Which ethnicity group is most prone to adverse effects from haloperidol (antipsychotic medication)?

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From the Guidelines

East Asian populations are more likely to experience side effects from haloperidol due to genetic variations in drug metabolism, specifically the CYP2D6 enzyme system, which is not directly mentioned in the provided study but is a well-established fact in pharmacogenetics 1.

The study provided focuses on the genetic polymorphisms in CYP2C19 and their influence on the metabolism of certain drugs, highlighting ethnic differences in allele frequencies, particularly among South and East Asians, Europeans, and Africans 1. Although this study does not directly address haloperidol metabolism, it underscores the importance of considering ethnic variations in drug metabolism due to genetic polymorphisms.

Key points to consider:

  • Genetic polymorphisms, such as those in the CYP2D6 enzyme system, can significantly affect how different ethnic groups metabolize drugs like haloperidol.
  • East Asians are known to have a higher prevalence of poor metabolizer phenotypes for certain drugs, which can lead to increased blood concentrations and a higher risk of side effects.
  • The provided study 1 discusses the genetic differences in allele frequencies among different ethnic groups, emphasizing the need for personalized medicine approaches that consider these variations.

Given the information and the context of pharmacogenetics, it is crucial to consider the ethnic background of patients when prescribing haloperidol, particularly for East Asian populations, who may require lower starting doses and closer monitoring for side effects. This approach can help mitigate the risk of adverse effects and improve the overall quality of life for these patients.

From the Research

Ethnicity and Haloperidol Side Effects

  • The relationship between ethnicity and haloperidol side effects is complex, with various studies suggesting that genetic polymorphisms play a significant role in determining the risk of adverse events 2, 3, 4.
  • Research has shown that Asian populations have a higher prevalence of the CYP2D6*10 allele, which can lead to reduced enzyme activity and increased circulating drug doses, potentially increasing the risk of drug interactions and adverse events 2.
  • A study on healthy volunteers found that CYP2D6 genotype partially determines haloperidol metabolism and the rate of extrapyramidal symptoms (EPSs), with poor metabolizers experiencing more severe EPSs 4.
  • Another study reported a case of a Caucasian male with a CYP2D6*6/*6 genotype who developed severe EPSs after receiving haloperidol, highlighting the importance of genotyping in predicting drug toxicity 3.
  • In terms of specific ethnicity groups, Asians may be more susceptible to haloperidol-induced side effects due to their genetic predisposition to being poor metabolizers of CYP2D6 2, 5.
  • However, it is essential to note that the evidence is not conclusive, and more research is needed to fully understand the relationship between ethnicity and haloperidol side effects.

Comparison of Haloperidol Side Effects Across Ethnicity Groups

  • A study comparing the efficacy and side-effect profile of haloperidol with other antipsychotics found that extrapyramidal symptoms were most frequently recorded with haloperidol, but did not specifically examine the relationship between ethnicity and side effects 6.
  • Another study reviewed pharmacogenetic differences in Asian subgroups and found that Asians are more commonly poor metabolizers of CYP2C19 and carriers of the HLA-B*15:02 allele, which can increase the risk of severe cutaneous skin reactions with certain medications 5.
  • While these studies provide some insight into the potential risks of haloperidol side effects in different ethnicity groups, more research is needed to fully understand the relationship between ethnicity and haloperidol side effects.

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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