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Published on: September 15, 2017
Exaggerated adrenarche in a cohort of Scottish children: clinical features and biochemistry
W F Paterson1, S F Ahmed, L Bath
1Royal Hospital for Sick Children, Glasgow, UK. wendy.paterson@clinmed.gla.ac.uk
Insights
Exaggerated adrenarche in Scottish children did not show reduced fetal growth but indicated a tendency towards overweight and mild hyperinsulinemia. Raised anti-Mullerian hormone levels in girls suggest advanced ovarian development.
Area of Science:
- Pediatric Endocrinology
- Reproductive Health
- Growth and Development
Background:
- Exaggerated adrenarche (EA) is a condition with potential links to fetal growth and future health risks.
- Understanding the clinical features and risk factors in children with EA is crucial for early intervention.
Purpose of the Study:
- To investigate the association between exaggerated adrenarche and reduced fetal growth.
- To identify potential risk factors for future morbidity in Scottish children exhibiting clinical features of EA.
Main Methods:
- A three-year prospective study involving auxological measurements, blood pressure monitoring, and biochemical analyses.
- Pelvic ultrasound was conducted in girls to assess reproductive development.
- Included assessment of serum dehydroepiandrosterone sulfate (DHEAS), androstenedione, insulin, and anti-Mullerian hormone (AMH).
Main Results:
- The study cohort included 42 girls and 8 boys with exaggerated adrenarche.
- No evidence of reduced fetal growth was found; instead, a tendency towards overweight was observed.
- Mild hyperinsulinemia and modest elevations in serum androgens were noted in some patients.
- Significantly raised AMH levels in girls indicated advanced ovarian follicular development.
Conclusions:
- The Scottish cohort with exaggerated adrenarche demonstrated a female predominance.
- Findings suggest overweight and mild hyperinsulinemia as associated factors, not reduced fetal growth.
- Raised AMH levels in girls point to advanced ovarian development, a key finding for understanding EA in females.
Objective:
To investigate the reported association between exaggerated adrenarche (EA) and reduced foetal growth and to identify possible risk factors for future morbidity in Scottish children with clinical features of EA.
Design:
Three-year prospective study.
Measurements:
Auxology, blood pressure (BP), biochemical analysis of blood and urine, pelvic ultrasound in girls.
Results:
Fifty-two patients were recruited of whom one girl had nonclassical congenital adrenal hyperplasia (17-OHP 17 nmol/l) and one had insufficient blood for analysis. The final cohort comprised 42 girls of mean (SD) age 7.7 (0.99) and eight boys of 8.8 (0.67) years. Mean (SD) birth weight was 3.27 (0.49) and 3.10 (0.76) kg in girls and boys respectively. Height/weight SDS were 1.13/1.69 in girls and 1.69/1.88 in boys. Mean systolic/diastolic BP was 107.8/60.4 (50th-75th centile) in girls and 115.5/63.9 (75th-91st centile) in boys. Uterine and ovarian development was prepubertal. Median serum dehydroepiandrosterone sulphate (DHEAS) was 2.1 and 4.1 mumol/l, androstenedione 3.1 and 3.8 nmol/l in girls and boys respectively, with DHEAS within the reference range/undetectable in 18/2 and androstenedione in 12/6 patients. Fasting insulin was 9.0 and 15.0 mU/l in girls and boys respectively, with concomitant low normal SHBG. Anti-Mullerian hormone (AMH) was 15.7 pmol/l in 27 girls, compared with 5.0 pmol/l in normal girls aged 5-8 years.
Conclusions:
Our Scottish EA cohort showed female predominance, no evidence of reduced foetal growth, a tendency to overweight with commensurate mild hyperinsulinaemia and modest elevation of serum androgens in some patients. We have found raised AMH levels in the girls, indicating advanced ovarian follicular development.
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