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Published on: July 5, 2017
Attenuated maximal muscle strength and peak power in children with sickle cell disease
Kelly A Dougherty1, Joan I Schall, Alisha J Rovner
1Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA 19104, USA. doughertyk@email.chop.edu
Insights
Children with sickle cell disease (SCD-SS) exhibit reduced muscle strength and peak power compared to healthy peers. These deficits exceed those explained by body composition, indicating additional contributing factors in anaerobic performance.
Area of Science:
- Pediatric Health
- Hematology
- Sports Medicine
Background:
- Sickle cell disease (SCD-SS) is a genetic blood disorder affecting red blood cells.
- Children with SCD-SS often experience growth and body composition differences.
- Assessing muscle function is crucial for understanding overall health in pediatric populations.
Purpose of the Study:
- To compare maximal handgrip strength and peak power in African-American children with and without SCD-SS.
- To determine if strength and power deficits in SCD-SS are solely due to body size and composition.
- To investigate potential additional factors contributing to reduced anaerobic performance in SCD-SS.
Main Methods:
- Maximal handgrip strength and peak power were measured in children aged 5-13 years.
- Measurements were taken using a handgrip dynamometer and a force plate.
- Data were adjusted for body size and composition (Z scores).
Main Results:
- Children with SCD-SS had significantly lower Z scores for height, weight, BMI, and various body composition measures.
- SCD-SS group showed significantly lower handgrip strength and peak power.
- Adjusted Z scores for handgrip strength and peak power were significantly lower in children with SCD-SS.
Conclusions:
- Maximal muscle strength and peak power are attenuated in children with SCD-SS.
- These deficits are greater than expected based on growth and body composition alone.
- Additional factors beyond physical growth contribute to impaired anaerobic performance in SCD-SS.
Abstract:
Dominant hand maximal handgrip strength evaluated with a handgrip dynamometer and peak power evaluated with a force plate, adjusted for body size and composition, were compared in African-American children aged 5 to 13 years, with and without type SS sickle cell disease (SCD-SS). Children with SCD-SS (n = 35; age, 9.0 ± 2.0 y) compared with healthy control children (n = 103; age, 8.6 ± 1.8 y) did not differ by age, sex, or pubertal status, yet had significantly lower Z scores for height, weight, body mass index, upper arm muscle area, upper arm fat area, fat mass-for-height and lean mass-for-height. Children with SCD-SS had significantly lower handgrip strength (12.7 ± 3.3 vs. 15.2 ± 5.1 kg, P < 0.008), peak power (882 ± 298 vs. 1167 ± 384 W, P < 0.001), and growth and body composition adjusted Z scores for handgrip strength (0.6 ± 1.3 standard deviations, P < 0.004) and peak power (male children = 1.0 ± 0.8 standard deviations, P < 0.0002; female children = 1.0 ± 1.7 standard deviations, P < 0.006). Maximal muscle strength and peak power are attenuated in children with SCD-SS compared with healthy control children beyond expectation for growth and body composition deficits suggesting that additional factors contribute to attenuation in anaerobic performance.
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