Evidence map›Paper›PMID 40663466›Full record

ArticleEuropean thyroid journal2025

Standardization of TSH and FT4 to gestational age in early pregnancy and associations with clinical outcomes.

Joris A J Osinga, Layal Chaker, Sjoerd van den Berg, Vincent W V Jaddoe, Eric A P Steegers, Henning Tiemeier, Robin P Peeters, Tim Korevaar

Abstract read
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Article in European thyroid journal, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Layal Chaker
Sjoerd van den Berg
Vincent W V Jaddoe
Eric A P Steegers
Henning Tiemeier
Robin P Peeters
Tim Korevaar

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To account for pregnancy-specific changes in thyroid physiology, international guidelines recommend the use of trimester-specific reference intervals. However, the pragmatic division in trimesters does not necessarily align with the changes in thyroid physiology. While the goal of treating gestational thyroid dysfunction is to prevent thyroid hormone-mediated adverse events, it remains unclear which method of standardizing to gestational age, if any, is most effective in identifying individuals at higher risk of adverse pregnancy events. Methods: We included 5,675 women participating in a population-based prospective cohort with data on thyroid-stimulating hormone (TSH), free thyroxine (FT4) and thyroperoxidase antibodies (TPOAbs) during early pregnancy (median: 13.2 weeks, 95% range: 9.8-17.6). We studied the association of TSH and FT4 with pre-eclampsia, premature delivery, birth weight and offspring IQ with or without full gestational age standardization of TSH and FT4 using multivariable regression models. Results: There was a positive association of gestational age at blood sampling with TSH (difference in mean TSH: +9.6%; P < 0.001) and a negative association with FT4 (difference in mean FT4: -20.2%; P < 0.001). Standardizing TSH to gestational age led to reclassification of 36 women as having normal TSH (9.9%) and 27 as having abnormal TSH (0.5%). For FT4, 62 women were reclassified as having normal FT4 (20.3%) and 57 as having abnormal FT4 (1.1%). Standardization of TSH and FT4 concentrations led to an attenuation of the associations with any outcome of up to 71% as compared to non-standardized TSH or FT4. Conclusions: Full standardization of TSH and FT4 to gestational age either does not affect or weakens their associations with clinical outcomes, suggesting that accounting for gestational age offers no benefit with regard to identifying high-risk thyroid dysfunction during early pregnancy.

Indexed as

Gestational AgeThyrotropinThyroxineAdultAutoantibodiesBirth WeightFemaleHumansPregnancyPregnancy ComplicationsPregnancy OutcomePregnancy Trimester, FirstPremature BirthProspective StudiesReference ValuesThyroid Function TestsAutoantibodiesThyrotropinThyroxineFT4gestational agepregnancythyroidTSH

Identifiers

PMID40663466
PMCPMC12284872

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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.