Evidence map›Paper›PMID 40964420›Full record

ArticleJOR spine2025

Plasma Pro- and Anti-Inflammatory Cytokines in an Observational Chronic Low Back Pain Cohort.

Valerio Tonelli Enrico, William Anderst, Kevin M Bell, J Paulo Coelho, Jessa Darwin, Anthony Delitto, Carol M Greco, Joon Y Lee, Gina P McKernan, Charity G Patterson and 5 more

Abstract read
In one paragraph

Article in JOR spine, 2025. 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. Trial
  2. Review
  3. Review
  4. Review
  5. Article
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

15 authors.

Valerio Tonelli EnricoFerguson Laboratory for Spine and Orthopaedic Surgery, Bethel Musculoskeletal Research Center, Department of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
William AnderstDepartment of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.ORCID https://orcid.org/0000-0002-0535-0953
Kevin M BellDepartment of Bioengineering University of Pittsburgh Swanson School of Engineering Pittsburgh Pennsylvania USA.ORCID https://orcid.org/0000-0003-2099-413X
J Paulo CoelhoFerguson Laboratory for Spine and Orthopaedic Surgery, Bethel Musculoskeletal Research Center, Department of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
Jessa DarwinDepartment of Physical Medicine and Rehabilitation University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.ORCID https://orcid.org/0000-0003-3360-2043
Anthony DelittoDepartment of Physical Therapy University of Pittsburgh School of Health and Rehabilitation Science Pittsburgh Pennsylvania USA.
Carol M GrecoDepartment of Physical Therapy University of Pittsburgh School of Health and Rehabilitation Science Pittsburgh Pennsylvania USA.ORCID https://orcid.org/0000-0002-3078-2918
Joon Y LeeFerguson Laboratory for Spine and Orthopaedic Surgery, Bethel Musculoskeletal Research Center, Department of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
Gina P McKernanDepartment of Physical Medicine and Rehabilitation University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
Charity G PattersonDepartment of Physical Therapy University of Pittsburgh School of Health and Rehabilitation Science Pittsburgh Pennsylvania USA.ORCID https://orcid.org/0000-0002-0060-0124
Sara R PivaDepartment of Physical Therapy University of Pittsburgh School of Health and Rehabilitation Science Pittsburgh Pennsylvania USA.
Michael J SchneiderClinical and Translational Science Institute, University of Pittsburgh Pittsburgh Pennsylvania USA.
Lauren WilcoxDepartment of Physical Medicine and Rehabilitation University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
Nam V VoFerguson Laboratory for Spine and Orthopaedic Surgery, Bethel Musculoskeletal Research Center, Department of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.
Gwendolyn A SowaFerguson Laboratory for Spine and Orthopaedic Surgery, Bethel Musculoskeletal Research Center, Department of Orthopaedic Surgery University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA.

Funding

Influence of inflammation-related genetic variants on PT treatment response in a population affected by CLBPU19AR076725 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SOWA, GWENDOLYN A, VO, NAM V · 2019 to 2023
$21.7M
NIAMS NIH HHS U19 AR076725
6 · The paper itself

Abstract

Background: Chronic low back pain (cLBP) is a multifactorial condition that can have various contributing factors, including biological, biomechanical, and behavioral. Recent evidence suggests that systemic inflammation may contribute to cLBP, impacting pain sensitivity and individuals' functional status. Circulatory pro- and anti-inflammatory cytokines are widely used to determine individuals' systemic inflammatory status. The University of Pittsburgh Mechanistic Research Center, part of the National Institutes of Health's (NIH) Helping to End Addiction Long-term Initiative, conducted a prospective, observational study to identify phenotypes in a large cohort of individuals with cLBP. The present work reports the quantification of key circulatory cytokines in this cLBP cohort. Methods: A total of 1007 individuals with cLBP were enrolled. Plasma samples were available from 936 participants, and concentrations of pro-inflammatory (IL-6, IFN-γ, TNF, IL-15, Leptin) and anti-inflammatory (IL-1ra, IL-10) cytokines were measured via immunoassays. Pain and functional status were assessed using validated self-reported numeric pain ratings scale and the Oswestry Disability Index. Descriptive statistics of analyzed cytokines were reported across the overall population, stratified by age (< 60 and ≥ 60 years old) and sex, and by pain levels as mild (0-5), moderate (6, 7), and severe (8-10), and ODI, categorized as minimal disability (0%-20%), moderate (21%-40%), and severe disability (> 40%). Results: The values of circulating cytokines assessed in this study aligned with those reported in the literature for other painful inflammatory conditions and, in most cases, exceeded those documented for healthy populations. IL-6, IL-1ra, and Leptin demonstrated higher concentrations with higher pain and disability severity. TNF showed higher concentration in participants with higher disability severity. Concentration levels of IFN-γ, IL-15, and IL-10 exhibited no differences across pain or ODI categories. Notably, TNF levels were higher in older adults (≥ 60 years), whereas Leptin levels were higher in females than in males. Conclusion: This study provides a snapshot of key circulating cytokines in a large cLBP cohort, revealing differences in pro- and anti-inflammatory cytokines across pain and disability for the overall population and in sex and age subgroups. Additional longitudinal and mechanistic studies are required to clarify how cytokines could serve as diagnostic, prognostic, or phenotyping markers, ultimately informing targeted, inflammation-focused therapies that may reshape current treatment approaches.

Indexed as

anti‐inflammatory cytokineschronic low back pain (cLBP)inflammatory cytokinesplasma protein biomarkers

Identifiers

PMID40964420
PMCPMC12439354

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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 OpenQuestion graph.