Evidence map›Paper›PMID 36411323›Full record

ArticleScientific reports2022

No associations between C-reactive protein and spinal pain trajectories in children and adolescents (CHAMPS study-DK).

Amber M Beynon, Niels Wedderkopp, Bruce F Walker, Charlotte Leboeuf-Yde, Jan Hartvigsen, Bobby Jones, Ian Shrier, Chinchin Wang, Jeffrey J Hébert

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 5 institutions in 4 countries.

Amber M BeynonDepartment of Chiropractic, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia. amber.beynon@mq.edu.au.
Niels WedderkoppResearch Unit of Pediatrics, Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.
Bruce F WalkerCollege of Science, Health, Engineering and Education, Murdoch University, Perth, WA, Australia.
Charlotte Leboeuf-YdeDepartment for Regional Health Research, University of Southern Denmark, Odense, Denmark.
Jan HartvigsenCenter for Muscle and Joint Health, Department of Sports Science and Clinical Biomechanics, University of Southern Denmark, Odense, Denmark.
Bobby JonesDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Ian ShrierCentre for Clinical Epidemiology, Lady Davis Institute, McGill University, Montreal, QC, Canada.
Chinchin WangCentre for Clinical Epidemiology, Lady Davis Institute, McGill University, Montreal, QC, Canada.
Jeffrey J HébertCollege of Science, Health, Engineering and Education, Murdoch University, Perth, WA, Australia.
University of Southern Denmark · DKMcGill University Health Centre · CAMurdoch University · AUMacquarie University · AUUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preliminary evidence points to a link between C-reactive protein (CRP) and spinal pain in adults. However, there is a paucity of research in younger populations. Therefore, we aimed to determine associations between CRP and spinal pain in childhood and adolescence. We identified trajectories of spinal pain from childhood to adolescence and investigated the associations between CRP and trajectory subgroups. Six- to 11-year-old children from 13 primary schools, were followed from October 2008 and until 2014. High-sensitivity CRP collected at baseline (2008) was measured using serum samples. The outcome was the number of weeks with non-traumatic spinal pain between November 2008 and June 2014. We constructed a trajectory model to identify different spinal pain trajectory subgroups. The associations between CRP and spinal pain trajectory subgroups were modelled using mixed-effects multinominal logistic regression. Data from 1556 participants (52% female), with a mean age of 8.4 years at baseline, identified five spinal pain trajectory subgroups: "no pain" (55.3%), "rare" (23.7%), "rare, increasing" (13.6%), "moderate, increasing" (6.1%), and "early onset, decreasing" (1.3%). There were no differences in baseline high-sensitivity CRP levels between spinal pain trajectory subgroups. Thus, the heterogeneous courses of spinal pain experienced were not defined by differences in CRP at baseline.

Indexed as

C-Reactive ProteinPainAdolescentAdultChildFemaleHumansLogistic ModelsMalePain MeasurementSpineC-Reactive Protein

Identifiers

PMID36411323
PMCPMC9678870
OpenAlexW4309495848

What OpenQuestion holds

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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 OpenQuestion graph.