# Keratin Expression in Podocytopathies, ANCA-Associated Vasculitis and IgA Nephropathy

## TL;DR

This study explores how keratin proteins in kidney cells relate to kidney disease severity and outcomes in various glomerular diseases.

## Contribution

The study identifies keratin expression patterns as potential biomarkers for predicting kidney function outcomes in glomerular diseases.

## Key findings

- ANCA vasculitis patients showed significantly higher glomerular keratin expression compared to controls and MCD patients.
- Tubular expression of keratins 7, 8, and 19 was associated with kidney outcomes across all groups.
- Patients with crescents exhibited elevated keratin expression in both glomeruli and tubulointerstitial areas.

## Abstract

Keratins are the main components of the cell cytoskeleton of epithelial cells. Epithelial cells under stressful stimuli react by modifying their keratin expression pattern. Glomerular diseases are pathological conditions that may lead to loss of kidney function if not timely diagnosed and treated properly. This study aims to examine glomerular and tubular keratin expression in podocytopathies, ANCA-associated vasculitis, and IgA nephropathy and how this expression correlates to clinical outcomes. We included 45 patients with podocytopathies (minimal change disease and focal segmental glomerulosclerosis), ANCA-associated vasculitis, and IgA nephropathy, with or without crescentic lesions, and healthy controls. All tissues were assessed by photon microscopy and immunohistochemistry. Biopsy sections were examined for keratins 7, 8, 18, and 19 expression in the glomerular and tubulointerstitial areas separately. Moreover, we examined how keratin expression was correlated with long-term kidney function outcomes. All four studied keratins had significantly increased glomerular expression in patients with ANCA vasculitis compared to controls and MCD patients. Tubular expression of keratins 7, 8, and 19 was related to kidney outcome in all groups. Patients with crescents had higher expression of all keratins in both glomeruli and tubulointerstitium. The presence of tubular atrophy, interstitial fibrosis, mesangial hyperplasia, and interstitial inflammation did not affect keratin expression. Keratins, an abundant component of renal epithelial cells, have the potential to be featured as a biomarker for kidney function prognosis in patients with glomerular diseases.