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Published on: September 15, 2017
Adrenocortical suppression in children with nephrotic syndrome treated with corticosteroids
Ganesh M Krishna1, Aashima Dabas1, Mukta Mantan2
1Department of Pediatrics, Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India.
Insights
Children with nephrotic syndrome on alternate day steroids show high rates of adrenal insufficiency. A cumulative steroid dose over 0.22 mg/kg/day indicates a risk for adrenocortical suppression.
Area of Science:
- Pediatric Endocrinology
- Pediatric Nephrology
- Endocrinology
Background:
- Children with nephrotic syndrome often receive prolonged alternate-day steroid therapy.
- This necessitates evaluating potential adrenocortical suppression using the adrenocorticotropic hormone (ACTH) stimulation test.
Purpose of the Study:
- To determine the prevalence of adrenocortical suppression in children with nephrotic syndrome on alternate-day steroids.
- To identify a predictive threshold for steroid dosage associated with adrenal insufficiency.
Main Methods:
- A cross-sectional study included 52 children (2-18 years) with steroid-sensitive or resistant nephrotic syndrome in remission.
- Adrenocortical function was assessed via baseline and post-ACTH stimulation serum cortisol levels.
- Adrenal insufficiency was diagnosed if 1-hour post-ACTH cortisol was <18.0 µgm/dl.
Main Results:
- The study found a 50% prevalence of adrenal insufficiency using baseline cortisol and 64% using post-stimulation levels.
- A cumulative annual prednisolone dose of >0.22 mg/kg/day predicted adrenocortical suppression with an AUC of 0.76.
- The predictive model demonstrated 63.9% sensitivity and 81.3% specificity.
Conclusions:
- A significant proportion of children with nephrotic syndrome exhibit adrenal insufficiency when treated with alternate-day steroids.
- Cumulative steroid intake exceeding 0.22 mg/kg/day on an alternate-day basis is a risk factor for predicting adrenocortical suppression.
Background:
Children with nephrotic syndrome are exposed to alternate day steroids for prolonged periods and this poses the need for evaluation of adrenocortical suppression using the adrenocorticotropic hormone (ACTH) stimulation test.
Methods:
This cross-sectional study enrolled children (2-18 years) both with steroid sensitive nephrotic syndrome (SSNS) (n = 27) and steroid resistant (SRNS) (n = 25); those on daily prednisolone or having serious bacterial infections or hospitalized were excluded. The primary objective was to determine prevalence of adrenocortical suppression in those on low dose alternate day steroids for more than 8 weeks or having received > 2 mg/kg/d for > 2 weeks in the past 1 year and currently in remission. A baseline morning fasting sample of serum cortisol was taken and 25 IU of ACTH (Acton Prolongatum*) injected intramuscularly and repeat serum cortisol sample taken after 1 h. All patients with 1 h post ACTH cortisol < 18.0 µgm/dl were diagnosed with adrenal insufficiency. Receiver operating characteristic curve was drawn to predict the prednisolone dose for adrenal insufficiency.
Results:
Fifty-two (33 males) children were enrolled (mean age 9.4 years); proportion of adrenal insufficiency was 50% and 64% using baseline and post stimulation cutoffs. The total cumulative annual dose of prednisolone 0.22 mg/kg/day predicted adrenocortical suppression with AUC 0.76 (95% CI 0.63-0.89), with sensitivity of 63.9% and specificity of 81.3%.
Conclusions:
A significant proportion of children with nephrotic syndrome were detected with adrenal insufficiency on ACTH stimulation test. A cumulative steroid intake of > 0.22 mg/kg/day on an alternate day basis emerged as a risk factor for predicting adrenocortical suppression.
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