IgA nephropathy is a glomerulonephritis that is characterised by macroscopic haematuria.
It is the most common cause of glomerulonephritis. The incidence peaks between 20 and 30 years, and is more common in men than women.
- Risk factors
- Young adult
- Family history
- Recent mucosal infection
- Pathophysiology
- Inherited or acquired defects in glycosylation → abnormal overproduction of galactose-deficient IgA1
- Increased production or reduced clearance of IgA-containing immunce complexes in chronic liver disease, coeliac disease, inflammatory bowel disease, and HIV
- Infection → deposition of IgA immune complexes in the mesangium
- Patient history
- Young adult
- Recent upper restpiratory tract or gastrointestinal infection
- Signs and symptoms
- Macroscopic haematuria
- Recurrent episodes
- Macroscopic haematuria
- Differentials
- Investigations
- Biopsy
- Mesangial IgA deposits on immunofluorescence
- Biopsy
- Treatment
- Regular monitoring of renal function and blood pressure
- Reduced protein intake if proteinuria is pressent
- Smoking cessation
- Weight management
- Blood pressure control with ACE inhibitors or ARBs
- These can also be used to reduce proteinuria
- Statins if dyslipidaemia is present
- Immunosuppresive treatment for patients with rapidly progressing disease or severe proteinuria
- Corticosteroids
- Complications
- Rapidly progressive glomerulonephritis