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Proteinuria 24th June 2011 Rachel Lennon The Spectrum of Glomerular Disease SLE Minimal change IgA nephropathy Membranous FSGS Diabetic nephropathy Anti-GBM disease MCGN Proteinuria Post infectious nephritis Small vessel vasculitis Endothelial cells GBM Podocyte 1 million in each adult human kidney Glomerular filtration barrier 180 litres of water and small solutes- almost no proteins Glomerular endothelial cells GBM Slit diaphragm Podocytes Mundel et al: Kidney International 2010 77 (7) p571-80 Definition • Protein:creatinine ratio (PCR) – 20mg/mmol – 200mg/mmol nephrotic range • Albumin: creatinine ratio (ACR) – 30mg/mmol Case-1 • • • • 13 year old boy No PMH/FH renal disease BP and renal function normal Incidental finding – Urinalysis: 2+protein – Mild proteinuria (PCR 20-50) • 3 early morning urines: PCR • Orthostatic proteinuria Case-2 • 5 year old boy • BP and renal function normal • Urinalysis 2+ protein, 2+ blood – – – – PCR 40-50 ACR 20 Calcium:creatinine: 1.5mmol/mmol USS: Nephrocalcinosis • NAG/RBP:creatinine • Dent’s disease: CLC5/OCRL-1 mutations Case-3 • 8 year girl – PMH: Bilateral VUR and recurrent UTI – FH: VUR • DMSA: Bilateral renal scarring • BP normal, eGFR 65ml/min/1.73m2 • Urinalysis 2+ protein PCR 30-50 • Enalapril 5mg od • Renal function before and at 2 weeks • Reflux nephropathy Case-4 • • • • • • 8 year old girl HSP Urinalysis: Protein 3+, blood 2+ PCR 100-150: Persistent at 4 weeks BP 95th centile Normal renal function • Renal biopsy: Crescentic GN, IgA deposition • Steroids/Azathioprine/Enalapril • HSP nephritis Summary • Investigate persistent proteinuria – Orthostatic – Tubular disease – Nephropathy • Use of anti-proteinuric agents to limit secondary injury