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Delayed puberty in males with chronic renal failure
Kidney International
|September 1, 1980
Summary
Chronic renal failure elevates follicle-stimulating hormone (FSH) in adolescent males, even before puberty. This suggests potential germinal epithelium damage, while Leydig cell function remains unaffected.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Reproductive Endocrinology
Background:
- Chronic renal failure (CRF) can impact endocrine function.
- The pituitary-testicular axis is crucial for male pubertal development.
Purpose of the Study:
- To investigate the effects of CRF on the pituitary-testicular axis in adolescent males.
- To assess hormonal profiles in relation to renal function and pubertal stage.
Main Methods:
- Studied 31 males (aged 11.7-20.0 yr) with CRF, divided into non-hemodialysis, hemodialysis, and post-renal transplant groups.
- Measured serum hormone levels including testosterone, androgens, luteinizing hormone, and follicle-stimulating hormone (FSH).
- Assessed pubertal development using Tanner staging and correlated hormone levels with serum creatinine and pubertal stage.
Main Results:
- Pubertal development was delayed in CRF patients.
- Testosterone and most androgens were normal for pubertal stage in non-dialysis and dialysis groups; adrenal androgens were decreased in transplant patients due to prednisone.
- Follicle-stimulating hormone (FSH) was significantly elevated in non-dialysis and hemodialysis groups, and in transplant patients with creatinine > 2 mg/dl, suggesting germinal epithelium damage.
Conclusions:
- Elevated FSH in adolescent males with CRF indicates potential damage to the germinal epithelium.
- Leydig cell function appears preserved despite chronic kidney disease.
- FSH elevation occurs early in CRF, even before significant pubertal maturation.