Evidence map›Paper›PMID 38461338›Full record

ArticlePediatric rheumatology online journal2024

Serum and salivary inflammatory biomarkers in juvenile idiopathic arthritis-an explorative cross-sectional study.

Lena Cetrelli, Anette Lundestad, Elisabet G Gil, Johannes Fischer, Josefine Halbig, Paula Frid, Oskar Angenete, Annika Rosén, Karin B Tylleskär, Keijo Luukko and 8 more

Open access · goldAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

18 authors at 6 institutions in 2 countries.

Lena CetrelliCenter for Oral Health Services and Research (TkMidt), Trondheim, Norway. lence@tkmidt.no.ORCID http://orcid.org/0000-0001-9643-517X
Anette LundestadDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Elisabet G GilKnarvik Orthodontics, Alver, Norway.
Johannes FischerDepartment of Clinical Dentistry, The Faculty of Medicine, University of Bergen (UiB), Bergen, Norway.
Josefine HalbigPublic Dental Health Service Competence Centre of Northern Norway (TkNN), Tromsø, Norway.
Paula FridPublic Dental Health Service Competence Centre of Northern Norway (TkNN), Tromsø, Norway.
Oskar AngeneteDepartment of Radiology and Nuclear Medicine, St. Olav Hospital HF, Trondheim University Hospital, Trondheim, Norway.
Annika RosénDepartment of Clinical Dentistry, The Faculty of Medicine, University of Bergen (UiB), Bergen, Norway.
Karin B TylleskärChild and Youth Clinic, Haukeland University Hospital, Bergen, Norway.
Keijo LuukkoDepartment of Clinical Dentistry, The Faculty of Medicine, University of Bergen (UiB), Bergen, Norway.
Ellen NordalDepartment of Clinical Medicine, The Arctic University of Norway (UiT), Tromsø, Norway.
Anne N ÅstrømDepartment of Clinical Dentistry, The Faculty of Medicine, University of Bergen (UiB), Bergen, Norway.
Marit S SkeieCenter for Oral Health Services and Research (TkMidt), Trondheim, Norway.
Astrid Kamilla StunesCenter for Oral Health Services and Research (TkMidt), Trondheim, Norway.
Athanasia BletsaDepartment of Clinical Dentistry, The Faculty of Medicine, University of Bergen (UiB), Bergen, Norway.
Abhijit SenCenter for Oral Health Services and Research (TkMidt), Trondheim, Norway.
Astrid J FeuerhermCenter for Oral Health Services and Research (TkMidt), Trondheim, Norway.
Marite RyggDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Norwegian University of Science and Technology · NOUniversity of Bergen · NOHaukeland University Hospital · NOUniversity Hospital of North Norway · NOWestern Norway University of Applied Sciences · NOCentre for Arctic Gas Hydrate, Environment and Climate · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiomarkers may be useful in monitoring disease activity in juvenile idiopathic arthritis (JIA). With new treatment options and treatment goals in JIA, there is an urgent need for more sensitive and responsive biomarkers.

objectiveWe aimed to investigate the patterns of 92 inflammation-related biomarkers in serum and saliva in a group of Norwegian children and adolescents with JIA and controls and in active and inactive JIA. In addition, we explored whether treatment with tumor necrosis factor inhibitors (TNFi) affected the biomarker levels.

methodsThis explorative, cross-sectional study comprised a subset of children and adolescents with non-systemic JIA and matched controls from the Norwegian juvenile idiopathic arthritis study (NorJIA Study). The JIA group included individuals with clinically active or inactive JIA. Serum and unstimulated saliva were analyzed using a multiplex assay of 92 inflammation-related biomarkers. Welch's t-test and Mann-Whitney U-test were used to analyze the differences in biomarker levels between JIA and controls and between active and inactive disease.

resultsWe included 42 participants with JIA and 30 controls, predominantly females, with a median age of 14 years. Of the 92 biomarkers, 87 were detected in serum, 73 in saliva, and 71 in both biofluids. A pronounced difference between serum and salivary biomarker patterns was found. Most biomarkers had higher levels in serum and lower levels in saliva in JIA versus controls, and in active versus inactive disease. In serum, TNF and S100A12 levels were notably higher in JIA and active disease. The TNF increase was less pronounced when excluding TNFi-treated individuals. In saliva, several biomarkers from the chemokine family were distinctly lower in the JIA group, and levels were even lower in active disease.

conclusionIn this explorative study, the serum and salivary biomarker patterns differed markedly, suggesting that saliva may not be a suitable substitute for serum when assessing systemic inflammation in JIA. Increased TNF levels in serum may not be a reliable biomarker for inflammatory activity in TNFi-treated children and adolescents with JIA. The lower levels of chemokines in saliva in JIA compared to controls and in active compared to inactive disease, warrant further investigation.

Indexed as

Arthritis, JuvenileAdolescentBiomarkersChildCross-Sectional StudiesFemaleHumansInflammationMaleSalivaBiomarkersAdolescentsBiomarkersChildrenDisease activityInflammationJuvenile idiopathic arthritisSalivaSerum

Identifiers

PMID38461338
PMCPMC10924355
OpenAlexW4392619262

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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.