Goracy I
Zakładu Biochemii Klinicznej i Diagnostyki Laboratoryjnej Instytutu Kardiologii Pomorskiej Akademii Medycznej w Szczecinie.
Ann Acad Med Stetin. 2000;46:97-108.
Due to its multifarious biological activity the renin-angiotensin system occupies a special position among risk factors of ischemic heart disease. The discovery of I/D polymorphism of the ACE gene led to a better understanding of genetic control of this enzyme. Hyperhomocysteinemia is an independent risk factor of ischemic heart disease. Elevated plasma levels of homocysteine may be due to improper diet (e.g. shortage of folic acid) and/or genetic influence. Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme in the metabolism of homocysteine. The present study was performed in 100 patients (14 women and 86 men, mean age 54.2 +/- 9.2 years) with a history of myocardial infarction. The control group included 100 patients (10 women and 90 men, mean age 52.3 +/- 10 years) without such history. PCR was used to detect I/D ACE and C677T MTHFR polymorphisms. Genomic DNA was isolated from peripheral blood nuclear cells and amplified by PCR with two pairs of primers flanking the polymorphic regions. The restriction enzyme Hinf I was used to identify genotypes of the MTHFR polymorphism. No difference between both groups was found concerning the distribution of I/D ACE genotypes (31% II, 51% ID, 18% DD in the study group; 30% II, 57% ID, 13% DD in the control group; Tab. 1) or the distribution of C677T MTHFR genotypes (46% CC, 45% CT, 9% TT in the study group; 39% CC, 50% CT, 11% TT in the control group; Tab. 2). There was a significant effect of I/D genotype on ACE activity (IU/L) in the study (II = 18.2 +/- 17.9; ID = 33.5 +/- 19.9; DD = 68.9 +/- 21.9) and in the control group (II = 24.2 +/- 18.1; ID = 31.5 +/- 20.9; DD = 51.4 +/- 19.5; Tab. 3). No correlation was confirmed between ACE or MTHFR genotypes and age at infarction or left ventricular mass (Tabs. 4, 5, 6). The results indicate that neither the I/D ACE nor the C677T MTHFR polymorphisms are associated with risk of myocardial infarction in the Polish population.
由于其多样的生物活性,肾素-血管紧张素系统在缺血性心脏病的危险因素中占据特殊地位。ACE基因I/D多态性的发现使人们对该酶的遗传控制有了更好的理解。高同型半胱氨酸血症是缺血性心脏病的一个独立危险因素。血浆同型半胱氨酸水平升高可能归因于饮食不当(如叶酸缺乏)和/或遗传影响。亚甲基四氢叶酸还原酶(MTHFR)是同型半胱氨酸代谢中的关键酶。本研究对100例有心肌梗死病史的患者(14名女性和86名男性,平均年龄54.2±9.2岁)进行。对照组包括100例无此类病史的患者(10名女性和90名男性,平均年龄52.3±10岁)。采用聚合酶链反应(PCR)检测ACE基因的I/D多态性和MTHFR基因的C677T多态性。从外周血核细胞中分离基因组DNA,并用两对位于多态性区域两侧的引物进行PCR扩增。用限制性内切酶Hinf I鉴定MTHFR多态性的基因型。两组之间在ACE基因I/D基因型分布(研究组中31%为II型、51%为ID型、18%为DD型;对照组中30%为II型、57%为ID型、13%为DD型;表1)或MTHFR基因C677T基因型分布(研究组中46%为CC型、45%为CT型、9%为TT型;对照组中39%为CC型、50%为CT型、11%为TT型;表2)方面未发现差异。在研究组(II型=18.2±17.9;ID型=33.5±19.9;DD型=68.9±21.9)和对照组(II型=24.2±18.1;ID型=31.5±20.9;DD型=51.4±19.5;表3)中,I/D基因型对ACE活性(IU/L)有显著影响。未证实ACE或MTHFR基因型与梗死年龄或左心室质量之间存在相关性(表4,5,6)。结果表明,在波兰人群中,ACE基因的I/D多态性和MTHFR基因的C677T多态性均与心肌梗死风险无关。