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Danazol and stanozolol in long-term prophylactic treatment of hereditary angioedema.

Abstract
Treatment with 17 alpha-methyltestosterone and with some synthetic androgens prevents attacks of hereditary angioedema (HAE). However, the potential hepatotoxicity of 17 alpha-alkylated androgens raises the problem of long-term prophylactic use of these agents. Therefore we compared the efficacy in preventing HAE attacks of 17 alpha-alkylated steroids (danazol and stanozolol) with non-17 alpha-alkylated derivatives (quinbolone, nandrolone decanoate and mesterolone). As the latter group proved ineffective, it seems that a drug's efficacy in preventing HAE attacks is connected to its 17 alpha-alkylation. Moreover, our long-term observations with the minimum effective dose of danazol seem to indicate the absence of important collateral effects.
AuthorsA Agostoni, M Cicardi, G C Martignoni, L Bergamaschini, B Marasini
JournalThe Journal of allergy and clinical immunology (J Allergy Clin Immunol) Vol. 65 Issue 1 Pg. 75-9 (Jan 1980) ISSN: 0091-6749 [Print] United States
PMID6765962 (Publication Type: Journal Article)
Chemical References
  • Androstadienes
  • Complement C1 Inactivator Proteins
  • Complement C4
  • Pregnadienes
  • Mesterolone
  • Stanozolol
  • Nandrolone
  • Danazol
  • quinbolone
Topics
  • Adult
  • Androstadienes (administration & dosage)
  • Angioedema (drug therapy, genetics)
  • Complement C1 Inactivator Proteins
  • Complement C4
  • Danazol (administration & dosage, adverse effects, therapeutic use)
  • Female
  • Humans
  • Long-Term Care
  • Male
  • Mesterolone (administration & dosage)
  • Middle Aged
  • Nandrolone (administration & dosage)
  • Pregnadienes (administration & dosage)
  • Stanozolol (administration & dosage, therapeutic use)

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