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      Aging is associated with quantitative and qualitative changes in circulating cell-free DNA: the Vitality 90+ study.

      Mechanisms of Ageing and Development
      Adult, Aged, Aged, 80 and over, Aging, blood, genetics, Base Sequence, DNA, chemistry, DNA Fragmentation, DNA Primers, Female, Humans, Molecular Weight, Oligonucleotide Array Sequence Analysis, Polymerase Chain Reaction, Young Adult, beta-Globins

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          Abstract

          As a marker of cellular death, cell-free DNA (cf-DNA) has a utility in diagnosis and prognosis of various disorders. Since aging accompanies increased cellular senescence and death, we aimed to characterize potential age-related alterations in cf-DNA. The study population consisted of 12 nonagenarian women (participants in the Vitality 90+ Study) and 11 healthy control women (aged 22-37 years). Some of the nonagenarians (n=8) were also recruited for follow-up after one year. cf-DNA was extracted using two different methods. Total cf-DNA was quantified directly in plasma and the amplifiable cf-DNA was assessed using quantitative PCR. Quality of cf-DNA was analysed with a DNA Chip assay. For all the quantification methods, the concentration of cf-DNA was significantly higher (p<0.05) in nonagenarians as compared to controls. The quality of the cf-DNA also displayed a marked difference between nonagenarians and controls; a fragmented pattern or appearance of low molecular weight cf-DNA was observed in the majority of the nonagenarians, whereas in controls, cf-DNA was intact and had a quasi-genomic, high molecular weight appearance. In nonagenarians, the quality of cf-DNA appeared similar in the original and follow-up samples. We propose that some, as yet uncharacterized, aspects of aging are reflected in the appearance of cf-DNA. Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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