(From Wikipedia, the free encyclopedia)
Genetic testing allows the genetic diagnosis of vulnerabilities to inherit diseases,
and can also be used to determine a person's ancestry.
Normally, every person carries two copies of every gene, one inherited from their mother,
one inherited from their father.
The human genome is believed to contain around 20,000 - 25,000 genes. In addition to studying
chromosomes to the level of individual genes, genetic testing in a broader sense includes
biochemical tests for the possible presence of genetic diseases, or mutant forms of genes
associated with increased risk of developing genetic disorders.
Genetic testing identifies changes in chromosomes, genes, or proteins.
Most of the time, testing is used to find changes that are associated with inherited disorders.
The results of a genetic test can confirm or rule out a suspected genetic condition or help
determine a person's chance of developing or passing on a genetic disorder.
Several hundred genetic tests are currently in use, and more are being developed.
Since genetic testing may open up ethical or psychological problems, genetic testing is often
accompanied by genetic counseling.
|Genetic testing "the analysis of RNA, chromosomes (DNA), proteins, and certain
metabolites in order to detect heritable disease-related genotypes, mutations, phenotypes,
or karyotypes for clinical purposes.
It can provide information about a person's genes and chromosomes throughout life.
Available types of testing include:
- Newborn screening: Newborn screening is used just after birth to identify genetic disorders
that can be treated early in life.
The routine testing of infants for certain disorders is the most widespread use of genetic
testing—millions of babies are tested each year in the United States.
All states currently test infants for phenylketonuria (a genetic disorder that causes mental
illness if left untreated) and congenital hypothyroidism (a disorder of the thyroid gland).
- Diagnostic testing: Diagnostic testing is used to diagnose or rule out a specific genetic or
In many cases, genetic testing is used to confirm a diagnosis when a particular condition is
suspected based on physical mutations and symptoms.
Diagnostic testing can be performed at any time during a person's life, but is not available
for all genes or all genetic conditions.
The results of a diagnostic test can influence a person's choices about health care and the
management of the disease.
- Carrier testing: Carrier testing is used to identify people who carry one copy of a gene
mutation that, when present in two copies, causes a genetic disorder.
This type of testing is offered to individuals who have a family history of a genetic disorder
and to people in ethnic groups with an increased risk of specific genetic conditions.
If both parents are tested, the test can provide information about a couple's risk of having
a child with a genetic condition.
- Prenatal testing: Prenatal testing is used to detect changes in a fetus's genes or
chromosomes before birth.
This type of testing is offered to couples with an increased risk of having a baby with a genetic or
In some cases, prenatal testing can lessen a couple's uncertainty or help them decide whether to
abort the pregnancy.
It cannot identify all possible inherited disorders and birth defects, however.
- Predictive and presymptomatic testing: Predictive and presymptomatic types of testing are used to
detect gene mutations associated with disorders that appear after birth, often later in life.
These tests can be helpful to people who have a family member with a genetic disorder,
but who have no features of the disorder themselves at the time of testing.
Predictive testing can identify mutations that increase a person's chances of developing
disorders with a genetic basis, such as certain types of cancer.
For example, an individual with a mutation in BRCA1 has a 65% cumulative risk of breast cancer.
Presymptomatic testing can determine whether a person will develop a genetic disorder, such as
hemochromatosis (an iron overload disorder), before any signs or symptoms appear.
The results of predictive and presymptomatic testing can provide information about a person’s
risk of developing a specific disorder and help with making decisions about medical care.
- Forensic testing: Forensic testing uses DNA sequences to identify an individual for legal purposes.
Unlike the tests described above, forensic testing is not used to detect gene mutations
associated with disease.
This type of testing can identify crime or catastrophe victims, rule out or implicate a crime
suspect, or establish biological relationships between people (for example, paternity).
- Research testing: Research testing includes finding unknown genes, learning how genes work and
advancing our understanding of genetic conditions.
The results of testing done as part of a research study are usually not available to patients or
their healthcare providers.
Genetic testing is often done as part of a genetic consultation and as of mid-2008 there were more
than 1,200 clinically applicable genetic tests available.
Once a person decides to proceed with genetic testing, a medical geneticist, genetic counselor,
primary care doctor, or specialist can order the test after obtaining informed consent.
Genetic tests are performed on a sample of blood, hair, skin, amniotic fluid
(the fluid that surrounds a fetus during pregnancy), or other tissue.
For example, a medical procedure called a buccal smear uses a small brush or cotton
swab to collect a sample of cells from the inside surface of the cheek.
The sample is sent to a laboratory where technicians look for specific
changes in chromosomes, DNA, or proteins, depending on the suspected disorder.
The laboratory reports the test results in writing to a person's doctor or genetic counselor.
Routine screening tests are done on a small blood sample, using a 'heel stick', by pricking
the baby's heel and blotting the blood on a special paper.
Unlike other types of genetic testing, a parent will usually only receive the result if it is positive.
|The results of genetic tests are not always straightforward, which often makes them challenging to
interpret and explain.
When interpreting test results, healthcare professionals consider a person’s medical history,
family history, and the type of genetic test that was done.
A positive test result means that the laboratory found a change in a particular gene,
chromosome, or protein of interest. Depending on the purpose of the test,
this result may confirm a diagnosis, indicate that a person is a carrier of a
particular genetic mutation, identify an increased risk of developing a disease (such as cancer) in the
future, or suggest a need for further testing.
Because family members have some genetic material in common, a positive test result may also have
implications for certain blood relatives of the person undergoing testing.
It is important to note that a positive result of a predictive or presymptomatic genetic test
usually cannot establish the exact risk of developing a disorder.
Also, health professionals typically cannot use a positive test result to predict the course or
severity of a condition.
A negative test result means that the laboratory did not find a dangerous copy of the gene,
chromosome, or protein under consideration.
This result can indicate that a person is not affected by a particular disorder, is not a
carrier of a specific genetic mutation, or does not have an increased risk of developing a certain
disease. It is possible, however, that the test missed a disease-causing genetic alteration
because many tests cannot detect all genetic changes that can cause a particular disorder.
Further testing may be required to confirm a negative result.
In some cases, a negative result might not give any useful information.
This type of result is called uninformative, indeterminate, inconclusive, or ambiguous.
Uninformative test results sometimes occur because everyone has common, natural variations in
their DNA, called polymorphisms, that do not affect health.
If a genetic test finds a change in DNA that has not been associated with a disorder in other people,
it can be difficult to tell whether it is a natural polymorphism or a disease-causing mutation.
An uninformative result cannot confirm or rule out a specific diagnosis, and it cannot
indicate whether a person has an increased risk of developing a disorder.
In some cases, testing other affected and E unaffected family members can help clarify this type of result.
Risks and limitations
|The physical risks associated with most genetic tests are very small, particularly for those tests
that require only a blood sample or buccal smear (a procedure that samples cells from the
inside surface of the cheek).
The procedures used for prenatal testing carry a small but real risk of losing the
pregnancy (miscarriage) because they require a sample of amniotic fluid or tissue
from around the fetus.
Many of the risks associated with genetic testing involve the emotional, social,
or financial consequences of the test results. People may feel angry, depressed,
anxious, or guilty about their results.
In some cases, genetic testing creates tension within a family because the results can reveal
information about other family members in addition to the person who is tested.
The possibility of genetic discrimination in employment or insurance is also a concern.
Some individuals avoid genetic testing out of fear it will affect their ability to purchase
insurance or find a job.
Health insurers do not currently require applicants for coverage to undergo genetic testing,
and when insurers encounter genetic information, it is subject to the same confidentiality
protections as any other sensitive health information.
Legislation in the United States called the Genetic Information Nondiscrimination
Act prohibits group health plans and health insurers from denying coverage to a healthy
individual or charging that person higher premiums based solely on a genetic predisposition to
developing a disease in the future.
The legislation also bars employers from using individuals’ genetic information when
making hiring, firing, job placement, or promotion decisions.
It was signed into law by President Bush on May 21, 2008.
Genetic testing can provide only limited information about an inherited condition.
The test often can't determine if a person will show symptoms of a disorder,
how severe the symptoms will be, or whether the disorder will progress over time.
Another major limitation is the lack of treatment strategies for many genetic disorders once they
A genetics professional can explain in detail the benefits, risks, and limitations of a particular test.
It is important that any person who is considering genetic testing understand and weigh these
factors before making a decision.
Many people are also concerned about the privacy implications of genetic testimony.
In the United States, federal law requires that this kind of medical information to be kept confidential.
Direct-to-Consumer (DTC) Genetic Testing
|Direct-to-Consumer (DTC) genetic testing is a type of genetic test that is accessible
directly to the consumer without having to go through a health care professional.
Usually, to attain a genetic test, health care professionals such as doctors acquire the
permission of the patient and order the desired test. DTC genetic tests, however, allow
consumers to bypass this process and order one themselves.
There are a variety of DTC tests, ranging from testing for breast cancer alleles to mutations
linked to cystic fibrosis.
Benefits of DTC testing are the accessibility of tests to consumers, promotion of proactive
healthcare and the privacy of genetic information.
Possible additional risks of DTC testing are the lack of governmental regulation and the
potential misinterpretation of genetic information.
|DTC genetic testing has been controversial due to outspoken opposition within the scientific community.
Critics of DTC testing argue against the risks involved, the unregulated advertising and marketing claims,
and the overall lack of governmental oversight.
DTC testing involves many of the same risks associated with any genetic test.
One of the more obvious and dangerous of these is the possibility of severe misreading of test results.
Without professional guidance, consumers can potentially misinterpret genetic information, causing them to
be deluded about their personal health.
Some advertising for direct-to-consumer genetic testing has been criticized as conveying an
exaggerated and inaccurate message about the connection between genetic information and disease risk,
utilizing emotions as a selling factor.
An advertisement for a BRCA-predictive genetic test for breast cancer stated: “There is no stronger
antidote for fear than information.”
|Currently, there is no strong federal regulation moderating the DTC market.
Though there are several hundred tests available, only a handful are approved by the FDA,
which are sold as at-home test kits.
Due to the nature of the majority of DTC tests as mailed in DNA samples, it is difficult
for the FDA to exercise a form of jurisdiction as the tests are completed in the laboratories
of providers, and are not in fact sold as medical devices.
Additionally, the FDA has not yet officially substantiated with scientific evidence the
claimed accuracy of the majority of direct-to-consumer genetic tests.
On April 24, 2008, the United States Senate passed the Genetic Information Nondiscrimination
Act with a vote of 95-0.
The act is the first of its kind in the U.S. to prevent discrimination against people based on
their genetic information.
This legislation will bar health insurance companies and employers from discriminating against
individuals on the basis of their genetic information.
|Some possible future ethical problems of genetic testing were considered in the science
fiction film Gattaca, and the science fiction anime series "Gundam Seed".
Also some films which include the topic genetic testing include, "The Island" and the "Resident Evil"