A new apolipoprotein E mutation, apoE Las Vegas, in a European-American with lipoprotein glomerulopathy
Author(s) -
Andrew S. Bomback,
Huijuan Song,
Vivette D. D’Agati,
Scott Cohen,
Alison Neal,
Gerald B. Appel,
Brad H. Rovin
Publication year - 2010
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfq389
Subject(s) - apolipoprotein e , medicine , lipoprotein , glomerulopathy , las vegas , apolipoprotein b , nephrotic syndrome , glomerulonephritis , disease , pathology , cholesterol , kidney , metropolitan area
Lipoprotein glomerulopathy is a rare disease diagnosed by unique histopathologic findings of glomerular capillary dilatation by lipoprotein thrombi. The disease is caused by mutations in apoE, the gene that encodes apolipoprotein E. To date, <80 cases have been reported in the medical literature, nearly all of which are from Japan or China. Only five cases from the United States have previously been reported, of which three patients were of European ancestry. Here, we present the fourth case of lipoprotein glomerulopathy in a European-American man. Whereas prior European-American patients with lipoprotein glomerulopathy were found to have the previously reported apoE Kyoto genotype, the patient presented here was found to have a novel mutation that we have named apoE Las Vegas.
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