月经周期和口服避孕药阶段对间歇性跑步时骨(再)塑形标志物的影响

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-27 DOI:10.1007/s00223-024-01259-4
Isabel Guisado-Cuadrado, Nuria Romero-Parra, Kirsty J. Elliott-Sale, Craig Sale, Ángel E. Díaz, Ana B. Peinado
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引用次数: 0

摘要

为了探索性激素波动如何影响骨代谢,本研究旨在检测跑步时月经周期和口服避孕药(OC)周期中 P1NP 和 β-CTX-1 的浓度。研究分析了 8 名处于卵泡早期、卵泡晚期和黄体中期的无月经女性在运动前后的 17β-雌二醇、孕酮、P1NP 和 β-CTX-1,并对 8 名处于停药期和服药活跃期的 OC 使用者进行了评估。跑步方案包括以最大有氧速度的 85% 进行 8 × 3 分钟的跑步机跑步。17β-雌二醇浓度(pg-ml-1)在卵泡早期(47.22 ± 39.75)低于卵泡晚期(304.95 ± 235.85;p = 0.001)和黄体中期(165.56 ± 80.6;p = 0.003),在停药期(46.51 ± 44.09)高于积极服药期(10.88 ± 11.24;p = 0.001)。黄体中期(13.214 ± 4.926)的孕酮(纳克-毫升-1)高于卵泡早期(0.521 ± 0.365; p <0.001)和卵泡晚期(1.677 ± 2.586; p <0.001)。与卵泡早期(60.96 ± 16.64;p = 0.006;)和黄体中期(59.122 ± 11.77;p = 0.002)相比,卵泡晚期(69.97 ± 17.84)和黄体中期(59.122 ± 11.77;p = 0.002)雌性雌激素的 P1NP 浓度(纳克-毫升-1)更高。β-CTX-1浓度(纳克-毫升-1)在黄体中期(0.376 ± 0.098)低于卵泡晚期(0.496 ± 0.166; p = 0.001)和卵泡早期(0.452 ± 0.148; p = 0.039)。与服药活跃期(45.45 ± 6;p = 0.001)相比,OC 使用者在停药期(61.75 ± 8.32)的运动后 P1NP 浓度更高。比较激素谱,运动后 P1NP 浓度在卵泡早期(66.91 ± 16.26;p <;0.001)、卵泡晚期(80.66 ± 16.35;p <;0.001)和黄体中期(64.57 ± 9.68;p = 0.002)高于服药活跃期。这些发现强调了研究具有不同卵巢激素特征的运动女性的重要性,因为性激素浓度的变化会影响骨代谢对跑步的反应,结果显示,与OC周期的服药活跃期相比,运动后P1NP浓度在所有月经周期阶段都较高。
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Influence of Menstrual Cycle and Oral Contraceptive Phases on Bone (re)modelling Markers in Response to Interval Running

To explore how sex hormone fluctuations may affect bone metabolism, this study aimed to examine P1NP and β-CTX-1 concentrations across the menstrual and oral contraceptive (OC) cycle phases in response to running. 17β-oestradiol, progesterone, P1NP and β-CTX-1 were analysed pre- and post-exercise in eight eumenorrheic females in the early-follicular, late-follicular, and mid-luteal phases, while 8 OC users were evaluated during the withdrawal and active pill-taking phases. The running protocol consisted of 8 × 3min treadmill runs at 85% of maximal aerobic speed. 17β-oestradiol concentrations (pg·ml−1) were lower in early-follicular (47.22 ± 39.75) compared to late-follicular (304.95 ± 235.85;p = < 0.001) and mid-luteal phase (165.56 ± 80.6;p = 0.003) and higher in withdrawal (46.51 ± 44.09) compared to active pill-taking phase (10.88 ± 11.24;p < 0.001). Progesterone (ng·ml−1) was higher in mid-luteal (13.214 ± 4.926) compared to early-follicular (0.521 ± 0.365; p < 0.001) and late-follicular phase (1.677 ± 2.586;p < 0.001). In eumenorrheic females, P1NP concentrations (ng·ml−1) were higher in late-follicular (69.97 ± 17.84) compared to early-follicular (60.96 ± 16.64;p = 0.006;) and mid-luteal phase (59.122 ± 11.77;p = 0.002). β-CTX-1 concentrations (ng·ml−1) were lower in mid-luteal (0.376 ± 0.098) compared to late-follicular (0.496 ± 0.166; p = 0.001) and early-follicular phase (0.452 ± 0.148; p = 0.039). OC users showed higher post-exercise P1NP concentrations in withdrawal phase (61.75 ± 8.32) compared to post-exercise in active pill-taking phase (45.45 ± 6;p < 0.001). Comparing hormonal profiles, post-exercise P1NP concentrations were higher in early-follicular (66.91 ± 16.26;p < 0.001), late-follicular (80.66 ± 16.35;p < 0.001) and mid-luteal phases (64.57 ± 9.68;p = 0.002) to active pill-taking phase. These findings underscore the importance of studying exercising females with different ovarian hormone profiles, as changes in sex hormone concentrations affect bone metabolism in response to running, showing a higher post-exercise P1NP concentrations in all menstrual cycle phases compared with active pill-taking phase of the OC cycle.

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