Why the study?
Does alipogene tiparvovec reduce triglycerides in patients with homozygous lipoprotein lipase deficiency?
Does alipogene tiparvovec reduce triglycerides in patients with homozygous lipoprotein lipase deficiency?
Alipogene tiparvovec represents the first possibly curative gene therapy for homozygous lipoprotein lipase deficiency, resulting in transient triglyceride reductions.
Does not support practice change in LPL deficiency; leaves open durable gene therapy efficacy and safety.
Homozygous lipoprotein lipase (LPL) deficiency is an ultra-orphan disease associated with increased rates of pancreatitis. Current treatments based on acute plasmapheresis allied with ultra-low fat diets are inadequate as responses to fibrates or other triglyceride-lowering therapies tend to be poor. Alipogene tiparvovec is an adeno-associated virus type I (AAV1) gene therapy using a hyper-functional LPL serine(447)-stop (S447X) insert administered intramuscularly under general anaesthetic with allied immunosuppression. Treatment results in histological muscle expression of LPL allied with a transient 40% reduction in triglycerides and improvements in postprandial chylomicron triglyceride content. Alipogene tiparvovec is the first possibly curative treatment for LPL deficiency.
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Wierzbicki et al. (2012) studied this question.
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