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Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro
Published on: March 17, 2023
Expression of adipokines in children with primary nephrotic syndrome and its association with hyperlipidemia
Ru-Xin Zhang1, Xuan Zhang1, Bi-Li Zhang1
1Department of Nephrology, Tianjin Children's Hospital, Tianjin 300074, China.
Insights
Primary nephrotic syndrome (PNS) in children is linked to altered adipokine levels, specifically lower omentin-1 and higher chemerin. These changes correlate with blood lipid abnormalities and cardiovascular risk, suggesting omentin-1
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Biochemistry
Background:
- Primary nephrotic syndrome (PNS) in children is a kidney disorder often associated with lipid metabolism disturbances.
- Adipokines, signaling molecules from adipose tissue, play a role in metabolic regulation and inflammation.
- Understanding adipokine profiles in PNS may offer insights into disease pathogenesis and associated complications like hyperlipidemia.
Purpose of the Study:
- To investigate the expression levels of adipokines in children with PNS during active disease and remission.
- To examine the correlation between adipokine levels and blood lipid profiles in children with PNS.
- To elucidate the role of adipokines in the development of hyperlipidemia in pediatric PNS.
Main Methods:
- A cohort of 90 children with PNS (active or remission stages) and 30 healthy controls were recruited.
- Serum samples were collected and analyzed for adipokine levels (omentin-1, chemerin) using ELISA.
- Blood lipid parameters, including total cholesterol, triglycerides, HDL, LDL, and various lipid ratios (e.g., atherogenic index, Castelli indices), were measured using an automatic biochemical analyzer.
Main Results:
- Children with PNS exhibited significantly lower omentin-1 and higher chemerin levels compared to controls, with levels differing between active and remission stages.
- PNS patients showed significantly elevated atherogenic indices, atherogenic coefficient, Castelli risk indices, and non-HDL cholesterol in both active and remission stages compared to controls.
- Omentin-1 levels correlated positively with high-density lipoprotein and negatively with atherogenic indices, suggesting a role in modulating lipid profiles and cardiovascular risk.
Conclusions:
- Omentin-1 levels are associated with disease activity, dyslipidemia, and proteinuria in pediatric primary nephrotic syndrome.
- Blood lipid ratios appear more sensitive than traditional lipid parameters for monitoring early cardiovascular risk in children with PNS.
- Adipokine dysregulation, particularly omentin-1, may contribute to the pathophysiology of hyperlipidemia in pediatric PNS.
Objectives:
To study the expression of adipokines in children with primary nephrotic syndrome (PNS) before and after treatment and its correlation with blood lipids, as well as the role of adipokines in PNS children with hyperlipidemia.
Methods:
A total of 90 children who were diagnosed with incipient PNS or recurrence of PNS after corticosteroid withdrawal for more than 6 months were enrolled as subjects. Thirty children who underwent physical examination were enrolled as the control group. Venous blood samples were collected from the children in the control group and the children with PNS before corticosteroid therapy (active stage) and after urinary protein clearance following 4 weeks of corticosteroid therapy (remission stage). ELISA was used to measure the levels of adipokines. An automatic biochemical analyzer was used to measure blood lipid levels.
Results:
Compared with the control group, the children with PNS had a significantly lower level of omentin-1 in both active and remission stages, and their level of omentin-1 in the active stage was significantly lower than that in the remission stage (P<0.001). For the children with PNS, the level of chemerin in the active stage was significantly higher than that in the remission stage, and the children with PNS in the active stage had a significantly higher level of chemerin than the control group (P<0.001). For the children with PNS, atherogenic index of plasma, atherogenic coefficient (AC), castelli risk index-1 (CRI-1), castelli risk index-2 (CRI-2), and non-high-density lipoprotein in the active stage were significantly higher than those in the remission stage (P<0.001), and these indices in the children with PNS in the active stage were significantly higher than those in the control group (P<0.001). The children with PNS in the remission stage had significantly higher atherogenic index of plasma, AC, CRI-1, and non-high-density lipoprotein than the control group (P<0.001). Compared with the control group, the children with PNS in the remission stage had significantly higher serum levels of total cholesterol, triglyceride, high-density lipoprotein, low-density lipoprotein, apolipoprotein B, and apolipoprotein A (P<0.01). In the children with PNS, the ratio of omentin-1 before and after corticosteroid therapy was positively correlated with that of high-density lipoprotein, 24-hour urinary protein excretion, and high-density lipoprotein/apolipoprotein A before and after treatment, and it was negatively correlated with the ratio of AC and CRI-1 before and after treatment (P<0.05). The PNS children with low omentin-1 levels in the active stage had significantly higher levels of CRI-1, CRI-2, AC, and apolipoprotein B/apolipoprotein A ratio than those with high omentin-1 levels (P<0.05).
Conclusions:
Omentin-1 may be associated with disease activity, dyslipidemia, and proteinuria in children with PNS. Blood lipid ratios may be more effective than traditional blood lipid parameters in monitoring early cardiovascular risk in children with PNS.
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