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Published on: January 31, 2013
Peripheral muscle strength in young males with cystic fibrosis
1School of Physiotherapy, Trinity Centre for the Health Sciences, St. James's Hospital, James's Street, Dublin 8, Ireland. jmhussey@tcd.ie
Insights
Children with cystic fibrosis (CF) exhibit reduced muscle strength compared to healthy peers. This decreased strength, particularly in knee and shoulder muscles, is linked to reduced lung function in CF patients.
Area of Science:
- Pediatric exercise physiology
- Pulmonary medicine
- Musculoskeletal health
Background:
- Children with cystic fibrosis (CF) demonstrate reduced peak work capacity and oxygen consumption during exercise.
- Peripheral muscle force is diminished in pediatric CF patients, even with mild lung function impairment.
- Previous research has not utilized isokinetic dynamometry to assess peripheral muscle strength in this population.
Purpose of the Study:
- To evaluate peripheral muscle strength in children with cystic fibrosis using isokinetic dynamometry.
- To compare isokinetic muscle strength between children with CF and age-matched healthy controls.
- To investigate the correlation between lung function (FEV1) and peripheral muscle strength in pediatric CF patients.
Main Methods:
- Isokinetic muscle strength of knee and shoulder flexors/extensors was measured in 13 children with CF and 13 controls at two movement speeds.
- Peak torque was calculated and normalized to body weight.
- Activity levels were assessed in both groups.
Main Results:
- Children with CF showed significantly lower peak torque normalized to body weight compared to controls.
- A significant correlation was found between FEV1 and knee muscle strength.
- FEV1 also correlated significantly with shoulder flexion strength at 90 degrees/s in CF subjects.
Conclusions:
- Pediatric patients with cystic fibrosis possess lower muscle strength than their healthy counterparts.
- Reduced airflow limitation in CF is associated with diminished peripheral muscle strength.
- Further research is needed to understand the link between muscle strength and exercise tolerance in CF.
Background:
In children with cystic fibrosis there is a decrease in peak work capacity and oxygen consumption on maximal exercise testing when compared to controls. Previous studies have shown that peripheral muscle force is decreased in children with cystic fibrosis even in those with minimal changes in lung function. However, no studies have examined peripheral muscle strength using isokinetic dynamometry which permits measurement of muscle strength throughout range and is considered the gold standard in orthopaedics and sports medicine.
Methods:
Isokinetic muscle strength was measured in the knee flexors and extensors and shoulder flexors and extensors at two speeds of movement in children with cystic fibrosis and matched controls. Activity levels in both groups were calculated.
Results:
Thirteen subjects and 13 age and height matched controls were assessed. Average peak torque was calculated and expressed in terms of body weight. There was a significant difference in peak torque/body weight in children with cystic fibrosis when compared to controls. FEV1 was significantly correlated with knee muscle strength and shoulder flexion at 90 degrees /s in subjects with CF.
Conclusion:
Children with CF had lower muscle strength than control subjects. Airflow limitation was associated with decreased muscle strength. The relationship between muscle strength and exercise tolerance requires investigation.
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