Evidence map›Paper›PMID 42620123›Full record

ArticleResearch square2026

Blood immune profiles in chronic low back pain patients with type 1 Modic changes are associated with intradiscal propionic acid levels.

Jan Devan, Jiamin Zhou, Po-Hung Wu, Noah Bonnheim, Conor O'Neill, Jeffrey C Lotz, Thomas M Link, Abel Torres-Espin, Oliver Distler, Stefan Dudli and 1 more

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Jan DevanUniversity of Zurich.
Jiamin ZhouUniversity of California, San Francisco.
Po-Hung WuAtrium Health Musculoskeletal Institute Wake Forest University School of Medicine.
Noah BonnheimUniversity of California, San Francisco.
Conor O'NeillUniversity of California, San Francisco.
Jeffrey C LotzUniversity of California, San Francisco.
Thomas M LinkUniversity of California, San Francisco.
Abel Torres-EspinUniversity of Waterloo.
Oliver DistlerUniversity of Zurich.
Stefan DudliUniversity of Zurich.
Aaron J FieldsUniversity of California, San Francisco.

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
Skeletal Biology and Biomechanics (SBB) CoreP30AR075055 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Wenhan Chang · 2019 to 2026
$7.1M
Novel imaging of endplate biomarkers in chronic low back painUH3AR076719 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FIELDS, AARON J · 2021 to 2021
$1.9M
Novel imaging of endplate biomarkers in chronic low back painUH2AR076719 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FIELDS, AARON J, KRUG, ROLAND · 2019 to 2019
$1.1M
NIAMS NIH HHS P30 AR075055NIAMS NIH HHS U19 AR076737NIAMS NIH HHS UH2 AR076719NIAMS NIH HHS UH3 AR076719
6 · The paper itself

Abstract

Background: Modic type 1 changes (MC1) are vertebral endplate bone marrow lesions associated with chronic low back pain (CLBP), but their underlying pathobiology remains unclear. Disc-bone marrow crosstalk that includes Methods: In a prospective analysis of patients from the UCSF comeBACK cohort, we quantified intradiscal propionic acid (PA) - a metabolic product of Results: High intradiscal PA was associated with distinct systemic immune responses in patients with MC1 but not in patients with Modic type 2 changes or without Modic changes. Transcriptomic analysis revealed enrichment of adaptive immune pathways and B cell activation signatures in PA-high MC1. Flow cytometry identified the expansion of immunosuppressive ectonucleotidases CD39 and CD73-expressing B cells in PA-high MC1 patients. Finally, intradiscal PA levels were correlated with circulating B cells and serum cytokine concentrations. Conclusions: Intradiscal PA levels measured by MRS associate with biologically distinct blood profiles characterised by systemic B cell activation in patients with MC1. These findings suggest a systemic immune component in the pathobiology of MC1 and highlight the potential of MRS-derived intradiscal PA levels to stratify patients with MC1-related chronic low back pain into biologically distinct subgroups.

Indexed as

B cellslow back painmagnetic resonance spectroscopyModic changes

Identifiers

PMID42620123
PMCPMC13484845

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.