Evidence map›Paper›PMID 31513095›Full record

Observational studySpine2020

Increased Fibrogenic Gene Expression in Multifidus Muscles of Patients With Chronic Versus Acute Lumbar Spine Pathology.

Bahar Shahidi, Kathleen M Fisch, Michael C Gibbons, Samuel R Ward

Registry-linked trialOpen access · greenAbstract readComparative StudyObservational Study
In one paragraph

Observational study in Spine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04290221 (Comparing Effectiveness Two Intratissue Percutaneous Electrolysis), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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.

NCT04290221 nacompletednot on this mapstarted 2021, after this paper: background citation

Comparing Effectiveness Two Intratissue Percutaneous Electrolysis (EPI) Interventions for Chronic Low Back Pain: Lumbar Nerve Root Stimulation vs Trigger Points Stimulation

TypeinterventionalSponsorUniversidad de AlmeriaRan2021 to 2023Enrolled64ConditionsChronic Low-back PainArmsUltrasound-guided percutaneous electrolysis in the lumbar nerve root, Electrical Dry Needling in trigger points
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Altered myogenic and lipid metabolism gene expression in paraspinal muscles of patients with adult spinal deformity who develop proximal junctional failure.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 · 2026
    Article
  2. Article
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  4. Review
  5. The relationship between muscle mass and low back pain: a cross-sectional study.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 · 2025
    Article
  6. Targeted multifidus muscle activation reduces fibrosis of multifidus muscle following intervertebral disc injury.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
    Article
  7. Article
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  9. Paraspinal muscle gene expression across different aetiologies in individuals undergoing surgery for lumbar spine pathology.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 · 2023
    Article
  10. Article
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  12. Spatial distribution of fat infiltration within the paraspinal muscles: implications for chronic low back pain.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 · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Bahar ShahidiDepartment of Orthopaedic Surgery, University of California San Diego, La Jolla, CA.
Kathleen M FischDepartment of Medicine, Center for Computational Biology & Bioinformatics, University of California San Diego, La Jolla, CA.
Michael C GibbonsDepartment of Bioengineering, University of California San Diego, La Jolla, CA.
Samuel R WardDepartment of Orthopaedic Surgery, University of California San Diego, La Jolla, CA.
University of California, San Diego · US

Funding

UC San Diego Clinical and Translational Research InstituteTL1TR001443 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DEPP, COLIN A. · 2015 to 2019
$3.4M
The contributions of neural control and mechanosensation to rehabilitation induced spine muscle recoveryR01HD088437 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Bahar Shahidi, Samuel Richard Ward · 2017 to 2026
$2.9M
NCATS NIH HHS TL1 TR001443NICHD NIH HHS R01 HD088437
6 · The paper itself

Abstract

STUDY

designProspective observational study-basic science (Level 1).

objectiveThe aim of this study was to compare expression of functional groups of genes within the atrophic, myogenic, fibrogenic, adipogenic, and inflammatory pathways between paraspinal muscle biopsies from individuals with acute and chronic lumbar spine pathology. SUMMARY OF BACKGROUND DATA: Low back pain is a complex and multifactorial condition that affects a majority of the general population annually. Changes in muscle tissue composition (i.e., fatty and fibrotic infiltration) are a common feature in individuals with lumbar spine pathology associated with low back pain, which often results in functional loss. Understanding the molecular underpinnings of these degenerative changes in different phases of disease progression may improve disease prevention and treatment specificity.

methodsIntraoperative biopsies of the multifidus muscle were obtained from individuals undergoing surgery for acute (<6-month duration) or chronic (>6-month duration) lumbar spine pathology. Expression of 42 genes related to myogenesis, atrophy, adipogenesis, metabolism, inflammation, and fibrosis were measured in 33 samples (eight acute, 25 chronic) using qPCR, and tissue composition of fat, muscle, and fibrosis was quantified using histology.

resultsWe found that tissue composition of the biopsies was heterogeneous, resulting in a trend toward lower RNA yields in biopsies with higher proportions of fat (r <-0.39, P < 0.1). There were no significant differences in gene expression patterns for atrophy (P > 0.635), adipogenesis (P > 0.317), myogenesis (P > 0.320), or inflammatory (P > 0.413) genes after adjusting for the proportion of muscle, fat, and connective tissue. However, in the fibrogenesis pathway, we found significant upregulation of CTGF (P = 0.046), and trends for upregulation of COL1A1 (P = 0.061), and downregulation of MMP1 and MMP9 (P = 0.061) in the chronic group.

conclusionThere is increased fibrogenic gene expression in individuals with chronic disease when compared to acute disease, without significant differences in atrophic, myogenic, adipogenic, or inflammatory pathways, suggesting increased efforts should be made to prevent or reverse fibrogenesis to improve patient function in this population. LEVEL OF EVIDENCE: N/A.

Indexed as

Acute DiseaseAdultAgedChronic DiseaseConnective TissueCross-Sectional StudiesFemaleGene ExpressionHumansLumbar VertebraeMaleMiddle AgedParaspinal MusclesProspective StudiesSpinal Diseases

Identifiers

PMID31513095
PMCPMC6994378
OpenAlexW2972819639

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.