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Licensed Unlicensed Requires Authentication Published by De Gruyter June 28, 2018

Clinical management of childhood hyperthyroidism with and without Down syndrome: a longitudinal study at a single center

  • Tiago Jeronimo Dos Santos ORCID logo , Gabriel Ángel Martos-Moreno , María Teresa Muñoz-Calvo , Jesús Pozo , Fernando Rodríguez-Artalejo and Jesús Argente ORCID logo EMAIL logo

Abstract

Background

The approach to the clinical management of Graves’ disease (GD) is debatable. This study aimed to identify predictors of remission in pediatric GD.

Methods

A longitudinal study of 36 children and adolescents with GD followed from 1997 to 2017 at a single tertiary hospital was performed. Clinical and biochemical parameters, including comorbidities, treatment with anti-thyroid drugs (ATD) or definitive therapy (radioiodine [RIT] and thyroidectomy), and remission as the main outcome were collected. We performed a multivariable logistic regression analysis to identify likely predictors of remission.

Results

Among patients, most were female, in late puberty, with exuberant symptoms at onset. Eleven also suffered from Down syndrome (DS). Thirty-four patients (94%) started on methimazole from disease onset, and 25 (69%) received it as the only therapy, with a mean duration of 2.7±1.8 years. Six changed to RIT and three underwent thyroidectomy; no DS patient received definitive therapy. Remission was higher in DS patients (45% vs. 25%, p=0.24), but afterwards (3.9±2.5 vs. 2.3±1.4 years, p<0.05); there was no significance in relapsing (20% vs. 15%). Females were less likely to reach remission (p<0.05); serum free thyroxine at onset was higher (p<0.05) in patients who required definitive therapy. Thyroid-stimulating immunoglobulin (TSI) values normalized in exclusively ATD therapy, especially from 2 years on (p<0.05).

Conclusions

Males were more likely to achieve remission. TSI values may normalize in GD, notably from the second year of treatment. DS children may benefit with conservative management in GD.


Corresponding author: Prof. Dr. Jesús Argente, Full Professor and Chairman, Department of Pediatrics and Pediatric Endocrinology, Hospital Infantil Universitario Niño Jesús. Instituto de Investigación La Princesa, Av. Menéndez Pelayo 65, 28009 Madrid, Spain

Acknowledgments

The authors wish to thank all the personal staff from the Department of Pediatric Endocrinology and from the Department of Preventive Medicine for their assistance to the issues raised during all the steps of the study.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization played no role in the study design, in the collection, analysis, and interpretation of data, in the writing of the report, or in the decision to submit the report for publication.

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Received: 2018-03-26
Accepted: 2018-04-23
Published Online: 2018-06-28
Published in Print: 2018-07-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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