Protein-Based Risk Score May Help Predict Cardiovascular Events in Stable CHD

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A 9-protein risk score may help predict CV events in stable coronary heart disease.
A 9-protein risk score may help predict CV events in stable coronary heart disease.

(HealthDay News) — A 9-protein risk score may help predict cardiovascular events among patients with stable coronary heart disease (CHD), according to a study published in the Journal of the American Medical Association.

Peter Ganz, MD, from the University of California, San Francisco, and colleagues conducted a prospective cohort study involving patients with stable CHD. They derived and validated a 9-protein risk score for 4-year probability of myocardial infarction, stroke, heart failure, and all-cause death in a derivation cohort that included 938 samples and a validation cohort with 971 samples. The risk score was compared with the Framingham secondary event model, refit to the cohorts in this study.

The researchers found that the C statistics were 0.66, 0.74, and 0.75 for refit Framingham, 9-protein, and refit Framingham plus 9-protein models, respectively, in the discrimination cohort. The corresponding C statistics were 0.64, 0.70, and 0.71, in the validation cohort.

Adding the 9-protein risk score to the refit Framingham correlated with a 0.09 and 0.05 increase in the C statistic in the derivation and validation cohorts, respectively. The integrated discrimination index for the 9-protein model compared with the refit Framingham model was 0.12 and 0.08 in the derivation and validation cohorts, respectively.

"Further research is needed to assess whether the score is more accurate in a lower-risk population," the researchers wrote.

Disclosures: Several authors disclosed financial ties to SomaLogic, which provided funding for and execution of the protein assays.

Reference

  1. Ganz P, Heidecker B, Hveem K, et al. Development and Validation of a Protein-Based Risk Score for Cardiovascular Outcomes Among Patients With Stable Coronary Heart Disease. JAMA. 2016;315(23):2532-2541. doi:10.1001/jama.2016.5951.
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