NAT2 polymorphisms as a cause of metamizole-induced agranulocytosis
Autor: | Christian Dohna-Schwake, Birte Möhlendick, Winfried Siffert, Michael M. Schündeln, Burcin Dogan, Ivana Radulovic |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Epstein-Barr Virus Infections Herpesvirus 4 Human Neutropenia Arylamine N-Acetyltransferase Dizygotic twin Tonsillitis Medizin Dipyrone CYP2C19 030226 pharmacology & pharmacy Gastroenterology 03 medical and health sciences 0302 clinical medicine Internal medicine Genetics medicine Humans General Pharmacology Toxicology and Pharmaceutics Molecular Biology Genetics (clinical) business.industry Anti-Inflammatory Agents Non-Steroidal medicine.disease Metamizole Hemolysis 030104 developmental biology Toxicity Molecular Medicine Female business Pharmacogenetics medicine.drug |
Zdroj: | Pharmacogenetics and genomics. 31(6) |
ISSN: | 1744-6880 |
Popis: | Metamizole is a widely prescribed NSAID with excellent analgesic and antipyretic properties. Although very effective, it is banned in some countries because of the risk for severe agranulocytosis. We here describe three patients with metamizole-associated agranulocytosis. Patient #1 suffered from agranulocytosis and tonsillitis followed by severe sepsis by Streptococcus pneumoniae and Epstein-Barr virus reactivation. Her dizygotic twin sister (patient #2) also suffered from agranulocytosis after a surgical intervention. Patient #3 initially had a tonsillitis and also developed neutropenia after metamizole intake. For all patients, pharmacogenetic diagnostic for the genes CYP2C9, CYP2C19 and NAT2, which are involved in metamizole metabolism and degradation of toxic metabolites, was initiated. Pharmacogenetic analysis revealed NAT2 slow acetylator phenotype in all three patients. Additionally, patient #2 is an intermediate metabolizer for CYP2C19 and patient #3 is a poor metabolizer for CYP2C9. Impairment of these enzymes causes a reduced degradation of toxic metabolites, for example, 4-methylaminoantipyrine (4-MAA) or 4-aminoantipyrine. The metabolite 4-MAA can complex with hemin, which is an early breakdown product during hemolysis. Hemolysis is often observed during invasive infections or after surgical procedures. It is known that the 4-MAA/hemin complex can induce cytotoxicity in the bone marrow and interrupt granulocyte maturation. In conclusion, metamizole-induced agranulocytosis most likely was a consequence of the underlying genetical predisposition, that is, polymorphisms in the genes NAT2, CYP2C9 and CYP2C19. Hemolysis may have increased the toxicity of metamizole metabolites. |
Databáze: | OpenAIRE |
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