Evidence map›Paper›PMID 32024769›Full record

ArticleMolecular & cellular proteomics : MCP2020

Decreased Immunoglobulin G Core Fucosylation, A Player in Antibody-dependent Cell-mediated Cytotoxicity, is Associated with Autoimmune Thyroid Diseases.

Tiphaine C Martin, Mirna Šimurina, Marta Ząbczyńska, Marina Martinic Kavur, Magdalena Rydlewska, Marija Pezer, Kamila Kozłowska, Andrea Burri, Marija Vilaj, Renata Turek-Jabrocka and 12 more

Open access · hybridAbstract readTwin Study
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.8field-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

32 citing papers in PubMed, 42 citations in OpenAlex.

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  20. Changes of IgGFrontiers in immunology · 2022
    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

22 authors at 7 institutions in 6 countries.

Tiphaine C MartinDepartment of Twin Research and Genetic Epidemiology, King's College, London, United Kingdom; School of Biomedical Sciences, University of Western Australia, Crawley, Western Australia, Australia.
Mirna ŠimurinaFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Marta ZąbczyńskaDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.
Marina Martinic KavurGenos, Glycoscience Research Laboratory, Zagreb, Croatia.
Magdalena RydlewskaDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.
Marija PezerGenos, Glycoscience Research Laboratory, Zagreb, Croatia.
Kamila KozłowskaDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.
Andrea BurriHealth and Rehabilitation Research Institute, Auckland University of Technology, Auckland, New Zealand; Waitemata Pain Service, Department of Anaesthesia and Perioperative Medicine, North Shore Hospital, Auckland, New Zealand.
Marija VilajGenos, Glycoscience Research Laboratory, Zagreb, Croatia.
Renata Turek-JabrockaChair and Department of Endocrinology, Jagiellonian University Medical College, Krakow, Poland; Department of Endocrinology, University Hospital in Krakow, Krakow, Poland.
Milena Krnjajić-TadijanovićGeneral Hospital "Dr. Josip Benčević", Slavonski Brod, Croatia.
Małgorzata Trofimiuk-MüldnerChair and Department of Endocrinology, Jagiellonian University Medical College, Krakow, Poland; Department of Endocrinology, University Hospital in Krakow, Krakow, Poland.
Ivo UgrinaFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia; Genos, Glycoscience Research Laboratory, Zagreb, Croatia.
Anna LityńskaDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.
Alicja Hubalewska-DydejczykChair and Department of Endocrinology, Jagiellonian University Medical College, Krakow, Poland; Department of Endocrinology, University Hospital in Krakow, Krakow, Poland.
Irena Trbojevic-AkmacicGenos, Glycoscience Research Laboratory, Zagreb, Croatia.
Ee Mun LimDepartment of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia; Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
John P WalshDepartment of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia; Medical School, The University of Western Australia, Crawley, Western Australia, Australia.
Ewa PochećDepartment of Glycoconjugate Biochemistry, Institute of Zoology and Biomedical Research, Jagiellonian University, Krakow, Poland.
Tim D SpectorDepartment of Twin Research and Genetic Epidemiology, King's College, London, United Kingdom.
Scott G WilsonDepartment of Twin Research and Genetic Epidemiology, King's College, London, United Kingdom; School of Biomedical Sciences, University of Western Australia, Crawley, Western Australia, Australia; Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Gordan LaucFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia; Genos, Glycoscience Research Laboratory, Zagreb, Croatia. Electronic address: glauc@pharma.hr.
Jagiellonian University · PLGenos (Croatia) · HRThe University of Western Australia · AUUniversity of Zagreb · HRKing's College London · GBNorth Shore Hospital · NZUniversity of Slavonski Brod · HR

Funding

Wellcome Trust
6 · The paper itself

Abstract

Autoimmune thyroid diseases (AITD) are the most common group of autoimmune diseases, associated with lymphocyte infiltration and the production of thyroid autoantibodies, like thyroid peroxidase antibodies (TPOAb), in the thyroid gland. Immunoglobulins and cell-surface receptors are glycoproteins with distinctive glycosylation patterns that play a structural role in maintaining and modulating their functions. We investigated associations of total circulating IgG and peripheral blood mononuclear cells glycosylation with AITD and the influence of genetic background in a case-control study with several independent cohorts and over 3,000 individuals in total. The study revealed an inverse association of IgG core fucosylation with TPOAb and AITD, as well as decreased peripheral blood mononuclear cells antennary α1,2 fucosylation in AITD, but no shared genetic variance between AITD and glycosylation. These data suggest that the decreased level of IgG core fucosylation is a risk factor for AITD that promotes antibody-dependent cell-mediated cytotoxicity previously associated with TPOAb levels.

Indexed as

Antibody-Dependent Cell CytotoxicityAdultAutoimmune DiseasesBlood CellsCohort StudiesFucoseGene Expression RegulationGlycomicsGlycosylationHumansImmunoglobulin GIodide PeroxidaseLinkage DisequilibriumModels, BiologicalPolymorphism, Single NucleotidePolysaccharidesFucoseImmunoglobulin GIodide PeroxidasePolysaccharidesantibodiesantibody-dependent cell-mediated cytotoxicity (ADCC)autoimmune thyroid diseasefucosylationglycoproteinsglycosylationIgGImmunologypatient cohortsthyroid peroxidase antibodies (TPOAb)

Identifiers

PMID32024769
PMCPMC7196582
OpenAlexW3005256423

What OpenQuestion 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 OpenQuestion graph.