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Published on: June 4, 2020
Grip Strength in Adults and Children with Cystinosis
Helina Iyob-Tessema1, Chia-Shi Wang1, Sabina Kennedy1
1Department of Pediatrics, Emory School of Medicine and Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Insights
Patients with cystinosis experience impaired muscle strength, particularly males and those with delayed cysteamine treatment. Lower physical activity also contributes to reduced grip strength in adults with cystinosis.
Area of Science:
- Nephrology
- Neurology
- Genetics
Background:
- Chronic kidney disease (CKD) is linked to reduced muscle strength.
- Cystinosis patients face higher risks of muscle weakness due to early CKD and myopathy.
- This study examines muscle strength and its risk factors in cystinosis patients.
Purpose of the Study:
- To assess muscle strength in individuals with cystinosis.
- To identify risk factors associated with decreased muscle strength in this population.
Main Methods:
- Recruited adult and pediatric patients from 2017-2019.
- Collected data via questionnaires on demographics, disease, activity, and neuromuscular symptoms.
- Measured grip strength using a dynamometer and analyzed z-scores for associations.
Main Results:
- Patients with cystinosis showed lower grip strength (mean z-score -2.1) than CKD patients without cystinosis.
- Male sex and delayed cysteamine initiation were linked to impaired grip strength.
- Low physical activity correlated with lower grip strength in adults; swallowing issues were also associated.
Conclusions:
- Cystinosis patients exhibit impaired muscle strength compared to controls and CKD patients.
- Muscle strength deficits are more pronounced in males and those with late cysteamine initiation.
- Further research is needed on physical activity, cysteamine optimization, and interventions.
Introduction:
Chronic kidney disease (CKD) is associated with impaired muscle strength. Patients with cystinosis have an increased risk for impaired muscle strength because of early development of CKD and cystinosis-induced myopathy. This study assesses muscle strength in patients with cystinosis and investigates risk factors of decreased muscle strength.
Methods:
Adult and pediatric patients were recruited from Cystinosis Research Network conferences and a large pediatric nephrology clinic between 2017 and 2019. Patients and caregivers completed questionnaires on demographic characteristics, disease course, daily physical activity, and neuromuscular symptoms. Grip strength was assessed using a dynameter and calculated z-scores for age and sex were assessed for associations with patient characteristics.
Results:
We included 76 patients with a mean grip strength z-score of -2.1 (SD, 1.1), which was lower than seen in patients with CKD without cystinosis. Male sex and delayed cysteamine initiation were independently associated with impaired grip strength. Among adults, a low level of physical activity was associated with lower grip strength z score, but no association was found in children. A third of the patients reported neuromuscular symptoms, with swallowing issues associated with lower grip strength. There was no significant correlation between eGFR and grip strength z-score.
Conclusion:
Patients with cystinosis have impaired muscle strength compared with healthy control subjects and patients with CKD. This impairment is greater in male patients and in patients with late initiation of cysteamine therapy and is associated with lower physical activity. Further studies investigating the effect of different types of physical activities, optimizing cysteamine therapy, and other interventions are needed.
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