Sebelipase Alfa Improves Aminotransferase Levels in Lysosomal Acid Lipase Deficiency: Data From an International Registry
Open Access
- 8 August 2025
- journal article
- research article
- Published by Wiley in Liver International
- Vol. 45 (9) , e70279
Abstract
Background and Aims: In patients with lysosomal acid lipase deficiency (LAL‐D), elevations in alanine and aspartate aminotransferases (ALT, AST) are associated with liver damage. The objective of this analysis was to evaluate aminotransferase levels in patients treated with sebelipase alfa enzyme replacement therapy and untreated patients. Methods: Patients in this observational study were from the International LAL‐D Registry and included untreated and treated patients who started sebelipase alfa at age ≥ 6 months. Patients in the longitudinal analysis must have had baseline and longitudinal measures of ALT or AST. A subanalysis was performed on data from patients with 3 consecutive annual follow‐up measures. Results: Of 186 patients included in this analysis, 125 were treated with sebelipase alfa. Median age at diagnosis was 9.1 y for treated patients and 20.6 y for untreated patients. Baseline ALT levels were above the upper limit of normal in 93% of children aged < 18 years and 68% of adults aged ≥ 18 years. Among 53 treated patients who had ALT results reported at 3 consecutive annual measurements, 22 (42%) had ALT levels within normal limits after 1 year of sebelipase alfa treatment. Results were similar for AST. A repeated measures regression model of data from treated patients showed significant reductions from baseline in both ALT and AST levels across 3 years of the study. Untreated patients had no appreciable changes in aminotransferase elevations over time. Conclusions: Aminotransferase levels were elevated in most patients with LAL‐D at baseline. There were sustained improvements with sebelipase alfa treatment. Trial Registration: International LAL‐D Registry: NCT01633489, EUPAS13276Keywords
Funding Information
- Alexion Pharmaceuticals
This publication has 20 references indexed in Scilit:
- Survival in infants treated with sebelipase Alfa for lysosomal acid lipase deficiency: an open-label, multicenter, dose-escalation studyOrphanet Journal of Rare Diseases, 2017
- Rapid progression and mortality of lysosomal acid lipase deficiency presenting in infantsGenetics in Medicine, 2016
- Clinical Features of Lysosomal Acid Lipase DeficiencyJournal of Pediatric Gastroenterology and Nutrition, 2015
- Sebelipase Alfa: First Global ApprovalDrugs, 2015
- Lysosomal Acid Lipase Deficiency — A New Therapy for a Genetic Lipid DiseaseNew England Journal of Medicine, 2015
- A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase DeficiencyNew England Journal of Medicine, 2015
- Lysosomal acid lipase deficiency – An under-recognized cause of dyslipidaemia and liver dysfunctionAtherosclerosis, 2014
- Alanine Aminotransferase-Old Biomarker and New Concept: A ReviewInternational Journal of Medical Sciences, 2014
- Cholesteryl ester storage disease: Review of the findings in 135 reported patients with an underdiagnosed diseaseJournal of Hepatology, 2013
- Small intestinal mucosa in cholesterol ester storage disease. A light and electron microscope study.1969