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Björn Peters, Joachim Beige, Justyna Siwy, Michael Rudnicki, Ralph Wendt, Alberto Ortiz, Ana Belen Sanz, Harald Mischak, Heather Reich, Salmir Nasic, Dana Mahmood, Anders Persson, Anders Fernström, Maria Weiner, Bernd Stegmayr, #2561 URINE PROTEOMICS FOR PREDICTION OF DISEASE PROGRESSION IN PATIENTS WITH IGA NEPHROPATHY, Nephrology Dialysis Transplantation, Volume 38, Issue Supplement_1, June 2023, gfad063c_2561, https://doi.org/10.1093/ndt/gfad063c_2561
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Abstract
IgA nephropathy (IgAN) may lead to kidney failure. The urinary proteomics biomarker-based classifier (IgAN237) may predict progression at the time of kidney biopsy [1]. We now studied whether IgAN237 predicts disease progression not only at the time of biopsy but also later in the course of IgAN.
Urine samples from 103 patients with biopsy-proven IgAN were analyzed using capillary electrophoresis-mass spectrometry at baseline (IgAN237 score-1) and 89 also at follow-up (IgAN237 score-2). Patients were grouped into ‘non-progressors’ (IgAN237 score ≤0.38 Units) and ‘progressors’ (IgAN237 score >0.38 Units). Historical and follow-up data included, e.g., estimated glomerular filtration rate (eGFR)-slopes, urinary albumin/creatinine ratio (UACR)-slopes and medication. Multiple logistic regression analysis, using a stepwise model, was done with progressors and non-progressors as dependent factors including explanatory variables age, sex, eGFR- and UACR-slopes.
Median age at biopsy was 44 years (range 11-92); 63% were male. Median interval between biopsy and IgAN237 score-1 was 65 months (0-606), and between IgAN237 score-1 and score-2 was 258 days (71-531). IgAN237 score-1 and score-2 values did not differ significantly and were correlated (rho = 0.44, p<0.001). Twenty-eight and 26% of patients were classified as progressors based on IgAN237 score-1 and score-2, respectively. The IgAN237 score inversely correlated with the chronic eGFR slopes (rho = -0.278, p = 0.02 for score-1; rho = -0.409, p = 0.002 for score-2) and with ±180days eGFR slopes (rho = -0.31, p = 0.009 and rho = -0.439, p = 0.001, respectively) (Figure 1). The ±180days eGFR-slopes were more reduced for progressors than non-progressors (median -5.98 versus -1.22 mL/min/1.73m2 per year for score-1, p<0.001; -3.02 vs 1.08 mL/min/1.73m2 per year for score-2, p = 0.047) (Figure 2). The only significant variable maintained in a multiple logistic regression analysis for IgAN237 score-1 (progressor vs non-progressor) was ±180days eGFR slope (p<0.001) and for IgAN237 score-2 the UACR (p = 0.002) and age at baseline (p = 0.016).

Correlation between IgAN237 score-1 (A) and IgAN237 score-2 (B) with ±180days eGFR-slope (eGFR180days-slope).

Boxplot of comparisons of progressors (IgAN237>0.38) vs non-progressors (IgAN237≤0.38) and ±180days eGFR-slope (eGFR180days-slope) (mL/min/1.73m2 per year) in IgAN237 score-1 (A) and IgAN237 score-2 (B).
The urinary IgAN237 classifier represents a risk stratification tool in IgAN not only at the time of biopsy but also later in the course of the disease. It may guide physicians in management and follow-up strategies in an individualized manner.
Reference
- albumins
- biopsy
- creatinine
- kidney failure
- biological markers
- disease progression
- electrophoresis
- follow-up
- iga glomerulonephritis
- urinary tract
- blood capillaries
- urine
- renal biopsy
- proteomics
- stratification
- urine albumin/creatinine ratio
- glomerular filtration rate, estimated
- box plot
- urine specimens
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