Evidence map›Paper›PMID 32232775›Full record

ArticleJournal of endocrinological investigation2020

Serum levels of advanced glycation end products (AGEs) are increased and their soluble receptor (sRAGE) reduced in Hashimoto's thyroiditis.

R M Ruggeri, M C Barbalace, M T Cristani, A Alibrandi, S Giovinazzo, G Giuffrida, F Trimarchi, S Cannavò, A Campennì

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Article in Journal of endocrinological investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

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  3. OmicsPred as a centralised resource for genetic prediction of multi-omic traits.medRxiv : the preprint server for health sciences · 2026
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  11. A genomic approach identifies sRAGE as a putatively causal protein for asthma.The Journal of allergy and clinical immunology · 2022
    Article
  12. Article
  13. Review
  14. Iodine nutrition optimization: are there risks for thyroid autoimmunity?Journal of endocrinological investigation · 2021
    Review
  15. 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 3 institutions in 1 country.

R M RuggeriDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy. rmruggeri@unime.it.
M C BarbalaceDepartment for Life Quality Studies, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
M T CristaniDepartment of Pharmaceutical Sciences and Health Products, University of Messina, Messina, Italy.
A AlibrandiUnit of Statistical and Mathematical Sciences, Department of Economics, University of Messina, Messina, Italy.
S GiovinazzoEndocrine Unit, University Hospital AOU Policlinico G. Martino, 98125, Messina, Italy.
G GiuffridaDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
F TrimarchiAccademia Peloritana dei Pericolanti, University of Messina, Messina, Italy.
S CannavòEndocrine Unit, University Hospital AOU Policlinico G. Martino, 98125, Messina, Italy.
A CampennìUnit of Nuclear Medicine, Department of Biomedical Sciences and Morphological and Functional Images, University of Messina, Messina, Italy.
University of Messina · ITAzienda Ospedaliera Universitaria Policlinico "G. Martino" · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAdvanced glycation end products (AGEs) are increased in conditions of oxidative stress and promote inflammation by interacting with their receptor RAGE on cell membrane. By contrast, the soluble receptor sRAGE exerts protective effects by competing with RAGE for ligand binding. AGEs/sRAGEs interaction is involved in the pathogenesis of several diseases related to oxidative stress. In the present study, we evaluated the AGEs/sRAGEs oxidative balance in Hashimoto' thyroiditis (HT).

methodsWe measured the levels of sRAGE, by ELISA, and AGEs, by spectrophotometric method, in the serum of 50 HT patients (5 M, 45 F; mean age 38.5 ± 12 years) and 50 age-, sex- and BMI-matched healthy controls. All subjects were euthyroid at recruitment and none was on LT-4 therapy.

resultsSerum sRAGEs were significantly lower (median 424 vs 738 pg/ml; p = 0.001) and AGEs higher (205 vs 114 AU/g prot; p = 0.001) in HT patients compared to controls, and the two parameters were inversely correlated (p = 0.016). Accordingly, the AGEs/sRAGEs ratio was threefold higher in HT patients than controls (0.48 vs 0.15; p = 0.0001). In regression analysis models, serum TPO-Ab were the main predictors for AGEs and sRAGEs levels and AGEs/sRAGEs ratio (p < 0.0001), irrespective of TSH and/or FT4 values.

conclusionsRAGEs were decreased and AGEs increased, suggesting a dysregulation of AGE/sRAGEs-related oxidative homeostasis in HT patients, even when in euthyroid status. Autoimmunity per se seems to play an important role in AGEs/sRAGE imbalance, irrespective of thyroid function alterations.

Indexed as

AdultBiomarkersCase-Control StudiesFemaleGlycation End Products, AdvancedHashimoto DiseaseHumansMaleMiddle AgedOxidative StressReceptor for Advanced Glycation End ProductsBiomarkersGlycation End Products, AdvancedReceptor for Advanced Glycation End ProductsAdvanced glycation end products (AGEs)AutoimmunityHashimoto’s thyroiditisOxidative stresssoluble Advanced Glycation End Products Receptor (sRAGE)

Identifiers

PMID32232775
OpenAlexW3013643844

What Socratic holds

Textmetadata
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 Socratic graph.