CYP2C9*3

From WikiMD's Wellness Encyclopedia


CYP2C9*3 is a variant allele of the CYP2C9 gene, which encodes an enzyme belonging to the cytochrome P450 superfamily. This enzyme is primarily involved in the metabolism of various drugs in the human body. The CYP2C9*3 allele is characterized by a single nucleotide polymorphism (SNP) that results in an amino acid substitution at position 144, where isoleucine is replaced by leucine (Ile144Leu). This genetic variation can significantly affect the enzyme's activity, leading to altered drug metabolism.

Function[edit | edit source]

The CYP2C9 enzyme plays a crucial role in the oxidative metabolism of a wide range of therapeutic drugs, including warfarin, phenytoin, tolbutamide, and nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen and celecoxib. The presence of the CYP2C9*3 allele is associated with reduced enzymatic activity, which can lead to slower drug clearance and increased risk of adverse drug reactions.

Clinical Significance[edit | edit source]

Individuals carrying the CYP2C9*3 allele may require dose adjustments for medications metabolized by CYP2C9 to avoid toxicity. For example, patients with this allele who are prescribed warfarin may need lower doses to achieve therapeutic anticoagulation without increasing the risk of bleeding. Pharmacogenetic testing for CYP2C9 variants, including CYP2C9*3, can help guide personalized medicine approaches to optimize drug therapy and minimize adverse effects.

Genetic Testing[edit | edit source]

Genetic testing for CYP2C9*3 is available and can be performed using various methods, including polymerase chain reaction (PCR) and DNA sequencing. Testing is particularly recommended for patients who are starting medications with a narrow therapeutic index that are metabolized by CYP2C9.

Population Genetics[edit | edit source]

The frequency of the CYP2C9*3 allele varies among different populations. It is more commonly found in individuals of European descent compared to those of African or Asian ancestry. Understanding the distribution of this allele can help in assessing the risk of drug interactions and adverse effects in diverse populations.

Also see[edit | edit source]



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