Rossi G P, Narkiewicz K, Cesari M, Winnicki M, Bigda J, Chrostowska M, Szczech R, Pawlowski R, Pessina A C
Department of Clinical and Experimental Medicine, University of Padua Medical School, Azienda Ospedaliera di Padova, Italy.
J Hypertens. 1999 May;17(5):647-55. doi: 10.1097/00004872-199917050-00008.
We investigated the determinants of plasma renin activity (PRA) and plasma levels of angiotensin-converting enzyme (pACE), including the effect of the D/I polymorphism of the angiotensin-converting enzyme (ACE) gene, in monozygotic (MZ) and dizygotic (DZ) twins.
Sixty-nine pairs of twins underwent measurements of blood pressure, pACE and ACE D/I genotyping. In addition, in 30 pairs ambulatory blood pressure (ABP) monitoring was carried out. To ascertain twin's zygosity, some highly discriminating variable number of tandem repeats micro- and mini-satellite systems were analysed by polymerase chain reaction (PCR) followed by polyacrylamide gel electrophoresis and silver staining. The D/I polymorphism was assessed by PCR; pACE was measured in triplicate with a colorimetric assay, and PRA by a commercial kit. In DZ twins, identity by descent of the D/I alleles was examined by PCR amplification of a highly polymorphic simple sequence repeat at the human growth hormone gene.
pACE levels were significantly (P < 0.01) higher in DD (9.27 +/- 2.60 IU/l, mean +/-SD) than in II (6.68 +/- 3.0), with DI having intermediate levels (7.93 +/- 2.7). No difference of PRA between different D/I genotypes was found. Twin data analysis showed a statistically significant heritability of pACE, but not of PRA. No differences between MZ and DZ twins in PRA, pACE and the relationship of the D/I genotype with pACE was found. Besides showing that the D/I genotype was the most important predictor of pACE, a multivariate analysis demonstrated that identity by descent of the D/I allele, as assessed by growth hormone (GH) genotyping, also significantly affected pACE.
In this study of normotensive twins, pACE and not PRA showed significant heritability, the former being tightly associated with the D/I ACE gene polymorphism, and/or with a quantitative trait locus in linkage disequilibrium with it.
我们在单卵双胞胎(MZ)和双卵双胞胎(DZ)中研究了血浆肾素活性(PRA)和血浆血管紧张素转换酶水平(pACE)的决定因素,包括血管紧张素转换酶(ACE)基因D/I多态性的影响。
69对双胞胎接受了血压、pACE测量及ACE D/I基因分型。此外,对30对双胞胎进行了动态血压(ABP)监测。为确定双胞胎的合子性,通过聚合酶链反应(PCR)分析了一些高分辨率的可变串联重复微卫星和小卫星系统,随后进行聚丙烯酰胺凝胶电泳和银染。通过PCR评估D/I多态性;采用比色法对pACE进行三次测量,使用商业试剂盒测量PRA。在双卵双胞胎中,通过对人类生长激素基因高度多态性简单序列重复进行PCR扩增,检测D/I等位基因的同源性。
DD型(9.27±2.60 IU/l,均值±标准差)的pACE水平显著高于II型(6.68±3.0)(P<0.01),DI型处于中间水平(7.93±2.7)。不同D/I基因型之间的PRA无差异。双胞胎数据分析显示pACE具有统计学显著的遗传力,但PRA没有。在PRA、pACE以及D/I基因型与pACE的关系方面,单卵双胞胎和双卵双胞胎之间没有差异。除了表明D/I基因型是pACE的最重要预测因子外,多变量分析还表明,通过生长激素(GH)基因分型评估的D/I等位基因同源性也显著影响pACE。
在这项对血压正常双胞胎的研究中,pACE而非PRA显示出显著的遗传力,前者与D/I ACE基因多态性紧密相关,和/或与与其处于连锁不平衡的数量性状位点紧密相关。