Urban Alehagen, Jan Alexander, Jan O Aaseth, Anders Larsson, Erland Svensson, Trine B Opstad
Journal: Cells 2023;12(13):1773
PMID: 37443807
Ageing is associated with multiple pathological processes including inflammation and oxidative stress which increases the risk of developing serious health issues such as cardiovascular diseases (CVD). There are many biomarkers associated with CVD and the ageing process. This sub-analysis of a previous prospective double-blind placebo-controlled randomised clinical trial investigated five of the biomarkers that are associated with CVD and the ageing process, including the intercellular adhesion molecule (ICAM-1), adiponectin, leptin, stem cell factor (SCF) and osteoprotegerin (OPG). This study also looked at the effects of selenium and Coenzyme Q10 supplementation over four years on ageing and markers of inflammation, endothelial dysfunction and fibrosis in elderly people. The levels of selenium were not adequate in participants before the intervention. The elderly participants received 200 mg/day of coenzyme Q10 capsules and 200 µg/day of organic selenium yeast tablets or placebo over 48 months. The results of this study showed that ICAM-1 and adiponectin were significantly related to age and all the biomarkers of ageing except leptin were associated with ageing. The supplementation with selenium and Coenzyme Q10 led to an anti-ageing effect. Healthcare professionals can use the results of this study to understand the beneficial effects of selenium and Coenzyme Q10 supplementation in elderly people with low selenium levels. Further robust studies are required to confirm the generalisability of the intervention.
Ageing is associated with cardiovascular disease (CVD). As no single biomarker reflects the full ageing process, we aimed to investigate five CVD- and age-related markers and the effects of selenium and coenzyme Q10 intervention to elucidate the mechanisms that may influence the course of ageing. This is a sub-study of a previous prospective double-blind placebo-controlled randomized clinical trial that included 441 subjects low in selenium (mean age 77, 49% women). The active treatment group (n = 220) received 200 µg/day of selenium and 200 mg/day of coenzyme Q10, combined. Blood samples were collected at inclusion and after 48 months for measurements of the intercellular adhesion molecule (ICAM-1), adiponectin, leptin, stem cell factor (SCF) and osteoprotegerin (OPG), using ELISAs. Repeated measures of variance and ANCOVA evaluations were used to compare the two groups. In order to better understand and reduce the complexity of the relationship between the biomarkers and age, factor analyses and structural equation modelling (SEM) were performed, and a structural model is presented. Correlation analyses of biomarker values at inclusion in relation to age, and relevant markers related to inflammation, endothelial dysfunction and fibrosis, demonstrated the biomarkers' association with these pathological processes; however, only ICAM1 and adiponectin were directly correlated with age. SEM analyses showed, however, that the biomarkers ICAM-1, adiponectin, SCF and OPG, but not leptin, all had significant associations with age and formed two independent structural factors, both significantly related to age. While no difference was observed at inclusion, the biomarkers were differently changed in the active treatment and placebo groups (decreasing and increasing levels, respectively) at 48 months ( ≤ 0.02 in all, adjusted), and in the SEM model, they showed an anti-ageing impact. Supplementation with selenium/Q10 influenced the analysed biomarkers in ways indicating an anti-ageing effect, and by applying SEM methodology, the interrelationships between two independent structural factors and age were validated.
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