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Cyclooxygenase-2 inhibitor-associated minimal-change disease
M Almansori1, T Kovithavongs, M U Qarni
1Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Selective cyclooxygenase-2 (COX-2) inhibitors, like celecoxib, can cause kidney damage, including minimal-change disease and acute tubular necrosis. Patients on these drugs presenting with nephrotic syndrome require careful renal monitoring.
Area of Science:
- Nephrology
- Pharmacology
- Internal Medicine
Background:
- Selective cyclooxygenase-2 (COX-2) inhibitors offer anti-inflammatory and analgesic benefits with reduced gastrointestinal risks compared to nonselective NSAIDs.
- However, data on the non-gastrointestinal toxicity, particularly nephrotoxicity, of COX-2 inhibitors remain limited.
- Nonsteroidal anti-inflammatory drugs (NSAIDs) are known for nephrotoxic effects, including minimal-change disease (MCD) with interstitial nephritis.
Observation:
- This report details a case of MCD and acute tubular necrosis (ATN) in a patient treated with celecoxib, a COX-2 inhibitor.
- Unlike a previous report, this case did not involve interstitial nephritis.
- While proteinuria resolved after celecoxib discontinuation, renal function did not fully recover.
Findings:
- Celecoxib, a selective COX-2 inhibitor, can induce minimal-change disease and acute tubular necrosis.
- Renal function may not recover completely even after drug withdrawal.
- This adverse renal effect highlights potential risks beyond the gastrointestinal tract.
Implications:
- Heightened clinical suspicion for COX-2 inhibitor-induced nephrotoxicity is warranted in patients presenting with nephrotic syndrome.
- Further research is needed to fully elucidate the spectrum of renal adverse effects associated with COX-2 inhibitors.
- This case underscores the importance of monitoring renal function in patients receiving selective COX-2 inhibitors.
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