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Published on: August 19, 2020
Urinary CD80 is elevated in minimal change disease but not in focal segmental glomerulosclerosis
Eduardo H Garin1, Wei Mu, John M Arthur
1Department of Pediatrics, University of Florida, Gainesville, Florida 32610, USA. garineh@peds.ufl.edu
Abstract:
Controversy exists as to whether minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) represent different diseases or are manifestations within the same disease spectrum. Urinary excretion of CD80 (also known as B7.1) is elevated in patients with MCD and hence we tested whether urinary CD80 excretion might distinguish between patients with MCD from those with FSGS. Urinary CD80 was measured in 17 patients with biopsy-proven MCD and 22 with proven FSGS using a commercially available enzyme-linked immunosorbent assay and its molecular size determined by western blot analysis. A significant increase in urinary CD80, normalized to urinary creatinine, was found in patients with MCD in relapse compared to those in remission or those with FSGS. No significant differences were seen when CD80 urinary excretion from MCD patients in remission were compared to those with FSGS. In seven of eight MCD patients in relapse, CD80 was found in glomeruli by immunohistochemical analysis of their biopsy specimen. No CD80 was found in glomeruli of two patients with FSGS and another MCD patient in remission. Thus, our study supports the hypothesis that MCD and FSGS represent two different diseases rather than a continuum of one disease. Urinary CD80 excretion may be a useful marker to differentiate between MCD and FSGS.
Insights
Urinary CD80 (B7.1) levels can help differentiate minimal change disease (MCD) from focal segmental glomerulosclerosis (FSGS). Elevated urinary CD80 in relapsed MCD patients suggests they are distinct diseases, not a spectrum.
Area of Science:
- Nephrology
- Immunology
- Biochemistry
Background:
- Minimal change disease (MCD) and focal segmental glomerulosclerosis (FSGS) are nephrotic syndromes with debated classification.
- Urinary CD80 (B7.1) is elevated in active MCD, prompting investigation into its diagnostic potential.
Purpose of the Study:
- To determine if urinary CD80 excretion can distinguish between MCD and FSGS.
- To investigate the presence of CD80 in renal glomeruli of patients with MCD and FSGS.
Main Methods:
- Urinary CD80 levels were measured in 17 MCD and 22 FSGS patients using ELISA.
- Molecular size of urinary CD80 was analyzed by western blot.
- Glomerular CD80 expression was assessed via immunohistochemistry on kidney biopsy specimens.
Main Results:
- Urinary CD80, normalized to creatinine, was significantly higher in relapsed MCD patients compared to MCD in remission or FSGS patients.
- No significant difference in urinary CD80 was observed between MCD patients in remission and FSGS patients.
- Glomerular CD80 was detected in 7/8 relapsed MCD patients but not in FSGS or remitted MCD patients.
Conclusions:
- MCD and FSGS likely represent distinct diseases, not a single disease spectrum.
- Urinary CD80 excretion may serve as a valuable biomarker for differentiating active MCD from FSGS.
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