CYP2A6
CYP2A6 is a gene in the human body that encodes the enzyme Cytochrome P450 2A6. This enzyme is part of the Cytochrome P450 family, a group of enzymes that are primarily located in the liver and are responsible for metabolizing various substances in the body, including drugs and toxins.
Function[edit | edit source]
The CYP2A6 enzyme is involved in the metabolism of several important substances. It plays a key role in the metabolism of nicotine, converting it into cotinine. It also metabolizes several carcinogens, including those found in tobacco smoke and certain types of food. In addition, CYP2A6 is involved in the metabolism of some medications, including the antipsychotic drug clozapine and the antidepressant nortriptyline.
Genetic Variability[edit | edit source]
There is significant genetic variability in the CYP2A6 gene among different individuals. This variability can affect the activity of the CYP2A6 enzyme and, consequently, how individuals metabolize certain substances. For example, some individuals have a version of the CYP2A6 gene that results in a less active enzyme, which can lead to slower metabolism of nicotine and certain drugs. This can have various implications for health and treatment outcomes.
Clinical Significance[edit | edit source]
The variability in the CYP2A6 gene has important clinical implications. For example, individuals with a less active CYP2A6 enzyme may be at lower risk for nicotine addiction, as they metabolize nicotine more slowly. However, they may also be at higher risk for certain side effects from medications that are metabolized by CYP2A6.
In addition, testing for CYP2A6 genetic variants can be used to guide treatment decisions for certain conditions. For example, individuals with certain CYP2A6 variants may require different dosages of medications that are metabolized by this enzyme.
See Also[edit | edit source]
References[edit | edit source]
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Contributors: Prab R. Tumpati, MD