Higher dose of methimazole causes frequent adverse effects in the management of Graves’ disease in children and adolescents
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Hirokazu Sato
, Nozomu Sasaki
Abstract
Objective: Methimazole (MMI) is used as a first-line antithyroid drug in children and adolescents with Graves’ disease (GD). The aim of this study was to evaluate the correlation between the initial dose of MMI and the clinical course of GD after treatment.
Design: Retrospective and collaborative study.
Setting: Nine facilities in Chiba prefecture, Japan.
Patients: Sixty-four children and adolescents with GD were analyzed. The subjects were divided into three groups by the initial daily dose of MMI: group A, 0.4±0.1 mg/kg (mean±SD, n=11); group B, 0.7±0.2 (n=37); group C, 0.9±0.2 (n=16).
Main outcome measures: The duration of time required for normalization of serum free T4 on initial treatment and the incidence of adverse effects for 1 year after the start of MMI were compared. Outcomes were compared among patients who were followed more than 3 years (group A, n=7; group B, n=24; group C, n=12).
Results: Mean duration of times for normalization of T4 was 1.9±1.5 months in group A, 1.6±0.9 in group B and 1.9±1.5 in group C (NS). No major adverse reactions were observed. Minor adverse effects occurred in 9.1% of cases in group A, 13.5% in group B and 62.0% in group C (p<0.01). Remission rates did not differ among the three groups.
Conclusions: Higher doses of MMI are harmful for initial use in children and adolescents with GD.
©2012 by Walter de Gruyter Berlin Boston
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Articles in the same Issue
- Masthead
- Masthead
- Editorial
- Growth hormone mortality: will history repeat itself?
- Review articles
- Interval training and the GH-IGF-I axis – a new look into an old training regimen
- Bone health in children and adolescent with Turner syndrome
- Metabolic alterations in pregnant women: gestational diabetes
- Short communication
- A method to determine the likelihood of transition to puberty in a heterogeneous prepubertal age group
- Images in pediatric endocrinology
- Hypopituitarism occurring in neonatal sepsis
- Original articles
- In congenital hypothyroidism, an initial L-thyroxine dose of 10–12 μg/kg/day is sufficient and sometimes excessive based on thyroid tests 1 month later
- TSH suppression after intravenous glucocorticosteroid administration in preterm infants
- Frequency of subclinical hypothyroidism in 5- to 15-year-old children with migraine headache
- Higher dose of methimazole causes frequent adverse effects in the management of Graves’ disease in children and adolescents
- Water deprivation test in children with polyuria
- Training increases anabolic response and reduces inflammatory response to a single practice in elite male adolescent volleyball players
- Positive effects of zinc supplementation on growth, GH, IGF1, and IGFBP3 in eutrophic children
- A novel intronic mutation in SHOX causes short stature by disrupting a splice acceptor site: direct demonstration of aberrant splicing by expression of a minigene in HEK-293T cells
- Increased growth hormone receptor (GHR) degradation due to over-expression of cytokine inducible SH2 domain-containing protein (CIS) as a cause of GH transduction defect (GHTD)
- Japanese growth prediction model for prepubertal children with growth hormone deficiency
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- Relationship between left ventricular mass and carotid intima media thickness in obese adolescents with non-alcoholic fatty liver disease
- Serum ischemia-modified albumin level and its association with cardiovascular risk factors in obese children and adolescents
- Obesity, insulin resistance, and the risk of an elevated alanine aminotransferase activity in the Korean adolescent population
- Leptin and IGF-I/II during the first weeks of life determine body composition at 2 years in infants born with very low birth weight
- Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele
- Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia
- Low bone status in Indian growth hormone-deficient children
- Gender related differences in glucocorticoid therapy and growth outcomes among pubertal children with 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH)
- Elevated serum anti-Müllerian hormone in adolescents with polycystic ovary syndrome: relationship to ultrasound features
- Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome
- Patient reports
- Intrathyroidal ectopic thymic tissue may mimic thyroid cancer: a case report
- Hypercortisolism and hypothyroidism in an infant with Smith-Lemli-Opitz syndrome
- Peripheral precocious puberty due to inadvertent exposure to testosterone: case report and review of the literature
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- Letters to the editor
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