Abstract | BACKGROUND: METHODS: We studied 199 patients with idiopathic MN followed up for 3.7 ± 3.2 years. We enrolled 33 patients with secondary MN and 356 subjects with normal blood pressure and no proteinuria. PLA2R single nucleotide polymorphisms (SNPs) were genotyped. RESULTS: The allele frequencies of C in rs35771982 and G in rs3828323 were 73.6 and 73.9%, respectively. Subjects with the CC genotype in rs35771982 had a higher susceptibility to idiopathic MN compared to subjects with other genotypes (odds ratio 2.6; 95% confidence interval 1.8-4.0). Patients with secondary MN were not different from controls with regard to PLA2R genotype. No impact of genetic polymorphisms on renal survival was detected. CONCLUSION: The findings of this study suggest that PLA2R SNPs might be associated with the risk of developing MN.
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Authors | Sejoong Kim, Ho Jun Chin, Ki Young Na, Suhnggwon Kim, Jieun Oh, Wookyung Chung, Jung Woo Noh, Young Ki Lee, Jong Tae Cho, Eun Kyoung Lee, Dong-Wan Chae, Progressive Renal Disease and Medical Informatics and Genomics Research (PREMIER) members |
Journal | Nephron. Clinical practice
(Nephron Clin Pract)
Vol. 117
Issue 3
Pg. c253-8
( 2011)
ISSN: 1660-2110 [Electronic] Switzerland |
PMID | 20805699
(Publication Type: Comparative Study, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2010 S. Karger AG, Basel. |
Chemical References |
- Receptors, Phospholipase A2
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Topics |
- Adult
- Aged
- Female
- Follow-Up Studies
- Genetic Predisposition to Disease
(genetics)
- Glomerulonephritis, Membranous
(diagnosis, genetics)
- Humans
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
(genetics)
- Receptors, Phospholipase A2
(genetics)
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