Evidence map›Paper›PMID 42333396›Full record

ArticleJournal of Korean medical science2026

Predictors of Treatment Outcomes in Pediatric Graves' Disease.

Do Young Shin, Eungu Kang, Hyo-Kyoung Nam, Kee-Hyoung Lee, Young-Jun Rhie

Abstract read
In one paragraph

Article in Journal of Korean medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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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

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No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Do Young ShinDepartment of Pediatrics, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.ORCID https://orcid.org/0000-0001-7723-5199
Eungu KangDepartment of Pediatrics, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.ORCID https://orcid.org/0000-0001-6544-3599
Hyo-Kyoung NamDepartment of Pediatrics, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-1512-2062
Kee-Hyoung LeeDepartment of Pediatrics, Seongbuk Woori Children's Hospital, Seoul, Korea.ORCID https://orcid.org/0000-0002-4319-9019
Young-Jun RhieDepartment of Pediatrics, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Korea. human21@korea.ac.kr.ORCID https://orcid.org/0000-0002-1250-6469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGraves' disease (GD), the most common cause of hyperthyroidism in children, is primarily treated with antithyroid drugs (ATDs). The aim of this study was to evaluate factors that could predict remission, relapse, and the need for persistent high doses of methimazole (MMI) in pediatric GD.

methodsThis was a retrospective study of medical records that included GD diagnosed before 19 years of age from January 2004 to December 2023. Remission was defined as maintaining the euthyroid state for more than 6 months after stopping ATDs. The high-dose group was defined as those receiving MMI doses of more than 5 mg/day at last follow-up, regardless of euthyroid status.

resultsOf the 113 patients (95 girls and 18 boys), 47 (41.6%) achieved remission at a mean of 37.17 ± 29.01 months after treatment. Compared to the non-remission group, the remission group showed significant differences in T3, fT4 and thyroid-stimulating hormone-binding inhibitor immunoglobulin (TBII) at diagnosis (330.92 ± 177.72 vs. 413.75 ± 179.09 ng/dL,

conclusionThyroid hormone and TBII levels at diagnosis, time to thyroid hormone and TBII normalization, and the TBII ratio after ATD treatment can be used to predict remission, relapse, and the persistent need for high-dose MMI in pediatric GD patients.

Indexed as

Antithyroid AgentsGraves DiseaseMethimazoleAdolescentChildChild, PreschoolFemaleHumansImmunoglobulins, Thyroid-StimulatingMaleRecurrenceRemission InductionRetrospective StudiesThyroxineTreatment OutcomeTriiodothyronineAntithyroid AgentsImmunoglobulins, Thyroid-StimulatingMethimazolethyrotropin-binding inhibitory immunoglobulinThyroxineTriiodothyronineAntithyroid DrugsGraves' DiseaseHyperthyroidismMethimazoleThyroid-Stimulating Hormone-Binding Inhibitory Immunoglobulin

Identifiers

PMID42333396
PMCPMC13287842

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