'DNA mutation causes heart disease in whites

WASHINGTON, May 4 (Reuters) A treasure hunt for genes has found that up to three-quarters of people of European descent have DNA that raises their risk for heart disease -- and these genes are close to a stretch of DNA linked to diabetes.

The findings, made by two independent groups of researchers, may help explain why so many people have heart disease even if they do not have clear risk factors such as smoking, high cholesterol or high blood pressure.

And they could lead to a test to predict the risk of heart disease, the biggest cause of death across the globe. ''I think this is a stunner,'' Dr Francis Collins, director of the National Human Genome Research Institute, told reporters.

''It seems like this one place carries all of that weight for two very common and very dangerous diseases.'' Both teams used a new method of combing the genome for disease genes called a genome-wide association study, which was not possible until the full human genome was published in 2003. Now scientists can map the DNA of people with a disease, compare them to this template genome or to people without a disease, and find what is different.

The two studies, using 40,000 people, found the same thing -- a stretch of DNA called 9q21 carried certain mutations in people with heart disease. It is an area that had not previously been identified as a gene, which may make it more difficult to determine how it causes disease, scientists said.

Dr Ruth McPherson of the University of Ottawa Heart Institute and colleagues scanned blood samples from 23,000 people.

Anna Helgadottir of Iceland-based deCODE Genetics Inc. in Reykjavik and US colleagues at Emory University in Atlanta, the University of Pennsylvania and Duke University in North Carolina tested 17,000 people.

HEART ATTACK RISK The deCODE team found that about 21 per cent of the people they tested had mutations in both copies of this DNA stretch, giving them a 64 per cent higher risk of a heart attack than people who carried no copies of the mutation.

McPherson's team said 20 to 25 per cent of Caucasians they tested carrying two mutated copies of 9q21 and had a 30 to 40 per cent higher risk of coronary heart disease than people without the mutation. Half the people had one copy and they had a 15 percent to 20 per cent higher risk of heart disease.

Africans did not appear to carry the mutations, and in African-Americans, the mutations were not associated with heart disease risk, McPherson's team wrote.

The region is not associated with inherited tendencies to have high cholesterol or high blood pressure.

But 9q21 is found near two genes called CDKN2A and CDKN2B, which four international teams of researchers last week reported they had identified in their own genome-wide association study looking for diabetes.

Collins said the coincidence was astonishing.

''We are in the same place in the genome. Here is CDKN2B and 2A, their signal, exactly in the same place as where we found an association for type-2 diabetes,'' Collins told reporters.

While diabetes raises the risk of heart disease, the heart disease researchers made sure that the patients they scanned did not have diabetes. Collins said researchers will now have to look for a mechanism that explains why a single stretch of DNA could cause both conditions.

In the meantime, deCODE plans to find practical uses.

''DeCODE plans to bundle this discovery with other genetic variants it has linked to risk of heart attack into a DNA-based test for gauging inherited risk of (heart attack),'' the company said in a statement.

REUTERS SLD ND0956