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dc.contributor.authorWard, Keira
dc.contributor.authorMulder, Edwin
dc.contributor.authorFrings-Meuthen, Petra
dc.contributor.authorO'Gorman, Donal J.
dc.contributor.authorCooper, Diane
dc.date.accessioned2020-10-21T13:06:11Z
dc.date.available2020-10-21T13:06:11Z
dc.date.copyright2020
dc.date.issued2020-10-19
dc.identifier.citationWard, K., Mulder, E., Frings-Meuthen, P., O'Gorman, D.J., Cooper, D. (2020). Fetuin-A as a potential biomarker of metabolic variability following 60 days of bed rest. Frontiers in Physiology. 11: 1297. doi.org/10.3389/fphys.2020.573581en_US
dc.identifier.issn1664-042X
dc.identifier.urihttp://research.thea.ie/handle/20.500.12065/3446
dc.description.abstractBackground: Fetuin-A is a hepatokine linked to the development of insulin resistance. The purpose of this study was to determine if 60 days head-down-tilt (HDT) bed rest increased circulating fetuin-A and if it was linked to whole body insulin sensitivity (IS). Additionally, we examined whether reactive jump training (RJT) could alleviate the metabolic changes associated with bed rest. Methods: 23 young men (29 ± 6 years, 181 ± 6 cm, 77 ± 7 kg) were randomized to a control (CTRL, n = 11) or RJT group (JUMP, n = 12) and exposed to 60 days of bed rest. Before and after bed rest, body composition and V.O2peak were measured and an oral glucose tolerance test was performed to estimate IS. Circulating lipids and fetuin-A were measured in fasting serum. Results: Body weight, lean mass, and V.O2peak decreased in both groups following bed rest, with greater reductions in CTRL (p < 0.05). There was a main effect of time, but not the RJT intervention, for the increase in fetuin-A, triglycerides (TG), area under the curve for glucose (AUCG) and insulin (AUCI), and the decrease in Matsuda and tissue-specific IS (p < 0.05). Fetuin-A increased in participants who became less insulin sensitive (p = 0.019). In this subgroup, liver IS and adipose IS decreased (p < 0.05), while muscle IS was unchanged. In a subgroup, where IS did not decrease, fetuin-A did not change. Liver IS increased (p = 0.012), while muscle and adipose tissue IS remained unchanged. Conclusions: In this study, we report an increase in circulating fetuin-A following 60 days of bed rest, concomitant with reduced IS, which could not be mitigated by RJT. The amount of fetuin-A released from the liver may be an important determinant of changes in whole body IS. In this regard, it may also be a useful biomarker of individual variation due to inactivity or lifestyle interventions.en_US
dc.formatPDFen_US
dc.language.isoenen_US
dc.publisherFrontiers Mediaen_US
dc.relation.ispartofFrontiers in Physiologyen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/ie/*
dc.subjectBed resten_US
dc.subjectFetuin-Aen_US
dc.subjectHepatokineen_US
dc.subjectInsulin sensitivityen_US
dc.subjectLiveren_US
dc.subjectMetabolismen_US
dc.titleFetuin-A as a potential biomarker of metabolic variability following 60 days of bed resten_US
dc.typeArticleen_US
dc.contributor.sponsorEuropean Space Agency PRODEX programme and Enterprise Ireland (C4000120081). HDT bed rest study was supported by the European Space Agency (4000113871/15/NL/PG).en_US
dc.description.peerreviewyesen_US
dc.identifier.doidoi.org/10.3389/fphys.2020.57358
dc.identifier.orcidhttps://orcid.org/0000-0001-6272-2840
dc.rights.accessOpen Accessen_US
dc.subject.departmentFaculty of Science & Health AITen_US


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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland