Evidence map›Paper›PMID 40746193›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Impact of Minimal Dose Strategy Before Antithyroid Drug Discontinuation on Relapse Risk in Graves' Disease.

Keitaro Miyamura, Mitsuru Ito, Hiroyuki Yamaoka, Mako Hisakado, Eijun Nishihara, Shuji Fukata, Mitsushige Nishikawa, Akira Miyauchi, Takashi Akamizu

Erratum issuedAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Keitaro MiyamuraCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Mitsuru ItoCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Hiroyuki YamaokaCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Mako HisakadoCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Eijun NishiharaCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.ORCID 0000-0003-1786-0077
Shuji FukataCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Mitsushige NishikawaCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.
Akira MiyauchiCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.ORCID 0000-0003-0041-197X
Takashi AkamizuCenter for Excellence in Thyroid Care, Kuma Hospital, Kobe 650-0011, Japan.ORCID 0000-0003-4960-8271

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough antithyroid drugs (ATDs) are widely used as the first-line therapy for Graves' disease, relapse after treatment discontinuation remains common. While a prolonged low-dose ATD therapy has been associated with improved remission rates, the impact of the minimal maintenance dose before discontinuation on relapse risk remains unclear.

methodWe conducted a retrospective cohort study using electronic medical records from a thyroid specialty hospital in Japan. Patients newly diagnosed with Graves' disease between 2008 and 2024 who had discontinued methimazole (MMI) after receiving a minimal maintenance dose (≤2.5 mg/day) were included. Patients were categorized into 4 groups based on their final maintenance dose before discontinuation: 2.5 mg/day, >1.25 to ≤2.5 mg/day, 1.25 mg/day, and <1.25 mg/day. We evaluated the association between the minimal MMI dose before discontinuation and the 1-year risk of relapse using multivariable regression and propensity score-matched analyses.

resultsAmong 4352 eligible patients, multivariable regression showed that, compared with the 2.5 mg/day group, the 1.25 mg/day group had a significantly lower risk of relapse within 1 year [risk ratio (RR) 0.46, 95% confidence interval (CI) 0.28-0.75], and the <1.25 mg/day group had the lowest risk (RR: 0.18, 95% CI: 0.05-0.73). The propensity score-matched analysis, consistent with the multivariable regression, showed that the 1.25 mg/day group had a lower risk of relapse compared with the 2.5 mg/day group (RR: 0.44, 95% CI: 0.23-0.85; 172 matched pairs).

conclusionLower minimum maintenance doses of MMI before discontinuation, particularly doses <2.5 mg/day, may be associated with a reduced risk of relapse in patients with Graves' disease. Clinicians should recognize the clinical relevance of the minimum maintenance dose in the treatment of Graves' disease.

Indexed as

Antithyroid AgentsGraves DiseaseMethimazoleAdultAgedDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansJapanMaleMiddle AgedRecurrenceRetrospective StudiesAntithyroid AgentsMethimazoleantithyroid drugsGraves’ diseasemaintenance dosemethimazolerelapse riskretrospective cohort study

Identifiers

PMID40746193
PMCPMC12819858

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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.