LFE Research Group, Department of Health and Human Performance. Faculty of Physical Activity and Sport Science (INEF), Universidad Politécnica de Madrid, Martín Fierro, 7, 28040, Madrid, Spain.
Department of Laboratory Medicine, Translational Metabolic Laboratory (TML 830), Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.
Eur J Appl Physiol. 2022 Dec;122(12):2683-2694. doi: 10.1007/s00421-022-05048-5. Epub 2022 Sep 21.
Menstrual cycle phase affects resting hepcidin levels, but such effects on the hepcidin response to exercise are still unclear. Thus, we investigated the hepcidin response to running during three different menstrual cycle phases.
Twenty-one endurance-trained eumenorrheic women performed three identical interval running protocols during the early-follicular phase (EFP), late-follicular phase (LFP), and mid-luteal phase (MLP). The protocol consisted of 8 × 3 min bouts at 85% of the maximal aerobic speed, with 90-s recovery. Blood samples were collected pre-exercise and at 0 h, 3 h and 24 h post-exercise.
Data presented as mean ± SD. Ferritin were lower in the EFP than the LFP (34.82 ± 16.44 vs 40.90 ± 23.91 ng/ml, p = 0.003), while iron and transferrin saturation were lower during the EFP (58.04 ± 19.70 µg/dl, 14.71 ± 5.47%) compared to the LFP (88.67 ± 36.38 µg/dl, 22.22 ± 9.54%; p < 0.001) and the MLP (80.20 ± 42.05 µg/dl, 19.87 ± 10.37%; p = 0.024 and p = 0.045, respectively). Hepcidin was not affected by menstrual cycle (p = 0.052) or menstrual cycle*time interaction (p = 0.075). However, when comparing hepcidin at 3 h post-exercise, a moderate and meaningful effect size showed that hepcidin was higher in the LFP compared to the EFP (3.01 ± 4.16 vs 1.26 ± 1.25 nMol/l; d = 0.57, CI = 0.07-1.08). No effect of time on hepcidin during the EFP was found either (p = 0.426).
The decrease in iron, ferritin and TSAT levels during the EFP may mislead the determination of iron status in eumenorrheic athletes. However, although the hepcidin response to exercise appears to be reduced in the EFP, it shows no clear differences between the phases of the menstrual cycle (clinicaltrials.gov: NCT04458662).
月经周期阶段会影响静止时的血红素水平,但运动对血红素反应的影响尚不清楚。因此,我们研究了三种不同月经周期阶段进行跑步时血红素的反应。
21 名训练有素的月经正常的女性在卵泡早期(EFP)、卵泡晚期(LFP)和黄体中期(MLP)进行了三次相同的间歇跑步方案。方案包括 8 次 3 分钟的冲刺,速度为最大有氧速度的 85%,恢复 90 秒。在运动前和运动后 0 小时、3 小时和 24 小时采集血样。
数据以平均值 ± 标准差表示。卵泡早期的铁蛋白低于卵泡晚期(34.82 ± 16.44 与 40.90 ± 23.91ng/ml,p = 0.003),而铁和转铁蛋白饱和度在卵泡早期较低(58.04 ± 19.70µg/dl,14.71 ± 5.47%),低于卵泡晚期(88.67 ± 36.38µg/dl,22.22 ± 9.54%;p < 0.001)和黄体中期(80.20 ± 42.05µg/dl,19.87 ± 10.37%;p = 0.024 和 p = 0.045)。血红素不受月经周期(p = 0.052)或月经周期*时间相互作用(p = 0.075)的影响。然而,当比较运动后 3 小时的血红素时,显示出中等且有意义的效应大小,表明黄体晚期的血红素高于卵泡早期(3.01 ± 4.16 与 1.26 ± 1.25 nMol/l;d = 0.57,CI = 0.07-1.08)。在卵泡早期,运动时间对血红素也没有影响(p = 0.426)。
在卵泡早期,铁、铁蛋白和转铁蛋白饱和度水平的降低可能会导致月经正常运动员铁状态的错误判断。然而,尽管运动对血红素的反应在卵泡早期似乎减少,但在月经周期的各个阶段之间没有明显的差异(clinicaltrials.gov:NCT04458662)。