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Thyroid outcome during long-term gonadotropin-releasing hormone agonist treatments for idiopathic precocious puberty
Francesco Massart1, Joshua Chuck Harrell, Giovanni Federico
1Pediatric Endocrine Center/Department of Pediatrics, University of Pisa, Pisa, Italy. massart@med.unipi.it
Insights
Long-term gonadotropin-releasing hormone agonist (GnRHa) treatment for central precocious puberty (CPP) in girls showed no thyroid dysfunction. Thyroid hormone levels changed, but monitoring is not required.
Area of Science:
- Pediatric Endocrinology
- Reproductive Endocrinology
- Thyroidology
Background:
- Central precocious puberty (CPP) is a condition where puberty begins unusually early.
- Gonadotropin-releasing hormone agonists (GnRHa) are used to suppress puberty in children with CPP.
- The long-term effects of GnRHa on thyroid function require further investigation.
Purpose of the Study:
- To assess the impact of long-term GnRHa administration on thyroid hormone levels in girls with idiopathic CPP.
- To compare the effects of two different GnRHa formulations, leuprorelin acetate (LA) and triptorelin (TR), on thyroid function.
Main Methods:
- A retrospective study of 73 girls with idiopathic CPP treated with GnRHa (LA or TR).
- Thyroid hormones (TSH, FT3, FT4) and antibodies were measured at baseline and over 40 months of treatment.
- Statistical analysis was performed to compare hormone levels between treatment groups and over time.
Main Results:
- Free triiodothyronine (FT3) levels significantly declined during both LA and TR treatments.
- The FT3/thyroxine (FT4) ratio showed significant differences between the LA and TR groups.
- Thyroid-stimulating hormone (TSH) secretion was not affected overall, but LA induced lower TSH values than TR.
Conclusions:
- Long-term GnRHa treatment for CPP in girls does not lead to evidence of thyroid dysfunction.
- While changes in TSH, FT3, and FT3/FT4 ratios were observed, they do not necessitate routine thyroid monitoring.
- The study suggests that thyroid activity monitoring is not required during GnRHa administration for CPP.
Purpose:
To examine the effects of long-term gonadotropin-releasing hormone agonist (GnRHa) administration on thyroid function in children affected by central precocious puberty (CPP).
Methods:
We retrospectively evaluated circulating thyroid hormones in 73 GnRHa-treated girls who were diagnosed with idiopathic CPP. Monthly depot injections (.1 mg/body kg) of leuprorelin acetate (LA) and of triptorelin (TR) were continuously administered for 40.4 +/- .7 months to 34 and 39 CPP patients, respectively. Serum levels of thyrotropin (TSH), free triiodothyronine (FT3), free thyroxine (FT4), and thyroid antibodies were determined at baseline and after 6, 12, 18, 24, 30, 36, and 40 months of GnRHa administration.
Results:
While there was no difference in FT4 release (p > .05), FT3 levels significantly declined during both LA and TR treatments from untreated baseline (p < .05). Opposite to circulating FT4 and FT3 values (p > .05), FT3/FT4 ratio was significantly different among LA and TR groups (p < .05). Both GnRHa treatments did not affect TSH secretion (p > .05); however, LA induced lower TSH values than TR (p < .05).
Conclusions:
There is no evidence of thyroid dysfunction during both GnRHa treatments, though changes in TSH, FT3, and FT3/FT4 ratios were noted. Finally, monitoring of thyroid activity during GnRHa administration is not required.
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