Evidence map›Paper›PMID 34142359›Full record

ReviewHormones (Athens, Greece)2021

Novel presentation of the c.1856A > G (p.Asp619Gly) TSHR gene-activating variant: relapsing hyperthyroidism in three subsequent generations manifesting in early childhood and an in vitro functional study.

Martin Bezdicka, Petra Kleiblova, Jiri Soucek, Marianna Borecka, Eva El-Lababidi, Daniel Smrz, Michal Rataj, Zdenek Sumnik, Jana Malikova, Ondrej Soucek

Abstract readCase ReportsReview
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In one paragraph

Review in Hormones (Athens, Greece), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 1 institution in 1 country.

Martin BezdickaVera Vavrova Laboratory/VIAL, Department of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Petra KleiblovaInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Jiri SoucekPrivate Paediatric Endocrinology Practice, Carlsbad, Czech Republic.
Marianna BoreckaInstitute of Biology and Medical Genetics, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Eva El-LababidiDepartment of Pediatrics, Third Faculty of Medicine, Charles University and Kralovske Vinohrady University Hospital, Prague, Czech Republic.
Daniel SmrzDepartment of Immunology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Michal RatajDepartment of Immunology, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Zdenek SumnikDepartment of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Jana MalikovaDepartment of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Ondrej SoucekVera Vavrova Laboratory/VIAL, Department of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic. Ondrej.Soucek@lfmotol.cuni.cz.ORCID http://orcid.org/0000-0002-6555-1802
Charles University · CZ

Funding

Ministerstvo Školství, Mládeže a Tělovýchovy CZ.1.05/4.1.00/16.0337Ministerstvo Zdravotnictví Ceské Republiky 00064203Ministerstvo Zdravotnictví Ceské Republiky NU20-03-00285
6 · The paper itself

Abstract

backgroundFamilial non-autoimmune hyperthyroidism is a rare disease caused by germline activating variants in the thyroid-stimulating hormone receptor (TSHR) gene. The c.1856A > G (p.Asp619Gly) pathogenic variant has been described in cases of toxic adenoma but never before, to our knowledge, in a case of familial non-autoimmune hyperthyroidism. PATIENT

findingsA 3-year-old boy was admitted for acute gastroenteritis presenting with goiter and tall stature. Laboratory findings revealed peripheral hyperthyroidism and negativity for thyroid autoantibodies. Antithyroid drug treatment was effective, but relapses occurred shortly after attempts to decrease the drug dose. As the boy's father and paternal grandmother also experienced relapsing hyperthyroidism manifesting in early childhood, genetic testing of TSHR was indicated. The c.1856A > G (p.Asp619Gly) pathogenic variant was found in all three affected family members. Functional in vitro characterization of the variant verified that it enhances constitutional activation of the receptor, leading to increased production of cyclic adenosine monophosphate. Total thyroidectomy was indicated in the boy due to an unsatisfactory prognosis. Due to persistent positive thyroglobulin serum concentration, a diagnostic radioiodine scan was performed approximately 2 years later. Residual thyroid tissue was revealed; therefore, radioiodine ablative therapy was performed. Despite adequate thyroxine substitution over a long period of follow-up, TSH remained suppressed.

conclusionsUnlike Graves' disease, familial non-autoimmune hyperthyroidism cases present with antithyroid drug-dependence. Not ultrasound but positive thyroglobulin serum concentration indicated residual thyroid tissue. Early detection of residual thyroid tissue and radioiodine ablation prevented the subject from experiencing relapsing hyperthyroidism and undergoing unnecessary repeated surgery. Life-long hormone substitution should be adjusted to free thyroxine rather than TSH serum concentrations.

Indexed as

Graves DiseaseHyperthyroidismAntithyroid AgentsChild, PreschoolHumansIodine RadioisotopesMaleNeoplasm Recurrence, LocalReceptors, ThyrotropinThyroglobulinThyrotropinThyroxineAntithyroid AgentsIodine RadioisotopesReceptors, ThyrotropinThyroglobulinThyrotropinThyroxineActivating TSHR pathogenic variantCase reportFamilial non-autoimmune hyperthyroidismFunctional studyRadioiodine ablative treatmentRepeated thyroid surgery

Identifiers

PMID34142359
OpenAlexW3171682262

What OpenQuestion holds

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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 OpenQuestion graph.