This cancer of the blood is rarely passed down, but genetics can help determine risk
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Genetics can increase your risk of leukemia, a cancer of the blood, but that doesn’t mean the disease is hereditary. In fact, leukemia running in families is rare. The cellular mutations that can lead to the disease aren’t typically passed from generation to generation.
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But your family tree and DNA can offer hints about your chances of getting leukemia, as oncologist Akriti Jain, MD, explains.
Researchers have identified only a few families with an inheritable form of leukemia, says Dr. Jain. So, what causes the disease? That’s still somewhat of a mystery. But there are known risk factors.
Certain genetic mutations, for instance, can increase your leukemia risk. These include:
The likelihood of a future leukemia diagnosis also increases with the following genetic conditions:
If you or a relative have any of these conditions, your doctor may suggest taking action. “If we know someone has a genetic defect, we can send them and their family members to get genetic counseling,” says Dr. Jain.
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Because the more you know, the better you and your doctor can monitor and treat the situation for you and your relatives.
Leukemia comes in many forms and can affect anybody. It develops in children and adults (mostly older adults and men). It accounts for more than 3% of new cancer diagnoses.
In most cases, healthcare providers can’t pinpoint an exact cause for leukemia. But certain life circumstances appear to be connected to the disease. You’re more at risk for leukemia if you have:
The search for biological processes and interactions that may lead to leukemia is ongoing.
“There has been an explosion in research into trying to find out how certain changes in DNA can cause normal bone marrow cells to become leukemia cells,” says Dr. Jain.
“We are finding more answers as we get better at performing genetic testing and more about the biological processes that can lead to leukemia.”
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