Abstract

Background: The increase in exercise levels in the last few years among professional and recreational female athletes has led to an increased scientific interest about sports health and performance in the female athlete population. The purpose of the IronFEMME Study described in this protocol article is to determine the influence of different hormonal profiles on iron metabolism in response to endurance exercise, and the main markers of muscle damage in response to resistance exercise; both in eumenorrheic, oral contraceptive (OC) users and postmenopausal well-trained women. Methods: This project is an observational controlled randomized counterbalanced study. One hundered and four (104) active and healthy women were selected to participate in the IronFEMME Study, 57 of which were eumenorrheic, 31 OC users and 16 postmenopausal. The project consisted of two sections carried out at the same time: iron metabolism (study I) and muscle damage (study II). For the study I, the exercise protocol consisted of an interval running test (eight bouts of 3 min at 85% of the maximal aerobic speed), whereas the study II protocol was an eccentric-based resistance exercise protocol (10 sets of 10 repetitions of plate-loaded barbell parallel back squats at 60% of their one repetition maximum (1RM) with 2 min of recovery between sets). In both studies, eumenorrheic participants were evaluated at three specific moments of the menstrual cycle: early-follicular phase, late-follicular phase and mid-luteal phase; OC users performed the trial at two moments: withdrawal phase and active pill phase. Lastly, postmenopausal women were only tested once, since their hormonal status does not fluctuate. The three-step method was used to verify the menstrual cycle phase: calendar counting, blood test confirmation, and urine-based ovulation kits. Blood samples were obtained to measure sex hormones, iron metabolism parameters, and muscle damage related markers. Discussion: IronFEMME Study has been designed to increase the knowledge regarding the influence of sex hormones on some aspects of the exercise-related female physiology. Iron metabolism and exercise-induced muscle damage will be studied considering the different reproductive status present throughout well-trained females’ lifespan. Trial registrationThe study was registered at Clinicaltrials.gov NCT04458662 on 2 July 2020.

Highlights

  • Female endogenous hormonal fluctuations during the menstrual cycle or exogenous hormones from an oral contraceptive cycle may have potential effects on exercise performance [1,2,3]

  • One hundred and four (104) physically active and healthy women were selected to participate in the IronFEMME Study, 57 of whom were eumenorrheic, 31 were oral contraceptive (OC) users and 16 were postmenopausal women

  • The fact, including women in research has been seen as a barrier due to the complexity of studying hormone fluctuations associated with the menstrual cycle [92]

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Summary

Introduction

Female endogenous hormonal fluctuations during the menstrual cycle or exogenous hormones from an oral contraceptive cycle may have potential effects on exercise performance [1,2,3]. The female reproductive system involves numerous hormonal and regulatory components, affecting the reproductive system, and with an impact on female metabolism, thereby influencing exercise performance [1] It is important know how the hypothalamic-pituitary-ovarian axis works and affects other systems and metabolism related to exercise, in order to adapt and optimise training sessions and competitions. The average menstrual cycle length is 28 days, with an interindividual variation of 21–35 days in healthy adult women [5], and it involves repetitive cycles of follicle development, ovulation, and preparation of the endometrium for possible implantation of an embryo [6] This process begins in the hypothalamus, with the pulsatile secretion of gonadotropin-releasing hormone (GnRH). These two gonadotropins targets the ovaries, where stimulates the secretion of sex steroid hormones 17β-estradiol and progesterone [6,7]

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