Key result
Sebelipase alfa cuts elevated LDL-C rates by ~32 percentage points in LAL-D at 1 year.
Why the study?
Dyslipidemia is common among patients with lysosomal acid lipase deficiency, and the lipid profile response to sebelipase alfa treatment needed assessment.
Does sebelipase alfa enzyme replacement therapy improve lipid abnormalities in patients with lysosomal acid lipase deficiency?
Cohort (n=144)
Yes
Does sebelipase alfa enzyme replacement therapy improve lipid abnormalities in patients with lysosomal acid lipase deficiency?
Absolute Event Rate: 46% vs 78%
Sebelipase alfa enzyme replacement therapy provides sustained improvements in the lipid profile, including reductions in LDL-C and triglycerides, in patients with lysosomal acid lipase deficiency.
BACKGROUND AND AIMS: Dyslipidemia, including elevated low-density lipoprotein cholesterol (LDL-C) and decreased high-density lipoprotein cholesterol (HDL-C), is common among patients with lysosomal acid lipase deficiency (LAL-D). The aim of this analysis was to assess the lipid profile of patients with LAL-D treated with sebelipase alfa enzyme replacement therapy. METHODS: Children and adults enrolled in the International LAL-D Registry who had a confirmed diagnosis of LAL-D were treated with sebelipase alfa, and had not received lipid-modifying medications were included. The proportions of patients with lipid parameters outside the limits of normal or clinically relevant cutoffs were analyzed before first treatment (baseline) and for up to 3 years of follow-up. RESULTS: Data from 144 patients (median age at diagnosis, 9.5 years; 92% White; 54% male) were analyzed. From baseline to after 1 year of sebelipase alfa treatment, decreases were observed in the proportion of patients with LDL-C >160 mg/dL (78% to 46%), non-HDL-C >190 mg/dL (70% to 47%), and triglycerides above the upper limit of normal (63% to 32%); the proportion of patients with HDL-C at or above the lower limit of normal increased (21% to 35%). Results were sustained through 3 years of follow-up and were similar in a cohort of patients who had results for all lipid components over 3 consecutive years of treatment. CONCLUSIONS: In patients with LAL-D not receiving lipid-modifying medication, sebelipase alfa treatment improved lipid abnormalities, with sustained reductions of LDL-C and triglycerides and elevations of HDL-C.
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Wilson et al. (2026) conducted a cohort in lysosomal acid lipase deficiency (LAL-D) (n=144). Sebelipase alfa vs. Baseline (before first treatment) was evaluated on Proportion of patients with LDL-C >160 mg/dL. In patients with LAL-D, sebelipase alfa treatment reduced the proportion of patients with LDL-C >160 mg/dL from 78% at baseline to 46% at 1 year, with sustained results through 3 years.
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