High impact loading on the skeleton is associated with a decrease in glucose levels in young men
2012 (English)In: Clinical Endocrinology, ISSN 0300-0664, E-ISSN 1365-2265, Vol. 77, no 6, 823-827 p.Article in journal (Refereed) Published
Objective The skeleton has been suggested to be involved in energy metabolism through osteocalcin (OC), an osteoblast-specific molecule. The objective of this study was to investigate whether high impact exercise stimulating bone formation would lead to changes in glucose and lipid metabolism independent of cardiorespiratory effects, and if OC mediates this association.
Design Prospective intervention study.
Methods Fifty men aged 20-32 years were allocated to an intervention group or a control group. The intervention group completed six different types of jumps in sets of five, with the frequency of these exercises gradually increasing over 8 weeks. At baseline and after 8 weeks, glycerol concentrations were measured in fat tissue as a marker of lipolysis by using microdialysis. Blood samples were assayed for OC and markers of glucose and lipid metabolism. Physical activity was measured using an accelerometer.
Results After adjustment for confounders at baseline and changes in physical activity during the intervention period, the intervention was associated with a decrease in levels of glucose (p = 0.04), adrenalin (p = 0.03) and OC (p=0.04) after adjusting for baseline levels and changes in physical activity. No other differences between the groups were significant, although the trends of the metabolic variables favored the intervention group.
Conclusions The results of this study suggest that high impact loading on the skeleton may affect glucose metabolism independent of the level of aerobic exercise.
Place, publisher, year, edition, pages
Blackwell Publishing, 2012. Vol. 77, no 6, 823-827 p.
High impact loading, skeleton, osteocalcin, glucose
Endocrinology and Diabetes
IdentifiersURN: urn:nbn:se:umu:diva-42508DOI: 10.1111/j.1365-2265.2012.04461.xOAI: oai:DiVA.org:umu-42508DiVA: diva2:409437