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

Abstract 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 biom...

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Main Authors: Akihiko Hiyama, Daisuke Sakai, Satoshi Nomura, Hiroyuki Katoh, Masahiko Watanabe
Format: Article
Language:English
Published: Wiley 2022-06-01
Series:JOR Spine
Subjects:
Online Access:https://doi.org/10.1002/jsp2.1189
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author Akihiko Hiyama
Daisuke Sakai
Satoshi Nomura
Hiroyuki Katoh
Masahiko Watanabe
author_facet Akihiko Hiyama
Daisuke Sakai
Satoshi Nomura
Hiroyuki Katoh
Masahiko Watanabe
author_sort Akihiko Hiyama
collection DOAJ
description Abstract 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 doaj.art-63a146a83f6341e1b1da43f1bf3f502a2022-12-22T02:32:44ZengWileyJOR Spine2572-11432022-06-0152n/an/a10.1002/jsp2.1189Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosisAkihiko Hiyama0Daisuke Sakai1Satoshi Nomura2Hiroyuki Katoh3Masahiko Watanabe4Department of Orthopaedic Surgery, Surgical Science Tokai University School of Medicine Isehara Kanagawa JapanDepartment of Orthopaedic Surgery, Surgical Science Tokai University School of Medicine Isehara Kanagawa JapanDepartment of Orthopaedic Surgery, Surgical Science Tokai University School of Medicine Isehara Kanagawa JapanDepartment of Orthopaedic Surgery, Surgical Science Tokai University School of Medicine Isehara Kanagawa JapanDepartment of Orthopaedic Surgery, Surgical Science Tokai University School of Medicine Isehara Kanagawa JapanAbstract 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.https://doi.org/10.1002/jsp2.1189cell‐free circulating DNAlateral lumbar interbody fusionlow back painlumbar canal stenosisnumeric rating scale
spellingShingle Akihiko Hiyama
Daisuke Sakai
Satoshi Nomura
Hiroyuki Katoh
Masahiko Watanabe
Analysis of cell‐free circulating DNA fragment size and level in patients with lumbar canal stenosis
JOR Spine
cell‐free circulating DNA
lateral lumbar interbody fusion
low back pain
lumbar canal stenosis
numeric rating scale
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 cell‐free circulating DNA
lateral lumbar interbody fusion
low back pain
lumbar canal stenosis
numeric rating scale
url https://doi.org/10.1002/jsp2.1189
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