Apolipoprotein E ɛ4 allele and nephrotic glomerular diseases in children

被引:0
作者
T. Asami
T. Ciomartan
H. Hayakawa
M. Uchiyama
S. Tomisawa
机构
[1] Department of Pediatrics,
[2] School of Medicine,undefined
[3] Niigata University,undefined
[4] Asahimachi-dori 1–757,undefined
[5] Niigata,undefined
[6] Japan e-mail: asamitds@med.niigata-u.ac.jp Tel.: +81-25-227-2216,undefined
[7] Fax: +81-25-227-0778,undefined
[8] Department of Pediatrics,undefined
[9] Niigata Sanitation Hospital,undefined
[10] Niigata,undefined
[11] Japan,undefined
来源
Pediatric Nephrology | 1999年 / 13卷
关键词
Key words Apolipoprotein E phenotype; Nephrotic syndrome; Focal segmental glomerulosclerosis;
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摘要
 Hyperlipidemia is a well-recognized complication of the nephrotic syndrome and is a factor contributing to the progression of the initial glomerular injury and the development of glomerulosclerosis. Apolipoprotein E (apoE) is a plasma protein and apoE ɛ 4 allele is associated with higher plasma cholesterol levels. With this in mind, we studied apoE phenotypes and alleles in children with nephrotic glomerular diseases (NGD, n=29), including idiopathic nephrotic syndrome (n=16), membranoproliferative glomerulonephritis (n=7), and focal segmental glomerulosclerosis (FSGS, n=6). Children with NGD had a higher ɛ 4 allele frequency (20.7%) than controls (10.8%), and those with FSGS had both higher apoE4/3 (66.7%) and ɛ 4 allele (33.3%) frequencies than controls (20.4% and 10.8%, respectively). In IgA nephropathy (n=30, disease controls), no significant association with specific apoE was found. Further studies are needed to clarify the significance of the observed high frequencies of apoE ɛ 4 allele in children with NGD and apoE4/3 phenotype distribution in FSGS.
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页码:233 / 236
页数:3
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