Exploratory study of autophagy inducer sirolimus for childhood cerebral adrenoleukodystrophy

ObjectivesX-linked adrenoleukodystrophy (ALD) is a peroxisomal disease caused by mutations in the ABCD1 gene. Childhood cerebral ALD (CCALD) is characterized by inflammatory demyelination, rapidly progressing, often fatal. Hematopoietic stem cell transplant only delays disease progression in patient...

Full description

Saved in:
Bibliographic Details
Main Authors: Xiao-Mei Luo (Author), Li-Ying Liu (Author), Qiu-Hong Wang (Author), Yang-Yang Wang (Author), Jing Wang (Author), Xiao-Yan Yang (Author), Shi-Jun Li (Author), Li-Ping Zou (Author)
Format: Book
Published: Frontiers Media S.A., 2023-06-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_ff5643aac6f34022a0ca64b8eabf5512
042 |a dc 
100 1 0 |a Xiao-Mei Luo  |e author 
700 1 0 |a Xiao-Mei Luo  |e author 
700 1 0 |a Li-Ying Liu  |e author 
700 1 0 |a Li-Ying Liu  |e author 
700 1 0 |a Qiu-Hong Wang  |e author 
700 1 0 |a Yang-Yang Wang  |e author 
700 1 0 |a Jing Wang  |e author 
700 1 0 |a Xiao-Yan Yang  |e author 
700 1 0 |a Shi-Jun Li  |e author 
700 1 0 |a Li-Ping Zou  |e author 
245 0 0 |a Exploratory study of autophagy inducer sirolimus for childhood cerebral adrenoleukodystrophy 
260 |b Frontiers Media S.A.,   |c 2023-06-01T00:00:00Z. 
500 |a 2296-2360 
500 |a 10.3389/fped.2023.1187078 
520 |a ObjectivesX-linked adrenoleukodystrophy (ALD) is a peroxisomal disease caused by mutations in the ABCD1 gene. Childhood cerebral ALD (CCALD) is characterized by inflammatory demyelination, rapidly progressing, often fatal. Hematopoietic stem cell transplant only delays disease progression in patients with early-stage cerebral ALD. Based on emergency humanitarianism, this study aims to investigate the safety and efficacy of sirolimus in the treatment of patients with CCALD.MethodsThis was a prospective, single-center, one-arm clinical trial. We enrolled patients with CCALD, and all enrolled patients received sirolimus treatment for three months. Adverse events were monitored and recorded to evaluate the safety. The efficacy was evaluated using the neurologic function scale (NFS), Loes score, and white matter hyperintensities.ResultsA total of 12 patients were included and all presented with CCALD. Four patients dropped out and a total of eight patients in the advanced stage completed a 3-month follow-up. There were no serious adverse events, and the common adverse events were hypertonia and oral ulcers. After sirolimus treatment, three of the four patients with an initial NFS > 10 showed improvements in their clinical symptoms. Loes scores decreased by 0.5-1 point in two of eight patients and remained unchanged in one patient. Analysis of white matter hyperintensities revealed a significant decrease in signal intensity (n = 7, p = 0.0156).ConclusionsOur study suggested that autophagy inducer sirolimus is safe for CCALD. Sirolimus did not improve clinical symptoms of patients with advanced CCALD significantly. Further study with larger sample size and longer follow-up is needed to confirm the drug efficacy.Clinical Trial registration:https://www.chictr.org.cn/historyversionpuben.aspx, identifier ChiCTR1900021288. 
546 |a EN 
690 |a childhood cerebral adrenoleukodystrophy 
690 |a autophagy 
690 |a sirolimus 
690 |a white matter hyperintensities 
690 |a demyelination 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pediatrics, Vol 11 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fped.2023.1187078/full 
787 0 |n https://doaj.org/toc/2296-2360 
856 4 1 |u https://doaj.org/article/ff5643aac6f34022a0ca64b8eabf5512  |z Connect to this object online.