Halitosis in cystinosis patients after administration of immediate-release cysteamine bitartrate compared to delayed-release cysteamine bitartrate

Mol Genet Metab. 2012 Sep;107(1-2):234-6. doi: 10.1016/j.ymgme.2012.06.017. Epub 2012 Jul 6.

Abstract

Halitosis due to dimethylsulfide (DMS) generation is a major side effect of cysteamine in the treatment of cystinosis. Recently, an enteric coated formulation of cysteamine bitartrate (RP103) administered twice daily was demonstrated to be non-inferior for lowering WBC cystine levels compared to the non-enteric coated formulation (Cystagon®), administered 4 times per day. Since both formulations had different pharmacokinetic profiles, we compared DMS breath levels after administration of either RP103 or Cystagon® in four cystinosis patients. Although cysteamine areas under the curve (AUCs) were comparable, AUC of DMS was lower after the administration of RP103 compared to Cystagon®. This observation is of importance in cystinosis patients, since halitosis hampers compliance with cysteamine therapy.

MeSH terms

  • Adolescent
  • Child
  • Cysteamine / administration & dosage
  • Cysteamine / pharmacokinetics
  • Cysteamine / therapeutic use*
  • Cystinosis / complications*
  • Cystinosis / drug therapy*
  • Exhalation
  • Halitosis / diagnosis
  • Halitosis / etiology*
  • Humans
  • Male
  • Sulfides / metabolism
  • Young Adult

Substances

  • Sulfides
  • Cysteamine
  • dimethyl sulfide