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Bioleptin as a useful marker of metabolic status in children with diabetes mellitus type 1
Katarzyna Jakubek-Kipa1, Sabina Galiniak2, Katarzyna Łagowska3
1Department of Pediatrics, Institute of Medical Sciences, Medical College of Rzeszów University, Rzeszów, Poland.
Insights
Children with type 1 diabetes have lower leptin levels than healthy children. Biologically active leptin (bioLEP) levels varied significantly based on diabetes diagnosis, duration, and metabolic control.
Area of Science:
- Pediatrics
- Endocrinology
- Metabolic Disorders
Background:
- Leptin plays a role in regulating metabolism.
- Understanding leptin's role in type 1 diabetes is crucial for metabolic management.
- Biologically active leptin (bioLEP) is a key indicator of leptin's function.
Purpose of the Study:
- To measure serum leptin and bioLEP levels in children with type 1 diabetes.
- To analyze these levels based on diabetes duration and metabolic control.
- To compare levels between diabetic children and healthy controls.
Main Methods:
- Study included 94 children with type 1 diabetes and 14 healthy controls.
- Diabetic children were categorized into newly diagnosed and long-term groups (good/poor control).
- Serum leptin and bioLEP were quantified using sandwich enzyme-linked immunosorbent assay.
Main Results:
- Children with type 1 diabetes exhibited lower leptin levels than healthy children.
- Newly diagnosed diabetic children had higher leptin than poorly controlled diabetic children.
- Well-controlled diabetic children showed lower leptin levels than healthy children.
Conclusions:
- Leptin and bioLEP levels differ significantly in children with type 1 diabetes based on disease status.
- Further research on bioLEP in diabetes can elucidate metabolic regulation mechanisms.
- Findings highlight the complex relationship between leptin, diabetes, and metabolic control in children.
Introduction:
The purpose of our study was tomeasure the level of leptin and biologically active leptin (bioLEP) in children with type 1 diabetes, depending on the duration of diabetes and its degree of metabolic control.
Methods:
The study included 94 children (58 boys and 36 girls). In a group of children with diabetes, 40 patients were newly diagnosed with type 1 diabetes, 40 children who have diabetes for more than a year (20 with good metabolic control and 20 with poor metabolic control). The control group consisted of 14 healthy children. The serum level of leptin and bioLEP was measured using a sandwich enzyme-linked immunosorbent assay. To our knowledge, this is the first study to describe bioLEP levels among diabetic children with different forms of disease control.
Results:
Lower levels of leptin were found in children with diabetes compared to healthy children. Furthermore, we found a statistically higher concentration of leptin in the group of children with newly diagnosed diabetes compared to children from the diabetic group with poor metabolic control and lower than healthy children (11.19 vs. 7.84 and 20.94 ng/mL). Moreover, children in the metabolically well-controlled group had statistically lower levels of this hormone (5.11 ng/mL) than healthy children. Leptin concentrations differed significantly between underweight, overweight, and obese children.
Discussion:
In our study, the level of bioLEP differed significantly between children in the newly diagnosed diabetes group and children in the long-term, poorly controlled diabetes group and healthy controls. Despite many studies published in recent years, many aspects of leptin secretion, action, and mechanisms of its influence on carbohydrate and fat metabolism are still to be clarified. In our opinion, studies evaluating the status of bioLEP in diabetes can also contribute to a better understanding of the mechanisms regulating metabolism.
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