Author:
Oikawa S,Matsunaga A,Saito T,Sato H,Seki T,Hoshi K,Hayasaka K,Kotake H,Midorikawa H,Sekikawa A,Hara S,Abe K,Toyota T,Jingami H,Nakamura H,Sasaki J
Abstract
Lipoprotein glomerulopathy (LPG) is a novel disease characterized by proteinuria, lipoprotein thrombi in the glomeruli, and increased concentration of plasma apolipoprotein (apo) E. It is believed that a genetic disorder of apo E may be present and associated with the disease. Three patients with LPG were examined in this study. The patients' DNA sequences were analyzed, and a nucleotide G to C point mutation in exon 4 of the apo E gene was confirmed in each patient. This missense mutation denotes amino acid substitution of the proline residue for arginine residue at position 145 of apo E. This variant (apo E Sendai) may cause a marked molecular conformational change of the apo E. These findings suggest that a novel variant is etiologically related to LPG.
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
Cited by
52 articles.
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