Literature DB >> 24263531

CD80 and suPAR in patients with minimal change disease and focal segmental glomerulosclerosis: diagnostic and pathogenic significance.

Gabriel Cara-Fuentes1, Changli Wei, Alfons Segarra, Takuji Ishimoto, Christopher Rivard, Richard J Johnson, Jochen Reiser, Eduardo H Garin.   

Abstract

BACKGROUND: Minimal change disease (MCD) is characterized by increased urinary excretion of CD80, whereas focal segmental glomerulosclerosis (FSGS) is associated with increased serum soluble urokinase-type plasminogen activator receptor (suPAR). The aim of the study was to assess whether the simultaneous measurement of urinary CD80 and serum suPAR helps differentiate MCD and FSGS.
METHODS: Urine and sera were collected from patients with MCD in relapse or in remission, from FSGS patients with nephrotic syndrome, and from healthy individuals. CD80 and suPAR were measured by ELISA.
RESULTS: Urinary CD80 was significantly increased in MCD patients in relapse compared with those in remission and with FSGS patients and control individuals. Serum suPAR levels were significantly higher in patients with FSGS when compared with MCD patients in relapse. Urinary suPAR showed a positive correlation with proteinuria in MCD in relapse and FSGS patients, whereas urinary CD80 correlated with proteinuria only in MCD patients in relapse.
CONCLUSION: Urinary CD80 is elevated in MCD patients in relapse compared with FSGS patients. In contrast, serum suPAR is significantly elevated in FSGS patients. The consistent pattern of these two biomarkers in MCD and FSGS suggests that these two conditions represent different entities rather than a continuum spectrum of one disease.

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Year:  2013        PMID: 24263531      PMCID: PMC4136522          DOI: 10.1007/s00467-013-2679-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  18 in total

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5.  "The FSGS factor:" enrichment and in vivo effect of activity from focal segmental glomerulosclerosis plasma.

Authors:  M Sharma; R Sharma; E T McCarthy; V J Savin
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7.  Primary nephrotic syndrome in children: clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children.

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Review 8.  A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases.

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  29 in total

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2.  CD80 and suPAR: diagnostic and pathogenic value in minimal change disease and focal segmental glomerulosclerosis?

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Review 3.  Pathogenesis of childhood idiopathic nephrotic syndrome: a paradigm shift from T-cells to podocytes.

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4.  Urinary CD80 levels as a diagnostic biomarker of minimal change disease.

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Review 5.  Minimal change disease and idiopathic FSGS: manifestations of the same disease.

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6.  Urinary CD80 excretion is a predictor of good outcome in children with primary nephrotic syndrome.

Authors:  Chen Ling; Xiaorong Liu; Ying Shen; Zhi Chen; Jianfeng Fan; Yeping Jiang; Qun Meng
Journal:  Pediatr Nephrol       Date:  2018-03-22       Impact factor: 3.714

7.  CD80 and suPAR in patients with minimal change disease and focal segmental glomerulosclerosis: diagnostic and pathogenic significance: response.

Authors:  Gabriel Cara-Fuentes; Richard J Johnson; Jochen Reiser; Eduardo H Garin
Journal:  Pediatr Nephrol       Date:  2014-05-11       Impact factor: 3.714

8.  Podocyte Expression of B7-1/CD80: Is it a Reliable Biomarker for the Treatment of Proteinuric Kidney Diseases with Abatacept?

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Review 10.  Biomarkers in pediatric glomerulonephritis and nephrotic syndrome.

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