Key result
Free cholesterol transfer to HDL upon TGRL lipolysis was significantly decreased in patients with acute myocardial infarction (by 45%), type 2 diabetes (by 25%), and extremely high HDL-C (by 20%) compared to healthy controls.
Why the study?
Extremely high HDL-C levels are paradoxically associated with elevated cardiovascular risk in a U-shape relationship, but the underlying mechanisms remain unknown.
Observational (n=123)
Yes
Effect estimate: 45% reduction
Absolute Event Rate: 57% vs 103%
p-value: p=<0.001
May refine CVD risk assessment beyond HDL-C levels; extends mechanistic understanding of HDL-triglyceride interactions.
Background Low concentrations of high-density lipoprotein cholesterol (HDL-C) represent a well-established cardiovascular risk factor. Paradoxically, extremely high HDL-C levels are equally associated with elevated cardiovascular risk, resulting in the U-shape relationship of HDL-C with cardiovascular disease. Mechanisms underlying this association are presently unknown. We hypothesised that the capacity of high-density lipoprotein (HDL) to acquire free cholesterol upon triglyceride-rich lipoprotein (TGRL) lipolysis by lipoprotein lipase underlies the non-linear relationship between HDL-C and cardiovascular risk. Methods To assess our hypothesis, we developed a novel assay to evaluate the capacity of HDL to acquire free cholesterol (as fluorescent TopFluor® cholesterol) from TGRL upon in vitro lipolysis by lipoprotein lipase. Results When the assay was applied to several populations markedly differing in plasma HDL-C levels, transfer of free cholesterol was significantly decreased in low HDL-C patients with acute myocardial infarction (−45%) and type 2 diabetes (–25%), and in subjects with extremely high HDL-C of >2.59 mmol/L (>100 mg/dL) (−20%) versus healthy normolipidaemic controls. When these data were combined and plotted against HDL-C concentrations, an inverse U-shape relationship was observed. Consistent with these findings, animal studies revealed that the capacity of HDL to acquire cholesterol upon lipolysis was reduced in low HDL-C apolipoprotein A-I knock-out mice and was negatively correlated with aortic accumulation of [ 3 H]-cholesterol after oral gavage, attesting this functional characteristic as a negative metric of postprandial atherosclerosis. Conclusions Free cholesterol transfer to HDL upon TGRL lipolysis may underlie the U-shape relationship between HDL-C and cardiovascular disease, linking HDL-C to triglyceride metabolism and atherosclerosis.
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Ma et al. (2019) conducted an observational in Cardiovascular disease and dyslipidemia (n=123). Abnormal HDL-C levels (low or extremely high) vs. Normal HDL-C levels (healthy normolipidaemic controls) was evaluated on Capacity of HDL to acquire free cholesterol from TGRL upon in vitro lipolysis (45% reduction, p=<0.001). Free cholesterol transfer to HDL upon TGRL lipolysis was significantly decreased in patients with acute myocardial infarction (by 45%), type 2 diabetes (by 25%), and extremely high HDL-C (by 20%) compared to healthy controls.
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