| Literature DB >> 27986629 |
Fabiola Olivieri1, Miriam Capri2, Massimiliano Bonafè3, Cristina Morsiani4, Hwa Jin Jung5, Liana Spazzafumo6, Jose Viña7, Yousin Suh5.
Abstract
Human aging is a lifelong process characterized by a continuous trade-off between pro-and anti-inflammatory responses, where the best-adapted and/or remodeled genetic/epigenetic profile may develop a longevity phenotype. Centenarians and their offspring represent such a phenotype and their comparison to patients with age-related diseases (ARDs) is expected to maximize the chance to unravel the genetic makeup that better associates with healthy aging trajectories. Seemingly, such comparison is expected to allow the discovery of new biomarkers of longevity together with risk factor for the most common ARDs. MicroRNAs (miRNAs) and their shuttles (extracellular vesicles in particular) are currently conceived as those endowed with the strongest ability to provide information about the trajectories of healthy and unhealthy aging. We review the available data on miRNAs in aging and underpin the evidence suggesting that circulating miRNAs (and cognate shuttles), especially those involved in the regulation of inflammation (inflamma-miRs) may constitute biomarkers capable of reliably depicting healthy and unhealthy aging trajectories.Entities:
Keywords: Aging trajectories; Centenarians; Circulating microRNAs; Offspring of centenarians; miR-21-5p
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Year: 2016 PMID: 27986629 PMCID: PMC5481482 DOI: 10.1016/j.mad.2016.12.004
Source DB: PubMed Journal: Mech Ageing Dev ISSN: 0047-6374 Impact factor: 5.432