Literature DB >> 25305309

The different requirement of L-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic-pituitary level.

Brunella Bagattini1, Caterina Di Cosmo1, Lucia Montanelli1, Paolo Piaggi1, Mariella Ciampi1, Patrizia Agretti1, Giuseppina De Marco1, Paolo Vitti1, Massimo Tonacchera2.   

Abstract

BACKGROUND: Levothyroxine (l-T4) is commonly employed to correct hormone deficiency in children with congenital hypothyroidism (CH) and in adult patients with iatrogenic hypothyroidism.
OBJECTIVE: To compare the daily weight-based dosage of the replacement therapy with l-T4 in athyreotic adult patients affected by CH and adult patients with thyroid nodular or cancer diseases treated by total thyroidectomy. DESIGN AND METHODS: A total of 36 adult patients (27 females and nine males) aged 18-29 years were studied; 13 patients (age: 21.5±2.1, group CH) had athyreotic CH treated with l-T4 since the first days of life. The remaining 23 patients (age: 24±2.7, group AH) had hypothyroidism after total thyroidectomy (14 patients previously affected by nodular disease and nine by thyroid carcinoma with clinical and biochemical remission). Patient weight, serum free thyroid hormones, TSH, thyroglobulin (Tg), anti-Tg, and anti-thyroperoxidase antibodies were measured. Required l-T4 dosage was evaluated. At the time of the observations, all patients presented free thyroid hormones within the normal range and TSH between 0.8 and 2 μIU/ml.
RESULTS: Patients had undetectable Tg and anti-thyroid antibodies. The daily weight-based dosage of the replacement therapy with l-T4 to reach euthyroidism in patients of group CH was significantly higher than that in those of group AH (2.16±0.36 vs 1.73±0.24 μg/kg, P<0.005). Patients of group CH treated with l-T4 had significantly higher serum TSH levels than patients of group AH (P=0.05) as well as higher FT4 concentrations.
CONCLUSIONS: To correct hypothyroidism, patients of group CH required a daily l-T4 dose/kg higher than group AH patients, despite higher levels of TSH. The different requirement of replacement therapy between adult patients with congenital and those with surgical athyroidism could be explained by a lack of thyroid hormones since fetal life in CH, which could determine a different set point of the hypothalamus-pituitary-thyroid axis.
© 2014 European Society of Endocrinology.

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Year:  2014        PMID: 25305309     DOI: 10.1530/EJE-14-0621

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  9 in total

1.  In children with acquired hypothyroidism levothyroxine requirements may be significantly conditioned by the etiology of thyroid failure.

Authors:  Laura Cannavò; Tommaso Aversa; Domenico Corica; Giorgia Pepe; Giovanni Battista Pajno; Angela Alibrandi; Filippo De Luca; Malgorzata Wasniewska
Journal:  Endocrine       Date:  2019-07-03       Impact factor: 3.633

2.  Liothyronine Improves Biochemical Control of Congenital Hypothyroidism in Patients with Central Resistance to Thyroid Hormone.

Authors:  Laura Paone; Abby F Fleisch; Henry A Feldman; Rosalind S Brown; Ari J Wassner
Journal:  J Pediatr       Date:  2016-05-11       Impact factor: 4.406

3.  Similar age-dependent levothyroxine requirements of schoolchildren with congenital or acquired hypothyroidism.

Authors:  Martin Perlsteyn; Johnny Deladoëy; Guy Van Vliet
Journal:  Eur J Pediatr       Date:  2016-02-09       Impact factor: 3.183

4.  Pre- and Postnatal Polybrominated Diphenyl Ether Concentrations in Relation to Thyroid Parameters Measured During Early Childhood.

Authors:  Whitney J Cowell; Andreas Sjödin; Richard Jones; Ya Wang; Shuang Wang; Robin M Whyatt; Pam Factor-Litvak; Gary Bradwin; Abeer Hassoun; Sharon Oberfield; Julie B Herbstman
Journal:  Thyroid       Date:  2019-05       Impact factor: 6.568

5.  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 6.  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

7.  Thyroid Function across the Lifespan: Do Age-Related Changes Matter?

Authors:  John P Walsh
Journal:  Endocrinol Metab (Seoul)       Date:  2022-04-14

Review 8.  Neuropsychological Alterations in Patients with Congenital Hypothyroidism Treated with Levothyroxine: Linked Factors and Thyroid Hormone Hyposensitivity.

Authors:  Karla Cristina Razón-Hernández; Norma Osnaya-Brizuela; Armando Valenzuela-Peraza; Esperanza Ontiveros-Mendoza; Luis Miguel Rodríguez-Serrano; Jorge Pacheco-Rosado; Gerardo Barragán-Mejía; Karla Sánchez-Huerta
Journal:  J Clin Med       Date:  2022-06-15       Impact factor: 4.964

9.  Tissue sensitivity to thyroid hormones may change over time.

Authors:  Giorgio Radetti; Franco Rigon; Alessandro Salvatoni; Irene Campi; Tiziana De Filippis; Valentina Cirello; Silvia Longhi; Fabiana Guizzardi; Marco Bonomi; Luca Persani
Journal:  Eur Thyroid J       Date:  2022-02-16
  9 in total

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