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.
| Original language | English |
|---|---|
| Pages (from-to) | 304-311 |
| Number of pages | 8 |
| Journal | Pharmacogenomics Journal |
| Volume | 17 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Jul 2017 |
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
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