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Glomerulonephritis (GN)

Written and reviewed by practising UK GPs, overseen by our Clinical Advisory Officer.

🧭 When to suspect

Glomerulonephritis (GN) is a group of mostly immune-mediated disorders in which inflammation damages the glomeruli – the kidney's filtering units. It is not one disease but a final common pathway for conditions ranging from IgA nephropathy (immunoglobulin A nephropathy, the commonest primary GN) to lupus and the small-vessel vasculitides.

The two cardinal urinary findings are haematuria (visible or non-visible) and proteinuria, and their combination – particularly with reduced kidney function – should always raise the possibility of glomerular disease. GN usually declares itself as one of two clinical pictures: a nephritic syndrome (an inflammatory, “active” urine) or a nephrotic syndrome (a heavy-protein-leak picture). Many patients sit between the two, and some are picked up only on an incidental abnormal urine dip or blood test.

The job in primary care is fourfold: recognise the pattern, never miss rapidly progressive disease, refer for the diagnosis (kidney biopsy), and start supportive treatment that protects the kidney while specialists decide on immunosuppression.

Nephritic syndrome (inflammatory) Nephrotic syndrome (heavy proteinuria)

Haematuria – often visible, smoky or “coca-cola”; dysmorphic red cells and red-cell casts.

Proteinuria, usually sub-nephrotic.

Hypertension and oliguria.

Rising creatinine / AKI is common.

• Typical causes: IgA nephropathy, post-streptococcal GN, ANCA or anti-GBM vasculitis, lupus nephritis.

Heavy proteinuria – uPCR > 300 mg/mmol (≈ > 3.5 g/24h); frothy urine.

Hypoalbuminaemia (albumin < 30 g/L).

Marked oedema – periorbital, peripheral, ascites.

Hyperlipidaemia; kidney function often preserved early.

• Typical causes: minimal change disease (children), membranous nephropathy (adults), FSGS, diabetic kidney disease.

Suspect GN in anyone with unexplained haematuria and proteinuria, unexplained acute kidney injury (AKI) or chronic kidney disease (CKD), new oedema, or new hypertension in a young person. A history of recent infection (streptococcal sore throat or skin infection) or features of systemic disease – rash, joint pain, haemoptysis – points towards a specific cause.

Source: UK Kidney Association · NICE NG203


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