Nutritional status in girls with juvenile chronic arthritis
Insights
Juvenile chronic arthritis (JCA) in girls is linked to lower selenium and impaired growth. Nutritional status changes, including reduced muscle mass, were more severe with higher disease activity.
Area of Science:
- Pediatric Rheumatology
- Nutritional Science
- Immunology
Background:
- Juvenile chronic arthritis (JCA) is an inflammatory condition affecting children.
- Nutritional status, particularly micronutrients involved in inflammation, may be altered in JCA.
- Understanding these alterations is crucial for managing disease progression and growth.
Purpose of the Study:
- To investigate the nutritional status of girls with JCA, focusing on key nutrients.
- To assess the relationship between nutritional status and disease activity in JCA.
- To evaluate growth parameters and muscle mass in JCA patients.
Main Methods:
- Compared nutritional markers (selenium, glutathione peroxidase, ascorbic acid, tocopherol, folate, cobalamin) in 26 JCA girls and healthy controls.
- Assessed plasma, blood, platelet, mononuclear cell, and granulocyte nutrient levels.
- Measured growth parameters, serum creatinine, and arm muscle circumference.
Main Results:
- JCA patients showed decreased plasma selenium and slightly depressed blood glutathione peroxidase activity, more pronounced with higher disease activity.
- A slight decrease in granulocyte ascorbic acid was noted in JCA patients.
- Arthritic patients exhibited impaired growth, lower serum creatinine, and reduced arm muscle circumference, particularly in systemic or polyarticular JCA.
Conclusions:
- JCA is associated with specific nutritional deficiencies and reduced muscle mass.
- Disease activity correlates with the severity of certain nutritional and physical changes.
- Dietary supplementation may help correct these nutritional deficits, warranting further research.
Abstract:
Nutritional status, with emphasis on nutrients involved in inflammatory processes, was investigated in 26 girls with juvenile chronic arthritis (JCA) and in healthy controls. Children with JCA had decreased plasma selenium compared to controls. Glutathione peroxidase activity in plasma was similar in both groups but the activity in blood was slightly depressed in JCA. The decrease in blood glutathione peroxidase was more pronounced in patients with high to medium disease activity. Ascorbic acid was measured in plasma, platelets, mononuclear cells and granulocytes. A slight decrease in granulocyte ascorbic acid was observed in patients but in plasma, platelets and mononuclear cells no difference was observed. Serum alpha-tocopherol, blood folate and serum cobalamine was the same in both groups. Several patients, especially in the youngest group, exhibited impaired growth. Serum creatinine and arm muscle circumference were lower in the arthritic patients indicating a lower muscle mass. These changes were more pronounced in patients with systemic or polyarticular onset of the disease. The possibility that the changes in nutritional status in patients with JCA can be corrected by dietary supplementation needs further investigation.
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