ROCHESTER, Minn. -- Mayo Clinic researchers have found that carrying a common genetic disorder doubles the risk of developing lung cancer in smokers and nonsmokers.
The study is published in the May 26 issue of the Archives of Internal Medicine, a journal published by the American Medical Association.
Researchers found that the genetic disorder, alpha-1 antitrypsin deficiency (1ATD), could explain up to about 12 percent of lung cancer patients in this study and likely represents the same widespread risk in the general population. "This is a seriously underdiagnosed disorder and suggests that people who have lung cancer and chronic obstructive pulmonary diseases (COPD) in their families should be screened for these gene carriers," says Ping Yang, M.D., Ph.D., a Mayo Clinic epidemiologist and lead investigator on the study.
The current standard diagnostic test measures protein produced by the gene. Because of the cost and limited availability of the test, it's not suitable for general screenings. A less expensive DNA-based gene panel test is being developed.
The World Health Organization estimates that at least 10 million Americans and 120 million people worldwide are 1ATD carriers. According to Dr. Yang, this study shows that the disorder "is among the highest for major gene effects on the risk of a common cancer."
A normal 1AT gene produces a protein that stops enzymes from breaking down elastin, which keeps lung tissue elastic for normal function. Carriers of 1ATD commonly develop emphysema and/or chronic obstructive pulmonary disease (COPD). Prior to this study, the connection between 1ATD, COPD and lung cancer risk had not been established.
"It has been suspected that 1ATD increased susceptibility to lung cancer," says Dr. Yang, "but this is the first solid evidence that supports and quantifies this risk.
"Importantly, our results support the hypothesis that the excess risk of lung canc
'/>"/>
| Contact: Traci Klein newsbureau@mayo.edu 507-284-5005 Mayo Clinic Source:Eurekalert |