# Acute Biochemical Responses to Competitive Tournament Load in Female Handball Players: Hormonal, Inflammatory and Muscle Damage Markers

**Authors:** Zarife Pancar, Yücel Makaracı, Celal Gençoğlu, Burak Karaca, Hasan Ulusal

PMC · DOI: 10.3390/life16030523 · Life · 2026-03-21

## TL;DR

This study examines how female handball players' bodies respond to the stress of a tournament, showing increased stress and muscle damage markers and decreased recovery-related hormones.

## Contribution

The study provides new insights into the combined hormonal, inflammatory, and muscle damage responses in female handball players during competitive tournaments.

## Key findings

- Tournament load increased cortisol, IL-6, CK, and osteocalcin, indicating stress and muscle damage.
- IGF-1 and testosterone decreased, showing a shift to a catabolic state.
- LDH decreased, while irisin remained unchanged.

## Abstract

Background: Congested tournament schedules impose substantial physiological stress in team sports; however, the integrated endocrine and inflammatory responses to real competitive match load in female handball players remain insufficiently characterized. Objective: This study aimed to characterize the acute biochemical responses, including hormonal, inflammatory, muscle damage, and bone metabolism markers, elicited by competitive tournament load in female handball players and to provide practical insights for optimizing recovery strategies and load management during short-term competitive periods. Methods: In a pre–post study design, venous blood samples were collected from competitive female athletes (n = 8; age 20.83 ± 2.93 years) before the first match and after the fourth consecutive match of an official university qualification tournament. Biochemical analyses included cortisol, insulin, IL-6, creatine kinase (CK), IGF-1, irisin, lactate dehydrogenase (LDH), osteocalcin, and testosterone. Pre-to-post changes were assessed using paired t-tests and effect sizes. Results: Tournament load induced substantial multisystem physiological perturbations. Significant increases were observed in cortisol (p < 0.001), insulin (p = 0.044), IL-6 (p < 0.001), CK (p < 0.001), and osteocalcin (p = 0.005), indicating activation of the hypothalamic–pituitary–adrenal axis, systemic inflammation, muscle membrane disruption, and enhanced bone turnover. Conversely, IGF-1 (p < 0.001) and testosterone (p = 0.004) significantly decreased, reflecting suppression of anabolic signaling and a shift toward a catabolic hormonal environment under cumulative match stress. LDH significantly decreased (p = 0.002), while irisin showed no significant change (p > 0.05). Conclusions: These findings demonstrate that congested tournament schedules provoke an integrated endocrine–inflammatory stress response in female handball players. Importantly, the observed anabolic–catabolic imbalance highlights the need for individualized recovery strategies, optimized load management, and adequate recovery periods to mitigate maladaptation and reduce injury risk during short-term competitive tournaments.

## Linked entities

- **Proteins:** PIN (insulin precursor), IL6 (interleukin 6), IGF1 (insulin like growth factor 1), bglap2 (bone gamma-carboxyglutamate (gla) protein (osteocalcin) 2), FNDC5 (fibronectin type III domain containing 5)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995] {aka FRCP2, irisin}, BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** Muscle Damage (MESH:D009133), Inflammatory (MESH:D007249)
- **Chemicals:** cortisol (MESH:D006854), testosterone (MESH:D013739)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028009/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028009/full.md

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Source: https://tomesphere.com/paper/PMC13028009