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2
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本文引用的文献

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Molecular biology of the angiotensin I converting enzyme: I. Biochemistry and structure of the gene.
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Polymorphism of the angiotensin I converting enzyme gene is apparently not related to high blood pressure: Dutch Hypertension and Offspring Study.血管紧张素I转换酶基因多态性显然与高血压无关:荷兰高血压与后代研究。
J Hypertens. 1993 Apr;11(4):345-8. doi: 10.1097/00004872-199304000-00003.
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The angiotensin I converting enzyme gene and predisposition to high blood pressure.血管紧张素I转换酶基因与高血压易感性
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Angiotensin I-converting enzyme in human circulating mononuclear cells: genetic polymorphism of expression in T-lymphocytes.人循环单核细胞中的血管紧张素I转换酶:T淋巴细胞中表达的基因多态性
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Relationships between angiotensin I converting enzyme gene polymorphism, plasma levels, and diabetic retinal and renal complications.血管紧张素I转换酶基因多态性、血浆水平与糖尿病视网膜及肾脏并发症之间的关系。
Diabetes. 1994 Mar;43(3):384-8. doi: 10.2337/diab.43.3.384.
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Short report: insertion variant in intron 9, but not microsatellite in intron 2, of the insulin receptor gene is associated with essential hypertension.简短报告:胰岛素受体基因第9内含子的插入变异而非第2内含子的微卫星与原发性高血压相关。
J Hypertens. 1993 Nov;11(11):1283-8.
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A potent genetic risk factor for restenosis.再狭窄的一个强大遗传风险因素。
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Cross-sectional analysis of Met235-->Thr variant of angiotensinogen gene in severe, familial hypertension.血管紧张素原基因Met235→Thr变异在重度家族性高血压中的横断面分析
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ApoE and ACE genes: impact on human longevity.载脂蛋白E基因和血管紧张素转换酶基因:对人类长寿的影响
Nat Genet. 1994 Jan;6(1):4-5. doi: 10.1038/ng0194-4.
10
Genetic associations with human longevity at the APOE and ACE loci.载脂蛋白E(APOE)和血管紧张素转换酶(ACE)基因座与人类长寿的遗传关联。
Nat Genet. 1994 Jan;6(1):29-32. doi: 10.1038/ng0194-29.

老年高血压患者中血管紧张素转换酶基因型的不同频率

Different frequencies of angiotensin-converting enzyme genotypes in older hypertensive individuals.

作者信息

Morris B J, Zee R Y, Schrader A P

机构信息

Department of Physiology, School of Medicine, University of Sydney, N.S.W., Australia.

出版信息

J Clin Invest. 1994 Sep;94(3):1085-9. doi: 10.1172/JCI117423.

DOI:10.1172/JCI117423
PMID:8083349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC295169/
Abstract

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.

摘要

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。