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Random luteinizing hormone often remains pubertal in children treated with the histrelin implant for central
Katherine A Lewis1, Erica A Eugster
1Section of Pediatric Endocrinology, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Insights
Random ultrasensitive luteinizing hormone (LH) monitoring in children with central precocious puberty (CPP) on histrelin implants is unreliable. Many patients show elevated LH despite effective treatment, indicating a need for revised monitoring strategies.
Area of Science:
- Pediatric Endocrinology
- Reproductive Medicine
- Clinical Chemistry
Background:
- Central precocious puberty (CPP) requires effective treatment to prevent adverse outcomes.
- Histrelin implants are a common treatment for CPP, aiming to suppress the hypothalamic-pituitary-gonadal axis.
- Monitoring treatment efficacy is crucial for managing CPP.
Purpose of the Study:
- To evaluate the utility of random ultrasensitive luteinizing hormone (US LH) levels for monitoring children with CPP treated with histrelin implants.
- To compare random US LH levels with gonadotropin-releasing hormone analog (GnRHa) stimulation tests.
Main Methods:
- Prospective, uncontrolled, observational study at a pediatric endocrinology tertiary center.
- Thirty-three children with CPP treated with histrelin implants were enrolled.
- Random US LH measurements at 6 months and GnRHa stimulation tests at 12 months were performed.
Main Results:
- In 59% of patients, 6-month random US LH levels exceeded the prepubertal range.
- All patients who underwent GnRHa stimulation tests showed complete axis suppression (peak LH <4 IU/L).
- US LH levels correlated with peak stimulated LH, with higher levels in those with pubertal random LH.
Conclusions:
- Random US LH levels do not consistently revert to prepubertal ranges in over half of patients with histrelin implants and suppressed axes.
- Current random US LH monitoring may not accurately reflect treatment efficacy in CPP.
- Further long-term studies are necessary to establish optimal monitoring strategies for CPP treatment.
Objective:
To investigate the use of random ultrasensitive (US) luteinizing hormone (LH) levels to monitor children being treated with a histrelin implant for central precocious puberty (CPP).
Study Design:
This was a prospective, uncontrolled, observational study at a pediatric endocrinology tertiary center. Thirty-three children (26 girls; mean age 7.2 ± 2.5 years) treated with a histrelin implant for CPP were enrolled. A random US LH measurement was obtained at 6 months, and a gonadotropin-releasing hormone analog stimulation test was performed at 12 months. Clinic visits occurred at baseline and at 6-month intervals.
Results:
In 59% of the patients (17 of 29), the 6-month random US LH exceeded the prepubertal range of ≤0.3 IU/L. In contrast, gonadotropin-releasing hormone analog stimulation tests revealed complete hypothalamic-pituitary-gonadal axis suppression (peak LH <4 IU/L) in all 31 patients who underwent testing. US LH levels were highly correlated with peak stimulated LH levels. The mean peak stimulated LH level was higher in patients with a pubertal random LH than in those with a prepubertal random LH (1.2 ± 0.5 IU/L vs 0.5 ± 0.1 IU/L; P < .01). No patient had clinical evidence of pubertal progression.
Conclusion:
The random US LH level does not revert to a prepubertal range in more than one-half of patients with a histrelin implant and documented hypothalamic-pituitary-gonadal axis suppression. Long-term studies are needed to elucidate the optimal strategy for monitoring treatment in children with CPP.
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