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HDL biology

CETP activity runs 2-3 times higher in hyperlipoproteinemia patients, peaking in Type V dyslipidemia (Atherosclerosis 2001)

Original title: Studies on the plasma lipid profiles, and LCAT and CETP activities according to hyperlipoproteinemia phenotypes (HLP)

Atherosclerosis · · 6

Lee M, Kim JQ, Kim J, Oh H, Park M

Classifying 196 hyperlipoproteinemia (HLP) patients and 19 non-HLP subjects by phenotype (Type IV most predominant at 58.6%, no Type I found), plasma lipids other than apoA-I and Lp(a) differed significantly between HLP and non-HLP groups (P<0.001). Type III and V, which impair clearance of triglyceride-rich lipoproteins, had higher triglyceride and VLDL-cholesterol, while Type II had higher triglyceride and LDL-cholesterol from LDL receptor defects. LCAT activity was lowest in Type III and IV and highest in Type V, tracking closely with free cholesterol and apoB/apoA and LDL/HDL ratios. CETP activity was highest in Type V, driven by its high VLDL-cholesterol, triglyceride, and low HDL-cholesterol, and CETP activity overall was elevated 2-3 fold in HLP patients compared with non-HLP, while the LCAT/CETP ratio was significantly lower in HLP than non-HLP.

Read the paper (DOI)PubMed

Original abstract

Hyperlipoproteinemia phenotypes (HLP), one of genetic disorders with an estimated prevalence of 0.5-2% in the general population, is responsible for 10% of premature CHD. After first screening with the high cholesterol (>6.47 mM/l) and triglyceride (TG) (>2.6 mM/l) levels without medication, subjects were typed for HLP classification. Differential metabolic effects of HLP types on plasma lipid profiles and the reverse cholesterol transport system (RCT) were studied in 196 HLP types (91.2%) and 19 non-HLP (8.8%). A total of 45% of subjects had primary HLP and the others had NIDDM (10.7%), hypertension (9.3%) and other chronic diseases. Type IV HLP (58.6%) was most predominant and Types IIa, IIb, III and V comprised 16.7, 12.1, 2.3 and 1.4% of the HLP. Type I was not found. Plasma lipids excluding apo A-I and Lp(a) were significantly different among HLP compared to non-HLP (P<0.001). Since Type V and III impact the clearance of TG-riched lipoproteins, TG and VLDL-C levels were higher in V and III. TG and LDL-C were higher in Type II than those in the others because of defect of LDL receptors. LCAT activity, lower in Type III and Type IV and highest in Type V, was highly associated with plasma free cholesterol levels and the ratio of apoB/apoA and LDL/HDL. CETP activity was highest in Type V due to high VLDL-C and TG and low HDL-C. The ratio of LCAT/CETP was not different among HLP types but was significantly lower in HLP than in non-HLP. CETP increased 2-3 times as well as LCAT decreased among HLP patients compared to non-HLP. We conclude non-HLP subjects with high cholesterol and TG levels do not always mean high risk of CHD and the intervention effects of HLP types would lead to impose the risk of CHD by the impact of RCT.

HDL biologymechanisms

Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.