Evidence map›Paper›PMID 38222805›Full record

ArticleJOR spine2024

Paraspinal muscles in individuals undergoing surgery for lumbar spine pathology lack a myogenic response to an acute bout of resistance exercise.

Bahar Shahidi, Bradley Anderson, Angel Ordaz, David B Berry, Severin Ruoss, Vinko Zlomislic, R Todd Allen, Steven R Garfin, Mazda Farshad, Simon Schenk and 1 more

Open access · goldAbstract 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
1.0field-weighted citation impact, top 22% 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.

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, 4 citations in OpenAlex.

  1. Article
  2. 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
  3. The multifaceted impact of physical exercise on FoxO signaling pathways.Frontiers in cell and developmental biology · 2025
    Review
  4. Article
  5. Artificial Intelligence in Spine and Paraspinal Muscle Analysis.Advances in experimental medicine and biology · 2024
    Review
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 at 2 institutions in 2 countries.

Bahar ShahidiUC San Diego Department of Orthopaedic Surgery La Jolla California USA.ORCID https://orcid.org/0000-0002-7532-6940
Bradley AndersonUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
Angel OrdazUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
David B BerryUC San Diego Department of Orthopaedic Surgery La Jolla California USA.ORCID https://orcid.org/0000-0001-8275-8322
Severin RuossUC San Diego Department of Orthopaedic Surgery La Jolla California USA.ORCID https://orcid.org/0000-0001-8896-635X
Vinko ZlomislicUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
R Todd AllenUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
Steven R GarfinUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
Mazda FarshadBalgrist University Hospital University of Zurich Zürich Switzerland.
Simon SchenkUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
Samuel R WardUC San Diego Department of Orthopaedic Surgery La Jolla California USA.
UC San Diego Health System · USUniversity of Zurich · CH

Funding

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
NICHD NIH HHS R01 HD088437
6 · The paper itself

Abstract

Background: Lumbar spine pathology (LSP) is a common source of low back or leg pain, and paraspinal muscle in these patients demonstrates fatty and fibrotic infiltration, and cellular degeneration that do not reverse with exercise-based rehabilitation. However, it is unclear of this lack of response is due to insufficient exercise stimulus, or an inability to mount a growth response. The purpose of this study was to compare paraspinal muscle gene expression between individuals with LSP who do and do not undergo an acute bout of resistance exercise. Methods: Paraspinal muscle biopsies were obtained from 64 individuals with LSP undergoing spinal surgery. Eight participants performed an acute bout of machine-based lumbar extension resistance exercise preoperatively. Gene expression for 42 genes associated with adipogenic/metabolic, atrophic, fibrogenic, inflammatory, and myogenic pathways was measured, and differential expression between exercised and non-exercised groups was evaluated for (a) the full cohort, and (b) an age, gender, acuity, and etiology matched sub-cohort. Principal components analyses were used to identify gene expression clustering across clinical phenotypes. Results: The exercised cohort demonstrated upregulation of inflammatory gene IL1B, inhibition of extracellular matrix components (increased MMP3&9, decreased TIMP1&3, COL1A1) and metabolic/adipogenic genes (FABP4, PPARD, WNT10B), and downregulation of myogenic (MYOD, ANKRD2B) and atrophic (FOXO3) genes compared to the non-exercised cohort, with similar patterns in the matched sub-analysis. There were no clinical phenotypes significantly associated with gene expression profiles. Conclusion: An acute bout of moderate-high intensity resistance exercise did not result in upregulation of myogenic genes in individuals with LSP. The response was characterized by mixed metabolic and fibrotic gene expression, upregulation of inflammation, and downregulation of myogenesis.

Indexed as

degenerationinjurypain

Identifiers

PMID38222805
PMCPMC10782077
OpenAlexW4388044430

What OpenQuestion holds

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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.