Evidence map›Paper›PMID 42388365›Full record

ArticleJournal of the Endocrine Society2026

Efficacy and safety of propylthiouracil protocols: high-dose monotherapy vs combination of low-dose with iodine.

Nami Suzuki, Jaeduk Yoshimura Noh, Natsuko Watanabe, Ai Yoshihara, Miho Fukushita, Masako Matsumoto, Masakazu Koshibu, Miki Kawai, Aiko Kitao, Kiminori Sugino and 1 more

Abstract read
In one paragraph

Article in Journal of the Endocrine Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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

1 citing paper in PubMed.

  1. 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

11 authors.

Nami SuzukiDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0003-2877-6647
Jaeduk Yoshimura NohDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0001-7340-8603
Natsuko WatanabeDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0003-2297-5004
Ai YoshiharaDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0003-1323-4722
Miho FukushitaDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0001-6815-5891
Masako MatsumotoDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0009-0000-7265-6787
Masakazu KoshibuDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0009-0007-0170-2804
Miki KawaiDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0009-0004-7106-6688
Aiko KitaoDepartment of Internal Medicine, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0009-0000-7417-2751
Kiminori SuginoDepartment of Surgery, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0002-9692-9871
Koichi ItoDepartment of Surgery, Ito Hospital, Shibuya, Tokyo 150-0001, Japan.ORCID https://orcid.org/0000-0002-2341-3620

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Propylthiouracil (PTU) use has decreased due to adverse events (AEs), but it is still needed for patients who cannot tolerate thiamazole. Objective: To compare the efficacy and safety of the PTU protocol between high-dose monotherapy and low-dose combination therapy with potassium iodide (KI). Methods: This is a retrospective observational study including patients who were newly diagnosed with Graves disease (GD) and received PTU as initial therapy between January 2005 and October 2024. Patients who received an initial dose of 300 mg (high-dose group) and those who received 150 mg of PTU combined with 50 mg of KI (low-dose group) were included. The propensity-score matching method was employed to adjust for confounders. Results: A total of 1171 patients (high-dose: low-dose = 1133: 38, all female) with a median age of 32 (interquartile range [IQR]: 28-36) years were included. Median levels of free-thyroxine (FT4) and thyroid-stimulating hormone receptor antibody were 4.97 (IQR: 3.67-7.31) ng/dL, 12.4 (IQR: 6.4-26.8) IU/L. Adverse events occurred in 294 patients (high-dose: low-dose = 289:5). Free-thyroxine levels were significantly lower at Week 2 in the low-dose group than in the high-dose group ( Conclusion: Despite a lower rate of efficacy from the initial dose, the low-dose protocol was effective in controlling hyperthyroidism with up-titration in young women with GD, with the potential for fewer AEs.

Indexed as

adverse eventsanti-thyroid drugsGraves diseasepotassium iodidepropylthiouracil

Identifiers

PMID42388365
PMCPMC13320707

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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.