Key result
Apolipoprotein A5 acts as a potent regulator of triglyceride metabolism, and its genetic variants are associated with an increased risk of obesity and metabolic syndrome.
Understanding the genetic and molecular mechanisms of apoA5 in triglyceride regulation highlights its potential as a therapeutic target for managing obesity and metabolic syndrome.
ApoA5 variants may increase metabolic risk; leaves open therapeutic targeting pending interventional validation.
Apolipoprotein A5 (apoA5) has been identified to play an important role in lipid metabolism, specifically in triglyceride (TG) and TG-rich lipoproteins (TRLs) metabolism. Numerous evidence has demonstrated for an association between apoA5 and the increased risk of obesity and metabolic syndrome, but the mechanism remains to be fully elucidated. Recently, several studies verified that apoA5 could significantly reduce plasma TG level by stimulating lipoprotein lipase (LPL) activity, and the intracellular role of apoA5 has also been proved since apoA5 is associated with cytoplasmic lipid droplets (LDs) and affects intrahepatic TG accumulation. Furthermore, since adipocytes provide the largest storage depot for TG and play a crucial role in the development of obesity, we could infer that apoA5 also acts as a novel regulator to modulate TG storage in adipocytes. In this review, we focus on the association of gene and protein of apoA5 with obesity and metabolic syndrome, and provide new insights into the physiological role of apoA5 in humans, giving a potential therapeutic target for obesity and associated disorders.
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Su et al. (2018) conducted a review in Obesity and metabolic syndrome. Apolipoprotein A5 (apoA5) was evaluated. Apolipoprotein A5 acts as a potent regulator of triglyceride metabolism, and its genetic variants are associated with an increased risk of obesity and metabolic syndrome.
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