Inazu A, Brown M L, Hesler C B, Agellon L B, Koizumi J, Takata K, Maruhama Y, Mabuchi H, Tall A R
Department of Medicine, Columbia University, College of Physicians and Surgeons, New York, NY 10032.
N Engl J Med. 1990 Nov 1;323(18):1234-8. doi: 10.1056/NEJM199011013231803.
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.
血浆胆固醇酯转运蛋白(CETP)催化胆固醇酯从高密度脂蛋白(HDL)转移至其他脂蛋白。我们最近描述了一个因CETP基因剪接缺陷导致HDL水平升高和CETP缺乏的日本家族。为评估这种情况的发生率和表型,我们通过CETP放射免疫测定和DNA分析,对另外11个HDL水平较高的家族进行了筛查。
我们在来自日本三个不同地区的4个家族中发现了相同的CETP基因突变。对突变的CETP等位基因进行限制性片段长度多态性分析表明,所有先证者对于相同单倍型均为纯合子。CETP缺乏的纯合子家族成员(n = 10)有中度高胆固醇血症(平均总胆固醇水平[±标准差],7.01±0.83 mmol/L),HDL胆固醇水平显著升高(4.24±1.01 mmol/L)和载脂蛋白A-I升高,而低密度脂蛋白胆固醇水平(1.99±0.80 mmol/L)和载脂蛋白B降低。缺乏的杂合子成员(n = 20),其CETP水平处于正常范围下限,与未受影响的家族成员相比,HDL胆固醇和载脂蛋白A-I水平中度升高,HDL亚类2与HDL亚类3的比例增加(1.5±0.8对0.7±0.4)。在美国不同地区的6名HDL胆固醇水平升高的无关受试者中未发现CETP缺乏。
CETP缺乏似乎是日本人群中HDL水平升高的常见原因,可能是由于奠基者效应。我们在杂合子中观察到的结果表明,CETP通常在HDL亚类2水平的调节中起作用。在CETP缺乏的家族中没有过早动脉粥样硬化的证据。事实上,CETP缺乏者的脂蛋白谱可能具有抗动脉粥样硬化作用,并且可能与寿命延长有关。