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Aerobic physical capacity and health-related quality of life in children with sickle cell disease

  • Corentin Laurent-Lacroix,
  • Marie Vincenti,
  • Stefan Matecki,
  • Perrine Mahé,
  • Lionel Moulis,
  • Gregoire De La Villeon,
  • Sophie Guillaumont,
  • Anne Requirand,
  • Johan Moreau,
  • Muriel Lalande,
  • Marie-Christine Picot,
  • Pascal Amedro,
  • Arthur Gavotto

摘要

Background

Aerobic fitness is a predictor of cardiovascular health which correlates with health-related quality of life in the general population. The aim is to evaluate the aerobic capacity by cardiopulmonary exercise test (CPET) in children with sickle cell disease in comparison with healthy matched controls.

Methods

Controlled cross-sectional study.

Results

A total of 72 children (24 with sickle cell disease and 48 healthy controls), aged 6–17 years old were enrolled. Children with sickle cell disease had a poor aerobic capacity, with median VO2max Z-score values significantly lower than matched controls (−3.55[−4.68; −2.02] vs. 0.25[−0.22; 0.66], P < 0.01, respectively), and a high proportion of 92% children affected by an impaired aerobic capacity (VO2max Z-score < −1.64). The VO2max decrease was associated with the level of anemia, the existence of a homozygote HbS/S mutation, restrictive lung disease and health-related quality of life.

Conclusion

Aerobic capacity is poor in children with sickle cell disease. VO2max decrease is associated with the level of anemia, the existence of a homozygote HbS/S mutation, lung function, and health-related quality of life. These results represent a signal in favor of early initiation of cardiac rehabilitation in patients with sickle cell disease.

Clinical trials

NCT05995743.

Impact

Aerobic fitness is a predictor of cardiovascular health which correlates with health-related quality of life in the general population.

Aerobic capacity (VO2max) is poor in children with sickle cell disease, despite the absence of any pattern of heart failure.

VO2max decrease was associated with the level of anemia, the existence of a homozygote HbS/S mutation, restrictive lung disease, and health-related quality of life.

These results are in favor of early initiation of cardiac rehabilitation in children with sickle cell disease.