Menstrual Cycle Phase-Based Interval Training Yields Distinct Muscle Changes in Female Athletes

Abstract

Advances in mass-spectrometry(MS)-based technologies have leveraged our understanding of skeletal muscle responsiveness to exercise in humans. However, there is a lack of such data in females, particularly pertaining to female athletes and menstrual cycle phase-based sprint interval training(SIT) despite its efficacy and popularity. Here, we present a comprehensive proteomic analysis of skeletal muscle adaptations to high-frequency SIT during different menstrual cycle phases in female athletes. We randomized 49 eumenorrheic females to either high-frequency SIT in the follicular(FB) or luteal phase(LB) over one menstrual cycle comprising eight sessions of 6×30-s all-out efforts. Twenty-five completed the intervention with verified cycles. MS-based proteomics revealed notable differences in muscle adaptations to phase-based SIT. LB suppressed mitochondrial pathways of the tricarboxylic acid cycle and electron transport chain while enriching ribosomal complexes. Conversely, FB enriched filament organization and skeletal system development. Mitochondrial repression during LB was linked to reduced VO2max, whereas exercise capacity improved in FB only. Our findings show that synching high-frequency SIT with menstrual cycle phases induces distinct muscle adaptations and affects phenotype in eumenorrheic female athletes.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

NCT04136457

Funding Statement

The study was supported as part of the Novo Nordisk Foundation grant to Team Danmark to the research network "Training strategies and competition preparation". Mass spectrometry analyses: supported by the Novo Nordisk Foundation (NNF).

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study was approved by the regional ethics committee of Copenhagen, Denmark (H-20052639).

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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data generated or analyzed during this study are included in this published article. Raw data and additional datasets can be accessed by request.

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