American Heart Association rapid access journal report
A simple blood test may identify people who have an increased risk of dying from cardiovascular disease, researchers report in Circulation: Journal of the American Heart Association.
The test measures gamma-glutamyl transferase (GGT) – an enzyme produced primarily by the liver and catalyzes glutathione, the main antioxidant in the body. The enzyme is elevated in some forms of liver disease, so physicians use GGT levels to detect liver damage and alcohol abuse.
In analyzing data from a long-term study involving more than 160,000 Austrian adults, the researchers found that the higher a persons blood level of GGT, the greater the risk of cardiovascular death. The levels are given in units per liter (U/l) of blood. Normal low is less than 9 U/l for women and less than 14 U/l for men. A moderately high value for GGT is 18 U/I for women and 28 U/I for men. High levels (twofold elevated) are more than 36 U/I for women and 56 U/I for men.
"People with high GGT had more than a 1.5-fold risk of dying from cardiovascular diseases in comparison to people with normal low levels of GGT," said senior author Hanno Ulmer, Ph.D. "For people under 60 years of age, this risk is even higher, amounting to more than two-fold. "Over the past decade, some small studies have suggested a link between high GGT and cardiovascular disease," said Ulmer, associate professor of medical statistics at the Innsbruck Medical University in Austria.
Several years ago, Italian researchers reported that elevated GGT could indicate early atherosclerosis. Ulmer and his colleagues investigated the researchers findings. They examined medical data collected from 1985–2001 from 163,944 (98.4 percent) of the then-enrolled volunteers in the Vorarlberg Health Monitoring and Promotion Program. This is an ongoing study in Austrias westernmost province that examines risk factors for chronic diseases.
The participants included 74,830 men and 89,114 women, age 19 or older when they entered the study, and had been followed for an average of 11 to 12 years.
After controlling for known cardiovascular risk factors, the team found that GGT was an independent predictor of fatal heart disease or stroke.
Among the studys other key findings:
Ulmer cited two mechanisms that might explain why GGT can indicate cardiovascular disease. The first, originally proposed by the Italian researchers, is that high GGT shows the presence of atherosclerosis. The second is that its related to the ill effects of heavy drinking on blood vessels.
"Beyond its role as an indicator of liver function, GGT is very likely to predict cardiovascular disease," Ulmer said. "Since GGT is correlated with established risk factors, the known ways of preventing the disease might also be effective in lowering GGT levels." Because the study participants were overwhelmingly white Austrians, the team could not say whether their findings hold true for other racial and ethnic groups.
"Both epidemiologic and experimental studies should be performed to confirm these findings," Ulmer said. "GGT should be included as a major parameter in future cardiovascular intervention studies."
In an accompanying editorial, Michele Emdin, M.D., of the cardiovascular medicine department at the National Research Council in Pisa, Italy, wrote that elevated GGT might help identify people with "the most risky combination for the vulnerable plaque, and the best medical strategies for the stabilization of lesions, rather than percutaneous or surgical."
Carole Bullock | Source: EurekAlert!
Further information: www.heart.org
More articles from
Life Sciences:
Caught in a trap: bumblebees vs. robotic crab spiders
05.09.2008 | Queen Mary, University of London
Do 68 molecules hold the key to understanding disease?
05.09.2008 | University of California - San Diego
Theory of the sun's role in formation of the solar system questioned
05.09.2008 | Earth Sciences
Caught in a trap: bumblebees vs. robotic crab spiders
05.09.2008 | Life Sciences
Do 68 molecules hold the key to understanding disease?
05.09.2008 | Life Sciences