Hodgkin's diseaseRisk Factors |
Physician-developed and -monitored. Original Date of Publication: 15 Aug 1999
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Original Source: http://www.oncologychannel.com/hodgkins/riskfactors.shtml | |
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Risk Factors
Although scientists have studied the many cellular changes associated with lymphoma, no one really knows why such changes occur. It is likely that certain risk factors make individuals more prone to developing Hodgkin's disease (HD). Many factors, such as age and genetics, are beyond our control. Other factors, such as environmental or lifestyle-related variables, may be more correctable.
It is now known that all cancers, including lymphoma, begin as a mutation (change) in the genetic materialthe DNA (deoxyribonucleic acid)within certain cells. The external or internal causes of such change probably add up over a lifetime. DNA errors may occur in the form of translocationsdamage produced when part of one chromosome becomes displaced and attached to another chromosome. Translocations disrupt the normal sequencing of the genes.
As a result, oncogenes (cancer-promoting genes) on the chromosomes may be switched on, whereas tumor suppressors (cancer-preventing genes) may be switched off. These changes often occur in cases of lymphoma. Physicians test for these translocations to help diagnose the type of lymphoma, determine a patient's prognosis (outcome), and identify cancer recurrence.
Numerous risk factors may be responsible for DNA damage within the body's lymphocytes (specialized white blood cells). The risk factors now believed to have the strongest associations with lymphoma are:
Age
The rate of HD is high in two age groups: young adults (age 15 - 40) and older adults (age 55+).
Sex
In general, both HD and NHL affect more men than women.
Infections
The risk of HD is increased somewhat in people who have been infected with viruses such as Epstein-Barr virus (EBV). EBV infects the B-cells and causes an illness known as infectious mononucleosis (sometimes referred to as "mono"). Eventually, the infected B-cells are sought out and killed by the body's T-cells. But if an individual has a T-cell shortage, the EBV-infected B-cells build up within the bloodstream and are at increased risk of developing the genetic mutations that can cause lymphomas.
It is important to note that there is no evidence of infection in many HD patients, so its role in cancer development remains uncertain.
Medical Conditions
Specific medical conditions may make a person more likely to develop HD or NHL. In particular, HD and NHL are more common among people with a weakened immune system, such as those with:
- Acquired immunodeficiency syndrome (AIDS)—disease caused by human immunodeficiency virus (HIV);
- Autoimmune diseases (e.g., rheumatoid arthritis, lupus, multiple sclerosis, under- or overactive thyroid)—disease caused by the body's immunologic attacks against its own tissues;
- Inherited immune deficiency syndromes (e.g., ataxia telangiectasia); or
- Organ transplants that require the use of immunosuppressant drugs.
Some experts believe that HD is caused by a complex deficiency in cellular immunity. Such a deficiency may be due to chronic overstimulation by cytokinessubstances that draw germ-fighting white blood cells to areas of infection.
Genetics
The rates of lymphoma and leukemia (e.g., chronic lymphocytic leukemia, CLL) are especially high in some Jewish populations, whereas Asian populations rarely develop CLL. Among first-degree relatives (parents, children, siblings) of CLL patients there is a two- to four-fold increased risk for this cancer.
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