Soylu Ozer, Yildirim Aydin, Coker Ajda, Tezel Tuna, List Edward O, Arman Ahmet
The Department of Cardiology, Dr. Siyami Ersek Hospital, Istanbul, Turkey.
Eur Cytokine Netw. 2008 Mar;19(1):42-8. doi: 10.1684/ecn.2008.0119. Epub 2008 Feb 26.
acute coronary syndrome (ACS) is defined as an inflammatory disease associated with development of atherosclerosis and instability. IL-1 is a candidate inflammatory cytokine that is thought to trigger ACS. The purpose of this study was to determine the relationship between IL-1 gene family polymorphisms (IL-1RN, IL-1B in positions -511 and +3953) and ACS in the Turkish population.
a total of 381 people participated in the study, with 117 control subjects and 264 ACS patients. Of the 264 ACS patients, 112 were diagnosed with stable angina pectoris (SAP) and 152 were diagnosed with unstable angina pectoris (USAP). The polymerase chain reaction (PCR) was used to determine the genotype of IL-1RN. The genotypes of IL-1B (-511 and +3953) were determined by PCR, followed by restriction enzyme digestion of the PCR products.
there were no significant differences in both IL-1RN, IL-1B (-511 and +3953) genotype distributions and IL-1RN allele frequencies between ACS patients and the control subjects. In addition, no association was observed in the allele frequency of IL-1B (-511 and +3953) between ACS patients and controls (p = 0.113 and p = 0.859, respectively), or between SAP patients and controls (p = 0.575 and p = 0.359, respectively). However, IL-1B allele 1 (C) (-511) polymorphism in USAP patients was found to be significantly different from that of control subjects (p = 0.041, OR: 2.01; 95% CI: 1.985-3.933). A significant difference was also observed between USAP and SAP patients for IL-1B (+3953) allele 1 (C) polymorphism; (p = 0.043, OR: 1.522; 95% CI: 1.012-2.88).
these results show that IL-1RN gene polymorphism has no association with ACS. However, the allele 1 (C) of IL-1B (-511) may be a risk factor for susceptibility to USAP in the Turkish population.
急性冠状动脉综合征(ACS)被定义为一种与动脉粥样硬化发展和不稳定性相关的炎症性疾病。白细胞介素-1(IL-1)是一种被认为可引发ACS的炎性细胞因子。本研究的目的是确定土耳其人群中IL-1基因家族多态性(IL-1RN、-511和+3953位点的IL-1B)与ACS之间的关系。
共有381人参与本研究,其中117名对照受试者和264例ACS患者。在264例ACS患者中,112例被诊断为稳定型心绞痛(SAP),152例被诊断为不稳定型心绞痛(USAP)。采用聚合酶链反应(PCR)确定IL-1RN的基因型。通过PCR确定IL-1B(-511和+3953)的基因型,随后对PCR产物进行限制性内切酶消化。
ACS患者与对照受试者之间在IL-1RN、IL-1B(-511和+3953)基因型分布以及IL-1RN等位基因频率方面均无显著差异。此外,在ACS患者与对照之间(分别为p = 0.113和p = 0.859),或在SAP患者与对照之间(分别为p = 0.575和p = 0.359),均未观察到IL-1B(-511和+3953)等位基因频率存在关联。然而,发现USAP患者中IL-1B等位基因1(C)(-511)多态性与对照受试者存在显著差异(p = 0.041,OR:2.01;95% CI:1.985 - 3.933)。在USAP与SAP患者之间,对于IL-1B(+3953)等位基因1(C)多态性也观察到显著差异;(p = 0.043,OR:1.522;95% CI:1.012 - 2.88)。
这些结果表明IL-1RN基因多态性与ACS无关。然而,IL-1B(-511)的等位基因1(C)可能是土耳其人群中USAP易感性的一个危险因素。