Universidad Francisco de Vitoria, Faculty of Health Sciences, Research Unit, Pozuelo de Alarcón, Madrid, Spain; SPORTNOMICS S.L., Madrid, Spain.
J Trace Elem Med Biol. 2024 Jul;84:127470. doi: 10.1016/j.jtemb.2024.127470. Epub 2024 May 11.
Nutritional strategies with iron supplementation have been shown to be effective in preventing the decline of blood biochemical parameters and sports performance. The aim of the study was to describe biochemical iron metabolism parameters in association with iron supplementation and HFE and AMPD1 polymorphisms in a Union Cycliste Internationale (UCI) World Tour cycling team to evaluate performance during a whole season METHODS: Twenty-eight professional men cyclists took part in this longitudinal observational pilot study. AMPD1 c.34 C>T (rs17602729) and HFE c.187 C>G (rs1799945) polymorphisms were genotyped using Single Nucleotide Primer Extension (SNPE). All the professional cyclists took oral iron supplementation throughout the season. Four complete blood analyses were carried out corresponding to UCI controls in January (1st), April (2nd), June (3rd) and October (4th). Data on participation in three-week Grand Tours, kms of competition and wins were analyzed.
In performance, especially in wins, there was a significant effect in HFE on biochemical hemoglobin (F = 4.255; p = 0.021) and biochemical hematocrit (F = 5.335; p = 0.009) and a hematocrit biochemical × genotype interaction (F = 3.418; p = 0.041), with higher values in professional cyclist with GC genotype. In AMPD1 there were significant effects in the biochemical iron x genotype interaction in three-week Grand Tours (F = 3.874; p = 0.029) and wins (F = 3.930; p = 0.028) CONCLUSIONS: Blood biochemical iron metabolism parameters could be related to performance in the season due to increasing hemoglobin and hematocrit concentration under iron supplementation, associated with winning in the professional cyclists with GC genotype of the HFE polymorphism.
补充铁的营养策略已被证明能有效防止血液生化参数和运动表现下降。本研究的目的是描述 UCI 世界巡回赛自行车队中与铁补充和 HFE 和 AMPD1 多态性相关的生化铁代谢参数,以评估整个赛季的表现。
28 名职业男子自行车运动员参加了这项纵向观察性试点研究。使用单核苷酸引物延伸(SNPE)对 AMPD1 c.34 C>T(rs17602729)和 HFE c.187 C>G(rs1799945)多态性进行基因分型。所有职业自行车运动员在整个赛季都服用口服铁补充剂。共进行了 4 次全血分析,分别对应于 1 月(1 月)、4 月(2 月)、6 月(3 月)和 10 月(4 月)的 UCI 控制。分析了参加三周大环赛、比赛公里数和获胜次数的数据。
在表现方面,尤其是在获胜方面,HFE 对生化血红蛋白(F = 4.255;p = 0.021)和生化血细胞比容(F = 5.335;p = 0.009)有显著影响,并且生化血细胞比容×基因型相互作用(F = 3.418;p = 0.041),GC 基因型的职业自行车运动员有更高的值。在 AMPD1 中,生化铁×基因型相互作用在三周大环赛(F = 3.874;p = 0.029)和获胜(F = 3.930;p = 0.028)中均有显著影响。
由于铁补充增加了血红蛋白和血细胞比容浓度,血液生化铁代谢参数可能与赛季表现有关,与 HFE 多态性 GC 基因型的职业自行车运动员的获胜有关。