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PMID: 2215607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Increased high-density lipoprotein levels caused by a common cholesteryl-ester transfer protein gene mutation.

The New England journal of medicine ·Vol. 323 ·No. 18 ·1990-11-01 ·Pages 1234-8

Inazu A, Brown ML, Hesler CB, Agellon LB, Koizumi J, Takata K, Maruhama Y, Mabuchi H, Tall AR

Abstract

The plasma cholesteryl-ester transfer protein (CETP) catalyzes the transfer of cholesteryl esters from high-density lipoprotein (HDL) to other lipoproteins. We recently described a Japanese family with increased HDL levels and CETP deficiency due to a splicing defect of the CETP gene. To assess the frequency and phenotype of this condition, we screened 11 additional families with high HDL levels by means of a radioimmunoassay for CETP and DNA analysis. We found the same CETP gene mutation in four families from three different regions of Japan. Analysis of restriction-fragment-length polymorphisms of the mutant CETP allele showed that all probands were homozygous for the identical haplotype. Family members homozygous for CETP deficiency (n = 10) had moderate hypercholesterolemia (mean total cholesterol level [+/- SD], 7.01 +/- 0.83 mmol per liter), markedly increased levels of HDL cholesterol (4.24 +/- 1.01 mmol per liter) and apolipoprotein A-I, and decreased levels of low-density lipoprotein cholesterol (1.99 +/- 0.80 mmol per liter) and apolipoprotein B. Members heterozygous for the deficiency (n = 20), whose CETP levels were in the lower part of the normal range, had moderately increased levels of HDL cholesterol and apolipoprotein A-I and an increased ratio of HDL subclass 2 to HDL subclass 3, as compared with unaffected family members (1.5 +/- 0.8 vs. 0.7 +/- 0.4). CETP deficiency was not found in six unrelated subjects with elevated HDL cholesterol levels who were from different parts of the United States. CETP deficiency appears to be a frequent cause of increased HDL levels in the population of Japan, possibly because of a founder effect. The results that we observed in heterozygotes suggest that CETP normally plays a part in the regulation of levels of HDL subclass 2. There was no evidence of premature atherosclerosis in the families with CETP deficiency. In fact, the lipoprotein profile of persons with CETP deficiency is potentially antiatherogenic and may be associated with an increased life span.

MeSH Terms
Adolescent Adult Aged Aged, 80 and over Apolipoproteins/deficiency,genetics Arteriosclerosis/blood,genetics Carrier Proteins/genetics Cholesterol Ester Transfer Proteins Cholesterol Esters/genetics Cholesterol, HDL/blood,genetics Cholesterol, LDL/blood DNA/analysis Female Glycoproteins Homozygote Humans Hypolipoproteinemias/blood,genetics Lipoproteins, HDL/blood,genetics Male Middle Aged Mutation
Chemicals
Apolipoproteins CETP protein, human Carrier Proteins Cholesterol Ester Transfer Proteins Cholesterol Esters Cholesterol, HDL Cholesterol, LDL Glycoproteins Lipoproteins, HDL DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Inazu A
Department of Medicine, Columbia University, College of Physicians and Surgeons, New York, NY 10032.
Brown M L
Hesler C B
Agellon L B
Koizumi J
Takata K
Maruhama Y
Mabuchi H
Tall A R
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1990-11-01
Pages
1234-8
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Grants
NHLBI NIH HHS · HL-21006 · United States
NHLBI NIH HHS · HL-22682 · United States
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