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Prominence of slow acetylator phenotype among patients with sulfonamide hypersensitivity reactions
Author(s) -
Rieder Michael J,
Shear N H,
Kanee A,
Tang B K,
Spielberg Stephen P
Publication year - 1991
Publication title -
clinical pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.941
H-Index - 188
eISSN - 1532-6535
pISSN - 0009-9236
DOI - 10.1038/clpt.1991.3
Subject(s) - sulfonamide , caffeine , acetylation , detoxification (alternative medicine) , phenotype , pharmacology , medicine , metabolism , pharmacogenetics , population , chemistry , biochemistry , genotype , pathology , gene , stereochemistry , alternative medicine , environmental health
Delayed hypersensitivity reactions are among the most severe adverse effects of the sulfonamides in current clinical use. These reactions appear to occur because of differences in the metabolism and detoxification of reactive metabolites of the sulfonamides. N ‐Acetylation is a major metabolic pathway for the sulfonamides. Slow acetylation phenotype might be a risk factor for the development of these reactions. We determined the acetylation phenotype of 21 patients who had suffered hypersensitivity reactions to the sulfonamides. There were 11 females and 10 males in the group, with a mean age of 15 years (age range, 1.8 to 50 years). Their acetylator phenotype was determined by determining the ratio of urinary caffeine metabolites (1‐methylxanthine to 5‐amino‐6‐formylmethyluracil after an oral dose of 50 mg caffeine). Nineteen (90%) of the patients were slow acetylators compared to a 55% incidence of slow acetylators in a race‐matched control population (p < 0.008). This suggests that a slow acetylator phenotype is a risk factor for the development of sulfonamide hypersensitivity reactions and provides further support for the role of imbalances in genetically determined pathways of metabolism and detoxification of the sulfonamides in the pathogenesis of these reactions. Clinical Pharmacology and Therapeutics (1991) 49 , 13–17; doi: 10.1038/clpt.1991.3