Genetic factors have long been known to make a significant contribution to CHD risk. Recent advances in genetics have led to the identification of many Single Nucleotide Polymorphisms (SNPs) - very small differences in our DNA that vary from person to person.
By looking at over 49,000 SNPs, researchers created a score, known as a genomic risk score (GRS) and showed that the higher the GRS the higher the future risk of CHD.
The study from University of Leicester in the UK is the first to look at a much larger number of SNPs to give a fuller picture of an individual's genetic risk of developing CHD.
Currently, clinical risk scores are based on known risk factors for CHD such as cholesterol level, having high blood pressure or diabetes and smoking.
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However, such scores are imprecise and unable to identify a large proportion of people who develop CHD. The researchers showed that the GRS was independent of the clinical risk scores and by combining the two risk score tools they were better able to predict people who were at risk of developing CHD in the next 10 years.
"We already know that CHD starts at an early age, several decades before symptoms develop, and preventative measures should ideally be applied much earlier, especially to those who are at increased risk," Samani said.
"Current clinical risk scores are not good at evaluating risk until middle-age. On the other hand the GRS, which is based on your DNA, can be applied at any age," he said.
The research was published in the European Heart Journal.