Cited by 25Renal Diseases and GlomerulopathiesChronic Kidney Disease and DiabetesSystemic Lupus Erythematosus Research

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis

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Bruschi, Maurizio, Catarsi, Paolo, Candiano, Giovanni, Rastaldi, Maria Pia, Musante, Luca, Scolari, Francesco, Artero, Mary, Carraro, Michele +8 more·2003·Kidney International

Abstract

Background Hyperlipemia characterizes nephrotic syndrome (NS) and contributes to the progression of the underlying nephropathy. The data in the literature support an implication of apolipoprotein E (apoE) in both hyperlipemia and focal segmental glomerulosclerosis (FSGS), a malignant condition associated with NS. Methods The apoE genotype was determined in 209 nephrotic patients, who were classified according to age and their response to steroids as resistant children (N = 96) and adults (43), and steroid dependent (33) and steroid responder (37) children. A total of 123 presented the histological features of FSGS. In a subgroup of 28 patients, serum and urinary levels of apoE and renal deposits were evaluated by immunofluorescence. Results The allelic frequencies of the three major haplotypes epsilon2, epsilon3, and epsilon4 were the same in nephrotic patients versus controls, and homozygosity for epsilon3epsilon3 was comparably the most frequent genotype (70 vs. 71%) followed by epsilon3epsilon4, epsilon2epsilon3, epsilon2epsilon4, epsilon4epsilon4. Serum levels of apoE were fivefold higher in NS and in FSGS patients than in controls, with a direct correlation with hypercholesterolemia and proteinuria. ApoE genotypes did not influence serum levels. Urinary levels were 1/10,000 of serum with an increment in nephrotic urines. Finally, immunofluorescence demonstrated the absence of apoE in sclerotic glomeruli, while comparably nephrotic patients with membranous nephropathy had…

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Crossref · 10.1046/j.1523-1755.2003.00777.x

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Authors
Bruschi, M., Catarsi, P., Candiano, G., Rastaldi, M. P., Musante, L., Scolari, F., Artero, M., Carraro, M., Carrea, A., Caridi, G., Zennaro, C., Sanna-Cherchi, S., Viola, F. B., Ferrario, F., Perfumo, F., & Ghiggeri, G. M.
Affiliations
Istituto Giannina Gaslini (IT)
Corresponding author
Ghiggeri, Gian Marco
Venue
Kidney International
Publisher
Elsevier BV
Published
2003-02
Volume
63
Issue
2
Pages
686-695
ISSN
0085-2538 (ISSN-L)
OpenAlex
W1991473040
Cited by
25
References
1
Citations by year
2026: 1 · 2023: 2 · 2022: 2 · 2021: 3 · 2020: 1 · 2018: 1 · 2017: 1 · 2015: 1 · 2014: 2 · 2013: 1 · 2012: 2
FWCI
0.42
Type
journal article
Language
en
Open access
Locations
  • Kidney International (publishedVersion)
  • PubMed (publishedVersion)
  • ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/) (submittedVersion)
  • Institutional Research Information System (Università degli Studi di Brescia) (submittedVersion)
  • CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion)
  • INFM-OAR (INFN Catania) (submittedVersion, other-oa)
  • Zenodo (CERN European Organization for Nuclear Research) (other-oa)
Topics
  • Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
  • Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
  • Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
Keywords
apolipoprotein E, idiopathic nephrotic syndrome, focal segmental glomerulosclerosis, hyperlipidemia, hypercholesterolemia, proteinuria, APOE genotype, membranous nephropathy, steroid resistance, lipid metabolism
MeSH terms
Adolescent, Adult, Apolipoproteins E, Child, Child, Preschool, Female, Genotype, Glomerulosclerosis, Focal Segmental, Humans, Kidney, Male, Nephrotic Syndrome, Cohort Studies

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