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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Evaluation of adipocytokines in children with chronic kidney disease
Maria Szczepańska1, Edyta Machura, Piotr Adamczyk
1Chair and Department of Paediatrics, Zabrze, Medical University of Silesia, School of Medicine with the Division of Dentistry, Poland. dializy_dzieciece_zabrze@poczta.onet.pl.
Insights
Serum adipocytokine levels are altered in children with chronic kidney disease (CKD). These changes may indicate cardiovascular risks and outcomes, highlighting the role of adipocytokines in pediatric kidney dysfunction.
Area of Science:
- Endocrinology
- Nephrology
- Metabolic research
Background:
- Adipose tissue functions as a metabolic and endocrine organ through secreted adipocytokines.
- Adipocytokine levels in children with chronic kidney disease (CKD) may predict cardiovascular complications and long-term outcomes.
- Evaluating adipocytokines can offer insights into the progression of CKD and post-transplant health.
Purpose of the Study:
- To simultaneously measure serum concentrations of six adipocytokines in children with CKD.
- To compare adipocytokine levels in children with CKD undergoing dialysis against a control group.
- To investigate the relationship between specific adipocytokines and kidney dysfunction.
Main Methods:
- Serum concentrations of adiponectin, apelin, chemerin, omentin, resistin, and vaspin were measured.
- The study included 28 children with CKD stage 5 on hemodialysis or peritoneal dialysis.
- Statistical analysis was performed, including adjustments for body mass index (BMI) and body surface area (BSA).
Main Results:
- Children with CKD showed significantly higher levels of apelin, omentin, and resistin, and lower levels of vaspin, adiponectin, and chemerin compared to controls.
- These differences persisted after adjusting for BMI.
- Adjusting for BSA revealed no significant difference in vaspin, adiponectin, and chemerin levels between groups.
- Correlations indicated negative relationships between omentin-apelin and omentin-vaspin, and positive relationships between adiponectin-chemerin and adiponectin-resistin.
Conclusions:
- Altered serum adipocytokine concentrations are linked to kidney dysfunction in pediatric CKD.
- Further longitudinal studies in larger pediatric cohorts are needed.
- Investigating the role of adipocytokines in CKD development and progression is crucial for understanding risk factors.
Introduction:
Adipose tissue through the many secreted adipocytokines creates a highly active metabolic and endocrine organ. The evaluation of serum adipocytokine concentration in children with chronic kidney disease (CKD) could serve as a marker of cardio-vascular complication progression and an index of outcome in adulthood and after kidney transplantation.
Material And Methods:
The aim of the study was to evaluate simultaneously the serum concentrations of six different adipocytokines: adiponectin, apelin, chemerin, omentin, resistin, and vaspin, in 28 children with CKD stage 5 on haemodialysis and peritoneal dialysis.
Results:
The concentration of apelin, omentin, and resistin in children with CKD was significantly higher and the concentration of vaspin, adiponectin, and chemerin was significantly lower than in the control group. After adjusting to body mass index (BMI), the same results were obtained. After adjusting to body surface area (BSA), the concentration of vaspin, adiponectin, and chemerin did not differ between children with CKD and the control group. In analysis of the correlation between serum total adipocytokine levels in children with CKD we found a negative relationship in pairs: omentin-apelin and omentin-vaspin, and positive in pairs: adiponectin-chemerin and adiponectin-resistin.
Conclusions:
Our results show that changes in serum adipocytokines concentration are associated with the kidney dysfunction in CKD in children. Longitudinal studies on larger groups of paediatric cohorts would be helpful in investigating whether adipocytokines play a harmful role in the development of CKD and would enable further understanding of the risk factors for CKD progression.
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