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Elevated serum β₂-GPI-Lp(a) complexes levels in children with nephrotic syndrome
Chunni Zhang1, Yang Luo, Zhongwei Huang
1Department of Clinical Laboratory, Jinling Hospital, Clinical School of Medical College, Nanjing University, 210002 Nanjing, P. R. China.
Insights
Elevated beta-2 glycoprotein I-lipoprotein(a) complexes are a significant risk factor in pediatric nephrotic syndrome. Enhanced lipoprotein(a) oxidation contributes to their formation, suggesting a potential new biomarker.
Area of Science:
- Immunology
- Nephrology
- Cardiovascular Research
Background:
- Beta-2 glycoprotein I (β₂-GPI) complexes with lipoprotein(a) [β₂-GPI-Lp(a)] are found in circulation and elevated in autoimmune diseases.
- These complexes may play a role in pediatric idiopathic nephrotic syndrome (NS).
Purpose of the Study:
- To investigate β₂-GPI-Lp(a) concentrations in children with NS.
- To explore the relationship between β₂-GPI-Lp(a), serum lipids, oxidized lipoprotein, and renal function in pediatric NS.
- To assess the potential of β₂-GPI-Lp(a) as a biomarker for pediatric NS.
Main Methods:
- Serum concentrations of β₂-GPI-Lp(a) and oxidized Lp(a) [ox-Lp(a)] were measured using ELISAs in 80 NS children and 82 controls.
- Serum lipids and kidney function parameters were determined.
- Multivariate logistic regression analyzed the association between β₂-GPI-Lp(a) and NS.
Main Results:
- Children with NS showed significantly higher β₂-GPI-Lp(a) (0.95 U/ml vs 0.28 U/ml) and ox-Lp(a) (14.55 mg/l vs 2.60 mg/l) levels compared to controls (P<0.0001 for both).
- β₂-GPI-Lp(a) positively correlated with ox-Lp(a) (r=0.246, P=0.028) and ox-Lp(a) with Lp(a) (r=0.301, P=0.007) in NS children.
- Multivariate analysis revealed a strong independent association between NS and β₂-GPI-Lp(a) (OR=13.694, P<0.0001).
Conclusions:
- Elevated β₂-GPI-Lp(a) is an independent risk factor for pediatric NS.
- Increased Lp(a) oxidation contributes to the formation of β₂-GPI-Lp(a) complexes in pediatric NS.
Background:
The complexes of β₂-glycoprotein I (β₂-GPI) with lipoprotein(a) [β₂-GPI-Lp(a)] exist in human circulation and are increased in serum from patients with some autoimmune diseases. This study aims to investigate the concentration of β₂-GPI-Lp(a) in serum of children with idiopathic nephrotic syndrome (NS) and its relationship with serum lipids, oxidized lipoprotein and renal function parameters to explore the potential of the complexes as an additional marker for evaluating pediatric NS.
Methods:
Serum concentrations of β₂-GPI-Lp(a) complexes and oxidized Lp(a) [ox-Lp(a)] were measured by "Sandwich" ELISAs in 80 NS children and 82 age/sex-matched healthy controls. The levels of serum lipids and kidney parameters were also determined. Multivariate logistic regression analysis was performed to identify correlate of β₂-GPI-Lp(a) and NS.
Results:
The serum concentrations of β₂-GPI-Lp(a) complexes in children with NS were significantly higher than those in controls (median 0.95 U/ml vs 0.28 U/ml, P<0.0001). Ox-Lp(a) levels were also markedly elevated (median 14.55 mg/l vs 2.60 mg/l, P<0.0001] in NS children. The concentrations of β₂-GPI-Lp(a) were positively correlated with ox-Lp(a) (r=0.246, P=0.028), but not with Lp(a) level, and the concentrations of ox-Lp(a) were positively related with Lp(a) (r=0.301, P=0.007) in NS children. Multivariate logistic regression analysis identified a positive association between NS and β₂-GPI-Lp(a) (OR=13.694, 95% CI 6.400-29.299, P<0.0001), after adjusting for kidney function parameters, serum lipids and ox-Lp(a).
Conclusions:
Elevated β₂-GPI-Lp(a) level was an independent and significant risk factor for pediatric NS and, enhanced Lp(a) oxidation partly contributes to the formation of β₂-GPI-Lp(a) complexes.
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