# Exertional Rhabdomyolysis, Hyposthenuria, and Acute Kidney Injury: The Non-benign Side of Sickle Cell Trait

**Authors:** Ashley C Vincent, Irmina Swiostek, Rehaan Shaffie

PMC · DOI: 10.7759/cureus.103115 · Cureus · 2026-02-06

## TL;DR

This paper highlights how sickle cell trait can lead to severe health issues like rhabdomyolysis and kidney failure, challenging the belief that it is a harmless condition.

## Contribution

The paper presents a case showing that sickle cell trait can cause severe clinical complications, emphasizing the need for better patient education.

## Key findings

- A healthy young athlete with sickle cell trait experienced severe rhabdomyolysis and acute kidney injury.
- Sickle cell trait may increase the risk of exertional rhabdomyolysis due to microvascular occlusion and tissue ischemia.
- The case suggests that sickle cell trait is not a clinically silent condition and requires improved counseling.

## Abstract

Sickle cell trait (SCT) is largely understood to be a clinically silent disease that typically does not require intensive clinical monitoring or counseling of patients. In fact, many patients with SCT are unaware that they have this genetic condition. However, emerging studies, case reports, and reviews increasingly demonstrate that severe clinical pathology can be associated with SCT, showcasing the need for improved counseling and education. We present the case of a healthy young male patient who was admitted to the hospital with rhabdomyolysis, acute liver injury, extreme electrolyte disturbances, and acute renal failure necessitating emergent hemodialysis. Given that this was an otherwise healthy young athlete with no known risk factors, the gravity of his clinical condition led our team to question why he had such a severe presentation. Further evaluation revealed the diagnosis of SCT. SCT has been linked to an increased risk of exertional rhabdomyolysis, which causes muscle damage via microvascular occlusion as well as tissue ischemia, caused by endothelial damage. These processes predispose to a decreased ability to concentrate urine, increasing risk for dehydration, and more serious clinical presentations. The potential links between SCT and exertional rhabdomyolysis support the hypothesis that SCT is not a clinically silent condition.

## Linked entities

- **Diseases:** rhabdomyolysis (MONDO:0005290), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, MB (myoglobin) [NCBI Gene 4151] {aka MYOSB, PVALB}
- **Diseases:** Exertional rhabdomyolysis (MESH:D012206), microvascular occlusion (MESH:D017566), inflammatory (MESH:D007249), muscle damage (MESH:D009133), injury (MESH:D014947), anemia (MESH:D000740), alcohol (MESH:D000437), muscle breakdown (MESH:D019042), crush injury (MESH:D000071576), hematuria (MESH:D006417), hyperkalemia (MESH:D006947), leg pain (MESH:D010146), hypertension (MESH:D006973), weakness (MESH:D018908), renal medullary carcinoma (MESH:D018276), infection (MESH:D007239), nephrotoxic proteins (MESH:D011488), renal failure (MESH:D051437), electrolyte disturbances (MESH:D014883), acidosis (MESH:D000138), chronic kidney disease (MESH:D051436), acute liver injury (MESH:D017114), dehydration (MESH:D003681), numbness (MESH:D006987), renal dysfunction (MESH:D007674), organ failure (MESH:D009102), autoimmune conditions (MESH:D001327), myoglobinuria (MESH:D009212), hyperpigmented rash (MESH:D005076), liver injury (MESH:D017093), cardiac instability (MESH:D006331), muscle pain (MESH:D063806), AKI (MESH:D058186), sickle cell (MESH:D000755), myopathy (MESH:D009135), proteinuria (MESH:D011507), SCT (MESH:D012805), acute illness (MESH:D000208), enzymatic or genetic deficiencies (MESH:D030342), ischemia (MESH:D007511), acute pain (MESH:D059787), damage (MESH:D020263)
- **Chemicals:** lowering medications (-), ATP (MESH:D000255), coenzyme Q (MESH:D014451), Urea Nitrogen (MESH:C530477), lipid (MESH:D008055), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12968087/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968087/full.md

---
Source: https://tomesphere.com/paper/PMC12968087