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Adrenal steroids synthesis during acute infectious diseases in infants

C A Longui1, E R M Zlochevsky, T A S S Bachega

  • 1Department of Pediatrics, Pediatric Endocrinology Unit, Santa Casa de São Paulo School of Medicine, University of São Paulo School of Medicine, São Paulo, Brazil.

Insights

Elevated 17-hydroxyprogesterone (17OHP) in infants during infection may mimic congenital adrenal hyperplasia (CAH). Early glucocorticoid therapy and ACTH testing are suggested for suspected cases.

Area of Science:

  • Pediatric endocrinology
  • Infectious diseases

Background:

  • Elevated plasma 17-hydroxyprogesterone (17OHP) complicates differential diagnosis in infants with septic shock versus adrenal failure.
  • Understanding adrenal steroid patterns during infection is crucial for accurate diagnosis and management.

Purpose of the Study:

  • To investigate adrenal steroid profiles, specifically 17OHP and cortisol, in infants experiencing infections of varying severity.
  • To determine the correlation between infection severity and specific adrenal steroid levels.

Main Methods:

  • Studied 56 infants aged 1-6 months during infectious episodes.
  • Measured plasma levels of cortisol, 17OHP, androstenedione, DHEA, DHEA-S, and testosterone.

Main Results:

  • Cortisol elevation was observed in 24 infants; one showed low cortisol.
  • 41 infants had 17OHP levels above 6.0 nmol/l, with 10 exceeding 30.2 nmol/l.
  • Higher 17OHP concentrations correlated positively with increased disease severity.

Conclusions:

  • Infectious diseases can cause 17OHP elevations mimicking non-classic congenital adrenal hyperplasia (NC-CAH).
  • Consider initiating glucocorticoid therapy if 17OHP elevation is not typical for classic CAH (SL-CAH).
  • Perform ACTH testing post-recovery to rule out CAH when 17OHP levels are significantly elevated during infection.
Abstract

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