Glomerulonephritis (GN) involves inflammation of the kidney's glomeruli. The complement system is part of the immune response. In certain types of GN, immune complexes activate the complement cascade, leading to its consumption and thus, low levels (hypocomplementemia), particularly C3 and C4.
Several conditions commonly present with glomerulonephritis and low complement levels due to immune complex deposition:
IgA nephropathy is characterized by deposits of Immunoglobulin A (IgA) in the glomeruli. While it is an immune-mediated glomerular disease, it is typically associated with normal or sometimes elevated complement levels. Unlike SBE, SLE, and cryoglobulinemia, significant complement consumption is not a hallmark feature of IgA nephropathy.
Therefore, IgA nephropathy is the condition listed that is NOT consistently associated with glomerulonephritis presenting with low complement levels.
A 40-year-old female with nephritic range proteinuria is found to have low serum complement levels. Which of the following can be the likely etiology?
1. Systemic lupus erythematosus
2. Post-infectious glomerulonephritis
3. Infective endocarditis
4. Mesangio-capillary glomerulonephritis
Select the correct answer using the code given below:
Match list I with list II and select the correct answer using the code given below the lists:
| List I (Urine exam) | List II (Disease) |
|---|---|
| A. Red cell casts | 1. Nephrotic syndrome |
| B. Microscopic haematuria | 2. Chronic renal failure |
| C. Proteinuria | 3. Polycystic kidney disease |
| D. Broad cell casts | 4. Glomerulonephritis |