Institute of Pathological Physiology, Masaryk University, Brno, Czech Republic.
Physiol Res. 2011;60(1):55-64. doi: 10.33549/physiolres.931976. Epub 2010 Oct 15.
Numerous association studies have been involved in studying the angiotensinogen (AGT) variants, AGT plasma levels and relations to cardiovascular diseases, such as hypertension, myocardial infarction, coronary heart disease. To investigate a role of AGT G(-6)A and M235T genetic variants for chronic heart failure (CHF) and advanced atherosclerosis (AA), a total of 240 patients with CHF and 200 patients with AA of the Czech origin were evaluated for the study. The study shows the role of polymorphism AGT G(-6)A in genetic background among advanced atherosclerosis patients and chronic heart failure patients (Pg=0.001). This difference was also observed in comparison of AA patients with subgroup of CHF with dilated cardiomyopathy (Pg=0.02; Pa=0.009), and ischemic heart disease (Pg=0.007). The greatest difference between triple-vessel disease and chronic heart failure groups was observed in frequency of GT haplotype (P<0.001) and GGMT associated genotype (P<0.001). Retrospectively, we found the same trend when the subgroups of CHF were compared to AA group (AA vs. IHD with CHF P<0.001; AA vs. DCM P<0.001). These results suggest AGT genetic variants as a risk factor for chronic heart failure compared to advanced atherosclerosis disease without heart failure, with a strong difference between IHD patients and chronic heart failure patients with ischemic heart disease, especially in haplotypes and associated genotypes.
已有大量的关联研究涉及血管紧张素原(AGT)变体、AGT 血浆水平与心血管疾病(如高血压、心肌梗死、冠心病)的关系。为了研究 AGT G(-6)A 和 M235T 遗传变异在慢性心力衰竭(CHF)和进展性动脉粥样硬化(AA)中的作用,对 240 例捷克裔 CHF 患者和 200 例 AA 患者进行了研究。研究表明,AGT G(-6)A 多态性在进展性动脉粥样硬化患者和慢性心力衰竭患者的遗传背景中起作用(Pg=0.001)。在比较伴有扩张型心肌病(Pg=0.02;Pa=0.009)和缺血性心脏病(Pg=0.007)的 CHF 亚组患者时,也观察到了这种差异。在三支病变组和 CHF 组之间,GT 单倍型(P<0.001)和 GGMT 相关基因型(P<0.001)的频率差异最大。回顾性分析发现,CHF 亚组与 AA 组比较时也存在相同的趋势(AA 与缺血性心脏病合并 CHF 比较 P<0.001;AA 与扩张型心肌病比较 P<0.001)。这些结果表明,与无心力衰竭的进展性动脉粥样硬化疾病相比,AGT 遗传变异是慢性心力衰竭的一个危险因素,在缺血性心脏病患者和伴有缺血性心脏病的慢性心力衰竭患者之间,尤其是在单倍型和相关基因型方面,差异很大。