Evidence map›Paper›PMID 40435173›Full record

ArticleEuropean thyroid journal2025

Insight into the metabolic shifts in Graves' hyperthyroidism: a study of acylcarnitine and lipid profiles.

Mikael Thomassen Neset, Arve Ulvik, Kristian Løvås, Johnny Laupsa-Borge, Lars Ertesvåg Breivik, Ann-Elin Meling Stokland, Bjørn Gunnar Nedrebø, Eyvind Rødahl, Eystein Husebye, Grethe Åstrøm Ueland and 1 more

Abstract read
In one paragraph

Article in European thyroid journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Mikael Thomassen NesetDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.
Arve UlvikBevital A/S, Laboratoriebygget, Bergen, Norway.
Kristian LøvåsDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Johnny Laupsa-BorgeBevital A/S, Laboratoriebygget, Bergen, Norway.
Lars Ertesvåg BreivikDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Ann-Elin Meling StoklandDepartment of Medicine, Stavanger University Hospital, Stavanger, Norway.
Bjørn Gunnar NedrebøDepartment of Medicine, Haugesund Hospital, Haugesund, Norway.
Eyvind RødahlDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.
Eystein HusebyeDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Grethe Åstrøm UelandDepartment of Medicine, Haukeland University Hospital, Bergen, Norway.
Hans Olav UelandDepartment of Ophthalmology, Haukeland University Hospital, Bergen, Norway.ORCID https://orcid.org/0000-0001-7993-9739

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Graves' disease increases metabolism and leads to net lipid degradation. Circulating acylcarnitines reflect lipid metabolism and the state of fatty acid oxidation in individuals. The aim of this study was to explore the lipid and acylcarnitine profiles in patients with Graves' disease. Methods: Seven lipids/apolipoproteins and 23 acylcarnitines were analysed in 100 newly diagnosed Graves' disease patients and validated in another 51 patients. Both groups were age- and sex-matched with healthy subjects. Results: The hyperthyroid Graves' disease patients (n = 88) from the main cohort (78 females, median age 42 (17-67) years) had significantly (P < 0.05) higher levels of medium- and long-chain acylcarnitines, and lower levels of short-chain acylcarnitines, compared with healthy subjects. Factor analysis showed that medium- and long-chain acylcarnitines explained most of the differences between the two groups. Serum levels of the five lipids/apolipoproteins were significantly lower in the hyperthyroid Graves' disease patients compared with healthy subjects. Patients (n = 21) treated with antithyroid drugs for 6 weeks had acylcarnitine levels closer to healthy subjects, compared with 79 treatment-naïve hyperthyroid patients. The main findings were confirmed in the validation group. Conclusion: Increased levels of medium- and long-chain acylcarnitines in patients with newly diagnosed Graves' disease may reflect accelerated catabolism. Lower levels of short-chain acylcarnitines point to Graves' disease being a catabolic condition, with a shift in energy source from carbohydrates to fat.

Indexed as

CarnitineGraves DiseaseLipid MetabolismLipidsAdolescentAdultAgedAntithyroid AgentsCase-Control StudiesFemaleHumansMaleMiddle AgedYoung AdultacylcarnitineAntithyroid AgentsCarnitineLipidsacylcarnitinesapolipoproteinsGraves' diseasehyperthyroidismlipidsmetabolism

Identifiers

PMID40435173
PMCPMC12160452

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.