Arq Bras Cardiol. 2013 Oct;101(4):352-8. doi: 10.5935/abc.20130167. Epub 2013 Aug 14.
Previous studies have analyzed the role of the genetic polymorphism of endothelial nitric oxide synthase on heart failure prognosis. However, there are no studies relating the G894T and heart failure in Brazil.
To evaluate the association between G894T GP and the prognosis of a sample of Brazilian outpatients with heart failure.
Cohort study included 145 patients with systolic heart failure, followed for up to 40 months (mean = 22), at two university hospitals, in the State of Rio de Janeiro. We evaluated the relationship between G894T and the following outcomes: reverse remodeling, improvement in functional class (NYHA), and mortality and hospitalization rates. The diameters of the left atrium and ventricle, as well as the ejection fraction of the left ventricle, were evaluated at baseline and at 6 months to assess reverse remodeling. The improvement in functional class was evaluated after 6 months, and mortality rate and hospitalization were evaluated during follow-up. Race was self-declared. G894T polymorphism was analyzed by polymerase chain reaction and restriction fragment length polymorphism.
The genotypic frequencies were GG (40%), GT (48.3%) and TT (11.7%). The allele frequency was guanine (64.1%) and thiamine (35.8%). There were no differences between the genotype or allelic frequencies according to self-declared race, either as baseline characteristics. There was no relationship between genotype or allele frequency and the outcome measures.
No association was observed between the G894T polymorphism (Glu298Asp) and prognosis in this sample of Brazilian outpatients with systolic heart failure.
先前的研究分析了内皮型一氧化氮合酶基因多态性对心力衰竭预后的影响。然而,在巴西,尚无关于 G894T 与心力衰竭的研究。
评估 G894T GP 与巴西心力衰竭门诊患者样本预后的相关性。
本队列研究纳入了 145 例收缩性心力衰竭患者,在两所大学附属医院进行了长达 40 个月(平均 22 个月)的随访。我们评估了 G894T 与以下结局之间的关系:逆转重构、心功能分级(NYHA)改善以及死亡率和住院率。在基线和 6 个月时评估左心房和心室直径以及左心室射血分数,以评估逆转重构。在 6 个月时评估心功能分级的改善,在随访期间评估死亡率和住院率。种族为自我报告。通过聚合酶链反应和限制性片段长度多态性分析 G894T 多态性。
基因型频率为 GG(40%)、GT(48.3%)和 TT(11.7%)。等位基因频率为鸟嘌呤(64.1%)和胸腺嘧啶(35.8%)。基因型或等位基因频率与自我报告的种族之间无差异,无论是在基线特征还是在随访期间的结局测量中。基因型或等位基因频率与结局测量之间无相关性。
在该巴西收缩性心力衰竭门诊患者样本中,未观察到 G894T 多态性(Glu298Asp)与预后之间存在关联。