Mendonça Maria Isabel, Dos Reis R Palma, Freitas A Isabel, Sousa Ana Célia, Pereira Andreia, Faria Paula, Gomes Susana, Silva Bruno, Santos Nuno, Serrao Marco, Ornelas Ilídio, Freitas Sónia, Freitas C, Araújo José Jorge, Brehm António, Cardoso A Almada
Unidade de Investigção, Hospital Central do Funchal, Funchal, Portugal.
Rev Port Cardiol. 2009 Apr;28(4):397-415.
Various studies have compared coronary artery disease (CAD) patients with controls in order to determine which polymorphisms are associated with a higher risk of disease. The results have often been contradictory. Moreover, these studies evaluated polymorphisms in isolation and not in association, which is the way they occur in nature.
Our purpose was to evaluate the risk of CAD in patients with associated polymorphisms in the same gene or in differen genes.
We evaluated the risk associated with ACE DD, ACE 8 CC, ACT 174MM, AGT 235TT, MTHFR 677TT, MTHFR 1298AA, PON1 192RR and PON1 55MM in 298 CAD patients and 298 healthy individuals. We then evaluated the risk of associated polymorphisms in the same gene (ACE DD + ACE 8GG; AGT 174MM + AGT 235TT; MTHFR 677TT + MTHFR 1298AA). Finally, for the isolated polymorphisms which were significant, we evaluated the risk of polymorphism associations at different functional levels (ACE + AGT; ACE + MTHFR; ACE + PON1). Multiple logistic regression was used to identify independent risk factors for CAD.
Isolated polymorphisms including ACE DD(p < 0.0001), ACE 8 gg (p=0.023), and MTHFR 1298AA (p = 0.049) presented with a significantly higher frequency in the CAD group. An association of polymorphisms in the same gene did not have an additive or synergistic effect, nor did it increase the risk of CAD. Polymorphic associations in different genes increased the risk of CAD, compared with the isolated polymorphisms. The association of ACE DD or ACE 8 GG with PON1 192RR increased the risk of CA fourfold (1.8 to 4.2). After logistic regression analysis, current smoking, family history, fibrinogen, diabetes, and the ACE DD or ACE 8 GG + MTHFR 1298AA and ACE DD or ACE 8 GG + PON1 192RR associations remained in the, model and proved to be independent predictors of CAD.
The association of polymorphisms in the same gene did not increase the risk of the isolated polymorphism. The association of polymorphisms in genes belonging to different enzyme systems was always linked to increased risk compared to the isolated polymorphisms. This study may contribute to a better understanding of overall genetic risk for CAD rather than that associated with each polymorphism in isolation.
多项研究对冠心病(CAD)患者与对照组进行了比较,以确定哪些基因多态性与更高的疾病风险相关。结果往往相互矛盾。此外,这些研究单独评估基因多态性,而非评估其关联性,然而在自然状态下它们是以关联形式出现的。
我们的目的是评估同一基因或不同基因中存在相关基因多态性的患者患CAD的风险。
我们评估了298例CAD患者和298例健康个体中与ACE DD、ACE 8 CC、ACT 174MM、AGT 235TT、MTHFR 677TT、MTHFR 1298AA、PON1 192RR和PON1 55MM相关的风险。然后我们评估了同一基因中相关基因多态性的风险(ACE DD + ACE 8GG;AGT 174MM + AGT 235TT;MTHFR 677TT + MTHFR 1298AA)。最后,对于具有显著性的单独基因多态性,我们评估了不同功能水平上基因多态性关联的风险(ACE + AGT;ACE + MTHFR;ACE + PON1)。采用多元逻辑回归来确定CAD的独立危险因素。
包括ACE DD(p < 0.0001)、ACE 8 gg(p = 0.023)和MTHFR 1298AA(p = 0.049)在内的单独基因多态性在CAD组中的出现频率显著更高。同一基因中基因多态性的关联没有相加或协同效应,也没有增加CAD风险。与单独的基因多态性相比,不同基因中的多态性关联增加了CAD风险。ACE DD或ACE 8 GG与PON1 192RR的关联使CAD风险增加了四倍(1.8至4.2)。经过逻辑回归分析,当前吸烟、家族史、纤维蛋白原、糖尿病以及ACE DD或ACE 8 GG + MTHFR 1298AA和ACE DD或ACE 8 GG + PON1 192RR关联仍保留在模型中,并被证明是CAD的独立预测因素。
同一基因中基因多态性的关联并未增加单独基因多态性的风险。与单独的基因多态性相比,属于不同酶系统的基因中基因多态性的关联总是与风险增加相关。本研究可能有助于更好地理解CAD的总体遗传风险,而非单独与每个基因多态性相关的风险。