When you take a medicine, your body needs way to handle it. One way is for drug transporters to carry the medicine to be broken down. A drug transporter called solute carrier organic anion transporter family member 1B1, known as SLCO1B1, helps the body get rid of certain medicines after they are no longer needed.
Each person differs from another at the DNA level. Genes are segments of that act as a set of instructions and tell the body how to work. The SLCO1B1 gene is a section of DNA that instructs how well the SLCO1B1 transporter will work.
The study of how genes like SLCO1B1 affect the way your body interacts with medicines is called pharmacogenomics. Differences in your DNA that make up the SLCO1B1 gene can affect how well you are able to handle certain medicines.
If you transport medicine too fast or too slow, the medicine may not work as well, or you may have more side effects.
A pharmacogenomic test can help your medical team know how well the SLCO1B1 transporter will work. The test results can help your doctor and pharmacist choose the correct type or dose of medicine to give you.
The results of your SLCO1B1 test will place you into one of four groups:
The SLCO1B1 transporter helps in the breakdown of many medicines, including statins, medicines used to lower cholesterol levels. Depending on what gene group you are in, you may need a lower dose of some medicines or a different medicine.
Scientists continue to find new information about which medicines are affected by gene test results. Talk to your doctor or pharmacist if you have questions about your medicines, side effects, or pharmacogenomic testing.
Find more information about genesLink Opens in a New Window that are being used to make medication therapy decisions for patients at St. JudeLink Opens in a New Window.
If you have questions about pharmacogenomic testing done at St. Jude, you can email the Clinical Pharmacogenomics Program at pharmacogenomics@stjude.org.
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Reviewed: September 2022