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Longitudinal differences in aerobic capacity between children with sickle cell anemia and matched controls
Andrew M Watson1, Robert I Liem, Zengqi Lu
1Department of Pediatrics, University of Wisconsin Hospital and Clinics, Madison, Wisconsin.
Insights
Children with sickle cell anemia (SCA) show lower maximal aerobic capacity (VO2peak) than healthy peers, with this gap widening during puberty. These differences persist even after accounting for key physiological factors.
Area of Science:
- Pediatric Hematology
- Cardiorespiratory Fitness
- Growth and Development
Background:
- Children with sickle cell anemia (SCA) often experience chronic health challenges.
- Maximal aerobic capacity (VO2peak) is a critical indicator of cardiorespiratory health.
- Understanding fitness trajectories in SCA is crucial for managing long-term health outcomes.
Purpose of the Study:
- To compare the longitudinal changes in maximal aerobic capacity (VO2peak) between children with SCA and healthy controls.
- To investigate the association of VO2peak trajectories with physiological variables like hemoglobin concentration and fat-free mass.
Main Methods:
- A longitudinal study involving 33 children with SCA and 30 matched healthy controls.
- Three annual fitness assessments measuring VO2peak.
- Statistical analysis using linear mixed models to compare changes over time, adjusting for covariates.
Main Results:
- Children with SCA had lower baseline VO2peak and hemoglobin levels compared to controls.
- Over time, children with SCA exhibited smaller increases in VO2peak, Tanner stage, and fat-free mass.
- The disparity in VO2peak trajectories between groups remained significant after adjusting for multiple physiological factors.
Conclusions:
- Children with SCA have significantly lower relative VO2peak than healthy children, and this difference exacerbates during puberty.
- These VO2peak trajectory differences are independent of age, sex, Tanner stage, fat-free mass, and hemoglobin concentration.
- The findings highlight potential long-term cardiorespiratory implications for children with SCA.
Background:
The purpose of this study was to compare longitudinal trajectories of maximal aerobic capacity in children with sickle cell anemia (SCA) and matched healthy controls, and explore whether these trajectories were associated with selected physiologic variables.
Procedure:
Children with SCA (n = 33) and healthy controls (n = 30) matched at baseline for race, sex, Tanner stage, height, and weight completed three consecutive annual fitness assessments (VO2peak ). Data were compared between the groups at each time point and within groups over time. Change in VO2peak between the two groups over time was assessed using a linear mixed model with age, sex, fat-free mass (FFM), Tanner stage, and hemoglobin (Hgb) concentration as covariates.
Results:
At baseline, children with SCA had significantly lower Hgb concentration (8.9 vs. 13.7 g/dL, P < 0.001) and relative VO2peak (24.2 vs. 27.9 ml/kg/min, P = 0.006) than healthy controls. Over time, children with SCA had smaller increases than healthy controls in VO2peak (-0.1 and +4.9 ml/kg/min, P < 0.001), Tanner stage at year 2 (15% and 66% Tanner 4, P < 0.001), and FFM (+4.0 and +6.8 kg, P = 0.02). Changes in Hgb concentration did not differ between groups (+0.03 and +0.09 g/dL, P = 1.0). After adjusting for age, sex, Tanner stage, FFM, and Hgb concentration the differences in change in VO2peak over time remained significant (P < 0.001).
Conclusion:
Children with SCA demonstrate lower relative VO2peak compared to healthy children and the difference increases over time. The difference in VO2peak trajectories between the two groups during puberty remains significant after adjusting for age, sex, FFM, Tanner stage, and Hgb concentration.
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