Complicated Relationship between Genetic Mutations and Phenotypic Characteristics in Transient and Permanent Congenital Hypothyroidism: Analysis of Pooled Literature Data

Long, Wei; Zhou, Lingna; Wang, Ying; Liu, Jiaxuan; Wang, Huaiyan; Yu, Bin

doi:https://doi.org/10.1155/2020/6808517

International Journal of Endocrinology

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 6808517 | https://doi.org/10.1155/2020/6808517

Complicated Relationship between Genetic Mutations and Phenotypic Characteristics in Transient and Permanent Congenital Hypothyroidism: Analysis of Pooled Literature Data

Wei Long,¹Lingna Zhou,¹Ying Wang,²Jiaxuan Liu,³Huaiyan Wang,²and Bin Yu¹

Academic Editor: Davide Francomano

Received10 Feb 2020

Revised17 Apr 2020

Accepted11 May 2020

Published29 May 2020

Abstract

Purpose. Mutations and phenotypic characteristics remain unclear in patients with congenital hypothyroidism (CH), and no study concerning whether the outcome of transient CH (TCH) or permanent CH (PCH) is determined by mutations has been reported. Methods. We searched the literature up to April 2019. Eligible studies and data extraction were performed. We estimated the relationship between mutations and phenotypic characteristics in pooled patients with CH. Results. Two hundred forty-one cases were pooled from 41 eligible studies. The thyroid morphology, classification of mutated genes, and types of mutations were different between 94 patients with TCH and 147 patients with PCH. Heterozygous missense mutations prevailed in PAX8, TSHR, FOXE1, and NKX2-5, and patients with these mutated genes had a higher risk of PCH (OR = 37.38, 95% CI 5.04–277.21, ). TCH and PCH have equal shares in patients with mutated DUOX2 or DUOXA2. Dual-site and multisite mutations were frequently detected in DUOX2. High phenotypic heterogeneity was observed in mutated DUOX2 even in the same mutations. However, there was no relationship found between mutations and transient or permanent outcome in patients with mutated DUOX2. Conclusion. Transient or permanent outcomes were influenced by the biological function of mutated genes instead of types of mutations among patients with CH. Patients whose mutations were related to thyroid dysgenesis (TD) were more likely to have PCH. The relationship between mutations and phenotypic characteristics is complicated, and phenotypic characteristics may be affected by mutations and other factors.

1. Introduction

Congenital hypothyroidism (CH), the condition of thyroid hormone deficiency present at birth, is the most common neonatal endocrine disorder with an incidence of 1 : 2,000 to 1 : 4,000 live births [1]. Based on the final outcome of thyroid hormone deficiency, CH can be classified into transient CH (TCH) and permanent CH (PCH) [2].

Genetic causes were reported in patients with CH [3, 4]. Thyroid dysgenesis (TD), one of the most common etiologies of CH, was reported to be linked with mutations in genes including thyroid-stimulating hormone receptor (TSHR), paired box gene 8 (PAX8), thyroid transcription factor 1 (TTF1/NKX2-1), thyroid transcription factor 2 (TTF2/FOXE1), and NK2 transcription factor-related locus 5 (NKX2-5) [4]. Thyroid dyshormonogenesis (TDH) was reported to be linked with mutations in the thyroid oxidase 2 (DUOX2), dual-oxidase maturation factor 2 (DUOXA2), thyroglobulin (TG), thyroid peroxidase (TPO), solute carrier family 5 member 5 (SLC5A5), solute carrier family 26 member 4 (SLC26A4), and iodotyrosine deiodinase (IYD) genes [5, 6]. It has been reported that TD or TDH can cause permanent or transient CH in unclear proportions [1]. However, the relationship between the underlying genotype of TD or TDH and CH outcome remains unclear.

Predicting the outcome of CH for patients is necessary to expeditiously determine whether he or she needs lifelong levothyroxine medication. Some potential indicators, such as the dose of levothyroxine and thyroid hormones at diagnosis or treatment, were studied to predict TCH or PCH [7, 8]. It is well established that the genotype plays an important role in thyroid morphology and the regulation of thyroid hormone levels [4]. However, little is known about whether mutations are related to CH outcomes. Previous case reports or small sample size studies reported patients with various mutations, while it is difficult to assess the relationship between genotype and phenotype resulting from the small sample size [9]. In the present study, we pooled the reported cases of the literature and performed an analysis, to examine (1) the characteristics of gene mutations in TCH and PCH populations and (2) the relationship between mutations and the outcome of PCH or TCH.

2. Materials and Methods

2.1. Literature Search and Inclusion Criteria

A literature search was performed by MEDLINE (via PubMed) and Web of Science (including Web of Science Core Collection, Chinese Science Citation Database, KCI-Korean Journal Database, MEDLINE, Russian Science Citation Index, and SciELO Citation Index) up to April 2019. The combined terms “congenital hypothyroidism OR thyroid dyshormonogenesis OR thyroid dysgenesis OR goiter OR ectopic OR ectopia” AND “mutation OR mutant OR variation OR variant” AND “permanent OR transient” were searched. Studies that fulfilled the following criteria were included: (1) published original studies, or studies that combined case reports and reviews; (2) clear final outcomes (TCH or PCH) could be inferred; and (3) complete information on the mutation.

2.2. Data Extraction

Eligible studies were reviewed by two reviewers, and selected articles were mutually agreed upon by the authors. The following information of the patients was collected: patients’ country or region (if not mentioned, the author’s region was replaced), sex, blood-spot TSH at newborn screening (bs-TSH), TSH at diagnosis (dTSH), FT3 or FT4 at newborn screening and diagnosis (the thyroid hormones data were not necessary due to the various detection methods and reference ranges), thyroid morphology, mutation information (including gene, position change of nucleotide and amino acid, and monoallelic or biallelic mutation), and clinical outcome (TCH or PCH, based on the thyroid function test results of the authors’ reevaluation when patients were over 3 years old [10]).

Studies about gene polymorphisms or patients with aneuploidy, chromosomal structural abnormalities, or undefined copy number variation were not included. For cases studied in multiple publications at different ages, the latest information was included. Repetitive cases in different studies were identified according to the information, including the same authors’ name or institution, the same levels of thyroid hormones at newborn screening or diagnosis, and the same mutation. Details of the assessment of CH outcome, the detection method of mutation, and the pathogenicity of mutations in the studies can be found in the original papers.

2.3. Statistical Analysis

All statistical analyses were performed by R (version. 3.4.3, http://www.r-project.org). We performed chi-square tests to compare the distribution of demographic and clinical characteristics as well as genetic mutation types between patients with TCH and those with PCH. Univariate analysis was performed to estimate the relationship between mutation and the final outcomes of patients with CH. Two-sided values of less than 0.05 were considered statistically significant.

3. Results

3.1. Literature Search and Case Inclusion

A total of 41 articles fulfilled the inclusion criteria, and 72 family cases and 176 single cases were identified after data extraction (Supplementary Table 1). In the process of data analyses, we identified seven repeat cases in different reports according to the same thyroid hormones and similar authors or authors’ institution. Finally, 241 patients with clear final outcomes were identified, including 94 patients with TCH and 147 patients with PCH, and details about included cases are listed in Supplementary Table 1. A flow chart of the article selection process is shown in Figure 1.

3.2. Characteristics of Gene Mutations in Patients with CH

According to the data of the included articles, we analyzed the clinical data and mutations. Patients with mutations of DUOX2, DUOXA2, TG, TPO, FOXE1, NKX2-5, PAX8, and TSHR were identified in our analysis, and DUOX2 was the most frequent mutation in both patients with TCH and those with PCH. Novel mutations were identified in 34 studies. In 20 of 34 studies, the pathogenicity of novel mutations was evaluated by in vitro functional characterization. Eleven other studies evaluated the pathogenicity of novel mutations according to the strategy that mutations were not detected in the healthy control subjects on the basis of in silico prediction analysis.

The TCH/PCH proportion of different gene mutations was distinct. Forty-one patients were identified with gene mutation-related TD, including 23 with PAX8, 17 with TSHR, one with FOXE1, and one with NKX2-5. One heterozygous PAX8 mutation patient was TCH, while all of the others were diagnosed with PCH. The result was complicated for genes related to TDH. In our analysis, five TG and 34 TPO mutation patients were identified, and all of them had PCH, while TCH and PCH had equal shares among the patients with mutations in DUOX2 or DUOXA2. In patients who harbored mutations of two different genes, four patients harboring heterozygous DUOX2 and TSHR were diagnosed with PCH, while two combinational DUOX2 and TPO mutation patients were diagnosed with TCH. In addition, one patient with compound heterozygous c.565T > C of DUOX2 and 43 kB deletion (encompassing DUOX2, DUOXA1, and DUOXA2) was TCH. The distributions of genotypes in the TCH and PCH groups are shown in Figure 2.

3.3. Characteristics of the Patients with TCH and with PCH

We compared the characteristics between patients with TCH and those with PCH, and the results are shown in Table 1. The proportion of area, thyroid morphology, gene classification, and type of mutation were different between patients with TCH and those with PCH, while no difference was observed in sex, mutation state, or location. We also evaluated the relationship between the patient data and the outcome. Compared to normal thyroid morphology, the abnormal morphology of TD, including small volume, hypoplasia, and ectopy, seemed to be a risk predictor of PCH (OR = 21.08, 95% CI: 2.70–164.37, ). Similar results were obtained in the gene classification, and patients with mutations associated with TD were more likely to have PCH than patients with mutations of TDH (OR = 37.38, 95% CI: 5.04–277.21, ). In terms of the types of mutations, patients with single non-missense mutations, dual-site mutations, or multisite mutations were less likely to have PCH than patients with single missense mutations.

According to the pathogenic mechanism and the distinct TCH/PCH proportion of gene mutations, we further divided genes into three subgroups, DUOX2/DUOXA2, TG/TPO, and PAX8/TSHR/FOXE1/NKX2-5, and studied the differences in the subgroup of gene classifications (results are shown in Table 2). Most mutations of PAX8, TSHR, FOXE1, and NKX2-5 were found in patients with PCH except for one PAX8 mutation in a patient with TCH. For those patients with PCH, heterozygote (78.05%) and single missense mutations (75.61%) prevailed. This characteristic may explain the unusual result that single missense mutations have a higher risk of PCH in all cases. The thyroid morphology of 67.57% of patients was small volume, hypoplasia, or ectopy. All mutations of TG and TPO, which are associated with TDH, were found in patients with PCH, 86.49% of whom had goiter. Among patients with DUOX2 mutations, Asian cases were overwhelmingly dominant, and a significant difference was found in the distribution of area between TCH and PCH patients, but no difference was observed in other characteristics. In addition, dual-site and multisite mutations were mainly detected in DUOX2/DUOXA2, while single mutations were more common in genes associated with TD. We also evaluated the relationship between the mutation data and the final outcome in DUOX2 mutation patients, but no statistical significance was observed (result is shown in Supplementary Table 2).

3.4. Phenotypic Heterogeneity of the DUOX2 Mutation

In the course of data analysis, we found phenotypic heterogeneity in consanguineous or nonconsanguineous patients with the same DUOX2 mutation. The different phenotypic cases with the same mutation are summarized in Supplementary Table 3. These mutations included seven missense mutation, one nonsense mutations, one multisite mutation, and one splice site mutation. All cases were reported in East Asia, including China, Korea, and Japan. The different phenotypes were reflected in the final outcome and thyroid morphology. Among those patients, 73.47% were goiter and 66.1% were TCH.

4. Discussion

To the best of our knowledge, this is the first study concerning the relationship between mutations and phenotype in previously reported patients with CH. We compared the mutation data between patients with TCH and patients with PCH, and the proportion of genes and mutation types between TCH and PCH was different. The outcome of patients with CH at reevaluation was influenced by the mutated gene. Compared to patients whose mutated gene is related to TDH, patients with mutations related to TD have a higher risk of developing PCH.

Recent evidence points to the possibility of a genetic component in patients with TD [4]. Transcription factors encoded by PAX8, FOXE1, and NKX2-5 are necessary for thyroid embryogenesis and are also expressed in other tissues of the developing fetus. Mutations in these genes lead to syndromes combined with TD [11, 12]. It is easy to understand that most patients with CH with mutations in PAX8, FOXE1, and NKX2-5 present with PCH and thyroid morphology of dysgenesis in our study. Characteristics of heterozygote or single missense mutations were obvious among those patients. However, some unusual cases were identified. Three PCH cases with normal thyroid but one TCH case with decreased thyroid were reported in the same study, and the authors found that the thyroid gland ranged from aplastic and hypoplastic to normal in patients with the same PAX8 mutation (p.R31H) and reported the first patient with PAX8 mutation with an enlarged thyroid gland [13]. TSHR, which is located on the surface of thyroid follicular cells and mediates the effects of TSH, is important for the development and function of the thyroid gland [14]. Although TSHR gene mutations were reported to be one of the causes of TD [15] and patients with mutations in TSHR all presented with PCH in our study, thyroid morphology was variable. Our results showed that eight of twelve patients with PCH with mutations in TSHR have eutopic thyroid glands. Previous studies demonstrated that inactivating TSHR mutations results in mild or severe thyroid hypoplasia [16, 17], and the heterogeneity was presumably due to different residual functions of TSHR mutations.

We concluded that patients with mutations of TPO or TG were permanent in our included cases. Both monoallelic and biallelic mutations of TPO were classically characterized by total iodide organification defect [18, 19]. Unlike TPO or TG, equal shares of TCH or PCH were found in the patients with mutations in DUOX2 or DUOXA2 in our review, and dual-site and multisite mutations were frequently detected in DUOX2. Mutation in DUOX2, which is responsible for TDH, was the most frequent mutation in both TCH and PCH patients, especially among Asian populations. Our previous study also demonstrated that DUOX2 was the most common genetic defect in Chinese patients with CH [20]. Most patients with DUOX2 pathogenic mutations have a thyroid gland with increased or normal size [21], but Fu et al. [22] reported one female PCH case with decreased thyroid size. In the original study [22], mutations of DUOX2 were screened by Sanger sequencing, while other genes were not screened. We presumed that a further study of gene test is necessary to interpret this unusual case.

The characteristics of the DUOX2 mutation and the phenotype-genotype correlations have not yet been fully understood. Our results showed that dual-site or multisite mutations were frequently reported in DUOX2 but rarely in other genes. We also found that variable phenotypes were caused by DUOX2 mutations, and there was no relationship between the mutation from DUOX2 and the outcome of patients with CH at reevaluation, which was controversial in previous studies. Previous studies demonstrated that biallelic DUOX2 mutations cause severe, permanent hypothyroidism, while monoallelic mutations result in milder, transient hypothyroidism [23, 24]. However, subsequent studies have reported biallelic mutations in DUOX2 in patients with TCH [25, 26], and monoallelic mutations in patients with PCH were also reported [27, 28]. We found that TCH and PCH have equal shares in patients with DUOX2 mutations, which demonstrated that monoallelic and biallelic DUOX2 mutations can both cause transient or permanent CH, while there was no correlation between the final outcome and the mutation type. Although a study showed that patients with one or two DUOX2 mutations turned out to have subclinical or transient CH and that patients with three or more DUOX2 mutations were mostly associated with permanent CH [29], another study showed that disease severity, neurodevelopment, and prognosis were not correlated with DUOX2 mutation types or numbers [30]. Our study confirmed that the number of DUOX2 mutations did not determine transient or permanent outcomes. It is difficult to predict the outcome by the number of mutations or mutated alleles in patients with DUOX2 mutations.

Phenotypic heterogeneity with the same DUOX2 mutation was found in consanguineous or nonconsanguineous patients, implying that the phenotype might be different in individuals with DUOX2 mutations, even in those with the same mutation. DUOX2 mutations result in variable phenotypes ranging from mild to severe CH [31], which could be explained by the compensation effect. The coexistence of two DUOX isoforms (DUOX1 and DUOX2) and their corresponding maturation factors could certainly constitute an efficient redundant mechanism to maintain sufficient H₂O₂ supply for thyroid hormone synthesis [32]. In addition, phenotypic heterogeneity could be explained by other mechanisms such as unidentified mutations in noncoding regions or other genes, nutrition, environment, or other epigenetic factors [33–36].

The genetic diagnosis of CH could provide great benefits not only to current patients but also in genetic counseling for the next birth or subsequent generations. In addition, it is also helpful to understand the genetic etiology of CH. Our study indicated that the transient or permanent outcome of patients with CH was influenced by the type of genes instead of the form of mutations and patients whose mutations related to TD were more likely to have PCH. However, the limitations of the present study need to be noticed. Although 41 studies were included in this study, the number of CH patients included in the final data analysis was relatively small. This limitation might affect the accurate analysis of relationship between mutations and phenotypes. In addition, it is difficult to predict the outcome by the mutation in patients with the DUOX2 mutation because of the variable phenotypes resulting from the DUOX2 mutation. Further study is necessary to understand the complicated relationship between the genetic etiology and phenotypic characteristics of CH.

5. Conclusions

The outcome of transient or permanent was influenced by the functional type of mutated genes instead of the form of mutations among patients with CH. Patients whose mutations were related to TD were more likely to have PCH. The relationship between mutations and phenotypic characteristics was complicated, and there was no relationship between mutations and transient or permanent outcome in patients with mutated DUOX2.

Data Availability

The data used to support the findings of this study are available from the corresponding authors upon request.

Conflicts of Interest

On behalf of all authors, the corresponding author states that there are no conflicts of interest.

Acknowledgments

The authors thank Dr. Rui Yang for comments and editing. This work was supported by the National Natural Science Foundation of China (grant number 81903400), Changzhou Key Laboratory of High-Tech Research (grant number: CM20193009), and Guiding Project of Changzhou Health Committee (grant number WZ201821).

Supplementary Materials

Supplementary Table 1: clinical data and mutation of included cases. Note: bsTSH: blood-spot TSH at newborn screening; dTSH: TSH at diagnosis; PCH: permanent CH; TCH: transient CH; fsX: frameshift with an early stop codon. Supplementary Table 2: univariate analysis for mutation data associated with the final outcome in patients with DUOX2 mutation. Supplementary Table 3: phenotypic heterogeneity in the patients with the same-site mutation of DUOX2 gene. (Supplementary Materials)

References

M. V. Rastogi and S. H. LaFranchi, “Congenital hypothyroidism,” Orphanet Journal of Rare Diseases, vol. 5, no. 1, p. 17, 2010.
View at: Publisher Site | Google Scholar
C. D. Cosmo and M. Tonacchera, “Congenital hypothyroidism,” in Thyroid Diseases: Pathogenesis, Diagnosis, and Treatment, P. Vitti and L. Hegedüs, Eds., pp. 333–371, Springer International Publishing, Cham, Switzerland, 2018.
View at: Publisher Site | Google Scholar
G. Szinnai, “Clinical genetics of congenital hypothyroidism,” Paediatric Thyroidology, vol. 26, pp. 60–78, 2014.
View at: Publisher Site | Google Scholar
L. Persani, G. Rurale, T. de Filippis, E. Galazzi, M. Muzza, and L. Fugazzola, “Genetics and management of congenital hypothyroidism,” Best Practice & Research Clinical Endocrinology & Metabolism, vol. 32, no. 4, pp. 387–396, 2018.
View at: Publisher Site | Google Scholar
C. E. Cherella and A. J. Wassner, “Congenital hypothyroidism: insights into pathogenesis and treatment,” International Journal of Pediatric Endocrinology, vol. 2017, no. 1, p. 11, 2017.
View at: Publisher Site | Google Scholar
H. Grasberger and S. Refetoff, “Genetic causes of congenital hypothyroidism due to dyshormonogenesis,” Current Opinion in Pediatrics, vol. 23, no. 4, pp. 421–428, 2011.
View at: Publisher Site | Google Scholar
I. S. Park, J. S. Yoon, C. H. So, H. S. Lee, and J. S. Hwang, “Predictors of transient congenital hypothyroidism in children with eutopic thyroid gland,” Annals of Pediatric Endocrinology & Metabolism, vol. 22, no. 2, pp. 115–118, 2017.
View at: Publisher Site | Google Scholar
N. Zdraveska, M. Zdravkovska, V. Anastasovska, E. Sukarova-Angelovska, and M. Kocova, “Diagnostic reevaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism,” Endocrine Connections, vol. 7, no. 2, pp. 278–285, 2018.
View at: Publisher Site | Google Scholar
M. Satoh, K. Aso, S. Ogikubo, A. Ogasawara, and T. Saji, “Genetic analysis in children with transient thyroid dysfunction or subclinical hypothyroidism detected on neonatal screening,” Clinical Pediatric Endocrinology, vol. 18, no. 4, pp. 95–100, 2009.
View at: Publisher Site | Google Scholar
J. Legér, A. Olivieri, M. Donaldson et al., “European society for paediatric endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism,” Hormone Research in Paediatrics, vol. 81, no. 2, pp. 80–103, 2014.
View at: Publisher Site | Google Scholar
S. S. Trueba, J. Augé, G. Mattei et al., “PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations,” The Journal of Clinical Endocrinology & Metabolism, vol. 90, no. 1, pp. 455–462, 2005.
View at: Publisher Site | Google Scholar
P. E. Macchia, P. Lapi, H. Krude et al., “PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis,” Nature Genetics, vol. 19, no. 1, pp. 83–86, 1998.
View at: Publisher Site | Google Scholar
C. Fu, R. Chen, S. Zhang et al., “PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism,” Clinica Chimica Acta, vol. 450, pp. 322–326, 2015.
View at: Publisher Site | Google Scholar
L. Li, W. Zhang, Y. Zang, S. Yan, B. Kong, and S. Liu, “Identification of a novel TSHR mutation from a Chinese baby with congenital hypothyroidism due to ectopy,” International Journal of Clinical and Experimental Pathology, vol. 9, no. 1, pp. 153–158, 2016.
View at: Google Scholar
L. Persani, D. Calebiro, D. Cordella et al., “Genetics and phenomics of hypothyroidism due to TSH resistance,” Molecular and Cellular Endocrinology, vol. 322, no. 1-2, pp. 72–82, 2010.
View at: Publisher Site | Google Scholar
S. Narumi, K. Muroya, Y. Abe et al., “TSHR mutations as a cause of congenital hypothyroidism in Japan: a population-based genetic epidemiology study,” The Journal of Clinical Endocrinology & Metabolism, vol. 94, no. 4, pp. 1317–1323, 2009.
View at: Publisher Site | Google Scholar
K. Tsunekawa, K. Onigata, T. Morimura et al., “Identification and functional analysis of novel inactivating thyrotropin receptor mutations in patients with thyrotropin resistance,” Thyroid, vol. 16, no. 5, pp. 471–479, 2006.
View at: Publisher Site | Google Scholar
H. M. Targovnik, C. E. Citterio, and C. M. Rivolta, “Iodide handling disorders (NIS, TPO, TG, IYD),” Best Practice & Research Clinical Endocrinology & Metabolism, vol. 31, no. 2, pp. 195–212, 2017.
View at: Publisher Site | Google Scholar
L. Fugazzola, N. Cerutti, D. Mannavola et al., “Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect,” The Journal of Clinical Endocrinology & Metabolism, vol. 88, no. 7, pp. 3264–3271, 2003.
View at: Publisher Site | Google Scholar
W. Long, G. Lu, W. Zhou et al., “Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism,” Endocrine Journal, vol. 65, no. 10, pp. 1019–1028, 2018.
View at: Publisher Site | Google Scholar
M. M. L. Kizys, R. A. Louzada, M. Mitne-Neto et al., “DUOX2 mutations are associated with congenital hypothyroidism with ectopic thyroid gland,” The Journal of Clinical Endocrinology & Metabolism, vol. 102, no. 11, pp. 4060–4071, 2017.
View at: Publisher Site | Google Scholar
C. Fu, S. Zhang, J. Su et al., “Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism,” Journal of Endocrinological Investigation, vol. 38, no. 11, pp. 1219–1224, 2015.
View at: Publisher Site | Google Scholar
J. C. Moreno, H. Bikker, M. J. E. Kempers et al., “Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism,” The New England Journal of Medicine, vol. 347, no. 2, pp. 95–102, 2002.
View at: Publisher Site | Google Scholar
H. Grasberger, “Defects of thyroidal hydrogen peroxide generation in congenital hypothyroidism,” Molecular and Cellular Endocrinology, vol. 322, no. 1-2, pp. 99–106, 2010.
View at: Publisher Site | Google Scholar
Y. Maruo, H. Takahashi, I. Soeda et al., “Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program,” The Journal of Clinical Endocrinology and Metabolism, vol. 93, no. 11, pp. 4261–4267, 2008.
View at: Publisher Site | Google Scholar
R. E. Enacan, M. E. Masnata, F. Belforte et al., “Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases,” Archivos Argentinos de pediatria, vol. 115, no. 3, pp. e162–e165, 2017.
View at: Publisher Site | Google Scholar
F. Wang, K. Lu, Z. Yang et al., “Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes,” Clinical Endocrinology, vol. 81, no. 3, pp. 452–457, 2014.
View at: Publisher Site | Google Scholar
M. Tan, Y. Huang, X. Jiang et al., “The prevalence, clinical, and molecular characteristics of congenital hypothyroidism caused by DUOX2 mutations: a population-based cohort study in Guangzhou,” Hormone and Metabolic Research, vol. 48, no. 9, pp. 581–588, 2016.
View at: Publisher Site | Google Scholar
C. Fu, S. Luo, S. Zhang et al., “Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients,” Clinica Chimica Acta, vol. 458, pp. 30–34, 2016.
View at: Publisher Site | Google Scholar
X. Chen, X. Kong, J. Zhu et al., “Mutational spectrum analysis of seven genes associated with thyroid dyshormonogenesis,” International Journal of Endocrinology, vol. 2018, Article ID 8986475, 14 pages, 2018.
View at: Publisher Site | Google Scholar
G. Dufort, S. Larrivée-Vanier, D. Eugéne et al., “Wide spectrum of DUOX2 deficiency: from life-threatening compressive goiter in infancy to lifelong euthyroidism,” Thyroid, vol. 29, no. 7, pp. 1018–1022, 2019.
View at: Publisher Site | Google Scholar
J. C. Moreno and T. J. Visser, “New phenotypes in thyroid dyshormonogenesis: hypothyroidism due to DUOX2 mutations,” Thyroid Gland Development and Function, vol. 10, pp. 99–117, 2007.
View at: Publisher Site | Google Scholar
G. D. Marco, P. Agretti, L. Montanelli et al., “Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism,” The Journal of Clinical Endocrinology & Metabolism, vol. 96, no. 8, pp. E1335–E1339, 2011.
View at: Publisher Site | Google Scholar
S. Narumi, K. Muroya, Y. Asakura, M. Aachi, and T. Hasegawa, “Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patients,” The Journal of Clinical Endocrinology & Metabolism, vol. 96, no. 11, pp. E1838–E1842, 2011.
View at: Publisher Site | Google Scholar
Y. Maruo, K. Nagasaki, K. Matsui et al., “Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty,” European Journal of Endocrinology, vol. 174, no. 4, pp. 453–463, 2016.
View at: Publisher Site | Google Scholar
C. Hoste, S. Rigutto, G. V. Vliet, F. Miot, and X. D. Deken, “Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H₂O₂-generating enzyme DUOX2 associated with transient congenital hypothyroidism,” Human Mutation, vol. 31, no. 4, pp. E1304–E1318, 2010.
View at: Publisher Site | Google Scholar

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