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In one of the grimmest public health research findings yet, researches have warned that a gene mutation that “almost guarantees the development of heart disease” is carried by 60 million people.

 

Around 4% people from the Indian subcontinent have the mutation, which increases the risk of heart disease 7-fold, Nature Genetics reports.
It is rare to find a gene which has such a big effect and is so common. It is almost like finding a time bomb in a large population but there is no means to defuse it! The researchers first identified the mutation in the heart protein gene MYBPC3 five years ago in two Indian families with cardiomyopathy - a disease causing deterioration of the heart muscle. And the increased risk of heart disease - seven times that of people without the mutation - is so high is almost guarantees the development of heart problems.

Heart disease is a massive global killer, and it is predicted that by 2010 India's population will suffer approximately 60% of the world's heart disease. Experts said it could lead to a screening test but it was not yet clear if it would aid treatment decisions.

Abnormal protein
In the test tube, cells with the mutation - where 25 letters of genetic code are missing - the MYBPC3 protein is abnormal and "messes up" the structure of the heart muscle.
The researchers said in younger people the body seemed to have an effective mechanism for breaking down and removing the mutated protein. But with age the mechanism stops working efficiently which is why heart disease in people carrying the gene develops in middle age.
Chris Tyler-Smith, a senior investigator at The Wellcome Trust Sanger Institute, Hinxton, UK, and one of the study authors said the mutation probably arose around 30,000 years ago and has been able to spread because its effects usually develop only after people have had their children.
"What we expect to find are common mutations with very small effects or rare mutations with big effects. The combination of big effects and high frequency is surprising."
He said "in principle" it would be extremely easy to test people at a young age for the gene but at the moment all that doctors could do would be to offer healthy lifestyle advice.

Professor Peter Weissberg, medical director at the British Heart Foundation, said the study underpins the strong genetic nature of heart disease. This news is made grimmer by the fact that besides counselling and rehabilitation, there is no remedy at disposal currently!
"It provides good grounds for screening people of South Asian origin with unexplained heart failure and screening their families if positive."
"However, there is no evidence yet that early detection will lead to improved outcome since we have no idea if the outlook for this group can be modified by conventional heart failure treatments."

Adapted from BBC News

 

 

 

 

 

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