Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the <i>TSHR</i> gene

Won Kyoung Cho; Moon-Bae Ahn; Woori Jang; Hyojin Chae; Myungshin Kim; Byung-Kyu Suh

doi:10.6065/apem.2018.23.4.235

Ann Pediatr Endocrinol Metab > Volume 23(4); 2018 > Article

Cho, Ahn, Jang, Chae, Kim, and Suh: Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene

Case report

Annals of Pediatric Endocrinology & Metabolism 2018;23(4): 235-239.

Published online: December 31, 2018

DOI: https://doi.org/10.6065/apem.2018.23.4.235

Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene

Won Kyoung Cho, MD, PhD¹, Moon-Bae Ahn, MD², Woori Jang, MD, PhD³, Hyojin Chae, MD, PhD³, Myungshin Kim, MD, PhD³, Byung-Kyu Suh, MD, PhD²

¹Department of Pediatrics, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea

²Department of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Korea

³Department of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Korea

Address for correspondence: Byung-Kyu Suh, MD, PhD Department of Pediatrics, Seoul St. Mary's hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea
Tel: +82-2-2258-6185 Fax: +82-2-537-4544 E-mail: suhbk@catholic.ac.kr

Received November 18, 2018 Revised December 6, 2018 Accepted December 14, 2018

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Most cases of congenital hyperthyroidism are autoimmune forms caused by maternal thyroid stimulating antibodies. Nonautoimmune forms of congenital hyperthyroidism caused by activating mutations of the thyrotropin receptor (TSHR) gene are rare. A woman gave birth to a boy during an emergency cesarean section at 33 weeks of gestation due to fetal tachycardia. On the 24th day of life, thyroid function tests were performed due to persistent tachycardia, and hyperthyroidism was confirmed. Auto-antibodies to TSHR, thyroid peroxidase, and thyroglobulin were not found. The patient was treated with propylthiouracil and propranolol, but hyperthyroidism was not well controlled. At 3 months of age, the patient had craniosynostosis and hydrocephalus, and underwent a ventriculoperitoneal shunt operation. Direct sequencing of the TSHR gene showed a heterozygous mutation of c.1899C>A (p.Asp633Glu) in exon 10. No mutations were discovered in any of the parents in a familial genetic study. We have reported a case of sporadic nonautoimmune congenital hyperthyroidism, by a missense mutation of the TSHR gene, for the first time in South Korea.

Keywords: Hyperthyroidism, Nonautoimmune, Thyrotropin receptor, Germ-line mutation

Introduction

Congenital hyperthyroidism caused by activating mutations of the thyrotropin receptor (TSHR) gene is a rare disorder. Most cases of congenital hyperthyroidism are autoimmune forms caused by maternal thyroid stimulating immunoglobulins. Autoimmune congenital hyperthyroidism shows a transient course, lasting approximately 4 months after birth, and resolving when maternal antibodies are eliminated from the blood of the infant. However, nonautoimmune congenital hyperthyroidism by activating germline mutations in the TSHR gene shows a persistent and severe hyperthyroidism. Clinical manifestations of nonautoimmune congenital hyperthyroidism might occur from the fetus and cause tachycardia, arrhythmia, intrauterine growth retardation and premature birth. There are 2 types of activating TSHR germline mutations. One is familial nonautoimmune hyperthyroidism (FNAH), an autosomal dominant disorder, and the other is sporadic nonautoimmune hyperthyroidism (SNAH), caused by de novo mutations [1]. Compared to FNAH, SNAH tends to occur at a younger age, present more severe clinical symptoms. These findings might be influenced by genetic, epigenetic or environmental factors including in vitro activity of TSHR mutations [2]. To date, a total of 17 patients with SNAH by 12 activating mutations of the TSHR gene have been reported in the literature [2-4]. Herein, we report a case of sporadic nonautoimmune congenital hyperthyroidism by a missense mutation of the TSHR gene for the first time in South Korea.

Case report

A woman gave birth to a boy during an emergency cesarean section at 33 weeks of gestation due to fetal tachycardia. The birth weight was 2,280 g (50th–75th percentile), height was 43 cm (10th–25th percentile), and head circumference was 31 cm (50th–75th percentile). After birth, the boy was treated with meconium aspiration syndrome in neonatal intensive care unit. Approximately 4 days later, the patient recovered with mechanical ventilation, but continued to have tachycardia. Electrocardiography and echocardiography was normal except sinus tachycardia. Thyroid function test showed hyperthyroidism with increased free thyroxine (fT₄, 3.98 ng/dL; normal reference value, 0.85–1.86 ng/dL), total triiodothyronine (T₃, 10.52 ng/mL; normal reference value, 0.78–1.82 ng/mL) and decreased thyroid-stimulating hormone (TSH, 0.05 mIU/L; normal reference value, 0.17–4.05 mIU/L). Test for antibodies to TSHR, thyroid peroxidase, and thyroglobulin were negative. A thyroid ultrasound revealed increased vascularity and a diffuse goiter. The patient's mother had no history of any thyroid disease.

The patient was treated with propylthiouracil (PTU, 5 mg/kg) and propranolol for short-term management of thyroid storm [5], but showed persistent hyperthyroidism even after 1 month of treatment. One more month of intensive treatment with an increased dose of PTU (7.5 mg/kg) could only lead to subclinical hyperthyroidism (fT₄, 1.07 ng/dL; T₃, 2.54 ng/mL; TSH, 0.01 mIU/L). At 3 months after birth, a forehead protrusion was observed and the anterior fontanelle could not be palpated on physical examination. Brain computed tomography revealed hydrocephalus due to craniosynostosis and the patient underwent surgery to place a ventriculoperitoneal shunt. After 6 more months of treatment, thyroid function tests recovered to normal and tachycardia improved. PTU treatment was replaced with methimazole and euthyroid state was maintained for 2 months. When the dose of methimazole was reduced (0.3 mg/kg), a relapse of hyperthyroidism occurred. At 12 months of age (corrected age of 10 months), the patient’s height and weight were in the 50th–75th and 25th–50th percentile, respectively, in addition to exhibiting delayed milestones (cognitive skills at 7 months, receptive communication at 5 months, expressive communication at 6 months, fine motor at 6 months, and gross motor at 7 months). Moreover, the patient’s bone age was estimated to be 2 years and 8 months, which was markedly advanced compared to his chronological age.

Molecular genetic analysis was performed by direct sequencing of TSHR. Genomic DNA was isolated from peripheral blood leukocytes using a QIAmp DNA Mini Kit (Qiagen, Hilden, Germany). Polymerase chain reaction (PCR) was performed using gene-specific primers for all coding exons and splice junctions of TSHR as previously described [6]. PCR amplicons were bi-directionally sequenced using the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA, USA) on an ABI PRISM 3100 Genetic Analyzer (Applied Biosystems). DNA chromatograms were analyzed using Sequencher software version 5.0 (Gene Codes, Ann Arbor, MI, USA) and the mutation was described according to the Human Genome Variation Society nomenclature. RefSeq ID: NM_000369.2 was used for reference sequences. Direct sequencing of the PCR products revealed the heterozygous missense mutation of c.1899C>A (p.Asp633Glu) in exon 10 of TSHR. No mutation was observed in all parents in a familial genetic study (Fig. 1). Therefore, c.1899C>A (p.Asp633Glu) was deemed a de novo mutation. The variant was neither found in ExAC nor 1000 genomes. In In silico analysis, the variant was predicted deleterious by SIFT (http://provean.jcvi.org/protein_batch_submit.php), probably damaging by Polyphen-2 (http://genetics.bwh.harvard.edu/pph2/) and disease causing by Mutation Taster (http://www.mutationtaster.org/). The patient continues to be treated with antithyroid medication and maintains a euthyroid state.

This report was approved by the Institutional Review Board (IRB) at the Catholic University of Korea, Seoul St. Mary’s Hospital. Informed consent was waived by the IRB.

Discussion

In 1995, SNAH was first reported by Kopp et al. [1], who characterized it as severe thyrotoxicosis during the neonatal period or infancy. Table 1 summarizes the clinical features of 17 patients with sporadic non-autoimmune congenital hyperthyroidism by 12 activating mutations of the TSHR gene. Most of the SNAH patients who have been reported to date have exhibited manifestations of hyperthyroidism during the newborn period [1,4,6-15]. Many of the reported SNAH patients were born prematurely or with a low birth weight [1,6,8-13]. In particular, the patient reported by Holzapfel et al. [16] presented with thyrotoxicosis during the fetal period. The patient in the present study was born prematurely as well and presented with tachycardia during the fetal period. In addition, the patient had thyroid hypertrophy, craniosynostosis with advanced bone age, poor weight gain, and mild developmental delay. These clinical features are similar to other SNAH patients. Specifically, craniosynostosis was reported in 7 patients, while advanced bone age was confirmed in 12 patients. Moreover, there have been five SNAH patients without goiter and proptosis was documented in 7 of the 17 patients. Additional symptoms that have been reported for SNAH patients include jaundice, diarrhea, apnea, asphyxia, and hepatosplenomegaly. To date, a total of 12 TSHR gene mutations in less than 20 cases have been reported; however, there is no definite genotype-phenotype relationship (Table 1).

Somatic mutations of TSHR residue 633 (p.Asp633Glu, p.Asp633Tyr, p.Asp633His, and p.Asp633Ala) have been reported for an autonomously functioning thyroid nodule as well as toxic thyroid adenoma tissue of patients with hyperthyroidism. The same amino acid residue was also reported to be altered in a previous case of nonautoimmune congenital hyperthyroidism, consisting of an aspartate to tyrosine substitution [9]. However, because of the different base substitution, the patient in this report has a novel missense variant. In addition, this is the first report of SNAH in South Korea. For treatment of nonautoimmune congenital hyperthyroidism, antithyroid drugs, such as PTU or methimazole, are used. However, several reported cases were not adequately treated with medication alone, eventually requiring ablative treatment such as radioiodine therapy or thyroidectomy [1,9,10,12,14]. At present, the patient in this report is being treated with antithyroid medication alone. If diagnosis and treatment are delayed, nonautoimmune congenital hyperthyroidism may cause irreversible complications such as mental retardation. Therefore, early diagnosis and prompt treatment with genetic counseling are necessary.

In conclusion, we identified a new case of SNAH caused by an activating mutation of the TSHR gene in a premature newborn with persistent tachycardia after birth. To date, a total of 12 activating mutations of the TSHR gene in less than 20 cases have been reported. Unlike autoimmune congenital hyperthyroidism, SNAH shows a persistent and severe hyperthyroidism. Furthermore, thyroidectomy and radioactive iodine therapy are inevitable to prevent long-term complications. The diagnosis is challenging due to lack of genotype-phenotype correlation, thus early genetic screening is a key to minimizing permanent sequelae.

Notes

Conflict of interest: No potential conflict of interest relevant to this article was reported.

Fig. 1.

Direct sequencing analysis of TSHR. The proband was heterozygous for the missense mutation c.1899C>A (p.Asp633Glu). The same base change was not present in his father or mother. The base substitution mutation is indicated by a red arrow.

Table 1.

Clinical features of 17 patients with sporadic nonautoimmune congenital hyperthyroidism by 12 activating mutation of the TSHR gene

Case	Onset of hyperthyroidism	Gestational age/birth weight	Clinical manifestation related to hyperthyroidism	Mutation	Treatment	Reference
1	Fetal period	38 wk/2,410 g	Fetal tachycardia, advanced bone age, poor weight gain	p.Ser281Asn	Antithyroid drugs	Scaglia et al. [17]
1	Fetal period	38 wk/2,410 g	Fetal tachycardia, advanced bone age, poor weight gain	p.Ser281Asn	Total thyroidectomy	Scaglia et al. [17]
2	Fetal period	38 wk/2,600 g	Goiter, craniosynostosis, proptosis, advanced bone age, growth retardation, mental retardation	p.Ser505Asn	Antithyroid drugs	Holzapfel et al. [16]
2	Fetal period	38 wk/2,600 g		p.Ser505Asn	Subtotal thyroidectomy	Holzapfel et al. [16]
3	Newborn period	39 wk/3,500 g	Poor weight gain, diarrhea, excessive sweating and irritability	p.Ala623Val	Antithyroid drugs	Aycan et al. [4]
4	Newborn period	32 wk/1,660 g	Goiter, hyperactivity, mental retardation, advanced bone age	p.Phe631Leu	Antithyroid drugs	Kopp et al. [1]
					Subtotal thyroidectomy
					Radioiodine treatment
5	Newborn period	36 wk/2,520 g	Craniosynostosis	p.Ser281Asn	Antithyroid drugs	Grüters et al. [14]
5	Newborn period	36 wk/2,520 g	Craniosynostosis	p.Ser281Asn	Total thyroidectomy	Grüters et al. [14]
6	Newborn period	34 wk/3,290 g	Tachycardia, tachypnea, craniosynostosis, dolichocephaly, advanced bone age, midface hypoplasia, proptosis	p.Ser281Asn	Antithyroid drugs	Chester et al. [13]
7	Newborn period	32 wk/1,690 g	Goiter, proptosis, advanced bone age, hepatosplenomegaly, jaundice	p.Met453Thr	Antithyroid drugs	de Roux et al. [18]
8	Newborn period	36 wk/3,040 g	Goiter, proptosis, advanced bone age, delayed pubertal and psychomotor development, mental retardation, splenomegaly	p.Met453Thr	Subtotal thyroidectomy	Lavard et al. [12]
8	Newborn period	36 wk/3,040 g		p.Met453Thr	Radioiodine treatment	Lavard et al. [12]
9	Newborn period	38 wk/2,600 g	Goiter, craniosynostosis, proptosis	p.Ser505Asn	Antithyroid drugs	Schwab et al. [15]
9	Newborn period	38 wk/2,600 g	Goiter, craniosynostosis, proptosis	p.Ser505Asn	Total thyroidectomy	Schwab et al. [15]
10	Newborn period	37 wk/2,250 g	Goiter	p. Ala428Val	Antithyroid drugs	Börgel et al. [7]
11	Newborn period	32 weeks/1,860 g	Goiter, craniosynostosis, advanced bone age	p.Leu512Gln	Antithyroid drugs	Nishihara et al. [8]
11	Newborn period	32 weeks/1,860 g	Goiter, craniosynostosis, advanced bone age	p.Leu512Gln	Radioiodine treatment	Nishihara et al. [8]
12	Newborn period	35 wk/2,050 g	Goiter, advanced bone age, accelerated statural growth, speech disturbance, mental retardation, eyelid retraction	p.Ile568Thr	Antithyroid drugs	Tonacchera et al. [11]
13	Newborn period	33 wk/1,450 g	Goiter, mental retardation, craniosynostosis, mild proptosis	p.Thr632Ile	Antithyroid drugs	Kopp et al. [10]
					Subtotal thyroidectomy
					Radioiodine treatment
14	Newborn period	36 wk/2,040 g	Goiter, craniosynostosis, dolichocephaly, proptosis, hepatomegaly, periorbital edema, advanced bone age	p.Asp633Tyr	Antithyroid drugs	Bircan et al. [9]
14	Newborn period	36 wk/2,040 g		p.Asp633Tyr	Subtotal thyroidectomy (3 times)	Bircan et al. [9]
15	Infancy	37 wk/2,500 g	Goiter, advanced bone age	p.Val597Met	Antithyroid drugs	Esapa et al. [19]
15	Infancy	37 wk/2,500 g	Goiter, advanced bone age	p.Val597Met	Total thyroidectomy	Esapa et al. [19]
16	Infancy	40 wk/2,540 g	Goiter, advanced bone age, atopic dermatitis, growth retardation	p.Ser505Asn	Antithyroid drugs	Fuhrer et al. [20]
17	14 Months	40 wk/4,000 g	Diarrhea, increased growth velocity, advanced bone age	p.Pro639Ser	Antithyroid drugs	Agretti et al. [3]

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