Paper Details 
Original Abstract of the Article :
Warfarin doses are greatly affected by polymorphism altering cytochrome P450 2C9 (CYP2C9) and vitamin K epoxide reductase complex subunit 1 (VKORC1) gene. This study evaluated the prevalence of alleles (either single or double) and carriers of single nucleotide polymorphisms (SNPs) in both genotypes...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933267/

データ提供:米国国立医学図書館(NLM)

Warfarin Dosing: The Importance of Genetic Testing

Warfarin is a commonly used blood thinner medication, but its effectiveness can vary widely among individuals. This variability is often attributed to genetic differences that affect the metabolism of warfarin. This study investigates the prevalence of specific gene variations in a Saudi Arabian population and their potential impact on warfarin dosing.

The research focused on two genes, CYP2C9 and VKORC1, which are known to influence warfarin metabolism. The researchers genotyped 112 individuals and found significant variations in the prevalence of these gene variations. They also assessed the potential impact of these variations on warfarin dosing, suggesting that individuals with specific genetic profiles may require lower warfarin doses to achieve therapeutic effects.

Personalized Warfarin Dosing: A Key to Safety and Effectiveness

This study underscores the importance of personalized medicine approaches to warfarin therapy. Genetic testing can help predict individual responses to warfarin, allowing for more accurate dosing and reducing the risk of bleeding or clotting complications. It highlights the benefits of incorporating genetic information into clinical decision-making to optimize patient outcomes.

Understanding Genetic Influences on Medication Response

This research provides a valuable example of the growing field of pharmacogenetics, which explores the genetic basis of individual drug responses. This understanding can improve patient safety and effectiveness of medication therapy, leading to better health outcomes. It emphasizes the crucial role of genetic testing in tailoring treatments to individual patient needs.

Dr. Camel's Conclusion

The desert of the human genome holds many secrets, and this study delves into the complex interplay between genetic variations and medication response. It reminds us that understanding these genetic influences is crucial for ensuring safe and effective drug therapy, paving the way for a more personalized approach to healthcare.

Date :
  1. Date Completed n.d.
  2. Date Revised 2020-09-28
Further Info :

Pubmed ID

31889870

DOI: Digital Object Identifier

PMC6933267

Related Literature

SNS
PICO Info
in preparation
Languages

English

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