Impact of Steroid Therapy on Early Growth in Infants with Biliary Atresia: The Multicenter Steroids in Biliary Atresia Randomized Trial
Estella M Alonso, Wen Ye, Kieran Hawthorne, Veena Venkat, Kathleen M Loomes, Cara L Mack, Paula M Hertel, Saul J Karpen, Nanda Kerkar, Jean P Molleston, Karen F Murray, Rene Romero, Philip Rosenthal, Kathleen B Schwarz, Benjamin L Shneider, Frederick J Suchy, Yumirle P Turmelle, Kasper S Wang, Averell H Sherker, Ronald J Sokol, Jorge A Bezerra, John C Magee, ChiLDReN Network, Estella M Alonso, Wen Ye, Kieran Hawthorne, Veena Venkat, Kathleen M Loomes, Cara L Mack, Paula M Hertel, Saul J Karpen, Nanda Kerkar, Jean P Molleston, Karen F Murray, Rene Romero, Philip Rosenthal, Kathleen B Schwarz, Benjamin L Shneider, Frederick J Suchy, Yumirle P Turmelle, Kasper S Wang, Averell H Sherker, Ronald J Sokol, Jorge A Bezerra, John C Magee, ChiLDReN Network
Abstract
Objective: To investigate the impact of corticosteroid therapy on the growth of participants in the Steroids in Biliary Atresia Randomized Trial (START) conducted through the Childhood Liver Disease Research Network. The primary analysis in START indicated that steroids did not have a beneficial effect on drainage in a cohort of infants with biliary atresia. We hypothesized that steroids would have a detrimental effect on growth in these infants.
Study design: A total of 140 infants were enrolled in START, with 70 randomized to each treatment arm: steroid and placebo. Length, weight, and head circumference were obtained at baseline and follow-up visits to 24 months of age.
Results: Patients treated with steroids had significantly lower length and head circumference z scores during the first 3 months post-hepatoportoenterostomy (HPE), and significantly lower weight until 12 months. Growth trajectories in the steroid and placebo arms differed significantly for length (P < .0001), weight (P = .009), and head circumference (P < .0001) with the largest impact noted for those with successful HPE. Growth trajectory for head circumference was significantly lower in patients treated with steroids irrespective of HPE status, but recovered during the second 6 months of life.
Conclusions: Steroid therapy following HPE in patients with biliary atresia is associated with impaired length, weight, and head circumference growth trajectories for at least 6 months post-HPE, especially impacting infants with successful bile drainage.
Trial registration: ClinicalTrials.gov: NCT00294684.
Keywords: chronic liver disease; failure to thrive; sarcopenia.
Conflict of interest statement
Conflicts of Interest:
The authors have no relevant conflicts of interest to declare
Copyright © 2018 Elsevier Inc. All rights reserved.
Figures
Source: PubMed