg pain, leg numbness severity in patients with an LCS. Blood samples were obtained from patients with LCS (n = 22) before and immediately after spinal surgery. Plasma DNA was isolated and examined for cfDNA fragment size and concentration. A cohort of healthy volunteers (n = 5) constituted the control group. The cfDNA fragment size tended to be shorter in patients than in healthy controls, but this difference was not significant (P = .186). cfDNA level was significantly higher in LCS patients (mean 0.614 ± 0.198 ng/μL, range 0.302‐1.150 ng/μL) than in healthy controls (mean 0.429 ± 0.064 ng/μL, range 0.366‐0.506 ng/μL) (P = .008). cfDNA level correlated positively with average pain (r = .435, P = .026) and leg numbness (r = .451, P = .018). cfDNA fragment size did not differ from before to after surgery, but cfDNA level increased postoperatively in patients with LCS. This was the first study investigating whether cfDNA fragment size and level are associated with pain in patients with LCS. Our findings suggest that cfDNA level may be an objective indicator of pain and surgical invasiveness in patients with LCS.
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spelling pubmed-92382772022-06-30 Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis Hiyama, Akihiko Sakai, Daisuke Nomura, Satoshi Katoh, Hiroyuki Watanabe, Masahiko JOR Spine Research Articles Cell‐free circulating DNA (cfDNA), extracted by liquid biopsy, has been studied as a noninvasive biomarker for various diseases. The potential of cfDNA fragment size and level as a marker in lumbar canal stenosis (LCS) patients has never been studied. We investigated whether cfDNA is a biomarker of low back pain, leg pain, leg numbness severity in patients with an LCS. Blood samples were obtained from patients with LCS (n = 22) before and immediately after spinal surgery. Plasma DNA was isolated and examined for cfDNA fragment size and concentration. A cohort of healthy volunteers (n = 5) constituted the control group. The cfDNA fragment size tended to be shorter in patients than in healthy controls, but this difference was not significant (P = .186). cfDNA level was significantly higher in LCS patients (mean 0.614 ± 0.198 ng/μL, range 0.302‐1.150 ng/μL) than in healthy controls (mean 0.429 ± 0.064 ng/μL, range 0.366‐0.506 ng/μL) (P = .008). cfDNA level correlated positively with average pain (r = .435, P = .026) and leg numbness (r = .451, P = .018). cfDNA fragment size did not differ from before to after surgery, but cfDNA level increased postoperatively in patients with LCS. This was the first study investigating whether cfDNA fragment size and level are associated with pain in patients with LCS. Our findings suggest that cfDNA level may be an objective indicator of pain and surgical invasiveness in patients with LCS. John Wiley & Sons, Inc. 2021-12-28 /pmc/articles/PMC9238277/ /pubmed/35783906 http://dx.doi.org/10.1002/jsp2.1189 Text en © 2021 The Authors. JOR Spine published by Wiley Periodicals LLC on behalf of Orthopaedic Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Hiyama, Akihiko
Sakai, Daisuke
Nomura, Satoshi
Katoh, Hiroyuki
Watanabe, Masahiko
Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title_full Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title_fullStr Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title_full_unstemmed Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title_short Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
title_sort analysis of cell‐free circulating dna fragment size and level in patients with lumbar canal stenosis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238277/
https://www.ncbi.nlm.nih.gov/pubmed/35783906
http://dx.doi.org/10.1002/jsp2.1189
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