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TLR2 and age-related diseases: potential effects of Arg753Gln and Arg677Trp polymorphisms in acute myocardial infarction.

机译:TLR2和年龄相关疾病:Arg753Gln和Arg677Trp多态性在急性心肌梗死中的潜在作用。

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摘要

Inflammation is a key component of immune system. It is involved in both defense and pathophysiological events maintaining the dynamic homeostasis of host organism. Its function is controlled by innate immunity genes. Both their polymorphisms and environmental conditions give rise to different phenotypes in human population. Proinflammatory genotype may be beneficial in early life but not in old people. With advancing age, indeed, it increases the vulnerability and the intensity to inflammatory reactions responsible for the chronic inflammatory diseases, such as atherosclerosis and myocardial infarction (MI). Several studies have looked for detecting a genetic risk profile that might allow a pharmacogenomic approach to prevent and treat age-related diseases such as MI. We have evaluated the possible association between two polymorphisms of TLR2 gene-Arg677Trp and Arg753Gln-and MI. However, we found no association between TLR2 polymorphisms and MI.
机译:炎症是免疫系统的关键组成部分。它参与防御和病理生理事件,维持宿主生物体的动态稳态。它的功能由先天免疫基因控制。它们的多态性和环境条件都导致了人类的不同表型。促炎基因型可能对早期生命有益,但对老年人却无济于事。实际上,随着年龄的增长,它增加了引起慢性炎性疾病(如动脉粥样硬化和心肌梗塞(MI))的炎性反应的脆弱性和强度。数项研究寻求寻找可用于预防和治疗与年龄相关的疾病(例如MI)的药物基因组学方法的遗传风险概况。我们已经评估了TLR2基因Arg677Trp和Arg753Gln-和MI的两个多态性之间的可能联系。但是,我们发现TLR2多态性与MI之间没有关联。

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