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Relationships between maximal oxygen uptake and endothelial function in healthy male adults: a preliminary study

Aerobic capacity, as indicated by maximal oxygen uptake ( V O 2 max) has an important role in contrasting the traditional cardiovascular risk factors and preventing cardiovascular morbidity and mortality. It is known that endothelial function, measured as flow-mediated dilation (FMD) of the brachial...

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Published in:Acta diabetologica 2013-04, Vol.50 (2), p.135-141
Main Authors: Buscemi, Silvio, Canino, Baldassare, Batsis, John A., Buscemi, Chiara, Calandrino, Vincenzo, Mattina, Alessandro, Arnone, Mariangela, Caimi, Gregorio, Cerasola, Giovanni, Verga, Salvatore
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Language:English
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Summary:Aerobic capacity, as indicated by maximal oxygen uptake ( V O 2 max) has an important role in contrasting the traditional cardiovascular risk factors and preventing cardiovascular morbidity and mortality. It is known that endothelial function, measured as flow-mediated dilation (FMD) of the brachial artery, is strictly linked to atherogenesis and cardiovascular risk. However, the relationship between V O 2 max and FMD has not been fully investigated especially in healthy non-obese subjects. This preliminary study cross-sectionally investigated the relationship between V O 2 max and FMD in 22 non-obese, healthy sedentary male subjects. Dividing the cohort in two subgroups of 11 subjects each according to the median value of V O 2 max, the FMD was significantly lower in the subgroup with lower V O 2 max (mean ± sem: 7.1 ± 0.7 vs. 9.5 ± 0.8 %; P  = 0.035). Absolute V O 2 max (mL min −1 ) was significantly and independently correlated with body fat mass ( r  = −0.50; P  = 0.018) and with FMD ( r  = 0.44; P  = 0.039). This preliminary study suggests that maximal oxygen uptake is independently correlated with endothelial function in healthy non-obese adults. These results are also in agreement with the possibility that improving maximal oxygen uptake may have a favorable effect on endothelial function and vice versa.
ISSN:0940-5429
1432-5233
DOI:10.1007/s00592-010-0229-x