Clinical course of infants with congenital heart disease who developed thyroid dysfunction within 100 days

Article information

Ann Pediatr Endocrinol Metab. 2017;22(4):253-258

Publication date (electronic) : 2017 December 31

doi : https://doi.org/10.6065/apem.2017.22.4.253

Hye Jin Lee, MD ¹, Hyeoh Won Yu, MD ², Gi Beom Kim, MD, PhD ², Choong Ho Shin, MD, PhD ², Sei Won Yang, MD, PhD ², Young Ah Lee, MD, PhD^,²

¹Department of Pediatrics, Hallym University Kangnam Sacred Heart Hospital, Seoul, Korea

²Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea

Address for correspondence: Young Ah Lee, MD, PhD https://orcid.org/0000-0001-9179-1247 Department of Pediatrics, Seoul National University Children’s Hospital, 103 Daehak-ro, Jongnogu, Seoul 110-799, Korea Tel: +82-2-2072-2082 Fax: +82-2-2072-3917 E-mail: nina337@snu.ac.kr

Received 2017 May 19; Revised 2017 June 19; Accepted 2017 August 17.

Abstract

Purpose

We investigated the clinical course of infants with congenital heart disease (CHD) who experienced thyroid dysfunction within 100 days of birth.

Methods

We performed retrospective medical reviews of 54 CHD patients (24 male patients) who underwent a thyroid function test (TFT) between January 2007 and July 2016. Data were collected on birth history, diagnosis of CHD, underlying chromosomal or genetic abnormalities, medication history, surgery, ventilator care, and exposure to iodine contrast media (ICM). Results of neonatal screening tests (NSTs) and TFTs were reviewed.

Results

A total of 36 patients (29 transient, 7 permanent) showed thyroid dysfunction. Among the seven patients with permanent hypothyroidism, three had an underlying syndrome, three showed abnormal NST results, and one was admitted to the intensive care unit for macroglossia and feeding cyanosis. We found that infants with transient thyroid dysfunction had a lower birth weight and were more commonly exposed to thyroid disrupting medication and/or ICM. However, these risk factors were not significant. A total of 8 patients with a history of ICM exposure showed thyroid dysfunction. Excluding 3 patients with elevated thyroid stimulating hormone before ICM exposure, 5 patients recovered from transient thyroid dysfunction.

Conclusions

We observed thyroid dysfunction in two-thirds of CHD infants (53.7% transient, 13.0% permanent) who had risk factors and received TFT screening within 100 days, despite normal NSTs. Further studies with larger sample sizes are required to revise the criteria for TFT screening in CHD infants.

Keywords: Thyroid function tests; Congenital; Heart; Infant; Hypothyroidism

Introduction

Congenital hypothyroidism is one of the most preventable causes of neurocognitive impairment because early treatment is possible in neonates [1,2]. The thyroid hormone is important for normal growth and development in infancy [3,4]. After introducing national screening test (NST) using capillary thyroid stimulating hormone (TSH) level, the incidence of untreated congenital hypothyroidism has significantly decreased [5].

According to the Italian Registry of Congenital Hypothyroidism, congenital heart disease (CHD) is the most frequent disease condition associated with congenital hypothyroidism [6]. CHD is also reported to be a risk factor for nonautoimmune hypothyroidism in children [7]. In addition, intravenous iodine contrast media (ICM) is frequently used for diagnostic imaging and therapeutic intervention in CHD patients. Excess iodine exposed by ICM may disturb thyroid function in adult and pediatric population [8-11]. However, there is no generally accepted guideline for screening thyroid dysfunction in CHD infants.

The 2014 European Society of Pediatric Endocrinology (ESPE) guideline recommends a second screening of thyroid function test (TFT) in neonates with the following high risk factors for hypothyroidism; preterm or low birth weight infants, critically ill infants who were admitted to intensive care unit (ICU), and monozygotic twins [12]. Currently, secondary TFT screening in CHD infants is not different from that in those without CHD. Meanwhile, ICM exposure is not an absolute indication for TFT screening to detect thyroid dysfunction yet.

In this study, we aimed to identify frequency and clinical course of thyroid dysfunction in CHD infants who received TFT screening within 100 days according to current ESPE guidelines. We also aimed to identify the role of ICM exposure on developing thyroid dysfunction in CHD infants.

Materials and methods

1. Subjects and methods

The medical records of infants diagnosed with CHD between January, 2007 and July, 2016 at Seoul National University Children’s Hospital were retrospectively reviewed. Those who had TFT results before 100 days of birth were included in this study. Early preterm infants (gestational age [GA]<34 weeks), late preterm infants (34 weeks≤GA<37 weeks) with spontaneously closed patent foramen ovale or patent ductus arteriosus, infants whose mother had a history of autoimmune thyroid disease, and patients who expired before 3 years of age were excluded. A total of 54 infants (24 male infants) were finally included in this study.

Clinical data were collected on GA, birth weight, type of cardiac disease, other congenital anomalies, underlying chromosomal or genetic abnormalities, and previous history of medication affecting the thyroid function (dopamine, dobutamine, amiodarone, steroid, and furosemide), exposure to ICM through cardiac computed tomography (CT) or catheterization, operation, and mechanical ventilator care.

Laboratory findings of serum free thyroxine (fT4) and TSH levels from the first to last follow-up were reviewed. Serum concentrations of fT4 and TSH were measured using immunoradiometric kits (RIAKEY; Shin Jin Medics, Seoul, Korea). The normal ranges of serum fT4 and TSH are 0.70–1.80 ng/dL (9.01–23.2 pmol/L) and 0.4–4.1 mIU/L, respectively. A capillary sample of blood was obtained from the heel to preform NST by chemiluminescent Immunoassay (Modular Analysis E 170 module, Roche, Germany). The cutoff values of TSH on NST were <12 mIU/L. NST results were also reviewed in infants who were transferred from outside hospital.

Patients were categorized into the 3 groups as follows; normal thyroid function, transient thyroid dysfunction, and permanent hypothyroidism. In infants who started levothyroxine medication, the dose, starting and ending dates of levothyroxine medication were reviewed. The transient thyroid dysfunction group included infants who showed transient hyperthyrotropinemia which spontaneously normalized or those who successfully discontinued levothyroxine during follow-up. Patients who failed to discontinue or withdraw levothyroxine medication till 3 years of age were categorized into permanent hypothyroidism.

2. Statistical analysis

Statistical analyses were performed using IBM SPSS Statistics ver. 24.0 (IBM Co., Armonk, NY, USA). Analysis for normality was performed first. All continuous variables were described as means±standard deviation. Binary logistic regression analysis was performed to investigate risk factors associated with transient thyroid dysfunction. A P-value of <0.05 was considered statistically significant.

3. Ethics statement

The present study was reviewed and approved by the Institutional Review Board of Seoul National University Hospital (approval number: 1702-021-829) and informed consent was waved.

Results

1. Clinical characteristics of total subjects

Table 1 shows the baseline characteristics of the total 54 infants. The mean age at initial TFT check-up was 32.2±27.7 (range, 3–98) days after birth. Thirty-two patients (59.3%) had NST results available and 6 of these patients had elevated TSH levels on their NST. The mean age at last follow-up was 5.3±2.9 years. Eighteen patients (33.3%) had normal thyroid function. Among 36 patients with thyroid dysfunction, 29 infants (53.7%) had transient thyroid dysfunction, and 7 patients (13.0%) had permanent hypothyroidism (Fig, 1, Table 1).

Table 1.

Characteristics of total subjects

Fig. 1.

Clinical course of total subjects.

Thirteen patients (24.1%) were late preterm (34 to 36 weeks of GA) and 11 patients (20.4%) were small for GA. The CHDs of the patients were as follows; ventricular septal defect (n=21), atrial septal defect (n=15), atrioventricular septal defect (n=1), tetralogy of Fallot (n=6), pulmonary stenosis (n=5), Ebstein anomaly (n=2), functional single ventricle (n=1), thoracic aorta widening (n=1), mitral regurgitation (n=1), and truncus arteriosus (n=1). Twenty-three patients (42.6%) were diagnosed with chromosomal anomaly or genetic syndrome as follows: Down syndrome (n=11), other chromosomal defects (n=2, 46, XY, del(9)(p22), and 45, XX, -14, der(18), t(14;18)(q11.2;q23)), Digeorge syndrome (n=5), Williams syndrome (n=3), Beckwith-Wiedemann syndrome (n=1), and Alagille syndrome (n=1). Before evaluation of TFTs, 5 infants (9.3%) received cardiac surgery, 8 infants (14.8%) had a history of ICM exposure, and 15 infants (27.8%) had a history of thyroid disrupting medication such as dopamine, dobutamine, amiodarone, steroids, and/or furosemide (Table 1).

2. Clinical characteristics of CHD patients with permanent hypothyroidism

Among 7 patients categorized into the permanent hypothyroidism group (Table 2), 3 patients with Down syndrome (n=2, cases 1 and 2), and Williams syndrome (n=1, case 3) were included. Three of the remaining 4 patients without an underlying genetic syndrome were detected by elevated TSH levels on NST (cases 4–6). However, 1 patient (case 7, Table 2) was diagnosed with hypothyroidism 92 days after birth since delayed TSH elevation was detected in the ICU during the evaluation of feeding cyanosis and macroglossia.

Table 2.

Congenital heart disease infants with permanent hypothyroidism

3. Factors associated with transient thyroid dysfunction in infants with CHD

Among 29 patients categorized into the transient thyroid dysfunction group, 8 patients initially started levothyroxine and successfully discontinued medication at a later follow-up. The remaining 21 patients showed transient hyperthyrotropinemia which was spontaneously normalized without medication (Fig. 1).

The transient thyroid dysfunction group (n=29) had higher proportions of patients with a chromosomal anomaly or genetic syndrome, preterm birth, small for GA, history of ICM exposure, and use of thyroid disrupting medication than the normal thyroid function group (n=18). However, none of aforementioned risk factors including ICM exposure was statistically significant as a result of binary logistic regression analysis (Supplementary Table 1).

4. Clinical course of patients who had a history of ICM exposure

A total of 8 patients who had a history of ICM exposure were categorized into permanent hypothyroidism (n=3) or transient thyroid dysfunction (n=5, Table 3) group. Three patients with permanent hypothyroidism had already elevated levels of TSH before ICM exposure, suggesting congenital defects regardless of ICM exposure. When we closely looked at the 5 patients with transient thyroid dysfunction, we observed TSH levels increased 3 to 24 days after ICM exposure. Three of these 5 patients started levothyroxine medication and successfully discontinued before 3 years of age (cases 1, 4, and 5; Table 3).

Table 3.

Congenital heart disease infants with transient thyroid dysfunction after exposure to iodine contrast media (ICM)

Discussion

The prevalence of vitamin D deficiency in pediatric patients Two-thirds of the 54 CHD infants who received TFT screening within 100 days according 2014 ESPE guideline showed thyroid dysfunction. Seven patients (13%) were categorized into permanent hypothyroidism requiring persistent levothyroxine medication. Twenty-one infants (53.7%) with transient thyroid dysfunction had lower birth weight, and had more exposure to ICM and/or thyroid disrupting medication than those with normal thyroid function; however, none of risk factors including ICM exposure were statistically significant in this study. Despite normal NST results, delayed TSH elevation was detected in critically ill patient with CHD during ICU care. Unless CHD infants had elevated TSH levels before ICM exposure, thyroid dysfunction was transient in this study.

Seven patients with permanent hypothyroidism received TFTs according to the 2014 ESPE guideline [12], since they had risk factors for thyroid dysfunction such as Down syndrome, Williams syndrome, low birth weight, and/or ICU admission. Despite normal results of NST, TFT needs to be evaluated if CHD infants had risk factors for thyroid dysfunction. This study supports the current guideline recommending second TFT screening in CHD infants who had known risk factors related to thyroid dysfunction.

Half of CHD infants (53.7%) with risk factors showed transient thyroid dysfunction. Preterm birth and/or low birth weight [13-15], thyroid disrupting medication [16-18], and exposure to disinfectant containing iodine and/or ICM [8-11,19-22] were included as candidate risk factors for developing transient thyroid dysfunction in this study. Intrauterine stress with growth restriction and compensatory response to mild suppression of the thyroid gland [23], a significant reduction of the expression of thyroid receptor isoforms in the fetal brain with intrauterine growth restriction and the resetting of TSH sensitivity [24] may affect thyroid function. Having a history of dopamine, dobutamine, furosemide, steroid [16,17] and amiodarone18) was known to affect thyroid function. Meanwhile, diagnostic tools using ICM such as cardiac CT, and catheterization are being increasingly performed, especially for evaluation of cardiac structural anomaly. Thyroid dysfunction after ICM exposure has been reported in adults [11,20] and infants with CHD [21,22]. However, none of candidate risk factors was statistically significant in our study.

Recently, three term CHD infant cases were reported, who developed iodine-induced hypothyroidism 5 to 11 days after exposure to ICM and/or disinfectant containing iodine [19], which emphasizes that the thyroid function needs to be evaluated after excess iodine exposure in CHD infants. Two of these 3 infants had transient hypothyroidism, and one had severe hypothyroidism requiring ongoing thyroid replacement in the aforementioned study [19]. Iodine induced hypothyroidism is explained by failure to escape the Wolff-Chaikoff effect [10]. In healthy individuals, despite iodine excess, thyroid hormone homeostasis is maintained by the acute Wolff-Chaikoff effect by transient inhibition of thyroid hormone synthesis through decreased organification. Typically, the thyroid escapes from the acute Wolff-Chaikoff effect within a few days through down regulation of the sodium-iodine symporter in thyroid cells, and then normal thyroid hormone synthesis resumes [10]. However, in CHD infants, the thyroid cannot escape the Wolff-Chaikoff effect, resulting in thyroid dysfunction [19]. Although all CHD infants who had a history of ICM showed thyroid dysfunction at 3 to 24 days after exposure in our study, the independent pathogenic role of ICM exposure on thyroid dysfunction was not found. Except 3 patients who already had elevated TSH levels before ICM exposure, 5 patients successfully recovered from transient thyroid dysfunction.

This study is limited by a retrospective design and small sample size. Since infants at high risk for developing thyroid dysfunction selectively received TFTs in our study, we could not know the incidence of congenital hypothyroidism for the total CHD infants due to selection bias. Since the possibility of common mechanisms such as the pathologic role of NKX2.5 or TBX1 coding sequences on the thyroid and heart development has been suggested [25,26], further study is needed to discover whether CHD itself is independently associated with congenital hypothyroidism.

In conclusion, thyroid dysfunction was detected in two-third of CHD infants who received TFT screening within 100 days according to current ESPE guidelines (53.7% transient, 13.0% permanent), although NST results were normal. The independent effect of ICM exposure on thyroid dysfunction was not identified in this study. Further studies with larger sample sizes are required to revise criteria for TFT screening in CHD infants.

Notes

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

Supplementary material

Supplementary Table 1 can be found via https://doi.org/10.6065/apem.2017.22.4.253.

apem-2017-22-4-253-supplementary.pdf

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Table 1.

Characteristics of total subjects

Characteristic	Total	Normal	Transient thyroid dysfunction	Permanent hypothyroidism
No. of patients	54	18 (33.3)	29 (53.7)	7 (13.0)
Male sex	24 (44.4)	6 (33.3)	14 (48.3)	4 (57.1)
Gestational age (wk)	37.8±1.7	38.2±1.7	37.6±1.8	37.7±1.0
Birth weight (kg)	2.9±0.7	3.1±0.6	2.9±0.7	2.5±0.5
Preterm	13 (24.1)	3 (16.7)	9 (31.0)	1 (14.3)
Small for gestational age	11 (20.4)	2 (11.1)	7 (24.1)	2 (28.6)
Chromosomal anomaly or genetic syndrome	23 (42.6)	6 (33.3)	14 (48.3)	3 (42.9)
Cyanotic heart disease	17 (31.5)	6 (33.3)	8 (27.6)	3 (42.9)
Ventilator care history	8 (14.8)	3 (16.7)	5 (17.2)	1 (14.3)
History of surgery	5 (9.3)	1 (5.6)	3 (10.3)	1 (14.3)
Exposure to iodine contrast media	8 (14.8)	0 (0)	5 (17.2)	3 (42.9)
Thyroid disrupting medication	15 (27.8)	2 (11.1)	10 (34.5)	3 (42.9)

Values are presented as number (%) or mean±standard deviation.

Table 2.

Congenital heart disease infants with permanent hypothyroidism

Case	Sex	Congenital heart disease	Underlying disease	GA (wk)	Birth weight (kg)	TSH (NST) (mIU/L)	Age at detection of elevated TSH (day)	Serum fT4 (ng/dL)	Serum TSH (mIU/L)	Age at start levothyroxine (day)	Imaging study	Age at last follow-up (yr)
1	M	TOF	Down syndrome	39	2.3	Normal (2.9)	26	1.7	8.9	628	NA	8.0
2	F	AVSD, PDA	Down syndrome	36	1.8	Normal (6.8)	7	1.9	8.2	21	NA	3.9
3	M	AS, PS	Williams syndrome	38	2.6	NA	83	1.0	5.5	130	NA	9.2
4	F	Large VSD, ASD, PDA	None	38	2.2	Elevated (44.8)	17	0.65	100	18	NA	8.3
5	M	Functional single ventricle	None	38	3.2	Elevated (14.5)	7	1.18	28.0	380	NA	3.7
6	F	IAA, PDA,VSD	None	37	2.6	Elevated (157)	17	0.10	801.0	17	Lingual thyroid	6.1
7	M	Large ASD	None	38	3.0	Normal (NA, outside)	92	0.89	22.3	92	NA	6.5

Normal values of TSH (NST), serum fT4, and serum TSH were ≤12 mIU/L, 0.70–1.80 ng/dL, and 0.4–4.1 mIU/L, respectively.

GA, gestational age; TSH, thyroid stimulating hormone; NST, neonatal screening test; fT4, free thyroxine; TOF, tetralogy of Fallot; AVSD, atrioventricular septal defect; PDA, patent ductus arteriosus; AS, aortic stenosis; PS, pulmonary stenosis; VSD, ventricular septal defect; ASD, atrial septal defect; IAA, interrupted aortic arch; NA, not available.

Table 3.

Congenital heart disease infants with transient thyroid dysfunction after exposure to iodine contrast media (ICM)

Case	Sex	Congenital heart disease	Underlying disease	Birth weight (kg)	TSH (NST) (mIU/L)	Serum TSH before exposure to ICM	Exposure to ICM (age [day] at exposure)	Serum TSH after exposure to ICM (age [day] at evaluation)	Levothyroxine medication (dose, age [day] at start)	Levothyroxine withdrawal (age [day] atdiscontinuation)	Imaging study
1	F	IAA, VSD, ASD	Digeorge syndrome	2.5	Normal (9.5)	4.0	CT angiography (13)	23.04 (25)	Yes (15.5 µg/kg/day at 25)	Yes (33)	NA
2	F	TOF	Digeorge syndrome	2.9	Normal (7.6)	NA	CT angiography (4)	5.4 (20)	No	-	NA
3	M	VSD, MR, ASD	46,XY,del(9) (p22)	3.7	NA	NA	CT angiography (71)	5.3 (74)	No	-	NA
4	F	AP window, ASD, VSD	None	1.7	Normal (1.7)	NA	CT angiography (6)	13.7 (30)	Yes (6.6 µg/kg/day, 30)	Yes (889)	Normal
5	M	VSD, MAPCA	None	2.3	NA	2.8	Cardiac catheterization (417)	22.6 (449)	Yes (3.8 µg/kg/day at 449)	Yes (894)	Normal

Normal values of TSH (NST), and serum TSH were ≤12 mIU/L, and 0.4-4.1 mIU/L, respectively.

TSH, thyroid stimulating hormone; NST, neonatal screening test; IAA, interrupted aortic arch; VSD, ventricular septal defect; ASD, atrial septal defect; CT, computed tomography; TOF, tetralogy of Fallot; MR, mitral regurgitation; AP window, aortopulmonary windrow; MAPCA, major aortopulmonary collateral arteries; NA, not available.