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The molecular biomarkers of vascular aging and atherosclerosis: telomere length and mitochondrial DNA4977 common deletion

机译:血管老化和动脉粥样硬化的分子生物标志物:端粒长度和线粒体DNA4977常见缺失

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摘要

Age is the dominant risk factor for the most prevalent atherosclerotic vascular diseases, including coronary artery disease, myocardial infarction, cerebrovascular disease and stroke. In human, telomere erosion and mitochondrial DNA (mtDNA) damage play a central role in the mechanisms leading to cellular aging decline. This review summarizes the most relevant findings on the role of telomere shortening and the common mtDNA~4977 deletion in the progression and evolution of atherosclerosis by combining insight from experimental models and human clinical studies. The current evidence shows a link between telomere erosion and compromised mitochondrial function and provides a new perspective regarding their potential role as clinical biomarkers and therapeutic targets.
机译:年龄是最普遍普遍的动脉粥样硬化血管疾病的主要风险因素,包括冠状动脉疾病,心肌梗塞,脑血管疾病和中风。 在人体,端粒侵蚀和线粒体DNA(MTDNA)损伤在导致细胞老化衰老的机制中起着核心作用。 本综述总结了通过实验模型和人类临床研究的洞察力结合洞察力缺失和演化中的端粒缩短和常见MTDNA〜4977缺失的最相关结果。 目前的证据表明了端粒侵蚀和受损的线粒体功能之间的联系,并提供了与临床生物标志物和治疗靶标的潜在作用的新视角。

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