Osmak G J, Sidko A R, Kiselev I S, Favorova O O
National Medical Research Center for Cardiology, Moscow, 121552 Russia.
Pirogov Russian National Research Medical University, Moscow, 117997 Russia.
Mol Biol (Mosk). 2020 Jul-Aug;54(4):699-704. doi: 10.31857/S0026898420040138.
Myocardial infarction (MI), one of the most common manifestations of cardiovascular system aging, is often fatal. The vast majority of studies on genetic susceptibility to age-dependent diseases are carried out using the case-control study design. However, its use involves a number of difficulties, most of which arise when establishing the control group of relatively healthy individuals. In this work, survival functions were analyzed for carriers of alternative polymorphic variants of 18 genes that had been tested for association with MI using the case-control approach in our previous study, and the magnitude of the shift in the age of the disease onset depending on individual variations of the genome was estimated. The following risk variants were associated with the age of MI: rs2430561A of IFNG (HR = 1.3, P = 0.043), rs17998895 of PAI-1 (HR = 1.3, P = 0.039), rs1800896GG of IL10 (HR = 1.5, P = 0.0048), rs1800471C of TGFB1 (HR = 1.5, P = 0.043), and rs11614913*TT of MIR196A2 (HR = 1.5, P = 0.035). In carriers of these variants, the disease developed 3-6 years earlier than in carriers of alternative variants. The results of this study were compared with data on the associations with MI previously obtained on the same sample using the case-control approach. It turned out that the estimates based on the two methods mostly disagreed. However, the age-dependent approach relies on fewer assumptions that can be additionally verified. In our opinion, it makes this approach more promising than the case-control design.
心肌梗死(MI)是心血管系统衰老最常见的表现之一,往往是致命的。绝大多数关于年龄依赖性疾病遗传易感性的研究都是采用病例对照研究设计进行的。然而,这种方法存在一些困难,其中大部分困难出现在建立相对健康个体的对照组时。在这项研究中,分析了18个基因的替代多态性变体携带者的生存函数,这些基因在我们之前的研究中已通过病例对照方法检测了与MI的关联性,并估计了疾病发病年龄根据基因组个体差异的变化幅度。以下风险变体与MI的发病年龄相关:IFNG的rs2430561A(风险比=1.3,P=0.043)、PAI-1的rs17998895(风险比=1.3,P=0.039)、IL10的rs1800896GG(风险比=1.5,P=0.0048)、TGFB1的rs1800471C(风险比=1.5,P=0.043)以及MIR196A2的rs11614913*TT(风险比=1.5,P=0.035)。在这些变体的携带者中,疾病的发生比替代变体的携带者早3至6年。本研究的结果与之前使用病例对照方法在同一样本上获得的与MI关联的数据进行了比较。结果发现,基于这两种方法的估计大多不一致。然而,年龄依赖性方法所依赖的假设较少,这些假设可以进一步验证。我们认为,这使得这种方法比病例对照设计更有前景。