More than 25 years of genetic studies of clozapine-induced agranulocytosis
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2017-07
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taverne
Abstract
Clozapine is one of the most effective atypical antipsychotic drugs prescribed to patients with treatment-resistant schizophrenia. Approximately 1% of patients experience potential life-threatening adverse effects in the form of agranulocytosis, greatly hindering its applicability in clinical practice. The etiology of clozapine-induced agranulocytosis (CIA) remains unclear, but is thought to be a heritable trait. We reviewed the genetic studies of CIA published thus far. One recurrent finding from early candidate gene study to more recent genome-wide analysis is that of the involvement of human leukocyte antigen locus. We conclude that CIA is most likely a complex, polygenic trait, which may hamper efforts to the development of a genetic predictor test with clinical relevance. To decipher the genetic architecture of CIA, it is necessary to apply more rigorous standards of phenotyping and study much larger sample sizes.
Keywords
Agranulocytosis/chemically induced, Antipsychotic Agents/adverse effects, Clozapine/adverse effects, Drug-Related Side Effects and Adverse Reactions/etiology, Genome-Wide Association Study/methods, HLA Antigens/metabolism, Humans, Schizophrenia/drug therapy, Taverne, Genetics, Molecular Medicine, Pharmacology, Review, Journal Article
Citation
de With, S A J, Pulit, S L, Staal, W G, Kahn, R S & Ophoff, R A 2017, 'More than 25 years of genetic studies of clozapine-induced agranulocytosis', Pharmacogenomics Journal, vol. 17, no. 4, pp. 304-311. https://doi.org/10.1038/tpj.2017.6