Evidence map›Paper›PMID 41659339›Full record

ArticleFrontiers in endocrinology2025

Circulating thyroid hormones and metabolites in children with autism spectrum disorder.

Michael Hancock, Rui Zhang, Suzanne J Brown, Conchita Boyder, Shelby Mullin, Purdey J Campbell, Scott G Wilson, Ee Mun Lim, Andrew J O Whitehouse, John P Walsh

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2025. 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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0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

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.

Michael HancockDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Rui ZhangPathWest Laboratory Medicine, Queen Elizabeth II (QEII) Medical Centre, Perth, WA, Australia.
Suzanne J BrownDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Conchita BoyderPathWest Laboratory Medicine, Queen Elizabeth II (QEII) Medical Centre, Perth, WA, Australia.
Shelby MullinDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Purdey J CampbellDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Scott G WilsonDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Ee Mun LimDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.
Andrew J O WhitehouseThe Kids Research Institute Australia, Perth Children's Hospital, Perth, WA, Australia.
John P WalshDepartment of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Perth, WA, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Context: Thyroid hormones affect neurological development and function, but detailed studies of thyroid hormones and metabolites in autism are lacking. Objective: To characterize thyroid function and metabolism in autistic children. Methodology: This cross-sectional study compared 788 autistic children (mean age 7.6 ± 3.9 years, 78% male) with 301 non-autistic children (mean age 7.8 ± 4.0 years, 48% male; comprising 215 (71.4%) non-autistic siblings of participants and 86 (28.6%) unrelated individuals). Plasma TSH, free T4 (FT4) and free T3 (FT3) were measured by automated immunoassay, and total T4, total T3 and thyroid hormone metabolites by customized liquid chromatography-tandem mass spectrometry (LCMS/MS). Regression analyses were adjusted for age and sex. Results: TSH concentrations were similar in autistic and non-autistic children (median 2.3 vs 2.1 mU/L, P = 0.64). FT4 was significantly lower in autistic children (18.4 vs 18.7 pmol/L, P = 0.0003), as was FT3 (7.0 vs 7.1pmol/L, P<0.0001), with no significant difference in the FT4:FT3 ratio (P = 0.24). Total T4 was lower in autistic children (178 vs 194 nmol/L, P = 0.0026, as was total T3 (2.2 vs 2.4 nmol/L, P = 0.018), with no significant difference in the T4:T3 ratio (P = 0.099). Two metabolites were significantly lower in autistic children: 3,5-T2 (0.010 vs 0.021 nmol/L, P<0.0001) and 3,3'-T2 (0.12 vs 0.16 nmol/L, P<0.0001), whereas T0 levels were higher (1.5 vs 1.1 nmol/L, P = 0.028). Conclusions: Circulating thyroid hormones and metabolites differ between autistic and non-autistic children, although the observed differences are small. The study demonstrates the utility of LCMS/MS for in-depth characterization of thyroid hormone economy, with potentially wide applications.

Indexed as

Autism Spectrum DisorderThyroid HormonesChildChild, PreschoolCross-Sectional StudiesFemaleHumansMaleTandem Mass SpectrometryThyrotropinThyroxineTriiodothyronineThyroid HormonesThyrotropinThyroxineTriiodothyronineAustralian autism biobankautism spectrum disorderliquid chromatography-tandem mass spectrometry (LCMS/MS)thyroid hormonesthyroid metabolites

Identifiers

PMID41659339
PMCPMC12872564

What Socratic holds

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LicenceCC BY
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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 Socratic graph.