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Glomerular Disease Quiz
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Which pathological process best explains the underlying cause of Berger disease?
- A IgA deposition in the mesangium causing inflammation You picked ✓
- B Amyloid protein deposition within the renal interstitium You picked ✕
- C Immune complex-mediated glomerular inflammation following streptococcal infection You picked ✕
- D Ischaemic damage to glomeruli due to chronic hypertension You picked ✕
- E Autoantibody-mediated destruction of the glomerular basement membrane You picked ✕
Correct!
Incorrect
The answer is A: IgA deposition in the mesangium causing inflammation
Explanation
Why A is correct
See IgA Nephropathy. Option A is correct: Berger disease (IgA nephropathy) is caused by IgA deposition in the mesangium of the glomerulus, which triggers an inflammatory response and damages the mesangium. The mesangium is the supporting tissue lying between the glomerular capillary loops. IgA (immunoglobulin A) is the antibody that protects the mucous membranes, such as those of the airways and gut, so the disease is often triggered by a mucosal infection. In a patient with an upper respiratory tract infection, over-activation of IgA can cause it to be deposited in the glomerulus. The deposits cause mesangial cell proliferation and damage, so the classic presentation is visible or invisible haematuria (blood in the urine, either seen by eye or found only on testing) one to two days after a throat infection, with or without proteinuria. Serum IgA is often raised and complement (C3 and C4, a group of immune proteins) is normal. IgA nephropathy is the most common cause of nephritic syndrome, although it can also present as nephrotic syndrome. There is no specific effective treatment, but ACE inhibitors or angiotensin receptor blockers help control proteinuria (protein in the urine) and blood pressure. Memory aid: IgA nephropathy brings IgA to the mesangium.
- Cause: deposition of IgA in the mesangium of the glomerulus, which triggers inflammation.
- Trigger: often a mucosal infection, such as an upper respiratory tract infection.
- Presentation: visible or invisible haematuria one to two days after a throat infection, with or without proteinuria.
- Tests: serum IgA is often raised and complement (C3 and C4) is normal.
Why the other options are incorrect
- B. Amyloid protein deposition within the renal interstitium: Amyloid deposition within the kidney describes amyloidosis, which causes nephrotic syndrome. It has no link to IgA deposition in the mesangium. Your answer
- C. Immune complex-mediated glomerular inflammation following streptococcal infection: Immune complex glomerulonephritis after a streptococcal infection describes post-streptococcal glomerulonephritis. It typically arises after a delay and is associated with a low complement level, unlike IgA nephropathy. Your answer
- D. Ischaemic damage to glomeruli due to chronic hypertension: Ischaemic damage from chronic hypertension causes hypertensive nephrosclerosis, a scarring process. It is not an immune-mediated nephritis. Your answer
- E. Autoantibody-mediated destruction of the glomerular basement membrane: Autoantibody attack on the glomerular basement membrane is the mechanism of anti-GBM disease (Goodpasture disease). IgA nephropathy is caused by deposits in the mesangium. Your answer
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1
Which of the following findings is most characteristic of nephritic syndrome?
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Which underlying immunological mechanism best explains why patients with systemic lupus erythematosus can present with either nephritic or nephrotic patterns of kidney disease?
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