Adrenal disease

Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study

Eur J EndocrinolPublished Retrospective cohort study

An erratum to this article was published (Eur J Endocrinol, 5 Jun 2024 ↗)

Main finding · TART diagnosisResult — go to the resultrisk 2.6 times higher

Authors' conclusion

A delayed CAH diagnosis of >1 year vs CAH diagnosis within 1 month after birth was associated with a higher risk of TART development, which may be attributed to poor disease control in early life.

Study context

Population
Male patients with congenital adrenal hyperplasia (CAH) (21-hydroxylase deficiency, n = 181; 11-hydroxylase deficiency, n = 7), median age 13 years (IQR 10–17), at least 1 testicular US; data of first 4 years of life
Participants
188 patients
Exposure
Delayed CAH diagnosis >1 year vs diagnosis within 1 month of life
Outcome
TART development
Methodological detailsmulticenter (n = 22), open cohort, I-CAH registry
  • Multicenter (n = 22)
  • Open cohort
  • I-CAH registry

Main finding

TART diagnosis

risk

2.6 times higher

As reported in the abstract

TART detected
72 (38%)

Observational data: associations, not effects.

Further findings

Biochemical disease control and bone age advancement in first 4 years · first 4 years of life

Did not predict TART onset

Height SD scores at end of 4-year period · end of 4-year study period

Increased height SD scores associated with higher risk of TART diagnosis
27%

Original publication

Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study. Eur J Endocrinol. Published 14 October 2023. doi:10.1093/ejendo/lvad143

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