Your doctor may use cytochrome P450 (CYP450) tests to help determine how your body processes (metabolizes) a drug. The human body contains P450 enzymes to process medications.
As a result of inherited (genetic) traits that cause variations in these enzymes, medications may affect each person differently.
Also known as pharmacogenetics or pharmacogenomics, drug-gene testing is the study of how genes affect your body’s response to medication.
Tests look for any changes and variations in these genes that determine whether a medication could be an effective treatment for you or whether you could have side effects from a certain medication.
The P450 enzyme with the most variation in different people is the CYP2D6, which processes a lot of antidepressants and antipsychotic medications.
By checking your DNA for specific gene variations, CYP450 test and give clues about how your body may respond to a particular antidepressant. Other CYP450 tests are available for other enzymes.
CYP450 and other genetic tests (genotyping test) are becoming more common as doctors try to understand why antidepressants help some people and not others. While their use might be increasing, there are also limitations.
There are many reasons to decide to undergo cytochrome P450 tests, including:
Medications for depression are usually prescribed based on one's symptoms and medical history. For example, the first antidepressant tried relieves depression symptoms and has tolerable side effects.
However, for many others, finding the right medication takes trial and error. It can take several months or longer for certain individuals to find the right antidepressant.
Genotyping tests, such as cytochrome P450 tests, may accelerate the identification of a medication that is more likely to be better processed by your body.
Ideally, better processing will lead to fewer side effects and improved effectiveness. CYP450 tests are generally used only when initial depressant treatment are not successful.
Genotyping tests are also used in other fields of medicine. For example, the CYP2D6 test can help determine whether certain cancer medications, such as tamoxifen for breast cancer, are likely to be more effective.
The CYP2C9 test can be helpful in determining appropriate dosing of the blood thinner warfarin to reduce the risk of adverse effects.
It normally takes several days to a week to get the results of cytochrome P450 tests. Once they are available, you and your doctor will discuss the results and how they might affect your treatment options.
CYP450 tests give clues to how well your body processes a drug by looking at specific enzymes. People can be classified according to how fast they metabolize medications.
For example, results of a CYP2D6 test may show which of these four types applies to you:
Poor metabolizers. If you process a certain drug more slowly than normal because of a missing enzyme, the medication can build up in your system.
This can increase the likelihood that it will cause side effects. You might still be able to benefit from these medications, but at lower dosages.
Intermediate metabolizers. If you have reduced enzyme function in processing drugs, you may not process some medications as well as normal metabolizers do. This can increase your risk of side effects and drug interactions.
Normal metabolizers (also known as extensive metabolizers). If the test shows that you process certain antidepressants normally, you're more likely to benefit from treatment and have fewer side effects than people who don't process those particular medications as well.
Ultrarapid metabolizers. In this case, medications leave your body too quickly — often before they have a chance to work properly. You'll likely need higher than usual doses of medications.
CYP450 testing isn't useful for all antidepressants, but it can provide information about how you're likely to process a number of them. For example:
The CYP2D6 enzyme is involved in metabolizing antidepressants such as fluoxetine (Prozac), paroxetine (Paxil, Pexeva) and venlafaxine (Effexor XR), as well as tricyclic antidepressants such as nortriptyline (Pamelor), amitriptyline, clomipramine (Anafranil), desipramine (Norpramin) and imipramine (Tofranil).
Some antidepressants, such as fluoxetine and paroxetine, can cause the CYP2D6 enzyme to slow down. The CYP2C19 enzyme is involved in metabolizing citalopram (Celexa) and escitalopram (Lexapro).
Test limitations Although they have potential, CYP450 tests have limitations:
Tests are available for only certain medications. Also, each test is specific to only one medication, so a change in medication may require another test.
Testing can't predict for certain which particular medication will work best for you — it can only provide clues.
Tests only look at some of the genes involved in how your body uses certain drugs — so factors out of the scope of the test may impact how an antidepressant will affect you.
Tests focus on how the body metabolizes a drug, but not on what the drug does to the body, such as how the drug might change the brain receptors to improve symptoms. It isn't entirely clear how useful tests are in choosing an antidepressant.
Even if you have tests, you may still need to try different antidepressants and different doses to identify what works best for you. Not all insurance companies cover the costs of these tests.
Despite the limitations, some doctors use CYP450 tests and think they're helpful. However, these tests aren't meant to be the only way to determine which antidepressants to try. They're just one tool that may help.
Trying antidepressants based on your medical history and symptoms is still the standard method for identifying the best medication for your needs.