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Treatment of focal segmental glomerulosclerosis.

Abstract
The prognosis of untreated patients with focal segmental glomerulosclerosis is poor, as the disease progress to end-stage renal disease in approximately 50--70% of nephrotic patients. Although focal segmental glomerulosclerosis was initially considered to be a steroid-resistant disease, several studies have shown a better responsiveness to more prolonged courses of steroids. For patients with steroid-resistant or -dependent focal segmental glomerulosclerosis, cyclosporine A and cytotoxic agents have shown efficacy in clinical trials. Plasmapheresis or LDL-apheresis may represent a rescue treatment in patients who do not respond to other therapies. The role of other agents used in focal segmental glomerulosclerosis, including azathioprine, mycophenolate mofetil, tacrolimus, pefloxacin or vitamin E is still poorly defined.
AuthorsP Passerini, C Ponticelli
JournalCurrent opinion in nephrology and hypertension (Curr Opin Nephrol Hypertens) Vol. 10 Issue 2 Pg. 189-93 (Mar 2001) ISSN: 1062-4821 [Print] England
PMID11224693 (Publication Type: Journal Article, Review)
Chemical References
  • Adrenal Cortex Hormones
  • Antineoplastic Agents
  • Purines
  • Vitamin E
  • Pefloxacin
  • Cyclosporine
  • Tacrolimus
Topics
  • Adrenal Cortex Hormones (therapeutic use)
  • Antineoplastic Agents (therapeutic use)
  • Blood Component Removal
  • Cyclosporine (therapeutic use)
  • Drug Resistance
  • Glomerulosclerosis, Focal Segmental (drug therapy, therapy)
  • Humans
  • Immunosorbent Techniques
  • Pefloxacin (therapeutic use)
  • Purines (biosynthesis)
  • Tacrolimus (therapeutic use)
  • Vitamin E (therapeutic use)

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