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Circulating cell-free DNA telomere length and bilirubin in the Vienna Active Ageing Study: exploratory analysis of a randomized controlled trial

机译:维也纳主动衰老研究中的循环无细胞DNA端粒长度和胆红素的研究:一项随机对照试验的探索性分析

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摘要

Telomere length (TL) in blood cells is widely used in human studies as a molecular marker of ageing. Circulating cell-free DNA (cfDNA) as well as unconjugated bilirubin (UCB) are dynamic blood constituents whose involvement in age-associated diseases is largely unexplored. To our knowledge, there are no published studies integrating all three parameters, especially in individuals of advanced age. Here we present a secondary analysis from the Vienna Active Aging Study (VAAS), a randomized controlled intervention trial in institutionalized elderly individuals (n = 101). Using an exploratory approach we combine three blood-based molecular markers (TL, UCB and cfDNA) with a range of primary and secondary outcomes from the intervention. We further look at the changes occurring in these parameters after 6-month resistance exercise training with or without supplementation. A correlation between UCB and TL was evident at baseline (p < 0.05), and both were associated with increased chromosomal anomalies such as nucleoplasmatic bridges and nuclear buds (p < 0.05). Of the three main markers explored in this paper, only cfDNA decreased significantly (p < 0.05) after 6-month training and dietary intervention. No clear relationship could be established between cfDNA and either UCB or TL. The trial was registered at ClinicalTrials.gov ().
机译:血细胞中的端粒长度(TL)在人类研究中被广泛用作衰老的分子标记。循环中的无细胞DNA(cfDNA)和未结合的胆红素(UCB)是动态的血液成分,其在与年龄相关疾病中的参与程度尚待探索。据我们所知,尚无已发表的研究综合了这三个参数,特别是在高龄人群中。在这里,我们提供了维也纳主动老龄化研究(VAAS)的第二项分析,这是一项针对制度化老年人的随机对照干预试验(n = 101)。使用探索性方法,我们将三种基于血液的分子标记(TL,UCB和cfDNA)与干预措施产生的一系列主要和次要结果结合在一起。我们将进一步研究在进行6个月的抵抗运动训练(有或没有补充)后,这些参数的变化。在基线时,UCB和TL之间存在明显的相关性(p <0.05),并且两者都与染色体异常的增加有关,如核质桥和核芽(p <0.05)。在本文探讨的三个主要指标中,经过6个月的训练和饮食干预后,仅cfDNA显着下降(p <0.05)。 cfDNA与UCB或TL之间无法建立明确的关系。该试验已在ClinicalTrials.gov()上注册。

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