- Open Access
Pregnancy outcomes and neonatal thyroid function in women with thyroid cancer: a retrospective study
BMC Pregnancy and Childbirth volume 23, Article number: 383 (2023)
Evidence regarding adverse pregnancy outcomes in patients with thyroid cancer has been conflicting, and the effect of thyroid dysfunction caused by thyroid hormone suppression therapy in terms of neonatal thyroid stimulating hormone (TSH) is unclear. This study aimed to investigate whether thyroid cancer was associated with adverse pregnancy outcomes and had an adverse effect on neonatal thyroid function.
This was a retrospective study of 212 singleton pregnancies with thyroid cancer and 35,641 controls without thyroid cancer. Data on maternal pregnancy outcomes and neonatal outcomes were analyzed.
The median TSH level in the thyroid cancer group was significantly lower than that in the control group (0.87 µIU/mL vs. 1.17 µIU/mL; P < 0.001), while the FT4 level was higher than that in the control group (17.16 pmol/L vs. 16.33 pmol/L; P < 0.001). The percentage of thyroid peroxidase antibodies (TPOAb) positive in the thyroid cancer group was significantly higher than that in the control group (25.0% vs. 11.8%; P < 0.001). Pregnancies with thyroid cancer had a higher risk of late miscarriage (OR 7.166, 95% CI: 1.521, 33.775, P = 0.013), after adjusting maternal TPOAb positive, there was no statistical significance (OR 3.480, 95% CI: 0.423, 28.614, P = 0.246). Pregnancies with thyroid cancer had higher gestational weight gain (GWG) (14.0 kg vs. 13.0 kg, P < 0.001). Although there was no significant difference in the prevalence of gestational diabetes mellitus (GDM) (20.8% vs. 17.4%, P = 0.194), the oral glucose tolerance test (OGTT) showed that fasting plasma glucose and 2-hour value in the thyroid cancer group were higher than those in the control group (P = 0.020 and 0.004, respectively). There was no statistically significant difference in TSH between the thyroid cancer group and the control group, regardless of full-term newborns or preterm newborns.
Thyroid cancer might not have substantial adverse effects on pregnancy outcomes except for excessive GWG. No adverse effect on neonatal TSH was found, but the effect on long-term thyroid function and neuropsychological function in offspring need further study.
Beijing Birth Cohort Study (ChiCTR220058395).
Thyroid cancer is one of the most common cancers diagnosed in young women . Figures from the National Cancer Center (NCC) of China annually report show that thyroid cancer experienced the largest increase in incidence among all cancer types in China and is the fourth most common cancer in Chinese women with age-standardized incidence rates of thyroid cancer at 17.7% . Differentiated thyroid cancer (DTC) is the most frequent subtype of thyroid cancer. In most patients, the standard treatment (thyroidectomy with or without radioactive iodine treatment) is effective [3, 4]. Thyroid hormone replacement therapy or thyroid hormone suppression therapy after thyroidectomy is needed [3, 4]. The main challenge in caring for women with previously treated thyroid cancer is maintaining the thyroid stimulating hormone (TSH) level within the suitable range. Thyroid hormones play an essential role in maintaining pregnancy and promoting optimal fetal development. According to the American Thyroid Association (ATA) recommendation, pregnant women with thyroid cancer should be managed at the same TSH goal as determined preconception . The importance of adequate thyroid hormonal status during pregnancy has been emphasized in association with pregnancy outcomes [6,7,8,9,10]. Several retrospective studies have discussed the effects of a history of thyroid cancer on pregnancy outcomes [11,12,13,14,15]. However, the evidence regarding adverse pregnancy outcomes in patients with thyroid cancer has been conflicting.
The formation and maturation of the newborn’s hypothalamic-pituitary-thyroid axis begin in utero with fetal dependence on maternal thyroid hormones early in the pregnancy and later on the direct supply of iodine from the mother for its thyroxine production . Studies have suggested that maternal thyroid dysfunction during development may induce a shift in the hypothalamic-pituitary-thyroid axis set point of the offspring [17,18,19]. It has been shown that maternal thyroid function was positively associated with offspring thyroid function at birth [19,20,21,22]. Nevertheless, the effect of thyroid dysfunction caused by thyroid hormone suppression therapy in terms of neonatal TSH is unclear.
Therefore, we aimed to evaluate the incidence of adverse pregnancy outcomes, including late miscarriage, stillbirth, and preterm delivery, in patients with thyroid cancer and to investigate whether patients with thyroid cancer had an increased risk of adverse pregnancy outcomes compared with those without thyroid cancer by conducting a retrospective study. Another aim of this study was to investigate whether the neonatal thyroid function of mothers with thyroid cancer differed from that of mothers without thyroid cancer.
The study was embedded in the Beijing Birth Cohort Study (ChiCTR220058395). The study included singleton pregnancy women who had a history of thyroid cancer or were diagnosed with thyroid cancer during pregnancy and received prenatal care at Beijing Obstetrics and Gynecology Hospital, Capital Medical University from January 2016 to December 2021. The control group was singleton pregnancy women who received care at Beijing Obstetrics and Gynecology Hospital between January 2016 to December 2021, with no history of thyroid cancer, other thyroid diseases, or other malignant tumors. Supplementary Fig. 1 shows the flow chart of the control group’s enrollment. This study has been performed in accordance with the Declaration of Helsinki and has been approved by the ethics committee of Beijing Obstetrics and Gynecology Hospital, Capital Medical University (2018-ky-009-01). Since the anonymous data were respectively extracted from the electronic record without any information that could identify particular individual, a waiver of informed consent was granted by the ethics committee of Beijing Obstetrics and Gynecology Hospital, Capital Medical University.
Baseline information, pregnancy outcomes, and neonatal data were obtained from the electronic database of Beijing Obstetrics and Gynecology Hospital, Capital Medical University. History of abnormal pregnancy includes early and late miscarriage, fetal loss, stillbirth, and preterm delivery. Thyroid cancer-related data were collected, including diagnosis time, duration, treatment modality, and levothyroxine (L-T4) treatment before and during pregnancy. The levels of maternal TSH, free thyroxine (FT4), and thyroid peroxidase antibodies (TPOAb) were recorded during the first prenatal visit before 16 weeks of gestation. The TPOAb concentration was considered positive when levels were above 60 U/mL. Plasma glucose and lipids were measured in the first trimester (before 16 weeks) and the third trimester (32–34 weeks). The 2-h 75-g oral glucose tolerance test (OGTT) was performed at 24–28 weeks’ gestation. In their offspring, TSH was measured in plantar blood samples on filter paper cards screening for congenital hypothyroidism 72 h to 7 days after birth.
Maternal outcomes of this study included late miscarriage (defined as the spontaneous loss of a pregnancy from 12 to 23+ 6 weeks of gestation) , stillbirth (defined as a baby who dies after 28 weeks of pregnancy, but before or during birth), preterm delivery (between gestational weeks 28 and 36+ 6); delivery by cesarean section; gestational diabetes mellitus (GDM, diagnosed according to a the 2-h 75-g OGTT between 24 and 28 week’s gestation, with plasma glucose thresholds for fasting, 1-, and 2- hour being 5.1, 10.0, and 8.5 mmol/L, respectively); hypertensive disorders in pregnancy (HDP, including chronic hypertension, gestational hypertension, preeclampsia/eclampsia, and preeclampsia superimposed on chronic hypertension) ; premature rupture of membranes (defined as rupture of membranes before the onset of labor) ; placenta previa (defined as the placenta lies directly over the internal os) ; placenta abruption (defined as the early separation of a placenta from the lining of the uterus before completion of the second stage of labor) ; abnormally invasive placentation (defined as previously described by Collins et al. ); postpartum hemorrhage (≥ 1000 mL for cesarean delivery or ≥ 500 mL for vaginal delivery). The neonatal outcomes of this study included macrosomia (defined as a newborn birth weight of more than 4000 g); low birth weight infant (LBW, defined as a newborn birth weight below 2500 g).
Quantitative data with non-normal distribution are shown as median (interquartile range), and categorical data are presented as percentages. Mann-Whitney U test, chi-square test, and general linear repeated-measures model were used to assess the differences between the control and study groups where appropriate. Multivariable logistic regression analysis was used to estimate the odds ratio (OR) and the confidence intervals (CIs) for the association of thyroid cancer with adverse pregnancy outcomes. For multivariable logistic analyses, a fixed set of known risk factors for adverse pregnancy outcomes was adjusted for potential confounding, including maternal TPOAb positive, maternal age, multiparity, pre-pregnancy diabetes mellitus (DM), and HDP. Multiple linear regression models were used to investigate the association between variables and GWG. Covariates included the maternal history of thyroid cancer, maternal age, maternal pre-pregnancy body mass index (BMI), multiparity, history of the polycystic ovarian syndrome (PCOS), pre-pregnancy DM, GDM, HDP, and gestational age of delivery. TSH and FT4 were log-transformed and were approximately normally distributed with these transformations. Multiple linear regression models were used to investigate the association between variables and neonatal TSH. Covariates were selected based on biological confounding plausibility, change in effect estimate of the variable of interest, or the reduction of the residual variance of the model. Covariates included the maternal history of thyroid cancer, maternal TSH, maternal FT4, maternal TPOAb positive, maternal age, maternal pre-pregnancy BMI, mode of conception, mode of delivery, birth month, and neonatal gender. When comparing neonatal TSH levels, we used propensity score matching to eliminate possible confounding factors. A 1:1 matching was performed on the propensity score with a maximum caliber of 0.05, and 205 cases in the thyroid cancer group and 205 controls were included in the statistical analysis. Matching variables include maternal age, pre-pregnancy BMI, gestational age of delivery, mode of delivery, birth month, neonatal gender, maternal history of pre-pregnancy DM, GDM, HDP. A P value < 0.05 was considered statistically significant. All analyses were performed using Statistical Package of Social Sciences version 25.0 for Windows (SPSS Inc).
From 2016 to 2021, 212 women with thyroid cancer were included in this study. Table 1 shows information about the thyroid cancer therapy of the patients. The median interval from diagnosis of thyroid cancer to conception was 3.0 (1.5, 4.0) years. Only two women were diagnosed during pregnancy. Most patients (98.1%) received thyroidectomy, among whom seven patients (3.3%) were treated with radioactive iodine therapy (RAIT) after surgery. Four patients were on an active surveillance management approach because of their papillary microcarcinomas without clinically evident metastases or local invasion. The median dosage of L-T4 pre-pregnancy was 1.63 µg/kg/day and it increased to 1.77 µg/kg/day during pregnancy. The median TSH and FT4 levels during early pregnancy were 0.87 µIU/mL and 17.16 pmol/L, respectively.
The basic characteristics of the two groups are presented in Table 2. Women with thyroid cancer tended to be older with a higher pre-pregnancy BMI and a higher prevalence of pre-pregnancy hypertension. The proportion of women with history of abnormal pregnancy in the thyroid cancer group was significantly higher than that in the control group (19.3% vs. 11.7%; P = 0.001). In terms of pre-pregnancy DM, history of HDP, history of GDM, and conceived by in vitro fertilization-embryo transfer (IVF-ET), no difference was observed between thyroid cancer patients and the control group.
When comparing the differences in the maternal thyroid function during early pregnancy between the two groups, we found that the median TSH level in the thyroid cancer group was significantly lower than that in the control group (0.87 µIU/mL vs. 1.17 µIU/mL; P < 0.001), while the FT4 level in the thyroid cancer group was significantly higher than that in the control group (17.16 pmol/L vs. 16.33 pmol/L; P < 0.001). The percentage of TPOAb positive in pregnant women with thyroid cancer was 25.0%, which was significantly higher than that in the control group (11.8%), P < 0.001.
The maternal outcomes between pregnant women with and without thyroid cancer was shown in Table 3. Most adverse obstetric outcomes such as stillbirth, preterm delivery, cesarean section, GDM, HDP, premature rupture of membranes, placenta previa, placenta abruption, abnormally invasive placentation, and postpartum hemorrhage had no difference between the two groups. Pregnant women with thyroid cancer had a higher risk of late miscarriage (0.9% vs. 0.0%; OR 7.166, 95% CI: 1.521, 33.775, P = 0.013). However, after adjusting maternal TPOAb positive, there was no statistical significance (OR 3.480, 95% CI: 0.423, 28.614, P = 0.246) (Table 4).
The differences in GWG and glucolipid levels
As shown in Table 3, no matter whether in all pregnant women or full-term pregnant women, the GWG in the thyroid cancer group was higher than that in the control group. Multiple linear regression analysis showed that GWG was related to the history of thyroid cancer after adjusting maternal age, pre-pregnancy BMI, multiparity, history of PCOS, pre-pregnancy DM, GDM, HDP, and delivery gestational age (Table 5).
When comparing the differences in the glucolipid levels in the first and third trimesters of pregnancy between the two groups (Supplementary Table 1), levels of total cholesterol (TCHO) and high-density lipoprotein cholesterol (HDL-C) in the thyroid cancer group were found to be significantly higher in the first trimester. However, there was no significant difference in glucolipid levels between the two groups in the third trimester. Although there was no significant difference in the prevalence of GDM between the two groups (20.8% vs. 17.4%; P = 0.194), OGTT showed that fasting plasma glucose and 2-hour value in the thyroid cancer group were higher than those in the control group (P = 0.020 and = 0.004, respectively) (Supplementary Table 1).
As shown in Table 3, the proportions of male newborns in the thyroid cancer group and the control group were 49.5% and 51.4%, respectively. The mean newborn birthweight of the thyroid cancer group was 3365 g which was similar to that of the control group (3370 g). And there was no significant difference in the proportion of macrosomia and the proportion of LBW between the two groups.
The differences in neonatal TSH levels
We found that there was no statistically significant difference in TSH of full-term newborns and preterm newborns between the thyroid cancer group and the control group (Table 3). We got the same results after propensity score matching (1:1) (Supplementary Table 2). Matching variables include maternal age, pre-pregnancy BMI, gestational age of delivery, mode of delivery, birth month, neonatal gender, maternal history of pre-pregnancy DM, GDM, and HDP. Multiple linear regression analysis showed that neonatal TSH was associated with maternal TSH, maternal FT4, maternal age, pre-pregnancy BMI, mode of delivery, and birth month (Table 6). No correlation was found between neonatal TSH and maternal history of thyroid cancer (Table 6).
Pregnant women with a history of thyroidectomy with or without radioactive iodine treatment were treated with supplementary LT4 throughout pregnancy. In this study, thyroid function status was significantly different in women with thyroid cancer in early pregnancy. However, the disease might not have substantial adverse effects on pregnancy outcomes except for GWG. Women with thyroid cancer had an excessive GWG. Considering that maternal thyroid function is a determinant of newborn thyroid function , we compared neonatal TSH levels between pregnancies with thyroid cancer and their controls. However, we found no significant difference in the level of neonatal TSH between the two groups. Further analysis observed an association between neonatal TSH and maternal FT4 and TSH levels in the first trimester of pregnancy, but no correlation was found between neonatal TSH and maternal history of thyroid cancer.
In this study, the proportion of late miscarriages of pregnant women with thyroid cancer was higher than that of their controls (0.9% vs. 0.0%; P = 0.001). A meta-analysis also demonstrated an increased risk of miscarriage or abortion in women with thyroid cancer . But the authors considered the result might be biased because of the small number of studies and considering the potentially significant publication bias. The percentage of TPOAb positive in pregnant women with thyroid cancer was significantly higher than that in the control group (25.0% vs. 12.9%; P < 0.001). After adjusting maternal TPOAb positive, the odds of late miscarriage with thyroid cancer were 3.480 (0.423, 28.614) and there was no statistical significance. There is evidence that the presence of maternal thyroid autoantibodies is strongly associated with miscarriage [30, 31], and animal study has found an increased proportion of fetal resorption in mice with induced thyroperoxidase antibodies . Considering the limited number of available patients, further studies are warranted to explore whether TPOAb is associated with increased late miscarriage in pregnant women with thyroid cancer.
The thyroid hormone has an important role in regulating metabolism, which influences key metabolic pathways that control energy balance. Our present study showed that pregnant women with thyroid cancer had an increased GWG. Liu et al. did not find differences in GWG between thyroid cancer survivors and the control group . However, a propensity score-matched cohort study showed that thyroid cancer survivors had reduced weight gain during pregnancy . Owing to the evidence regarding GWG in patients with thyroid cancer being few and conflicting, further studies are warranted to strengthen these conclusions. It has been reported that GWG may be related to the risk of pregnancy complications [33, 34]. Moreover, thyroid dysfunction has been suggested to play a role in the etiology of GDM [35,36,37,38,39]. There was no evidence of increased risk of GDM in patients with thyroid cancer confirmed by our present study and other studies [11, 14]. However, OGTT showed that fasting plasma glucose and 2-hour value in the thyroid cancer group were higher than those in the control group. No increased incidence of other major adverse pregnancy outcomes such as macrosomia, preterm delivery, and cesarean delivery was detected among women with thyroid cancer in our study. We analyzed the difference in total GWG rather than that of pre-OGTT weight gain, and the latter has a better correlation with the OGTT results. Whether there is a causal relationship between excessive GWG and the difference in OGTT needs to be further explored. Current evidence suggests that clinicians should pay attention to GWG in women with thyroid cancer.
Regarding other pregnancy outcomes assessed in our study, we found no statistically significant difference between the thyroid cancer group and the control group. The evidence regarding adverse pregnancy outcomes in patients with thyroid cancer has been conflicting. A retrospective cohort study reported by Liu et al. showed that pregnant women with a history of thyroid cancer had a higher risk of abnormally invasive placentation . Another retrospective cohort study revealed that pregnancies complicated by thyroid cancer have higher incidences of venous thromboembolism and need for transfusions, with comparable overall newborn outcomes . A study conducted by Cho and colleagues showed that women with a history of thyroid cancer had a slightly higher risk of preterm birth, high birth weight, preeclampsia, postpartum hemorrhage, and placenta previa . The results of the meta-analysis showed that the event rates for preterm labor and congenital anomalies in patients with DTC who underwent thyroidectomy were 0.07 (95% CIs, 0.05–0.09; 14 studies) and 0.03 (95% CIs, 0.02–0.06; 17 studies), respectively, which were similar to those previously reported in the general population . These valuable data should reassure both patients and physicians that a history of thyroid cancer does not meaningfully impact the risk of adverse pregnancy outcomes.
Previous studies have shown that maternal thyroid function is positively associated with offspring thyroid function at birth [20, 21]. Our present showed that the thyroid function status was significantly different in women with thyroid cancer in early pregnancy, which was consistent with other studies [11, 41]. João Anselmo et al. conducted a retrospective study concerning fetal loss associated with excess thyroid hormone exposure . Individuals with resistance to thyroid hormone (RTH) achieve euthyroidism by maintaining high serum levels of free thyroid hormone. They found that the levels of TSH in unaffected infants born to RTH mothers were suppressed, which indicated that the high maternal thyroid hormone levels produce fetal thyrotoxicosis . Another study showed that the amniotic fluid thyroxine level in patients with thyroid carcinoma who were placed on suppressive thyroxine treatment was lower than that in normal pregnancies and hypothyroid patients . Fan et al. also found that levels of neonatal TSH in the thyroid cancer group were significantly lower than those in the control group . However, we found no significant difference in the levels of neonatal TSH between the thyroid cancer group and the control group. Considering the limited number of available evidence, further studies are warranted to investigate the effect of LT4 suppression therapy during pregnancy on neonatal thyroid function in women with thyroid cancer.
We have for the first time performed a detailed analysis of glucolipid metabolism which deserves attention for pregnancies with thyroid cancer in the future. And our conclusion should reassure both patients and physicians that thyroid cancer does not meaningfully impact the risk of adverse pregnancy outcomes. Our study was limited by the retrospective and single-center study design. With regard to 212 women with thyroid cancer, more information could not be available, including initial risk stratification and response to therapy. Moreover, the laboratory data on thyroid function in the second and third trimesters especially in pregnancies without thyroid cancer were not available. Data on cases of miscarriage before 12 weeks of gestation were not included in the electronic database of our hospital. Therefore, we could not analyze whether pregnant women with thyroid cancer had an increased risk of early miscarriage. The lack of data on the Apgar score and the percentage of admissions to the neonatal unit was another limitation of our study.
In conclusion, thyroid cancer might not have substantial adverse effects on pregnancy outcomes except for excessive GWG. Although there was no significant difference in the prevalence of GDM, pregnant women with thyroid cancer had higher fasting plasma glucose and a 2-hour value in OGTT. Thyroid function status was significantly different in women with thyroid cancer in early pregnancy, however, we found no significant effect on neonatal TSH. The effect on long-term thyroid function and neuropsychological function in offspring need further study.
The datasets analyzed during the current study are available from the corresponding author on reasonable request.
The American Thyroid Association
Body mass index
Differentiated thyroid cancer
Gestational diabetes mellitus
Gestational weight gain
High-density lipoprotein cholesterol
Hypertensive disorders in pregnancy
In vitro fertilization-embryo transfer
Low birth weight
The National Cancer Center
Oral glucose tolerance test
Polycystic ovarian syndrome
Radioactive iodine therapy
Resistance to thyroid hormone
Thyroid peroxidase antibodies
Thyroid stimulating hormone
Araque DVP, Bleyer A, Brito JP. Thyroid cancer in adolescents and young adults. Future Oncol. 2017;13(14):1253–61.
Rongshou Zheng SZ, Hongmei Zeng S, Wang K, Sun Ru, Chen L, Li W, Wei, Jie He. Cancer incidence and mortality in China, 2016. J Natl Cancer Cent. 2022;2(1):1–9.
Haugen BR, Alexander EK, Bible KC, Doherty GM, Mandel SJ, Nikiforov YE, Pacini F, Randolph GW, Sawka AM, Schlumberger M, et al. 2015 american thyroid Association Management Guidelines for adult patients with thyroid nodules and differentiated thyroid Cancer: the american thyroid Association Guidelines Task Force on thyroid nodules and differentiated thyroid Cancer. Thyroid. 2016;26(1):1–133.
Schlumberger M, Leboulleux S. Current practice in patients with differentiated thyroid cancer. Nat Rev Endocrinol. 2021;17(3):176–88.
Alexander EK, Pearce EN, Brent GA, Brown RS, Chen H, Dosiou C, Grobman WA, Laurberg P, Lazarus JH, Mandel SJ, et al. 2017 guidelines of the american thyroid Association for the diagnosis and management of thyroid disease during pregnancy and the Postpartum. Thyroid. 2017;27(3):315–89.
Lee SY, Cabral HJ, Aschengrau A, Pearce EN. Associations Between Maternal Thyroid Function in Pregnancy and Obstetric and Perinatal Outcomes. J Clin Endocrinol Metab. 2020, 105(5).
Derakhshan A, Peeters RP, Taylor PN, Bliddal S, Carty DM, Meems M, Vaidya B, Chen L, Knight BA, Ghafoor F, et al. Association of maternal thyroid function with birthweight: a systematic review and individual-participant data meta-analysis. Lancet Diabetes Endocrinol. 2020;8(6):501–10.
Zhang Y, Sun W, Zhu S, Huang Y, Huang Y, Gao Y, Zhang J, Yang H, Guo X. The Impact of Thyroid Function and TPOAb in the First Trimester on Pregnancy Outcomes: A Retrospective Study in Peking. J Clin Endocrinol Metab. 2020, 105(3).
Toloza FJK, Derakhshan A, Mannisto T, Bliddal S, Popova PV, Carty DM, Chen L, Taylor P, Mosso L, Oken E, et al. Association between maternal thyroid function and risk of gestational hypertension and pre-eclampsia: a systematic review and individual-participant data meta-analysis. Lancet Diabetes Endocrinol. 2022;10(4):243–52.
Consortium on T, Pregnancy-Study Group on, Preterm B, Korevaar TIM, Derakhshan A, Taylor PN, Meima M, Chen L, Bliddal S, Carty DM, Meems M, et al. Association of thyroid function test abnormalities and thyroid autoimmunity with Preterm Birth: a systematic review and Meta-analysis. JAMA. 2019;322(7):632–41.
Liu D, Wei Y, Zhao Y, Li R, Yan J, Qiao J. Obstetric outcomes in thyroid cancer survivors: a retrospective cohort study. Int J Gynaecol Obstet. 2021;155(1):119–24.
Kim HO, Lee K, Lee SM, Seo GH. Association between pregnancy outcomes and Radioactive Iodine Treatment after Thyroidectomy among women with thyroid Cancer. JAMA Intern Med. 2020;180(1):54–61.
Cho GJ, Kim SY, Lee HC, Lee KM, Han SW, Oh MJ, Woodruff TK. Risk of adverse obstetric outcomes and the abnormal growth of offspring in women with a history of thyroid Cancer. Thyroid. 2019;29(6):879–85.
Cao Q, Zhu H, Zhang J, Li Y, Huang W. Pregnancy outcomes in thyroid Cancer survivors: a propensity score-matched cohort study. Front Endocrinol (Lausanne). 2022;13:816132.
Wu JX, Young S, Ro K, Li N, Leung AM, Chiu HK, Harari A, Yeh MW. Reproductive outcomes and nononcologic complications after radioactive iodine ablation for well-differentiated thyroid cancer. Thyroid. 2015;25(1):133–8.
Burrow GN, Fisher DA, Larsen PR. Maternal and fetal thyroid function. N Engl J Med. 1994;331(16):1072–8.
Pakkila F, Mannisto T, Surcel HM, Ruokonen A, Bloigu A, Pouta A, Hartikainen AL, Vaarasmaki M, Jarvelin MR, Suvanto E. Maternal thyroid dysfunction during pregnancy and thyroid function of her child in adolescence. J Clin Endocrinol Metab. 2013;98(3):965–72.
Peter F. Thyroid dysfunction in the offspring of mothers with autoimmune thyroid diseases. Acta Paediatr. 2005;94(8):1008–10.
Polak M, Le Gac I, Vuillard E, Guibourdenche J, Leger J, Toubert ME, Madec AM, Oury JF, Czernichow P, Luton D. Fetal and neonatal thyroid function in relation to maternal Graves’ disease. Best Pract Res Clin Endocrinol Metab. 2004;18(2):289–302.
Korevaar TI, Chaker L, Jaddoe VW, Visser TJ, Medici M, Peeters RP. Maternal and birth characteristics are determinants of offspring thyroid function. J Clin Endocrinol Metab. 2016;101(1):206–13.
Medici M, de Rijke YB, Peeters RP, Visser W, de Keizer-Schrama M, Jaddoe SM, Hofman VV, Hooijkaas A, Steegers H, Tiemeier EA. Maternal early pregnancy and newborn thyroid hormone parameters: the Generation R study. J Clin Endocrinol Metab. 2012;97(2):646–52.
Kuppens SM, Kooistra L, Wijnen HA, Vader HL, Hasaart TH, Oei SG, Vulsma T, Pop VJ. Neonatal thyroid screening results are related to gestational maternal thyroid function. Clin Endocrinol. 2011;75(3):382–7.
Giakoumelou S, Wheelhouse N, Cuschieri K, Entrican G, Howie SE, Horne AW. The role of infection in miscarriage. Hum Reprod Update. 2016;22(1):116–33.
Garovic VD, Dechend R, Easterling T, Karumanchi SA, McMurtry Baird S, Magee LA, Rana S, Vermunt JV, August P, American Heart Association Council on H. Hypertension in pregnancy: diagnosis, blood pressure goals, and Pharmacotherapy: A Scientific Statement from the American Heart Association. Hypertension. 2022;79(2):e21–e41.
American College of O. Gynecologists’ Committee on Practice B-O: practice Bulletin No. 172: premature rupture of membranes. Obstet Gynecol. 2016;128(4):e165–177.
Jain V, Bos H, Bujold E. Guideline No. 402: diagnosis and management of Placenta Previa. J Obstet Gynaecol Can. 2020;42(7):906–917e901.
Schmidt P, Skelly CL, Raines DA. Placental Abruption. StatPearls.edn. Treasure Island (FL); 2022.
Collins SL, Stevenson GN, Al-Khan A, Illsley NP, Impey L, Pappas L, Zamudio S. Three-Dimensional Power Doppler Ultrasonography for Diagnosing abnormally invasive placenta and quantifying the risk. Obstet Gynecol. 2015;126(3):645–53.
Moon S, Yi KH, Park YJ. Risk of Adverse Pregnancy Outcomes in Young Women with Thyroid Cancer: A Systematic Review and Meta-Analysis. Cancers (Basel)2022, 14(10).
Thangaratinam S, Tan A, Knox E, Kilby MD, Franklyn J, Coomarasamy A. Association between thyroid autoantibodies and miscarriage and preterm birth: meta-analysis of evidence. BMJ. 2011;342:d2616.
Dhillon-Smith RK, Coomarasamy A. TPO antibody positivity and adverse pregnancy outcomes. Best Pract Res Clin Endocrinol Metab. 2020;34(4):101433.
Lee YL, Ng HP, Lau KS, Liu WM, O WS, Yeung WS, Kung AW. Increased fetal abortion rate in autoimmune thyroid disease is related to circulating TPO autoantibodies in an autoimmune thyroiditis animal model. Fertil Steril. 2009;91(5 Suppl):2104–9.
Goldstein RF, Abell SK, Ranasinha S, Misso M, Boyle JA, Black MH, Li N, Hu G, Corrado F, Rode L, et al. Association of Gestational Weight Gain with maternal and infant outcomes: a systematic review and Meta-analysis. JAMA. 2017;317(21):2207–25.
LifeCycle Project-Maternal O, Childhood Outcomes Study G, Voerman E, Santos S, Inskip H, Amiano P, Barros H, Charles MA, Chatzi L, Chrousos GP, et al. Association of Gestational Weight Gain with adverse maternal and infant outcomes. JAMA. 2019;321(17):1702–15.
Li X, Zuo J, Li YH, Tang YP, Bao YR, Ying H. Association between thyroid function and risk of gestational diabetes mellitus in assisted pregnancies: a retrospective cohort study. Diabetes Res Clin Pract. 2021;171:108590.
Wang J, Gong XH, Peng T, Wu JN. Association of thyroid function during pregnancy with the risk of pre-eclampsia and gestational diabetes Mellitus. Endocr Pract. 2021;27(8):819–25.
Tang L, Li P, Zhou H, Li L. A longitudinal study of thyroid markers during pregnancy and the risk of gestational diabetes mellitus and post-partum glucose metabolism. Diabetes Metab Res Rev. 2021;37(4):e3441.
Tudela CM, Casey BM, McIntire DD, Cunningham FG. Relationship of subclinical thyroid disease to the incidence of gestational diabetes. Obstet Gynecol. 2012;119(5):983–8.
Rawal S, Tsai MY, Hinkle SN, Zhu Y, Bao W, Lin Y, Panuganti P, Albert PS, Ma RCW, Zhang C. A longitudinal study of thyroid markers across pregnancy and the risk of gestational diabetes. J Clin Endocrinol Metab. 2018;103(7):2447–56.
Spiegel E, Spence AR, Czuzoj-Shulman N, Abenhaim HA. Pregnancy outcomes after thyroid cancer. J Perinat Med. 2019;47(7):710–6.
Ding Z, Guo F, Zhou Y, Huang X, Liu Z, Fan J. Thyroxine supplementation in pregnant women after thyroidectomy for thyroid Cancer and neonatal Birth Weight. Front Endocrinol (Lausanne). 2021;12:728199.
Anselmo J, Cao D, Karrison T, Weiss RE, Refetoff S. Fetal loss associated with excess thyroid hormone exposure. JAMA. 2004;292(6):691–5.
Pekonen F, Teramo K, Ikonen E, Osterlund K, Makinen T, Lamberg BA. Women on thyroid hormone therapy: pregnancy course, fetal outcome, and amniotic fluid thyroid hormone level. Obstet Gynecol. 1984;63(5):635–8.
The authors gratefully acknowledge Chi Feng, Information Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal, and Child Health Care Hospital, for data collection.
This study was supported by grants from the Beijing Natural Science Foundation (No. 7214231), Scientific Research Common Program of Beijing Municipal Commission of Education (KM202110025007), and Beijing Hospitals Authority’ Ascent Plan (DFL20191402). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Ethics approval and consent to participate
This study has been performed in accordance with the Declaration of Helsinki and has been approved by the ethics committee of Beijing Obstetrics and Gynecology Hospital, Capital Medical University (2018-ky-009-01). Since the anonymous data were respectively extracted from the electronic record without any information that could identify particular individual, a waiver of informed consent was granted by the ethics committee of Beijing Obstetrics and Gynecology Hospital, Capital Medical University. All methods were carried out in accordance with relevant guidelines and regulations in the declaration.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Yuan, X., Zhao, J., Wang, J. et al. Pregnancy outcomes and neonatal thyroid function in women with thyroid cancer: a retrospective study. BMC Pregnancy Childbirth 23, 383 (2023). https://0-doi-org.brum.beds.ac.uk/10.1186/s12884-023-05588-4
- Thyroid cancer
- Pregnancy outcome
- Neonatal thyroid function