At a glance
Also known as
Thiopurine methltransferase, TPMT RBC, TPMT Genotype, TPMT Phenotype
Why get tested?
To detect a thiopurine methyltransferase (TPMT) deficiency and determine patients who are at risk of developing severe side effects if treated with the class of immune-supressing thiopurine drugs, azathioprine, mercaptopurine and thioguanine.
When to get tested?
Prior to thiopurine drug treatment
A single blood sample drawn from a vein in your arm
Test preparation needed?
For measuring TPMT enzyme activity (TPMT phenotyping), the test must be performed prior to taking a thiopurine drug since it may affect results; for the genetic test (TPMT genotyping), no specific test preparation is needed
Confused about genetics?
See our Genetics Information page
What is being tested?
Thiopurine methyltransferase (TPMT) is an that breaks down (metabolises) a class of drugs called thiopurines. These drugs are used to suppress the and are prescribed to treat various immune-related conditions or blood disorders (e.g., leukaemia). The activity level of the TPMT enzyme, or the genetics underlying the enzyme's activity, is tested before thiopurine drug therapy to make sure that individuals treated with the drugs can metabolise them.
Examples of thiopurines include azathioprine, mercaptopurine, and thioguanine. These medications are used to treat diseases such as acute lymphoblastic leukaemia, inflammatory bowel disease and autoimmune disorders. They may also be prescribed for organ transplant recipients to help delay or prevent organ rejection. If someone's TPMT activity is too low, the person may not effectively metabolise thiopurines, which can lead to severe side effects.
About one person in every 300 is severely deficient in TPMT, and about 10 per cent of the population have lower than normal levels of TPMT. Individuals in both categories are at an increased risk for thiopurine drug toxicity, which can include suppression of the (myelosuppression) and/or very reduced levels of blood cells, such as red blood cells, white blood cells and platelets (haematopoetic toxicity). This can lead to complications such as anaemia, serious infections, and/or excessive bleeding.
These side effects can cause an individual to become severely ill and may even be life-threatening. These side effects can be avoided if TPMT production is tested before starting thiopurine treatment.
There are two ways to determine whether an individual is at risk of side effects from thiopurine therapy:
- TPMT activity test ()—this method tests the activity level of the enzyme thiopurine S-methyltransferase (TPMT) in a person's red blood cells. Depending on the enzyme activity level, a person may be prescribed a standard dose of the thiopurine drug, a reduced dose of the thiopurine drug, or a different drug other than a thiopurine.
- TPMT genetic test ()—an alternative test to TPMT enzyme activity level is a genetic test that can identify genetic variations in the TPMT . This genetic test identifies individual genetic differences associated with risk for thiopurine toxicity. Each person has two copies of the TPMT gene. Most people have two copies of "wild type" TPMT that produce sufficient TPMT enzyme. Approximately 10 per cent of people have one wild-type gene and one gene variation associated with decreased TPMT () and intermediate activity. Approximately one in 300 individuals have two copies of TPMT with variations resulting in little or no enzyme activity (). While numerous variations can occur in TPMT, there are five variations in particular that have been proven to be associated with TPMT deficiencies. Most genetic tests look for these five variations, although depending on the method used, more variations can be detected.This genetic test provides information about a person's likely response to thiopurines, but it will not quantify how much TPMT enzyme is actually being made by the body. There can be significant person-to-person and ethnic variability in TPMT production, even in people with the same gene variations.
How is the sample collected for testing?
For both genetic and enzyme activity testing, a blood sample is taken by needle from a vein in the arm. Alternatively, for the genetic test alone, a swab of cells from the inside cheek (buccal swab) may be collected.
Is any test preparation needed to ensure the quality of the sample?
For the method that measures TPMT enzyme activity, taking a thiopurine drug could lead to falsely low results, so the test should be performed prior to starting therapy. For the genetic test (TPMT genotyping), no specific test preparation is needed.
What does TPMT normally do in the body?
No one really knows the answer to this. The is found in many cells but the interest in the enzyme is purely in looking at patients who are on thiopurine drugs.
My doctor ordered a test for thiopurine metabolites. What is it and how is it related to TPMT testing?
A doctor may order a blood test for thiopurine metabolites to monitor drug therapy. Measuring the metabolites is another way to ensure that toxic levels do not build up in the blood. Prior to administering the first dose, a doctor may test a person's TPMT enzyme activity or genotype to help determine risk of side effects as described in other sections of this article. The doctor can adjust the prescribed dose according to those results. After therapy begins, the level of metabolites can be measured and monitored, with subsequent doses adjusted as necessary to avoid toxicity.