Morris B J, Zee R Y, Schrader A P
Department of Physiology, School of Medicine, University of Sydney, N.S.W., Australia.
J Clin Invest. 1994 Sep;94(3):1085-9. doi: 10.1172/JCI117423.
The frequency of the D allele of an insertion/deletion (I/D) polymorphism of the angiotensin I-converting enzyme (ACE) gene has been reported to be elevated in myocardial infarction and other patients. We therefore hypothesized that death rate of DD individuals should be increased in the population as a whole and this should be evident as a decrease in DD frequency with age. This hypothesis was tested in 118 Caucasian subjects who were already at high risk of cardiovascular events by having severe, early onset, familial hypertension (HT). A group of 196 age-, sex- and body mass index-matched normotensives (NTs) was used as a control. In the NT group II, ID, and DD genotype frequencies were similar for different age groups. DD frequency was 0.42 in NTs, but in HTs was 0.28, 0.26, and 0.10 for the age groups < 50, 50-59, and > or = 60 yr, respectively. Corresponding D allele frequencies were 0.52, 0.46, and 0.40 in the respective age groups of HTs, compared with 0.61 in NTs (by chi 2-analysis, P = 0.1, 0.047, and 0.0006, respectively). In HTs aged > or = 60, DD frequency was only 14% of expected. Plasma ACE activity tracked similarly with I/D genotype in HTs (P = 0.027; n = 35) as in NTs (P = 0.0001; n = 94) and Michaelis constant was identical for DD and II. Neither blood pressure, body mass index, nor sex bore any relationship with I/D genotype. In conclusion, in a group of severely HT patients not selected for cardiac pathology, there appeared to be a marked, selective decrease, in subgroups of increasing age, in frequency of the ACE DD genotype. One possibility suggested by this data might be that DD increases risk of premature death, at least in HTs who have two HT parents.
据报道,血管紧张素I转换酶(ACE)基因插入/缺失(I/D)多态性的D等位基因频率在心肌梗死患者及其他患者中有所升高。因此,我们推测在整个人口中,DD个体的死亡率应该会增加,这应该表现为DD频率随年龄增长而降低。在118名患有严重早发性家族性高血压(HT)且已处于心血管事件高风险的白种人受试者中对这一假设进行了检验。将一组196名年龄、性别和体重指数匹配的血压正常者(NTs)作为对照。在NT组中,不同年龄组的II、ID和DD基因型频率相似。NTs中DD频率为0.42,但在HT患者中,年龄<50岁、50 - 59岁和≥60岁组的DD频率分别为0.28、0.26和0.10。HT患者相应年龄组的D等位基因频率分别为0.52、0.46和0.40,而NTs中为0.61(经卡方分析,P值分别为0.1、0.047和0.0006)。在≥60岁的HT患者中,DD频率仅为预期值的14%。HT患者中血浆ACE活性与I/D基因型的相关性与NTs相似(HT患者中P = 0.027;n = 35,NTs中P = 0.0001;n = 94),且DD和II的米氏常数相同。血压、体重指数和性别与I/D基因型均无任何关系。总之,在一组未因心脏病理情况而选择的严重HT患者中,随着年龄增长的亚组中,ACE DD基因型频率似乎出现了显著的选择性降低。该数据提示的一种可能性可能是,DD增加了过早死亡的风险,至少在有两位HT父母的HT患者中如此。