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Background: Exertional rhabdomyolysis is a condition resulting from skeletal muscle damage and release of intracellular toxins into the systemic circulation as a consequence of extreme physical effort. With increasing numbers of people partaking in high-intensity workouts, we hypothesized that the rate of presentation of exertional rhabdomyolysis was also increasing.
Methods: All presentations to the Princess Alexandra Hospital emergency department in Brisbane, Australia between March 2005 and December 2016 were identified from the electronic medical record. Records of patients with a serum creatine kinase value >1,000 U/L or a urinary myoglobin >5 mg/L were extracted for determination of whether the rhabdomyolysis was attributable to physical exertion.
Results: From a total of 1,957 rhabdomyolysis cases, 89 patients (70.8% male) were identified as having exertional rhabdomyolysis. The frequency of presentation increased from 0.28/10,000 presentations in 2005 to 3.5/10,000 in 2015. Gym-induced exertional rhabdomyolysis was the primary subcategory (53.9%) for these cases, and manual labor was the second most common subcategory (15.7%).
Conclusion: This study provides evidence for increasing instances of exertional rhabdomyolysis in the Brisbane, Australia metropolitan area and adds to the current knowledge about those who develop exertional rhabdomyolysis. Future studies are warranted to investigate if similar trends are being seen in other regions and to identify the circumstances leading to the presentation. Such knowledge would be valuable for devising strategies to prevent and mitigate injury.
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http://dx.doi.org/10.31486/toj.17.0112 | DOI Listing |
Genes (Basel)
August 2025
Consortium for Health and Military Performance, Department of Military and Emergency Medicine, F. Edward Hébert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA.
Background/objective: Exertional rhabdomyolysis (ER) is primarily driven by mechanical stress on muscles during strenuous or unaccustomed exercise, often exacerbated by environmental factors like heat and dehydration. While the general cellular pathway involving energy depletion and calcium overload is understood in horse ER models, the underlying mechanisms specific to the ER are not universally known within humans. This study aimed to evaluate whether patients with ER exhibited transcriptional signatures that were significantly different from those of healthy individuals.
View Article and Find Full Text PDFComp Biochem Physiol A Mol Integr Physiol
August 2025
Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort, Pretoria 0110, South Africa; Department of Production Animal Sciences, Faculty of veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort, Pretoria 0110,
Rhabdomyolyses is a clinical sign of capture myopathy in wild animals and may be linked to glycogen metabolism. To study potential mechanisms, 26 wild blesbok were chased for 15 min and immobilised, whereafter 12 of these blesbok were doused with ice-water (n = 14 chased only group; n = 12 chased + cooled group). An additional 12 blesbok served as resting (not chased) uncooled controls.
View Article and Find Full Text PDFMuscles
August 2024
ENFYRED Research Group, Faculty of Health and Sports, University of Zaragoza, 22002 Huesca, Spain.
Exertional rhabdomyolysis (ER) is a condition where muscle breakdown occurs after intense and unaccustomed exercise in healthy individuals. It is characterized by muscle pain, weakness, and myoglobinuria, potentially leading to acute kidney injury and worsening the patients' prognosis. Ultra-trail races (UT) necessitate high energy and extreme muscular exertion, which can result in significant muscle breakdown, leading to ER and elevated biomarkers such as creatine kinase (CK) and lactate dehydrogenase (LDH).
View Article and Find Full Text PDFCureus
June 2025
Neuromuscular Medicine, Cleveland Clinic Foundation, Cleveland, USA.
Introduction McArdle disease (glycogen storage disorder type 5) is an autosomal recessive metabolic myopathy caused by a myophosphorylase enzyme deficiency. Most patients develop symptoms during childhood; however, diagnosis is usually delayed until adulthood. Our study aimed to identify clues for an earlier recognition of this rare disease.
View Article and Find Full Text PDFCureus
June 2025
Internal Medicine, Burjeel Medical City, Abu Dhabi, ARE.
We report one of the first documented cases globally of a 24-year-old female presenting with recurrent episodes of muscle pain, weakness, and rhabdomyolysis. Although she initially improved with conservative management, her symptoms recurred, warranting further investigation. Comprehensive serologic and metabolic evaluations revealed a rare dual diagnosis of seropositive myasthenia gravis (MG) and aldolase A deficiency.
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