Reactive Oxygen Species Production and Mitochondrial Dysfunction in White Blood Cells Are Not Valid Biomarkers of Ageing in the Very Old

Laura Wiley(Newcastle University), Deepthi Ashok(Newcastle Hospitals - Campus for Ageing and Vitality), Carmen Martín-Ruiz(Newcastle Hospitals - Campus for Ageing and Vitality), Duncan Talbot(University of Bedfordshire), Joanna Collerton(Newcastle University), Andrew Kingston(Newcastle University), Karen Davies(Newcastle Hospitals - Campus for Ageing and Vitality), Patrick F. Chinnery(Newcastle University), Michael Catt(Newcastle University), Carol Jagger(Newcastle University), Thomas B. L. Kirkwood(Newcastle Hospitals - Campus for Ageing and Vitality), Thomas von Zglinicki(Newcastle Hospitals - Campus for Ageing and Vitality)
PLoS ONE
March 10, 2014
Cited by 14Open Access
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Abstract

Reliable and valid biomarkers of ageing (BoA) are needed to understand mechanisms, test interventions and predict the timing of adverse health events associated with ageing. Since increased reactive oxygen species (ROS) production and mitochondrial dysfunction are consequences of cellular senescence and may contribute causally to the ageing of organisms, we focused on these parameters as candidate BoA. Superoxide levels, mitochondrial mass and mitochondrial membrane potential in human peripheral blood mononuclear cells (PBMCs) and subpopulations (lymphocytes and monocytes) were measured in participants from the Newcastle 85+ study, a population-based study of the very old (aged 85 years and older). The intra- and inter-assay precision expressed as coefficient of variation (CV) for all parameters was acceptable (3% to 12% and 5 to 22% respectively). All parameters were stable in the short-term (1 week interval) in a sample of control individuals in the PBMCs and lymphocyte subpopulation, however they were unstable in the monocyte subpopulation; this rendered monocytes unreliable for further analysis. There was a significant association between superoxide levels and mitochondrial mass (positive in lymphocytes, p = 0.01) and between superoxide levels and mitochondrial membrane potential (negative in PBMCs, p = 0.01; positive in lymphocytes, p = 0.05). There were also significant associations between superoxide levels and mitochondrial parameters with other markers of oxidative stress-induced cellular senescence (p≤0.04), however some were in the opposite direction to expected. No associations were found between the measured parameters and age-related outcomes, including cognitive impairment, disability, co-morbidity and survival - questioning the validity of these parameters as candidate BoA in the very old.


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