Back to Search
Start Over
Common Apolipoprotein E Gene Mutations Contribute to Lipoprotein Glomerulopathy in China.
- Source :
- Nephron Clinical Practice; Apr2010, Vol. 114 Issue 4, pc260-c267, 8p, 1 Color Photograph, 3 Diagrams, 2 Charts
- Publication Year :
- 2010
-
Abstract
- Background: Lipoprotein glomerulopathy (LPG) is a unique disease characterized by thrombus-like lipoprotein deposition in glomeruli and an increased serum apolipoprotein E level (ApoE protein or APOE gene). Several APOE mutations contribute to the occurring of LPG. Methods: We confirmed LPG in 7 individuals by renal biopsy, and investigated families of 2 patients with urinalysis, serum creatinine and serum lipid examination. Exons of APOE of all individuals as well as their relatives were amplified and sequenced directly. Results: Two types of APOE mutations were identified in the 7 patients and their relatives. APOE Maebashi (Arg142-Leu144→0) heterozygotes were found in 5 individuals who were from 4 different families. APOE Kyoto (Arg25-Cys) was confirmed heterogeneous in another 2 individuals. Both mutations present incomplete penetrance. Conclusion: Our research indicates that APOE Maebashi (Arg142-Leu144→0) is a common mutation in Chinese LPG. However, not all carriers of the 2 mutations have LPG, although hyperlipidemia and high serum ApoE level are tested. There are likely other reasons, such as a local mechanism in the glomeruli, which participated in the renal injury. Copyright © 2010 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 16602110
- Volume :
- 114
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- Nephron Clinical Practice
- Publication Type :
- Academic Journal
- Accession number :
- 49158722
- Full Text :
- https://doi.org/10.1159/000276578