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ABSTRACT: Background
The familial chylomicronemia syndrome (FCS) is an ultra rare disease caused by lipoprotein lipase (LPL) deficiency associated with potentially lethal acute pancreatitis risk. Thrombocytopenia (platelet count < 150,000 × 109/L) has been reported in patients with FCS, treated or not with volanesorsen, a second generation APOC3 anti-sense oligonucleotide. Chylomicrons are the lipoproteins delivering fat after a meal and FCS thus has a post-prandial origin. Platelet count and function have not been studied post-prandially in FCS.Objective
To evaluate post-prandial fluctuations in the platelet count (PLC) and functional defects of hemostasis in FCS.Methods
PLC, functional defects in hemostasis and hematologic variables were measured up-to 5 h after
SUBMITTER: Larouche M
PROVIDER: S-EPMC10294360 | biostudies-literature | 2023 Jun
REPOSITORIES: biostudies-literature