Evidence map›Paper›PMID 41994489›Full record

ArticleJournal of the Endocrine Society2026

Impacts of new sex- and age-specific TSH and FT4 reference ranges on thyroid status and metabolic disorder associations.

Sayaka Yamada, Kazuhiko Horiguchi, Masako Akuzawa, Koji Sakamaki, Eijiro Yamada, Tetsuro Andou, Masanobu Yamada

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

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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. Review
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

7 authors.

Sayaka YamadaDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Gunma University Graduate School of Medicine, Maebashi, Gunma 3718511, Japan.ORCID https://orcid.org/0000-0002-9490-6983
Kazuhiko HoriguchiDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Gunma University Graduate School of Medicine, Maebashi, Gunma 3718511, Japan.
Masako AkuzawaHidaka Hospital, Takasaki, Gunma 3700001, Japan.
Koji SakamakiHidaka Hospital, Takasaki, Gunma 3700001, Japan.
Eijiro YamadaDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Gunma University Graduate School of Medicine, Maebashi, Gunma 3718511, Japan.
Tetsuro AndouHidaka Hospital, Takasaki, Gunma 3700001, Japan.
Masanobu YamadaDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Gunma University Graduate School of Medicine, Maebashi, Gunma 3718511, Japan.ORCID https://orcid.org/0000-0002-2142-633X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: Thyroid hormone levels vary by age, sex, and genetic background; yet most clinical reference ranges (RRs) do not account for these factors, potentially leading to misclassification of thyroid status and missed associations with metabolic disorders. Objective: The aim of this study was to evaluate the impact of newly established age- and sex-specific reference ranges for thyroid-stimulating hormone (TSH) and free thyroxine (FT4) on the prevalence of thyroid statuses and their associations with metabolic disorders. Methods: Cross-sectional observational studies were conducted, and we enrolled over 8000 participants who underwent thyroid status evaluation with Abbott and Siemens assay kits. We compared the prevalence of different thyroid statuses and corresponding metabolic disorders based on the new RRs with that based on the manufacturers' RRs. Results: New RRs significantly altered the prevalence of several thyroid statuses. Subclinical hypothyroidism increased in middle-aged individuals using Abbott kits but decreased in older individuals using Siemens kits. Syndrome of inappropriate secretion of TSH (SITSH, high FT4 with normal or elevated TSH) increased significantly with both kits when applying the new RRs. SITSH, defined by the new RRs, was significantly associated with increased risks of hypertension (Abbott: odds ratio [OR] 2.00; Siemens: OR 1.70) and diabetes (Abbott: OR 2.65; Siemens: OR 1.68), whereas no such associations were observed using the manufacturers' RRs. Conclusion: Age- and sex-specific RRs corrected the misclassification of thyroid status and uncovered a previously underdiagnosed group (SITSH) associated with cardiometabolic risks. These findings support the importance of new RRs for diagnostic accuracy and clinical risk stratification.

Indexed as

free-thyroxinemetabolic disordersreference rangesthyroid statusthyroid-stimulating hormone

Identifiers

PMID41994489
PMCPMC13079444

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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.