Evidence map›Paper›PMID 39015135›Full record

ArticleJOR spine2024

Proteomic analysis of serum in a population-based cohort did not reveal a biomarker for Modic changes.

Friederike Schulze, Juhani Määttä, Sybille Grad, Irina Heggli, Florian Brunner, Mazda Farshad, Oliver Distler, Jaro Karppinen, Jeffrey Lotz, Stefan Dudli

Abstract read
In one paragraph

Article in JOR spine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
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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

10 authors.

Friederike SchulzeCenter of Experimental Rheumatology, Department of Rheumatology University Hospital Zurich, University of Zurich Zurich Switzerland.ORCID https://orcid.org/0000-0002-1702-3255
Juhani MäättäResearch Unit of Health Sciences and Technology University of Oulu Oulu Finland.
Sybille GradAO Research Institute Davos Davos Switzerland.ORCID https://orcid.org/0000-0001-9552-3653
Irina HeggliCenter of Experimental Rheumatology, Department of Rheumatology University Hospital Zurich, University of Zurich Zurich Switzerland.ORCID https://orcid.org/0000-0002-3064-8364
Florian BrunnerDepartment of Physical Medicine and Rheumatology Balgrist University Hospital, Balgrist Campus, University of Zurich Zurich Switzerland.
Mazda FarshadDepartment of Orthopedics Balgrist University Hospital Zurich Switzerland.
Oliver DistlerCenter of Experimental Rheumatology, Department of Rheumatology University Hospital Zurich, University of Zurich Zurich Switzerland.
Jaro KarppinenResearch Unit of Health Sciences and Technology University of Oulu Oulu Finland.
Jeffrey LotzDepartment of Orthopaedic Surgery University of California San Francisco San Francsisco California USA.ORCID https://orcid.org/0000-0002-9654-0647
Stefan DudliCenter of Experimental Rheumatology, Department of Rheumatology University Hospital Zurich, University of Zurich Zurich Switzerland.

Funding

UCSF Core Center for Patient-centric Mechanistic Phenotyping in Chronic Low Back PainU19AR076737 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOTZ, JEFFREY C. · 2019 to 2023
$34.1M
NIAMS NIH HHS U19 AR076737
6 · The paper itself

Abstract

Introduction: Modic changes (MC) are bone marrow lesions of vertebral bones, which can be detected with magnetic resonance imaging (MRI) adjacent to degenerated intervertebral discs. Defined by their appearance on T1 and T2 weighted images, there are three interconvertible types: MC1, MC2, and MC3. The inter-observer variability of the MRI diagnosis is high, therefore a diagnostic serum biomarker complementing the MRI to facilitate diagnosis and follow-up would be of great value. Methods: We used a highly sensitive and reproducible proteomics approach: DIA/SWATH-MS to find serum biomarkers in a subset of the Northern Finland Birth Cohort 1966. Separately, we measured a panel of factors involved in inflammation and angiogenesis to confirm some potential biomarkers published before with an ELISA-based method called V-Plex. Results: We found neither an association between the serum concentrations of the proteins detected with DIA/SWATH-MS with the presence of MC, nor a correlation with the size of the MC lesions. We did not find any association between the factors measured with the V-Plex and the presence of MC or their size. Conclusion: Altogether, our study suggests that a robust and generally usable biomarker to facilitate the diagnosis of MC cannot readily be found in serum.

Indexed as

degenerative disc diseaselow back painModic changesnorthern Finland birth cohortproteomicsserum‐biomarker

Identifiers

PMID39015135
PMCPMC11250394

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Registered trials

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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.