Evidence map›Paper›PMID 38451373›Full record

ArticleEuropean spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society2024

Discovery of circulating blood biomarkers in patients with and without Modic changes of the lumbar spine: a preliminary analysis.

Khaled Aboushaala, Ana V Chee, Sheila J Toro, Rajko Vucicevic, Catherine Yuh, Jake Dourdourekas, Ishani K Patel, Alejandro Espinoza-Orias, Chundo Oh, Lena Al-Harthi and 10 more

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Article in European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Khaled AboushaalaDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Ana V CheeDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA. ana_chee@rush.edu.
Sheila J ToroDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Rajko VucicevicDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Catherine YuhDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Jake DourdourekasDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Ishani K PatelDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Alejandro Espinoza-OriasDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Chundo OhDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Lena Al-HarthiDepartment of Microbial Pathogens and Immunity, Rush Medical College, Chicago, IL, USA.
Jaro KarppinenMedical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
Edward J GoldbergDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Frank M PhillipsDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Matthew ColmanDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Frances M K WilliamsDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Jeffrey A BorgiaDepartments of Anatomy & Cell Biology and Pathology, Rush Medical College, Chicago, IL, USA.
Stefan GreenDepartment of Internal Medicine, Rush Medical College, Chicago, IL, USA.
Christopher ForsythDepartment of Internal Medicine, Rush Medical College, Chicago, IL, USA.
Howard S AnDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA.
Dino SamartzisDepartment of Orthopedic Surgery, Rush Medical College, 1611 W. Harrison St, Chicago, IL, 60612, USA. Dino_Samartzis@rush.edu.ORCID 0000-0002-7473-1311

Funding

Human Microbiome and its Role in the Development of Lumbar Spine Degeneration and Modic ChangesR21AR079679 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI SAMARTZIS, DINO · 2022 to 2023
$382k
NIAMS NIH HHS R21 AR079679
6 · The paper itself

Abstract

purposeThe following study aimed to determine the existence of blood biomarkers in symptomatic patients with or without lumbar Modic changes (MC).

methodsA cross-sectional sub-analyses of a prospective cohort was performed. Fasting blood samples were collected from patients with and without lumbar MC who had undergone spinal fusion or microdiscectomy. An 80-plex panel and CCL5/RANTES were used to assess preoperative plasma cytokine concentrations. Patient demographics and imaging phenotypes were also assessed.

resultsThirty-one subjects were analysed (n = 18 no MC; n = 13 MC). No significant differences were found in age, sex, body mass index, smoking and alcohol history, and surgical procedure (i.e. fusion, decompression) between the two groups (p > 0.05). Several statistically significant blood biomarkers in MC patients were identified, including elevated levels of C-C Motif Chemokine Ligand 5 (CCL5, p = 0.0006), while Macrophage Migration Inhibitory Factor (MIF) was significantly lower (p = 0.009). Additionally, C-X-C Motif Chemokine Ligand 5 (CXCL5, p = 0.052), Pentraxin 3 (PTX3, p = 0.06) and Galectin-3 (Gal-3, p = 0.07) showed potential relevance. Moreover, MC patients exhibited significantly higher levels of disc degeneration (p = 0.0001) and displacement severity (p = 0.020). Based on multivariate analyses and controlling for disc degeneration/displacement, CCL5 (OR 1.02; 95% CI 1.002-1.033; p = 0.028) and MIF (OR 0.60; 95% CI 0.382-0.951; p = 0.030) were independently associated with MC patients.

conclusionThis "proof-of-concept" study is the first to identify specific and significantly circulating blood biomarkers associated with symptomatic patients with lumbar MC, independent of disc alterations of degeneration and/or bulges/herniations. Specifically, differences in CCL5 and MIF protein levels were significantly noted in MC patients compared to those without MC.

Indexed as

Intervertebral Disc DegenerationIntervertebral Disc DisplacementBiomarkersChemokinesCross-Sectional StudiesHumansLigandsLumbar VertebraeMagnetic Resonance ImagingProspective StudiesBiomarkersChemokinesLigandsBiomarkersChangesDisc degenerationDisc herniationEndplateImagingModicMRI

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.