Literature DB >> 31287502

Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins?

Emanuela Medda1, Maria Cristina Vigone2, Alessandra Cassio3, Francesca Calaciura4, Pietro Costa5, Giovanna Weber2, Tiziana de Filippis6, Giulia Gelmini5, Marianna Di Frenna2, Silvana Caiulo2, Rita Ortolano3, Daniela Rotondi7, Monica Bartolucci5, Rossella Gelsomino4, Simona De Angelis7, Marco Gabbianelli7, Luca Persani6,8, Antonella Olivieri7.   

Abstract

CONTEXT: Newborn screening program for congenital hypothyroidism (CH) adopting rescreening in at-risk neonates.
OBJECTIVES: To estimate the concordance rate for CH in twin pairs discordant at the first screening; to verify whether long-term follow-up of healthy cotwins belonging to CH discordant pairs may be useful to diagnose thyroid hypofunction during development; to evaluate the importance of genetic and environmental influences on liability to permanent and transient CH. DESIGN AND PATIENTS: Forty-seven screening discordant twin pairs were investigated. Proband was defined as the twin in the pair with a positive test at the first screening and a confirmed diagnosis of CH.
RESULTS: Seven screening discordant twin pairs became concordant for CH within the first month of life (pairwise concordance of 14.9%) because seven screening negative cotwins showed high TSH values when retested. During long-term follow-up (range, 3 to 21 years), hypothyroidism was diagnosed in two monozygotic screening negative cotwins at the age of 9 months and 12 years, respectively. Furthermore, the twin analysis showed that 95% of liability to transient CH was explained by genetic factors and 5% by environmental (unshared) factors, whereas 64% of phenotypic variance of permanent CH was explained by common environmental factors (shared during the fetal life) and 36% by unshared environmental factors.
CONCLUSIONS: This study showed that the introduction of rescreening permits the diagnosis of CH in a greater number of twins. It also showed the importance of long-term follow-up in both twins in the pair, and the role of nongenetic factors in the etiology of permanent CH.
Copyright © 2019 Endocrine Society.

Entities:  

Mesh:

Year:  2019        PMID: 31287502     DOI: 10.1210/jc.2019-00900

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  8 in total

Review 1.  New genetics in congenital hypothyroidism.

Authors:  Athanasia Stoupa; Dulanjalee Kariyawasam; Marina Muzza; Tiziana de Filippis; Laura Fugazzola; Michel Polak; Luca Persani; Aurore Carré
Journal:  Endocrine       Date:  2021-03-01       Impact factor: 3.633

2.  Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism.

Authors:  D Gentilini; M Muzza; T de Filippis; M C Vigone; G Weber; L Calzari; A Cassio; M Di Frenna; M Bartolucci; E S Grassi; E Carbone; A Olivieri; L Persani
Journal:  J Endocrinol Invest       Date:  2022-09-07       Impact factor: 5.467

Review 3.  Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.

Authors:  Paul van Trotsenburg; Athanasia Stoupa; Juliane Léger; Tilman Rohrer; Catherine Peters; Laura Fugazzola; Alessandra Cassio; Claudine Heinrichs; Veronique Beauloye; Joachim Pohlenz; Patrice Rodien; Regis Coutant; Gabor Szinnai; Philip Murray; Beate Bartés; Dominique Luton; Mariacarolina Salerno; Luisa de Sanctis; Mariacristina Vigone; Heiko Krude; Luca Persani; Michel Polak
Journal:  Thyroid       Date:  2021-03       Impact factor: 6.568

4.  Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study.

Authors:  Maria Cristina Maggio; Saveria Sabrina Ragusa; Tommaso Silvano Aronica; Orazia Maria Granata; Eleonora Gucciardino; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2021-05-05       Impact factor: 2.638

5.  Age- and sex-specific reference intervals for thyroid hormones in a Chinese pediatrics: a prospective observational study of 1,279 healthy children.

Authors:  Cong Yao; Mo Wu; Mei Liu; Xiaoqian Chen; Hongmin Zhu; Chen Xiong; Dan Wang; Yun Xiang; Guori Suo; Jun Wang; Hong Sun; Chunhui Yuan; Yong Xia
Journal:  Transl Pediatr       Date:  2021-10

6.  The prevalence of hypothyroxinemia in premature newborns.

Authors:  Renata Stawerska; Marzena Nowak-Bednarek; Tomasz Talar; Marzena Kolasa-Kicińska; Anna Łupińska; Maciej Hilczer; Ewa Gulczyńska; Andrzej Lewiński
Journal:  Front Endocrinol (Lausanne)       Date:  2022-08-10       Impact factor: 6.055

7.  Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.

Authors:  Liangshan Li; Wenmiao Liu; Liqin Zhang; Fang Wang; Fengqi Wang; Maosheng Gu; Xiuli Wang; Shiguo Liu
Journal:  Endocrine       Date:  2020-08-15       Impact factor: 3.633

8.  Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China.

Authors:  Jinfu Zhou; Jinying Luo; Junyu Lin; Yinglin Zeng; Xiaolong Qiu; Wenbin Zhu; Guanghua Liu
Journal:  Medicine (Baltimore)       Date:  2020-06-26       Impact factor: 1.817

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.