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Apolipoprotein C-II is an essential regulator of lipid metabolism through its role as an activator of endothelial-bound lipoprotein lipase. Its proper concentration is critical—both deficiencies due to genetic mutations in APOC2 and excessive circulating levels disrupt normal lipid processing leading to significant metabolic disorders characterized by elevated blood fats. Genetic testing distinguishes between primary defects in apo-CII versus other causes like LPL deficiency. Therapeutically modulating apo-CII remains an area under active research given its central role in controlling plasma triglyceride levels.
Modulation of ApoC-II levels to influence LPL activity and triglyceride metabolism
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