Evidence map›Paper›PMID 42106713›Full record

ArticleBMC pregnancy and childbirth2026

Thyroid function changes in pregnant women with thyroid cancer and their association with adverse fetal outcomes: a parallel controlled study.

Zhi-Fen Hua, Juan Chen, Jiang-Nan Wu, Ting Peng

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Article in BMC pregnancy and childbirth, 2026. 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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5 · Who and what money

Authors and funding

4 authors.

Zhi-Fen Hua *Department of Obstetrics, Tongren Hospital, Shanghai Jiao Tong University, School of Medicine, 1111 Xian Xia Road, Shanghai, 200336, China.
Juan Chen *Department of Obstetrics, Tongren Hospital, Shanghai Jiao Tong University, School of Medicine, 1111 Xian Xia Road, Shanghai, 200336, China.
Jiang-Nan WuClinical Research Unit, Obstetrics and Gynecology Hospital of Fudan University, 566 Fangxie Road, Shanghai, 200011, China. wjnhmm@126.com.
Ting PengDepartment of Obstetrics, Tongren Hospital, Shanghai Jiao Tong University, School of Medicine, 1111 Xian Xia Road, Shanghai, 200336, China. qch1868@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe effects of thyroid hormone replacement or suppression therapy in women with thyroid cancer on thyroid function during pregnancy and subsequent adverse fetal outcomes are still largely unknown. To compare thyroid function at 8 weeks of gestation and its changes during pregnancy between the survivors and controls, and to assess the association of these differences with adverse fetal outcomes.

methodsThis was a retrospective cohort-based parallel control study. A total of 140 survivors and 280 controls delivery time-matched controls were extracted from 46,610 singleton pregnant women who received prenatal examinations in a second-level specialized hospital between January 2019 and March 2024. The primary outcomes were birth defects, small for gestational age (SGA, defined as birth weight < 10th percentile by gestational week), preterm birth (< 37 weeks), and neonatal asphyxia (defined as fetuses with a 1 min-Apgar score of < 7). Apgar scores at 1 and 5 min and umbilical arterial blood gas (ABG) indexes were surrogate indicators of neonatal asphyxia.

resultsCompared to the control group, FT3 was lower in the survivors, while FT4 was higher. Change of FT3 between 8 and 16 weeks of gestation in survivors was significantly smaller than that in the controls (-0.08 vs. -0.30, P < 0.005). The survivors had an insignificant association with SGA/preterm birth (adjusted OR 2.06, 0.68-6.23, P = 0.20), a slightly higher risk of fetal asphyxia (Peto OR, 6.49; 95% CI: 0.81-52.0; P = 0.078), and a lower 1 min Apgar score (β, -0.10; 95% CI: -0.16 to -0.03;P = 0.004). Change in FT3 between 8 and 16 weeks was associated with SGA/preterm birth (adjusted OR, 4.42, 95%CI: 1.32-14.84, P = 0.016). FT3 at 8 weeks of gestation and its changes between 16 and 32 weeks of gestation were negatively correlated with the umbilical ABG index, with both β of -0.02(p = 0.015 and 0.019, respectively).

conclusionsThis study found differences in FT3 and FT4 levels and their changes during pregnancy between the survivors and controls. These differences, especially the changes in FT3 during pregnancy, might suggest a potential biological link, though further studies are needed to establish causality.

Indexed as

Pregnancy Complications, NeoplasticThyroid GlandThyroid NeoplasmsAdultApgar ScoreAsphyxia NeonatorumCase-Control StudiesFemaleGestational AgeHumansInfant, NewbornInfant, Small for Gestational AgePregnancyPregnancy OutcomePremature BirthRetrospective StudiesThyroxineTriiodothyronineApgar scoresBirth weightPregnancyThyroid cancer survivorsThyroid functionUmbilical arterial blood gas

Identifiers

PMID42106713
PMCPMC13326337

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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.