Genetics
Heterozygous CETP D442G carrier shows apolipoprotein E trapped in HDL at triple the level of other carriers (Clin Chim Acta 2000)
Original title: Marked elevation in serum apolipoprotein E in a case of heterozygous cholesteryl ester transfer protein deficiency
A 57-year-old Japanese woman with total cholesterol 7.11 mmol/l, triglycerides 0.53 mmol/l, and HDL-cholesterol 2.05 mmol/l had a markedly elevated serum apolipoprotein E of 25 mg/dl with normal apo A-I, A-II, B, C-II, and C-III. Sequencing identified the heterozygous D442G mutation in the CETP gene, and ultracentrifugation showed her apo E concentrated in the HDL fraction with none detectable in VLDL, unlike normal controls. Eleven other unrelated D442G carriers averaged only 7 plus or minus 1.5 mg/dl apo E, about a third of the proband's level, with no structural abnormality found in her apo E or LDL receptor genes, suggesting impaired transfer or receptor-mediated uptake of apo E from HDL as the mechanism.
Original abstract
The subject was a 57-year-old Japanese woman with a body mass index of 21.2 kgm(-2). Her serum total cholesterol (TC), triglycerides (TG) and HDL-cholesterol levels were 7.11 mmoll(-1), 0.53 mmoll(-1) and 2.05 mmoll(-1), respectively. She had a marked increase of serum apolipoprotein (Apo) E concentration of 25 mgdl(-1) with normal concentrations of serum Apo A-I, A-II, B, C-II and C-III. Polymerase chain reaction-restriction fragments length polymorphism analysis of the cholesteryl ester transfer protein (CETP) gene from this subject revealed the heterozygous nucleotide change causing a Asp442 to Gly substitution (D442G) in the CETP protein. For comparison, 11 unrelated female subjects with this mutation (age, 57+/-5.1 years; BMI, 22+/-1.5 kgm(-2); TC, 7.23+/-1.16 mmoll(-1); TG, 1.44+/-0.80 mmoll(-1); HDL-C, 2.47+/-0.53 mmoll(-1)) were found to have a serum Apo E concentration of 7+/-1.5 mgdl(-1), about a third of the patient's concentration. The lipoprotein profile of the proband's serum analyzed by disk polyacrylamide gel electrophoresis showed a trace amount of VLDL. A vitamin A fat-loading test showed little increase in serum triglycerides and retinyl palmitate levels compared with control subjects at 2, 4 and 6 h after fat loading. Ultracentrifugation analysis of her serum revealed no detectable Apo E in the VLDL fraction but showed a large amount of Apo E in the HDL fraction, in contrast to a normal control, who had Apo E in the VLDL fraction as well as in the HDL fraction. Sequence analysis of the Apo E gene from the subject showed no nucleotide changes in exon 3 and exon 4, which code the mature Apo E protein, indicating there is no structural abnormality in the Apo E protein. Direct sequence analysis of the LDL receptor gene also did not show any nucleotide change. Based on these findings, it was hypothesized that the marked increase of Apo E in the patient's serum was caused by a decreased transfer of Apo E from HDL particles to TG-rich lipoproteins or impaired uptake of Apo E-containing HDL by LDL receptor or remnant receptor, due presumably to a dysfunction of these receptors in the patient.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.