Reduction of Skeletal Muscle Power in Adolescent Males Carrying H63D Mutation in the HFE Gene.
Marcin LuszczykBarbara Kaczorowska-HacEwa MiloszElzbieta Adamkiewicz-DrozynskaEwa ZiemannRadoslaw LaskowskiDamian Jozef FlisMagdalena Rokicka-HebelJędrzej AntosiewiczPublished in: BioMed research international (2017)
Iron overload resulting from the mutation of genes involved in iron metabolism or excess dietary intake has been reported to negatively influence human physical performance. The aim of this study was to test the hypothesis that adolescents bearing a hemochromatosis gene (HFE) mutation in contrast to adults with the same mutation will not experience iron accumulation and their aerobic capacity will be similar to that of age-matched controls. Thirteen boys participated in the study. Seven of them are carriers of H63D mutation in the HFE gene and six were wild type. Fitness levels were assessed using the cardiopulmonary exercise test. In addition, iron status and inflammatory markers were determined. We observed that cardiovascular fitness was significantly lower in the group bearing the HFE mutation compared to the control group. Moreover, the HFE mutation group achieved lower maximal power output compared to the control group. There were no differences in blood ferritin concentrations between the two groups which indicates similar amounts of stored iron. Obtained data do not confirm our hypothesis. On the contrary, it was demonstrated that HFE mutation is associated with a lower level of aerobic capacity, even in the absence of iron accumulation.
Keyphrases
- physical activity
- skeletal muscle
- iron deficiency
- young adults
- endothelial cells
- genome wide
- magnetic resonance
- body composition
- insulin resistance
- magnetic resonance imaging
- blood pressure
- dna methylation
- wild type
- computed tomography
- gene expression
- electronic health record
- big data
- genome wide identification
- room temperature
- genome wide analysis