Can hyperthyroidism be cured during pregnancy?
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The treatment of Graves’ disease during pregnancy will depend on your individual symptoms, the severity of the condition, as well as how far your pregnancy has progressed. Women with Graves’ disease are often advised to postpone conception and use contraception until the disease is controlled. Women with difficult to control Graves’ who are on high doses of antithyroid medications often choose definitive therapy, such as surgery to remove the thyroid gland, prior to conception. Show Anti-Thyroid MedicationsYour doctor may prescribe antithyroid medications if the benefits of taking them appear to outweigh the risks. Tapazole (methimazole) and propylthiouracil (PTU) are the two antithyroid drugs used in the United States to treat hyperthyroidism. Both of these medications can cross the placenta and potentially cause birth defects and hypothyroidism in the fetus. (2) Doctors often recommend the lowest possible dose of antithyroid medication to minimize the risks. “We used to think that the antithyroid drug methimazole caused birth defects and that PTU didn’t,” says Douglas Ross, MD, a professor of medicine at Harvard Medical School and co-director of thyroid associates at Massachusetts General Hospital. “A few years ago, a large study from Denmark also showed that PTU does cause birth defects, although they are much less severe than methimazole birth defects.” (5) Birth defects caused by methimazole are often life-threatening and can include choanal atresia (blockage of the nasal passage), esophageal atresia (the upper part of the esophagus does not connect with the lower part), aplasia cutis (absence of skin), umbilical cord defects, or omphalocele (abdominal organs outside the body). Birth defects caused by PTU can include anatomical anomalies (abnormalities) in the face or neck region and in the urinary system. Such abnormalities generally require surgical treatment but are less severe than the defects caused by methimazole. (6) “At least in my practice, this information has led most women to decide that they don’t want to take antithyroid drugs at all if they have Graves’ disease and they want to get pregnant,” says Dr. Ross. “And so they choose to do definitive therapy — more frequently the surgery, because they’re in a hurry to get pregnant, than radioactive iodine — to definitively get rid of their thyroid.” Beta-BlockersBeta-blockers, a class of drugs commonly used to lower blood pressure, are also used to control the so-called hyperadrenergic symptoms of Graves’ disease, such as anxiety, irritability, rapid heart rate, tremors, and sweating. While beta-blockers are commonly used during pregnancy, there’s conflicting evidence regarding the risks associated with taking them. If you are prescribed a beta-blocker during pregnancy or are already taking one when you become pregnant, discuss the relative risks and benefits of these drugs with your doctor. SurgeryA thyroidectomy (surgery to remove all or part of the thyroid gland) is sometimes performed to treat Graves’ disease. After surgery, patients may be prescribed thyroid hormones, as most people will develop hypothyroidism (underactive thyroid) after the surgery. Some women opt to have a thyroidectomy prior to trying to conceive. Surgery poses risks if performed at different points in a pregnancy, so talk to your doctor about the risks and alternatives. Radioactive IodineRadioactive iodine treatment is not recommended for pregnant or nursing women, although some women choose to undergo radioactive iodine treatment before they try to conceive. People who choose radioactive iodine therapy will develop hypothyroidism, which is easier to treat and causes fewer health complications than hyperthyroidism. If you’re a woman of childbearing age and are considering radioactive iodine treatment, make sure to take a pregnancy test before you begin it, and ask your doctor how long you should wait after the treatment is complete before you try to conceive. No TreatmentWhile treating Graves’ disease during pregnancy comes with risks, so does foregoing treatment during pregnancy. Women who do not control their Graves’ disease are almost 10 times more likely to have a baby with low birth weight. They are also 16 times more likely to deliver preterm and 5 times more likely to develop preeclampsia and experience stillbirth. If you have Graves’ disease and want to have a baby, speak to your doctor about the best way to have a healthy pregnancy while also managing your disease. Introduction Hyperthyroidism is defined by abnormally high levels of thyroid hormone caused by an increased synthesis and secretion of thyroid hormone from the thyroid gland.1 The term “thyrotoxicosis”, on the other hand, is used to describe “excess of thyroid hormone”, and this can be due to an increased synthesis of thyroid hormone in the thyroid gland (hyperthyroidism), but may also occur in the absence of hyperthyroidism, eg, in patients with leakage of thyroid hormone from the thyroid gland (thyroiditis) or in patients with excess intake of thyroid hormone.1 Careful management and control of patients suffering from hyperthyroidism are important to prevent the possible complications related to the disease itself or to the treatment.1–3 A special situation is hyperthyroidism in women of reproductive age who are or may in the future become pregnant.4,5 Hyperthyroidism in pregnancy is a special clinical situation because physiological changes related to the pregnant state challenge the interpretation of thyroid function test and because potential complications related to the disease and/or the treatment may compromise the health of the pregnant woman and also the developing fetus.4,5 Hyperthyroidism can be overt (suppressed thyroid-stimulating hormone [TSH] and elevated T3 [triiodothyronine] and/or T4 [tetraiodothyronine] in a blood sample) or subclinical (suppressed TSH and normal T3 and T4).2,3 This review focuses on the management of overt hyperthyroidism in pregnant women and discusses the following current perspectives: 1) the etiology and incidence of overt hyperthyroidism in pregnancy, 2) the diagnosis of overt hyperthyroidism in pregnancy, 3) the consequences of untreated overt hyperthyroidism in pregnancy, and 4) the treatment of overt hyperthyroidism in pregnancy. Etiology and incidence of hyperthyroidism in pregnancy Etiology of hyperthyroidism Overt hyperthyroidism can be divided into different subtypes from the underlying etiology, and the three most common subtypes are Graves’ disease, multinodular toxic goiter, and solitary toxic adenoma.6 All types show a female predominance (most pronounced for Graves’ disease and multinodular toxic goiter), but there is a notable difference in the typical age at onset of these various types of hyperthyroidism (Figure 1).6 In a Danish population-based study with individual review and subclassification of 1,682 new cases of overt hyperthyroidism, Graves’ disease was the predominant type of hyperthyroidism in young individuals, and the incidence of this subtype was stable with increasing age (Figure 1).6 On the other hand, multinodular toxic goiter and solitary toxic adenoma were rare in young individuals, and the incidence was increasing with age, particularly for multinodular toxic goiter, which is the predominant type of hyperthyroidism in older individuals in Denmark (Figure 1).6
Graves’ disease is an autoimmune disease in which hyperthyroidism is caused by the production of autoantibodies that are directed against the TSH receptor and stimulate the thyroid gland to an increased production of thyroid hormone.1 Biochemically, increased serum levels of TSH receptor antibodies (TRAb) are detectable in 95% of patients with Graves’ disease.7 Hyperthyroidism caused by multinodular toxic goiter or toxic solitary adenoma is not considered of autoimmune origin, but develops from thyroid autonomy, where the synthesis of thyroid hormone occurs independently of regulation by TSH.8 Such thyroid autonomy is often seen as a late consequence of iodine deficiency.8 Incidence of hyperthyroidism in pregnancy Graves’ disease is the predominant type of overt hyperthyroidism in women of reproductive age and thereby also the main type of overt hyperthyroidism in pregnancy.6 However, other types of thyrotoxicosis may occur in early pregnancy, and they should be distinguished from the hyperthyroidism of Graves’ disease.4,5 Physiological changes in the pregnant state affect the function of the thyroid gland. The steep increase in human chorionic gonadotropin (hCG) from early pregnancy stimulates the thyroid gland to an increased production of thyroid hormone. hCG is a glycoprotein synthesized in and released from the placenta, and it stimulates the TSH receptor due to structural similarities with TSH.9 Gestational hyperthyroidism is a nonautoimmune transient disorder that occurs in the first trimester of pregnancy and is caused by the peak in hCG levels during early pregnancy.4,5 Gestational hyperthyroidism is often associated with hyperemesis gravidarum, and clinically it may be difficult to distinguish from Graves’ hyperthyroidism. The presence of TRAb strongly supports a diagnosis of Graves’ disease.2–4 The incidence of Graves’ disease varies in and around pregnancy.10 Pregnancy is associated with profound changes in the maternal immune system, with a general immune suppression during the pregnancy followed by an immune rebound after the birth of the child.11 Such alterations may influence the onset of autoimmune diseases (Figure 2).10 In a Danish population-based study of 403,958 women, the incidence of nontransient hyperthyroidism (considered to be Graves’ disease) was high in early pregnancy, which was followed by a gradual decline during the pregnancy and then a considerable increase in incidence postpartum (Figure 2).10 The women identified with hyperthyroidism in early pregnancy did not suffer from transient hyperthyroidism,10 but it can be speculated that the hCG-medicated increase in thyroid hormone production in early pregnancy may trigger the development of Graves’ disease in susceptible individuals.12 Likewise, Graves’ disease that developed prior to a pregnancy may aggravate in early pregnancy.13
Diagnosis of hyperthyroidism in pregnancy Changes in thyroid hormone metabolism The diagnosis of overt hyperthyroidism is based on the measurement of a suppressed TSH and an elevated T3 and/or T4.1–3 The physiological changes during a pregnancy may, however, challenge the interpretation of thyroid function test results.9 One physiological mechanism is the increase of hCG in early pregnancy that stimulates the thyroid gland to increase production of thyroid hormone and tends to decrease TSH.9 Another physiological mechanism is the increased activity of the type-3-deiodinase enzyme in the placenta that inactivates T3 and T4 and tends to increase TSH.9 Finally, the pregnancy-associated high levels of estrogen increase thyroxine-binding globulin with a concomitant increase in total T3 and total T4.9 One consideration related to these physiological changes is how to evaluate the peripheral thyroid hormone concentrations in pregnant women. The change in thyroxine-binding globulin concentrations, and thereby in the concentration of total thyroid hormone, has led to the use of free thyroid hormone assays in many countries. Direct measurement of free thyroid hormone concentrations includes an initial separation of free and protein-bound thyroid hormone by ultrafiltration or equilibrium dialysis. However, in routine laboratories, free thyroid hormones are usually determined using automatic immunoassays, and all these provide an indirect measurement of free thyroid hormone concentrations with no initial separation. Thus, free thyroid hormone concentrations change in relation to the physiological changes during a pregnancy.14 Furthermore, the methods used to determine the free thyroid hormone concentrations in different immunoassays are not identical, and this diversity stresses the importance of laboratory-specific reference ranges.15 Another consideration is the changes in thyroid function test results during a pregnancy. It has often been recommended to use trimester-specific reference ranges in pregnant women.2–4 However, the physiological changes in the first trimester of pregnancy are so rapid that such a definition may be too simple.16 Figure 3 depicts the lower reference limit for TSH and upper reference limit for free T4 (fT4) during early pregnancy determined using the Dimension Vista (Siemens Healthcare Diagnostics GmbH, Eschborn, Germany) immunoassay in healthy Danish pregnant women stratified by week of pregnancy.16 The dashed horizontal lines indicate the reference limits for nonpregnant adults provided by the manufacturer. The diagnosis of overt hyperthyroidism in nonpregnant adults would be defined by TSH below this lower reference limit of 0.358 mU/L and fT4 above the upper reference limit of 18.8 pmol/L. As can be seen from Figure 3, these reference limits would not correctly classify pregnant women with overt hyperthyroidism.16 For TSH, the lower reference limit was higher in early pregnancy and lower in weeks 9–12 of pregnancy. For fT4, the difference between the upper reference limit in nonpregnant and pregnant women was less pronounced, however, with a tendency toward higher levels in gestational weeks 9–12 and lower levels from week 13 and onward. Thus, in the diagnosis of hyperthyroidism in pregnant women, week-to-week-specific reference ranges in early pregnancy would be preferable.16
Untreated hyperthyroidism in pregnancy Fetal programming? Correct diagnosis of hyperthyroidism in pregnant women is important to prevent adverse outcomes of pregnancy. Overt hyperthyroidism is considered as a clinical high-risk situation, and the disease should be carefully diagnosed, managed, and controlled.2–4 On the other hand, subclinical hyperthyroidism (suppressed TSH) has not been associated with pregnancy complications.17 Thyroid hormones are important developmental factors.18 Thyroid hormone receptors are present in the maternal–fetal unit,19 and normal levels of thyroid hormone are important in the maintenance of a normal pregnancy.20 Both the lack of thyroid hormone and thyroid hormone excess may interfere with the maternal–fetal unit, and women suffering from hyperthyroidism have an increased risk of both early and late pregnancy loss.21 Maternal hyperthyroidism is also associated with an increased risk of preterm delivery and low birth weight of the child and may seriously complicate the health of the pregnant women, eg, maternal heart failure and in rare cases even thyroid storm.5 Thyroid hormone receptors are also present in the fetal brain,22 and levels of maternal thyroid hormones play a crucial role in fetal brain development.23 The fetal thyroid gland is increasingly able to synthesize thyroid hormones in the second half of pregnancy, but maternal thyroid hormones are important for fetal development throughout pregnancy.24 Evidence from experimental studies have shown that high levels of maternal thyroid hormones may interrupt fetal brain development,25,26 and population-based epidemiological studies have shown an association between maternal hyperthyroidism and the later development of brain-related disease in the child.27 In a Danish nationwide study, children born to mothers with hyperthyroidism had an increased risk of developing seizure disorders28 and attention-deficit hyperactivity disorder later in life,29 particularly when the mother was first diagnosed with hyperthyroidism after the pregnancy and potentially had undetected high levels of thyroid hormones during the pregnancy. A proposed mechanism is that maternal thyroid disease may program the fetus to later development of disease via subtle structural and/or functional changes during fetal brain development.27 Further studies, including studies with actual measurement of maternal thyroid function in pregnancy, are needed to explore this hypothesis. Treatment of hyperthyroidism in pregnancy Early pregnancy Overt hyperthyroidism should be adequately treated to prevent maternal and fetal complications. A matter of clinical attention in early pregnancy is, however, that transient biochemical hyperthyroidism caused by the physiological hCG peak in early pregnancy should not be treated with antithyroid drugs (ATDs).2–4 There is no evidence that ATD treatment of this transient physiological hyperthyroidism improves the outcome of pregnancy.2–4 A physical examination and repeated thyroid function testing every 2–3 weeks are recommended, and in case of hyperemesis gravidarum, this should be managed with supportive therapy and management of dehydration. The treatment of choice for overt hyperthyroidism in pregnant women is ATD.5 Radioiodine treatment should not be used in pregnancy. If ATDs are not tolerated, the alternative treatment is thyroidectomy, preferably in the second trimester of pregnancy.2–4 ATDs are thioamides that block the synthesis of thyroid hormone in the thyroid gland.30 The available drugs include methimazole (MMI) and its prodrug carbimazole (CMZ) as well as propylthiouracil (PTU). The drugs are equally effective in the treatment of hyperthyroidism, and they all pass the placenta, which may lead to fetal hypothyroidism in late pregnancy (see “Late pregnancy” section).31–33 The major concern to the use of these drugs in early pregnancy is, however, the potential risk of birth defects.34 An association between the use of ATD in early pregnancy and birth defects was first reported in 1972.35 In a short publication, it was described that two of eleven mothers who had given birth to a child with a scalp defect had been treated with MMI during pregnancy.35 Following this, additional cases of birth defects after the use of MMI or CMZ were reported. Many of these birth defects were within a certain group of malformations, which led to the description of a specific MMI embryopathy that included special facial features, aplasia cutis, upper airway atresia, esophageal and other gastrointestinal atresias, abdominal wall defects, and also ventricular septal defects.36–39 In recent years, the risk of birth defects evident from case reports has been corroborated in large clinic- and population-based studies. Studies from Japan40 and Denmark41 both reported an increased risk of birth defects in children exposed to MMI/CMZ. The birth defects involved various organ systems, which are illustrated in the upper part of Figure 4, and includes data from the Danish study.41 Furthermore, both studies40,41 reported birth defects in line with the previously described MMI embryopathy.
Notably, the Danish study41 also found an increased risk of birth defects in children exposed to PTU (lower part of Figure 4). However, the types of birth defects after PTU exposure were different from those observed after MMI/CMZ (Figure 4) and less severe.42 PTU-associated birth defects were confined to the face and neck region (preauricular sinus, fistula, and cysts) and the urinary tract (Figure 4). Although less severe, the majority of cases had been surgically treated.42 Current international guidelines recommend the use of PTU in the first trimester of pregnancy considering the risk of birth defects after MMI/CMZ and to consider shifting from PTU to MMI/CMZ after the first trimester considering the risk of liver failure associated with the use of PTU.2–4 Liver failure during treatment with PTU has been a matter of concern because PTU was the third most common drug-related cause of liver transplantation in the USA.43,44 However, in a recent Danish population-based study, the frequency of severe side effects to the use of ATDs in the general population and in pregnancy specifically was compared. Both agranulocytosis and liver failure were very rare events in pregnancy, with birth defects being the predominant side effect.34 Further studies within this field are needed, including more studies on alternative treatments to the use of ATD in pregnancy. Table 1 summarizes the current proposals on the treatment of overt hyperthyroidism in early pregnancy. Notably, the critical window of ATD exposure and the risk of birth defects are from weeks 6 to 10 of pregnancy.45 An important aspect in the proposals is to discuss future pregnancy with a woman who may become pregnant, including the strategy to detect a pregnancy as early as possible. For the responsible physician, it is important to consider the clinical indication of continued ATD treatment when a pregnancy is detected. Such evaluation should be based on thyroid function test results, levels of TRAb, current dose and duration of ATD treatment, and clinical symptoms.9
Late pregnancy An important aspect in the management of maternal hyperthyroidism in late pregnancy is the thyroid function of the fetus.46 TRAb, which are the cause of Graves’ hyperthyroidism in the mother, cross the placenta, and the concentration of TRAb is similar in maternal and fetal blood in late pregnancy.47 Thus, TRAb can also stimulate the fetal thyroid gland to produce excess thyroid hormones. In the second half of pregnancy, when the fetal thyroid gland is capable of synthesizing thyroid hormones, fetal hyperthyroidism can occur. As already mentioned, all available ATDs pass the placenta, and when used for the treatment of maternal hyperthyroidism, these drugs will also treat the fetal hyperthyroidism. However, there is a risk of fetal hypothyroidism during such treatment.48,49 Thyroid autoimmunity tends to attenuate during the pregnancy50 in line with the general suppression of the immune system11 and the gradual decline in the incidence of maternal hyperthyroidism in late pregnancy (Figure 2).10 Following this, the dose of ATD needed to keep the mother euthyroid may change during the pregnancy, and it is important to reduce the dose if indicated, because both MMI/CMZ and PTU tend to overtreat the fetus with a risk of fetal hypothyroidism, when the mother is euthyroid.33 In nonpregnant patients with Graves’ hyperthyroidism, a treatment regimen called “block replacement therapy” may be used.2–4 This treatment is based on a combination of ATD and thyroid hormone, which makes it possible to overtreat the hyperthyroidism and to keep the patient euthyroid with thyroid hormone replacement. Block replacement therapy should not be used in pregnant women because the high dose of ATD will overtreat the fetus and the thyroid hormone replacement therapy will only have minimal effect in the fetus with a risk of severe fetal hypothyroidism.2–4 However, this treatment regimen can be used in the special situation of isolated fetal hyperthyroidism.46 Isolated fetal hyperthyroidism can be developed if a pregnant woman who previously received ablative therapy for Graves’ disease (radioiodine treatment or thyroidectomy) still produces high levels of TRAb.46 In such case, ATD will treat the fetal hyperthyroidism, and thyroid hormone replacement will keep the pregnant women euthyroid. The risk of such fetal hyperthyroidism can be evaluated from the measurement of maternal TRAb levels in early pregnancy. If TRAb level is elevated, a plan for biochemical and clinical monitoring should be made, including the measurement of TRAb in mid-pregnancy around week 20 and if still elevated again in the third trimester around week 30 of pregnancy. Another important aspect to consider in late pregnancy is the risk of hyperthyroidism in the newborn child.5 Neonatal hyperthyroidism is typically present immediately after birth in children born to mothers with untreated Graves’ hyperthyroidism or mothers with previous thyroid ablation who still produce TRAb. On the other hand, delayed neonatal hyperthyroidism can occur in children born to mothers who received ATD during pregnancy and up to delivery. In such case, ATD will disappear from the child immediately after birth, whereas TRAb are cleared more slowly, and so neonatal hyperthyroidism can be detected some days after birth.5 The risk of neonatal hyperthyroidism can be evaluated from the measurement of maternal TRAb levels in late pregnancy. Ultrasound monitoring of fetal growth, goiter, and fetal heart rate are recommended in such patients if TRAb levels are more than three times above upper reference limit. Future perspectives Hyperthyroidism in pregnancy is a high-risk clinical situation that both the responsible physician and the patient should be aware of. The disease should be carefully managed and controlled to prevent both maternal and fetal complications. Untreated maternal hyperthyroidism may program the fetus to the long-term development of disease, and further studies are needed to explore the hypothesis of fetal programming by maternal hyperthyroidism. The management of hyperthyroidism before, during, and after a pregnancy involves different medical specialists (eg, general practitioner, obstetrician, endocrinologist, and pediatrician) and pertinent information to the patient. Ongoing and debatable topics on the management of hyperthyroidism in pregnancy especially refer to the diagnosis and treatment of hyperthyroidism in the first half of pregnancy. Further studies are needed on the week-to-week variation in thyroid function in early pregnancy. In addition to this, more data are needed on the risk of birth defects associated with the current available ATDs and the possibility of developing other treatments with fewer and less severe side effects. Disclosure The authors report no conflicts of interest in this work. References
How is hyperthyroidism treated during pregnancy?Antithyroid drugs are the treatment of choice for hyperthyroidism during pregnancy (18). They inhibit thyroid hormone synthesis by reducing iodine organification and coupling of MIT and DIT. Methimazole (MMI), propylthiouracil (PTU), and carbimazole have been used for the treatment of hyperthyroidism during pregnancy.
What happens if you have hyperthyroidism during pregnancy?How does hyperthyroidism affect pregnancy? Uncontrolled hyperthyroidism has many effects. It may lead to preterm birth (before 37 weeks of pregnancy) and low birth weight for the baby. Some studies have shown an increase in pregnancy-induced hypertension (high blood pressure of pregnancy) in women with hyperthyroidism.
Does hyperthyroidism make you high risk pregnancy?There is greater risk to the pregnancy from an untreated overactive thyroid gland than from taking antithyroid medication. Untreated hyperthyroidism can also lead to complications of high blood pressure in pregnancy, poor growth of the baby and premature delivery.
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