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Published on: October 2, 2018
Children with isolated hypospadias have different hormonal profile compared to those with associated anomalies
Simmi K Ratan1, Satish Aggarwal, Tarun Kumar Mishra
1Department of Pediatric Surgery, Maulana Azad Medical College, New Delhi, India. drjohnsimmi@yahoo.com
Insights
Children with hypospadias and associated anomalies show lower androgen levels, potentially explaining other developmental issues. Isolated hypospadias cases exhibit hormonal differences, including higher FSH, suggesting potential long-term reproductive concerns.
Area of Science:
- Pediatric Endocrinology
- Urology
- Reproductive Medicine
Background:
- Hypospadias is a common congenital condition affecting the urethra.
- Hormonal imbalances may play a role in the development of hypospadias and associated anomalies.
Purpose of the Study:
- To compare the hormonal profiles of children with isolated hypospadias (H) versus those with hypospadias and associated anomalies (HO) and healthy controls (C).
Main Methods:
- Prospective study involving 100 children with isolated hypospadias, 23 with hypospadias and anomalies, and 100 controls (0-12 years).
- Serum hormone levels (gonadotropins, DHEA-S, estrogen, progesterone, testosterone, DHT) were measured pre- and post-hCG stimulation.
- Statistical analysis compared hormonal differences between groups (p < 0.05 significant).
Main Results:
- Isolated hypospadias (H) group showed higher FSH, lower estrogen, and lower DHEA-S compared to controls.
- Hypospadias with anomalies (HO) group exhibited higher FSH, lower basal and peak testosterone, and lower androgens compared to H.
- HO group also had higher estrogen and progesterone levels than the H group.
Conclusions:
- Lower androgen output in HO may link to associated anomalies like undescended testes.
- Elevated FSH in hypospadiacs suggests potential Sertoli cell dysfunction and future reproductive issues.
- Leydig cell function appears more compromised in children with hypospadias and associated anomalies.
Aim:
The objective of this study is to compare the hormonal profile of children with isolated hypospadias to controls and hypospadiacs with associated anomalies.
Study Design:
Prospective observation at a tertiary referral hospital.
Study Subjects:
One hundred consecutive children (0-12 years) with isolated hypospadias (H), 23 with hypospadias and associated anomalies (HO).
Controls:
One hundred children (0-12 years) without any genitourinary/endocrine abnormalities (C).
Procedure:
Prehuman chorionic gonadotropin (HCG) and post-HCG fasting blood samples were drawn for estimation of serum gonadotropins, dehydroepiandrosterone sulfate (DHEA-S), estrogen (E), progesterone (P), and testosterone (T) and dihydrotestosterone (DHT).
Statistical Analysis:
Differences in hormonal levels between controls and subjects were computed with p < or = 0.05 as significant.
Results:
Compared with controls, "H" had significantly higher follicular stimulating hormone (FSH) (1.37 vs. 1.29 mIU/mL p=0.01), lower estrogen (8.08 vs. 13.78 pg/mL, p=0.00), and lower DHEA-S (27.34 vs. 40.24 microg/dL, p=0.03) levels; HO had higher FSH, lower basal T (0.13 vs. 0.46 ng/mL, p=0.01), and lower peak testosterone (1.53 vs. 2.32 ng/mL, p=0.01). "HO" had lower androgens (basal T, 0.13 vs. 0.29 ng/mL, p=0.03; peak T, 1.53 vs. 2.36 ng/mL, p=0.01), and higher estrogen (12.56 vs. 8.08 pg/mL, p=0.001) and progesterone (0.46 vs. 0.31 ng/mL, p=0.04) levels in comparison with H.
Conclusion:
Consistently lower output of androgens among HO explains the association of other anomalies (generally undescended testes) in them. High FSH among hypospadiacs hints at the possibility of Sertoli cell dysfunction and may have long-lasting sequelae for reproductive functions during adulthood. However, Leydig cell functions are affected more among HO.
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