Plasminogen Activator Inhibitor Type 1 Gene Polymorphism in Patients with Minimal Change Nephrotic Syndrome.
- Author:
Young Min KIM
1
;
Hyun Kee HONG
;
Sung Do KIM
;
Byoung Soo CHO
Author Information
1. East-West Kidney Disease Research Institute, School of Medicine, College of Medicine, Kyung-Hee University, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Plasminogen activator inhibitor type 1;
Polymorphism;
Nephrotic Syndrome
- MeSH:
Child;
DNA;
Genotype;
Humans;
Nephrosis, Lipoid*;
Nephrotic Syndrome;
Plasminogen Activator Inhibitor 1;
Plasminogen Activators*;
Plasminogen*;
Polymerase Chain Reaction;
Polymorphism, Restriction Fragment Length;
Promoter Regions, Genetic;
Thrombophilia;
Urokinase-Type Plasminogen Activator
- From:Journal of the Korean Society of Pediatric Nephrology
2004;8(1):26-32
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Hypercoagulability is present in patients with nephrotic syndrome. Plasminogen activator inhibitor type 1(PAI-1) is a major inhibitor of plasminogen activators. PAI-1 inactivates both tissue plasminogen activator(tPA) and urokinase plasminogen activator(uPA) by rapid formation of inactive 1:1 stoichiometric complexes. Recently some studies showed that the enhanced PAI-1 expression may be involved in the intraglomerular fibrinogen/fibrin- related antigen deposition seen in nephrotic syndrome. METHODS: PAI-1 gene promoter -844(G/A) polymorphism was evaluated in 146 children with minimal change nephrotic syndrome(MCNS) and 230 control subjects. The patients with MCNS were subdivided into 85 infrequent-relapser(IR) group and 61 frequent relapser(FR) group. PCR of PAI-1 gene promoter region including -844(G/A) and RFLP using the restriction enzyme Xho1 were performed for each DNA samples extracted from the groups. RESULTS: The distribution of PAI-1 genotype in the control group was G/G 81(32.5%), A/A 42(16.9%), and G/A 126(50.6%). The distribution of PAI-1 genotypes in the IR group of MCNS was G/G 29(34.1%), A/A 15(17.7%), and G/A 41(48.2%). The distribution of PAI-1 genotype in the FR group of MCNS was G/G 17(27.9%), A/A 18(29.5%), and G/A 26(42.6 %). There was a significantly increased frequency of A/A genotype(P=0.0251) in the FR group of MCNS. CONCLUSION: Our results indicate that the PAI-1 gene promoter A/A genotype may be associated with the FR in MCNS.
