Synder S M, Terdiman J F, Caan B, Feingold K R, Hubl S T, Smith R S, Young S G
Department of Medicine, Kaiser Permanente Medical Center, South San Francisco, California.
Am J Med. 1993 Nov;95(5):480-8. doi: 10.1016/0002-9343(93)90330-r.
Persons with total cholesterol (TC) levels less than 130 mg/dL (less than 3.26 mmol/L) make up less than 1% of a healthy population. Causes of hypocholesterolemia include a diet very low in cholesterol and saturated fat, disease, genetic factors (including low apolipoprotein B-100 [apo B-100] and the apo E allele), and drug therapy. The purpose of this study was to determine the causes of hypocholesterolemia in a healthy Kaiser Foundation Health Plan (KFHP) population.
We conducted a dietary and health survey of 201 healthy hypocholesterolemic adults (range: 2.04 to 3.88 mmol/L [79 to 150 mg/dL]) and 200 matched control subjects with TC levels in the middle quintile of the population (range: 5.0 to 5.61 mmol/L [194 to 217 mg/dL]) who had routine health screening from 1983 through 1985. We did apo E phenotyping studies and lipid and apo A-1 and B-100 measurements in a subgroup of 45 hypocholesterolemic subjects (mean TC level: 3.26 mmol/L [126 mg/dL]) and in a comparison group of 49 unmatched volunteers (mean TC level: 5.04 +/- 0.75 mmol/L [195 +/- 29 mg/dL]).
We found no differences in dietary intake or clinically significant medical illness between hypocholesterolemic and control subjects. In the hypocholesterolemic subgroup, we found an increased frequency of the apo E2 allele (epsilon 2) and a decreased frequency of the apo E4 allele (epsilon 4); the frequencies of the epsilon 2, epsilon 3, and epsilon 4 alleles were 33.3%, 63.3%, and 3.3%, respectively. The corresponding apo E allele frequencies in the comparison subgroup were 8.2%, 73.5%, and 18.4%, similar to those previously reported for the general population and significantly different from those found in the hypocholesterolemic subgroup (p < 0.0001). One hypocholesterolemic subject (a 46th patient) had a mutation in the apo B gene that resulted in the synthesis of a truncated species of apo B (apo B-46).
Our study indicates that hypocholesterolemia in our KFHP urban population is usually not caused by diet or disease. Biochemical factors, including the increased frequency of the apo E-2 phenotype and the decreased frequency of the apo E-4 phenotype, are more important.
总胆固醇(TC)水平低于130mg/dL(低于3.26mmol/L)的人群在健康人群中所占比例不到1%。低胆固醇血症的病因包括胆固醇和饱和脂肪含量极低的饮食、疾病、遗传因素(包括载脂蛋白B-100[apo B-100]和载脂蛋白E等位基因水平低)以及药物治疗。本研究的目的是确定凯泽基金会健康计划(KFHP)健康人群中低胆固醇血症的病因。
我们对201名健康的低胆固醇血症成年人(范围:2.04至3.88mmol/L[79至150mg/dL])和200名匹配的对照对象进行了饮食和健康调查,这些对照对象的TC水平处于1983年至1985年进行常规健康筛查人群的中间五分位数范围内(范围:5.0至5.61mmol/L[194至217mg/dL])。我们对45名低胆固醇血症受试者(平均TC水平:3.26mmol/L[126mg/dL])的亚组以及49名不匹配志愿者的对照组(平均TC水平:5.04±0.75mmol/L[195±29mg/dL])进行了载脂蛋白E表型研究以及血脂、载脂蛋白A-1和B-100测量。
我们发现低胆固醇血症患者与对照对象在饮食摄入或具有临床意义的疾病方面没有差异。在低胆固醇血症亚组中,我们发现载脂蛋白E2等位基因(ε2)频率增加,载脂蛋白E4等位基因(ε4)频率降低;ε2、ε3和ε4等位基因的频率分别为33.3%、63.3%和3.3%。对照亚组中相应的载脂蛋白E等位基因频率分别为8.2%、73.5%和18.4%,与先前报道的一般人群相似,且与低胆固醇血症亚组中的频率有显著差异(p<0.0001)。一名低胆固醇血症患者(第46例患者)的载脂蛋白B基因发生突变,导致截短型载脂蛋白B(apo B-46)的合成。
我们的研究表明,我们的KFHP城市人群中的低胆固醇血症通常不是由饮食或疾病引起的。生化因素,包括载脂蛋白E-2表型频率增加和载脂蛋白E-4表型频率降低,更为重要。