Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Clinics (Sao Paulo). 2013;68(2):147-52. doi: 10.6061/clinics/2013(02)oa05.

Abstract

Objective: The protocols for glucocorticoid replacement in children with salt wasting 21-hydroxylase deficiency are well established; however, the current recommendation for mineralocorticoid replacement is general and suggests individualized dose adjustments. This study aims to retrospectively review the 9-α-fludrocortisone dose regimen in salt wasting 21-hydroxylase deficient children who have been adequately treated during infancy.

Methods: Twenty-three salt wasting 21-hydroxylase deficient patients with good anthropometric and hormonal control were followed in our center since diagnosis. The assessments of cortisone acetate and 9-α-fludrocortisone doses, anthropometric parameters, and biochemical and hormonal levels were rigorously evaluated in pre-determined intervals from diagnosis to two years of age.

Results: The 9-α-fludrocortisone doses decreased over time during the first and second years of life; the median fludrocortisone doses were 200 µg at 0-6 months, 150 µg at 7-18 months and 125 µg at 19-24 months. The cortisone acetate dose per square meter was stable during follow-up (median = 16.8 mg/m²/day). The serum sodium, potassium and plasma rennin activity levels during treatment were normal, except in the first month of life, when periodic 9-α-fludrocortisone dose adjustments were made.

Conclusions: The mineralocorticoid needs of salt wasting 21-hydroxylase deficient patients are greater during early infancy and progressively decrease during the first two years of life, which confirms that a partial aldosterone resistance exists during this time. Our study proposes a safety regiment for mineralocorticoid replacement during this critical developmental period.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Hyperplasia, Congenital / drug therapy*
  • Adrenal Hyperplasia, Congenital / genetics
  • Age Factors
  • Anthropometry
  • Anti-Inflammatory Agents / administration & dosage*
  • Cortisone / administration & dosage
  • Cortisone / analogs & derivatives
  • Female
  • Fludrocortisone / administration & dosage*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Retrospective Studies
  • Statistics, Nonparametric
  • Time Factors
  • Treatment Outcome

Substances

  • Anti-Inflammatory Agents
  • Fludrocortisone
  • Cortisone

Supplementary concepts

  • Congenital adrenal hyperplasia due to 21 hydroxylase deficiency