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Frequently Asked Questions About Genetic Testing
Overview
Genetic research is leading to more genetic tests that can be used for diagnosis and treatment of genetic conditions. Genetic testing is available during pregnancy, and for diagnosis and treatment of infants, children and adults.
What is genetic testing?
Genetic tests look for alterations in a person's genes or changes in the level of key proteins coded for by specific genes. Abnormal results on these tests could mean that someone has an inherited disorder.
Types of genetic tests include:
- Gene tests (when you test DNA)
- Chromosomal tests (called karyotype and FISH)
- Biochemical tests (when you test enzyme levels)
What is a gene test?
Gene tests look for signs of a disease or disorder in DNA taken from a person's blood, body fluids or tissues. The tests can look for large changes, such as a gene that has a section missing or added, or small changes, such as a missing, added, or altered chemical base within the DNA strand. Other important changes can be genes with too many copies, genes that are too active, genes that are turned off, or those that are lost entirely.
Gene tests examine a person's DNA in a variety of ways. Some tests use probes. These are short strings of DNA with base sequences complementary to those of an altered gene. Probes look for their complements within a person's genome. If the altered is found, the probe binds to it, identifying the alteration.
Another type of gene test directly compares the sequence of DNA bases in a patient's gene to a normal version of the gene.
What is a chromosomal test?
Chromosomes are structures in the nucleus of a cell that contain DNA. Chromosomal tests look at features of a person's chromosomes, including their structure, number, and arrangement. These tests look for changes, such as pieces of chromosomes being switched or being in a different location.
Types of chromosomal tests include:
- Karyotype - This test gives a picture of all of a person's chromosomes from the largest to the smallest.
- FISH analysis (fluorescent in situ hybridization) - This test identifies certain regions on chromosomes using fluorescent DNA probes. FISH analysis can find small pieces of chromosomes that are missing or have extra copies. These small changes can be missed by the karyotype test.
What is a biochemical test?
Biochemical tests look at the level of key proteins. This level signals genes that are not working normally. These types of tests are used for newborn screening. For example, this screening can detect infants who have metabolic conditions such as phenylketonuria (PKU).
What information can genetic testing give?
Genetic testing can:
- Give a diagnosis if someone has symptoms.
- Show whether a person is a carrier for a genetic disease. Carriers have an altered gene, but will not get the disease. However, they can pass the altered gene on to their children.
- Help expectant parents know whether an unborn child will have a genetic condition. This is called prenatal testing.
- Screen newborn infants for abnormal or missing proteins that can cause disease. This is called newborn screening.
- Show whether a person has an inherited disposition to a certain disease before symptoms start.
- Determine the type or dose of a medicine that is best for a certain person. This is called pharmacogenetics.
People in families at high risk for a genetic disease have to live with uncertainty about their future and their children's future. A genetic test result that can show that a known alteration causing disease is not present in a person can provide a sense of relief.
A genetic test result that shows a person has an alteration causing disease can also give benefits. Such a test result might lead a person to take steps to lower their chance of disease. For example, someone could screen for the disease or could make changes to their health habits like diet and exercise. A genetic test result showing that a person has an alteration causing disease can lower their uncertainty. This information can also help people to make informed choices about their future.
What are reasons to get different types of genetic tests?
- Diagnostic testing
is to confirm a diagnosis when a person has signs or symptoms of a genetic disease. The genetic test used depends on the disease for which a person is tested. For example, if a patient has physical features that suggest Down syndrome, a chromosomal test is used. To test for Duchenne muscular dystrophy a gene test is done to look for missing sections in the dystrophin gene.
- Predictive testing can show which people have a higher chance of getting a disease before symptoms appear. For example, one type of predictive test screens for inherited disposition to certain cancers, such as colon and breast cancer. Someone with an inherited disposition has an increased chance of getting a disease. This does not mean that the person will certainly get the disease.
- Presymptomatic testing shows which family members are at risk for a certain genetic condition. This type of testing is done with people who do not have symptoms when the alteration causing disease in the family is known. For some diseases, this type of testing can lead to prevention or treatment options. For example, when a disease-causing alteration is found in a family, testing is recommended for all close blood relatives (such as parents and siblings). Those family members with the alteration can be offered removal of the thyroid. With other types of diseases, there are no prevention or treatment options. For example, there is no treatment for family members who have an alteration causing Huntington disease and those who have this alteration are certain to get the disease.
- Carrier testing can tell individuals if they are carriers of a gene alteration for a type of inherited disorder called an autosomal recessive disorder. A person who has only one altered copy of a gene for this type of disorder is called a carrier. Carriers will not get the disease, but can pass on the alteration to their children. If both parents are carriers, their children might inherit an alteration from each parent and get the disease. Examples of this type of disorder are cystic fibrosis and Tay-Sachs.
- Prenatal testing is available to pregnant women:
- Who are age 35 or older. This is because they are at higher risk for having a child with a chromosomal abnormality.
- Who have a family history of an inherited condition such as Duchenne muscular dystrophy.
- When their ancestry or ethnic background means that they might have a higher chance of an inherited disorder such as sickle cell anemia, thalassemia, or Tay-Sachs disease.
- To screen for common genetic disorders such as spina bifida and Down syndrome.
Two diagnostic procedures are common in prenatal testing. Amniocentesis involves testing a sample of amniotic fluid from the womb. CVS (or chorionic villus sampling) involves taking a tiny tissue sample from outside the sac where the fetus grows.
- Newborn screening is the most widespread type of genetic testing. It is an important public health program which can find disorders in newborns that have long-term health effects. Newborn screening tests infant blood samples for abnormal or missing gene products. For example, infants are often screened for Phenylketonuria (PKU). This is an enzyme deficiency that can lead to severe mental retardation if the child is not treated.
Newborn screening now tests for more diseases. In the past, newborn screening focused on a few metabolic disorders that led to mental retardation. Newborn screening programs now test for disorders that can cause infectious disease, premature death, hearing disorders and heart problems.
A new technology called tandem mass spectrometry allows screening of up to 30 other metabolic disorders. The number of disorders screened for varies from state to state. Some states offer newborn screening for up to 30 diseases, while others offer newborn screening for the most common disorders.
- Pharmacogenetic Testing is a new type of genetic testing. This type of test examines a person's genes to look at how drugs would move through the body and be broken down. The goal of pharmacogenetic testing is to have drug treatments that are specific to each person. For example, a test used in patients who have chronic myelogenous leukemia can show which patients would benefit from a medicine called Gleevac. Another test looks at a liver enzyme called cytochrome P450, which breaks down certain types of drugs. Gene alterations can affect how well people's bodies break down certain drugs. People with a less active form of the enzyme might get too much of a drug. Pharmacogenetic testing can help make sure that people get the right amount of a medicine.
How do I decide whether to be tested?
People have many different reasons for being tested or not being tested. For many, it is important to know whether a disease can be prevented if a gene alteration causing a disease is found. For example, those who have inherited forms of breast or colon cancer have options such as screening or early treatment. Pharmacogenetic testing can find the best medicine or dose of a medicine for a certain person.
In other cases, there is no treatment. There are no preventive steps or cures for Huntington Disease. But test results might help a person make life decisions, such as career choice, family planning or insurance coverage.
People can seek advice from a genetic counselor (link to genetic counseling section). Genetic counselors help individuals and families think about the scientific, emotional and ethical factors that affect the testing decision.
What about direct-to-consumer genetic tests available on the Internet?
A variety of genetic tests are being offered directly to consumers, often over the Internet. Such genetic testing usually involves scraping a few cells from inside the cheek and mailing the sample to a test laboratory, which performs the test. If you are considering such genetic tests, it is a good idea to discuss the issue with your health-care provider or a genetic counselor first.
Here are some major types of direct-to-consumer genetic tests:
- Health-related: These tests scan all or selected parts of your genome, which is your complete set of genetic material, for variants that may influence your risk of developing certain diseases. Be aware that current tests provide just a partial picture of your disease risk. For most diseases, many pieces of the genetic puzzle remain to be discovered, along with how those pieces interact with lifestyle and environmental factors. That means today's tests may falsely reassure people with undiscovered risk factors and needlessly alarm those with undiscovered protective factors.
Also, your test results may show that you are at increased risk for a condition, such as Alzheimer's disease, for which there currently is no effective prevention or cure. Such knowledge may help you plan your life, but it may also make you and your loved ones anxious or depressed. Finally, ask yourself if you are prepared to make changes in your lifestyle based on the test results. If you are not willing to take actions like stopping smoking or exercising more, such tests may not be of much benefit to you.
- Nutrigenetic: These testing companies say they can use information about your genetic make-up to develop a individualized diet plan. A recent government report found that such tests may be misleading or even harmful because they make claims that cannot be scientifically proven. For more information, read the General Accounting Office's report, Nutrigenetic Testing: Tests Purchased from Four Web Sites Mislead Consumers
- Ancestry: These tests scan your genome for genetic variants that may provide information about your ancestral roots.
- General: This type of test scans your genome for genetic variants related to many aspects of your life " from your physical traits to your ancestry to your personality. Such tests often do not claim to provide specific information about disease risk. However, some of the results may have implications for your health.
Where can I find more information about genetic testing?
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Last Updated: August 19, 2008
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