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Predicting atherosclerotic cardiovascular disease using AI

Icelandic deCODE genetics and its collaborators employed artificial intelligence (AI) to develop a protein score to predict major atherosclerotic cardiovascular disease events.

In a large retrospective analysis using measurements of thousands of plasma proteins in primary and secondary event populations, scientists from deCODE genetics and collaborators from USA, Denmark, and Iceland, reported in The Journal of the American Medical Association (JAMA) how they employed AI to develop a protein score to predict major atherosclerotic cardiovascular disease events (ASCVD).

Over 13,500 Icelanders

The study is based on a large data set consisting of over 13,500 Icelanders who had not experienced major ASCVD before plasma sampling and over 6,000 participants in the FOURIER trial who had suffered ASCVD before plasma sampling. All of these samples had measurements of the levels of around 5,000 plasma proteins measured with the SomaScan platform.

The protein risk score

The protein risk score, which is solely based on proteomics data from a single plasma sample, predicts ASCVD events well in the absence of information on medical history and risk factors. A large part of the risk captured by the proteins is also captured by established risk factors, however, the protein score captures additional risk.

Protein risk scores could become an important tool in clinical trials to get an early assessment of the efficacy of therapeutic intervention or for monitoring risk.”

What is more, the protein risk score is a dynamic measure and as such has the potential of being modified upon treatment unlike some of the classic risk factors that are immutable, such as family history and prior ASCVD events, states deCODE. This dynamic feature of protein risk scores, that the levels of proteins rise and fall as a function of time to and from events, makes it well-suited to predict the timing of events. As a result, protein risk scores could become an important tool in clinical trials to get an early assessment of the efficacy of therapeutic intervention or for monitoring risk.

We may have a biomarker that will allow the world to conduct shorter clinical trials with fewer participants.”

“We believe that in the proteomic risk score, we may have a biomarker that will allow the world to conduct shorter clinical trials with fewer participants. This is going to make the development of new medicines less expensive and make them available sooner for those who need them. Furthermore, in clinical practice it may allow for more effective prevention of ASCVD,” says Kari Stefansson, CEO of deCODE genetics and one of the senior investigators of the study.

Photo: deCODe genetics lab

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