Glucose metabolism in systemic juvenile idiopathic arthritis
Papatsorn Suppasit1, Soamarat Vilaiyuk1, Preamrudee Poomthavorn1
1Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Bangkok, 10400, Thailand.
Insights
Systemic juvenile idiopathic arthritis (SJIA) in overweight/obese children is linked to higher insulin resistance and impaired glucose metabolism. This suggests an increased risk for developing diabetes in these young patients.
Area of Science:
- Pediatric Rheumatology
- Endocrinology
- Metabolic Disorders
Background:
- Systemic juvenile idiopathic arthritis (SJIA) is a chronic childhood inflammatory disease.
- Chronic inflammation in SJIA may lead to insulin resistance and abnormal glucose metabolism, similar to adult RA.
- Glucose metabolism in SJIA patients has not been previously studied.
Purpose of the Study:
- To investigate glucose metabolism and insulin sensitivity in children and young adults with SJIA.
- To compare metabolic parameters between SJIA patients and healthy controls.
Main Methods:
- Recruited 39 SJIA patients (aged 4-25 years) and obese normoglycemic controls.
- Conducted oral glucose tolerance tests (OGTT) for all participants.
- Calculated insulin sensitivity (HOMA-IR, WBISI) and beta-cell function (IGI, DI) indices.
Main Results:
- Overweight/obese (OW/OB) SJIA patients showed significantly higher insulin resistance (HOMA-IR) and lower insulin sensitivity (WBISI) compared to OW/OB controls.
- OW/OB SJIA patients also exhibited higher insulin secretion (IGI).
- Lean SJIA patients had comparable insulin sensitivity to lean controls.
Conclusions:
- Overweight/obese children with SJIA exhibit increased insulin resistance.
- These findings suggest a potential heightened risk for diabetes development in this population.
- Further research is warranted to confirm these metabolic alterations.
Background:
Systemic juvenile idiopathic arthritis (SJIA) is a chronic systemic inflammatory disease in children. Overproduction of inflammatory cytokines in SJIA resembles that in adult onset Still disease. Chronic inflammation causes insulin resistance and consequently leading to abnormal glucose metabolism. Adults with rheumatoid arthritis (RA) have increased risks of abnormal glucose metabolism and diabetes. To date, glucose metabolism in patients with SJIA has not been elucidated.
Methods:
Patients with SJIA aged 4-25 years were recruited. All patients underwent an oral glucose tolerance test (OGTT). Indices of insulin sensitivity [homeostasis model assessment for insulin resistance (HOMA-IR) and whole-body insulin sensitivity index (WBISI)] and β-cell function [insulinogenic index (IGI) and disposition index (DI)] were calculated. Obese children with normoglycemia who underwent the OGTT were served as a control group.
Results:
A total of 39 patients with SJIA, aged 4-25 years, median (IQR) BMI SDS was 0.1 (-0.5 to 1.7). Patients were divided into 2 groups, overweight/obese (OW/OB) (n = 11) and lean (n = 28). Only one obese patient had prediabetes and none had diabetes. In comparison with sex- and age-matched OW/OB controls (n = 33), OW/OB patients with SJIA had higher insulin resistance [median (IQR) HOMA-IR: 2.6 (2.1-3.3) vs 1.5 (0.8-2.0), p = 0.001], lower insulin sensitivity [median (IQR) WBISI: 3.7 (2.7-5.9) vs 5.4 (4.5-8.7), p = 0.024], and higher insulin secretion [median (IQR) IGI: 2.5 (2.0-3.5) vs 1.0 (0.8-1.9), p = 0.001]. In lean patients with SJIA, insulin sensitivity indices seemed to be comparable with those of lean controls.
Conclusions:
Overweight/obese children with SJIA seemed to have increased insulin resistance and thus may have an increased risk for developing diabetes.
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