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首页> 外文期刊>Scientific reports. >Circulating cell-free DNA, telomere length and bilirubin in the Vienna Active Ageing Study: exploratory analysis of a randomized, controlled trial
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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:维也纳活性老化研究中循环无细胞DNA,端粒长度和胆红素:随机,受控试验的探索性分析

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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 (NCT01775111).
机译:血细胞中的端粒长度(TL)被广泛用于人类研究中作为衰老的分子标记。循环无细胞DNA(CFDNA)以及未缀合的胆红素(UCB)是动态血液成分,其受累年龄相关疾病在很大程度上是未开发的。据我们所知,没有公布的研究整合了所有三个参数,特别是在高龄人的个人中。在这里,我们提出了维也纳活跃老化研究(VAAS)的二级分析,在制度化的老年人中,随机对照干预试验(N?=?101)。使用探索方法,我们将三种血基分子标记物(TL,UCB和CFDNA)结合在干预的一系列主要和二次结果中。我们进一步看看在6个月电阻运动训练和无补充后,在这些参数中发生的变化。在基线(p≤0.05)中,UCB和T1之间的相关性,两者都与增加的染色体异常(如核质桥和核芽)相关(P?<β05)。在本文探索的三个主要标志中,仅在6个月的培训和饮食干预后,只有CFDNA显着下降(P?<-05)。在CFDNA和UCB或TL之间无法建立明确的关系。该试验在ClinicalTrials.gov(NCT01775111)注册。

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