Evidence map›Paper›PMID 36611247›Full record

ArticleThe Journal of clinical endocrinology and metabolism2023

Systemic Activation of the Kynurenine Pathway in Graves Disease With and Without Ophthalmopathy.

Hans Olav Ueland, Arve Ulvik, Kristian Løvås, Anette S B Wolff, Lars Ertesvåg Breivik, Ann-Elin Meling Stokland, Eyvind Rødahl, Roy Miodini Nilsen, Eystein Husebye, Grethe Åstrøm Ueland

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Molecular Biomarkers in Thyroid Eye Disease: A Literature Review.Ophthalmic plastic and reconstructive surgery · 2023
    Review
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Hans Olav UelandDepartment of Ophthalmology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0001-7993-9739
Arve UlvikBevital A/S, Laboratoriebygget, 5021 Bergen, Norway.ORCID 0000-0003-1574-9690
Kristian LøvåsDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-8027-8031
Anette S B WolffDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-8485-2248
Lars Ertesvåg BreivikDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0001-8395-6611
Ann-Elin Meling StoklandDepartment of Medicine, Stavanger University Hospital, 4011 Stavanger, Norway.ORCID 0000-0003-4496-615X
Eyvind RødahlDepartment of Ophthalmology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0003-1025-4840
Roy Miodini NilsenDepartment of Health and Functioning, Western Norway University of Applied Sciences, 5063 Bergen, Norway.ORCID 0000-0002-0228-1550
Eystein HusebyeDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-7886-2976
Grethe Åstrøm UelandDepartment of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0001-6116-7689
Haukeland University Hospital · NOBevital (Norway) · NOStavanger University Hospital · NOWestern Norway University of Applied Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextGraves disease (GD) is one of the most common autoimmune disorders. Recent literature has shown an immune response involving several different inflammatory related proteins in these patients.

objectiveThis work aimed to characterize the kynurenine pathway, activated during interferon-γ (IFN-γ)-mediated inflammation and cellular (T-helper type 1 [Th1] type) immunity, in GD patients with and without thyroid eye disease (TED).

methodsWe analyzed 34 biomarkers by mass spectrometry in serum samples from 100 patients with GD (36 with TED) and 100 matched healthy controls. The analytes included 10 metabolites and 3 indices from the kynurenine pathway, 6 microbiota-derived metabolites, 10 B-vitamers, and 5 serum proteins reflecting inflammation and kidney function.

resultsGD patients showed significantly elevated levels of 7 biomarkers compared with healthy controls (omega squared [ω2] > 0.06; P < .01). Of these 7, the 6 biomarkers with the strongest effect size were all components of the kynurenine pathway. Factor analysis showed that biomarkers related to cellular immunity and the Th1 responses (3-hydroxykynurenine, kynurenine, and quinolinic acid with the highest loading) were most strongly associated with GD. Further, a factor mainly reflecting acute phase response (C-reactive protein and serum amyloid A) showed weaker association with GD by factor analysis. There were no differences in biomarker levels between GD patients with and without TED.

conclusionThis study supports activation of IFN-γ inflammation and Th1 cellular immunity in GD, but also a contribution of acute-phase reactants. Our finding of no difference in systemic activation of the kynurenine pathway in GD patients with and without TED implies that the local Th1 immune response in the orbit is not reflected systemically.

Indexed as

Graves DiseaseGraves OphthalmopathyBiomarkersHumansInflammationInterferon-gammaKynurenineBiomarkersInterferon-gammaKynurenineautoimmunecellular immunityGraves diseasekynurenine pathwayTh1 responsethyroid eye disease

Identifiers

PMID36611247
PMCPMC10188306
OpenAlexW4313706519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.