Evidence map›Paper›PMID 40622704›Full record

ArticleActa ophthalmologica2026

Exploring tear fluid biomarkers and the ocular surface in thyroid eye disease.

Mikael Thomassen Neset, Roy Miodini Nilsen, Kristian Løvås, Kathrine Halsøy, Håkon Reikvam, Ann-Elin Meling Stokland, Grethe Åstrøm Ueland, Anette S B Wolff, Hans Christian D Aass, Sjur Reppe and 4 more

Abstract read
In one paragraph

Article in Acta ophthalmologica, 2026. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. 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

14 authors.

Mikael Thomassen NesetDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.
Roy Miodini NilsenFaculty of Health and Social Sciences, Western Norway University of Applied Sciences, Bergen, Norway.
Kristian LøvåsDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Kathrine HalsøyDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.
Håkon ReikvamDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Ann-Elin Meling StoklandDepartment of Medicine, Stavanger University Hospital, Stavanger, Norway.
Grethe Åstrøm UelandDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Anette S B WolffDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Hans Christian D AassDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Sjur ReppeDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Eystein Sverre HusebyeDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Eyvind RødahlDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.
Tor Paaske UtheimDepartment of Medical Biochemistry, Oslo University Hospital, Oslo, Norway.
Hans Olav UelandDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.ORCID https://orcid.org/0000-0001-7993-9739

Funding

Novo Nordisk Foundation Center for Basic Metabolic ResearchThe Regional Health Authorities of Western Norway F-12130
6 · The paper itself

Abstract

purposeTo examine ocular surface changes and inflammatory tear fluid biomarkers in patients with thyroid eye disease (TED).

methodsWe included 106 Graves' disease (GD) patients (36 without TED, 32 with active and 38 with inactive TED) and 106 age- and sex-matched healthy subjects for ophthalmological evaluation, including ocular surface status and Meibomian gland function. Tear fluid was analysed for 40 inflammatory biomarkers by a Luminex multiplex bead assay. The parameters were compared across subgroups.

resultsGD patients with TED had significantly higher median (min-max) Ocular Surface Disease Index (OSDI) score than GD patients without TED, with a median score of 31.4 (0-86.4) compared to 7.3 (0-45.8) (p < 0.01). Eleven of 50 patients with moderate-to-severe and sight-threatening TED had a meibum quality score above seven, compared to none of the 20 patients with mild TED (p = 0.027). Tear fluid levels of chemokine (C-C motif) ligand 2 (CCL2) were significantly (p = 0.003) higher in GD patients compared to healthy subjects. CD40 ligand (CD40L) and CCL2 were higher in GD patients with TED compared with GD patients without TED (p = 0.002 and 0.013, respectively). As a combined biomarker to distinguish between GD patients with and without TED, OSDI score together with tear fluid levels of CCL2 and CD40L produced an area under the receiver operating characteristic (ROC) curve of 0.80, with sensitivity of 0.69 at a fixed specificity of 0.80.

conclusionsOur findings demonstrate increased tear fluid levels of CD40L and CCL2 in patients with TED, indicating their potential as diagnostic biomarkers. Increased ocular discomfort in patients with TED could be related to impaired meibum quality.

Indexed as

BiomarkersDry Eye SyndromesGraves OphthalmopathyMeibomian GlandsTearsAdultAgedChemokine CCL2FemaleHumansMaleMiddle AgedROC CurveBiomarkersChemokine CCL2CD40 ligandchemokine (C–C motif) ligand 2dry eye diseaseGraves' diseaseocular surface diseasethyroid eye disease

Identifiers

PMID40622704
PMCPMC12803598

What OpenQuestion holds

Textmetadata
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.