Author: GENinCode US inc

  • New Study From GENinCode Shows Polygenic Risk Scores Improve the Accuracy of Cardiovascular Disease Risk Prediction

    New Study From GENinCode Shows Polygenic Risk Scores Improve the Accuracy of Cardiovascular Disease Risk Prediction

    NEW ORLEANS, LOUISIANA / ACCESS Newswire / November 12, 2025 / American Heart Association (“AHA”) Conference 2025, GENinCode the predictive genetics company focused on the prevention of cardiovascular disease (“CVD”), announces the presentation by Kaiser Permanente of a major clinical utility study on CARDIO inCode-Score Polygenic Risk Score (“PRS”) for the prevention of coronary heart disease (“CHD”).

    • Cardiovascular disease (“CVD”) is the leading cause of death in the US and worldwide with over 82 million Americans living with CVD.

    • CVD accounts for one in every three deaths in the US, or more than 900,000 deaths per year.

    • The estimated annual cost of CVD to US healthcare is over $400Bn with a consequential productivity loss of over $350Bn per annum which is forecast to exceed $1Trillion by 2035.

    The presentation titled ‘Enhancing the PREVENT Equation with a Polygenic Risk Score: Clinical Utility‘ showed the latest ASCVD clinical prediction tool ‘PREVENT’ was significantly enhanced by the inclusion of CARDIO inCode-Score (PRS), improving the predictive accuracy in personalised risk assessment for prevention of CHD.

    CARDIO inCode-Score is a clinically validated, commercially available polygenic risk score based on DNA extracted from a simple saliva or blood sample. The risk score has been designed and optimized for multi-ethnic population-based risk prediction and primary prevention of CHD in healthcare systems.

    GENinCode has worked with Kaiser Permanente Departments of Research and Cardiology on the clinical research and development of CARDIO inCode-Score for over 15 years. The multi-ancestry population study based on the Northern California GERA cohort studied over 60,000 individuals, 30-74 years of age, with follow up of 14 years and represents the latest in a series of CARDIO inCode-Score clinical utility publications.

    • The AHA presentation showed that integrating CARDIO inCode-Score with the PREVENT equation improves prediction of CHD events with statistical significance.

    • The benefit was particularly evident among borderline and intermediate PREVENT risk individuals, where there is uncertainty in clinical decision-making regarding statin initiation or intensification.

    • Combining CARDIO inCode-Score PRS with the PREVENT equation improves the ability to detect those most likely to develop ASCVD (NRI of 10.7%).

    • In addition, there was incremental risk stratification by CARDIO inCode-Score within each PREVENT risk group, more evident in borderline and intermediate risk categories. Notably, event rates for those at intermediate PREVENT risk with high PRS were higher than those at high PREVENT risk but low PRS (14.4% vs 12.4%).

    • Moreover, 50.2% of individuals in the borderline/intermediate PREVENT risk group with a high PRS were not on statin treatment. These individuals represent 9.2% of all people in the borderline/intermediate group.

    The clinical utility of CARDIO inCode-Score has also been validated in the Framingham Risk Score and the Pooled Cohort Equations, and now the PREVENT equation. CARDIO inCode-Score has also been assessed with the interplay between lifestyle and family history of CHD. Individuals with a high PRS can prevent incidence of CHD by as much as 52% by changing their lifestyle. A high PRS has also been shown to increase CHD risk greater than a positive ‘family history’ alone (64% higher vs 42% higher). The joint effect of a positive family history and a high PRS increases the hazard ratio by 2.3x, considerably improving CHD risk assessment based on family history. In addition, CARDIO inCode-Score has been shown to modulate the association of LDL-C with CHD, showing significantly increased risk from LDL-C levels of 100 mg/dL and above among individuals with a high PRS.

    Dr. Richard Kovacs, Q.E. and Sally Russell Professor of Cardiology at the Indiana University School of Medicine and Chief Medical Officer of the American College of Cardiology and Past President of the American College of Cardiology said:These results provide further compelling clinical evidence for the inclusion of polygenic risk scores (PRS) in conjunction with clinical risk for improved risk assessment of CHD. The polygenic risk score is especially important in relation to patients clinically classified at borderline/intermediate risk and younger patients with a family history of CHD. The recent scientific statements and acknowledgment of the value of PRS by the American College of Cardiology and American Heart Association is also welcome.”

    Our thanks to Dr. Jamal Rana and Dr. Carlos Iribarren for leading this clinical research and to co-authors Dr. Meng Lu, Dr. Martha Gulati, Dr. Nathan Wong and Dr. Roberto Elosua and our clinical advisory team for advocating the inclusion of genetic risk assessment in CHD risk assessment.

    Contact Information

    Matthew Walls
    CEO
    mwalls@genincode.com
    00447887501998

    .

    SOURCE: GENinCode US inc

    View the original press release on ACCESS Newswire

  • Publication of Landmark Study in JACC: Advances

    Publication of Landmark Study in JACC: Advances

    CARDIO inCode-Score Genetic Risk Influences Cholesterol Risk and Prediction of Coronary Heart Disease

    IRVINE, CA / ACCESS Newswire / October 28, 2025 / GENinCode, the predictive genetics company focused on prevention of cardiovascular disease (“CVD”), announces the publication of a major clinical study in JACC: Advances evaluating its CARDIO inCode-Score Polygenic Risk Score (“PRS”) for coronary heart disease (“CHD”). The study (https://share.google/nQwFO73QgGTiRqK45), was conducted at Kaiser Permanente’s Departments of Research and Cardiology in Pleasanton and Oakland. CA.

    Study Overview

    The study followed over 47,000 individuals of diverse ancestry for 14 years, analysing the relationship between low-density lipoprotein cholesterol (LDL-C) and polygenic risk for CHD. Participants were assessed for incidence of CHD events including myocardial infarction.

    CARDIO inCode-Score was used to quantify each participant’s inherited CHD risk and whether the effect of LDL-cholesterol on CHD risk was modified by an individual’s underlying genetic risk.

    Key Findings

    The results demonstrated polygenic risk significantly influences the relationship between LDL-cholesterol and CHD, with the combination of elevated LDL-C and high PRS conferring substantially greater risk supporting its use in clinical decision-making and preventive care.

    • Individuals with high polygenic risk experienced a 75% increase in CHD risk at LDL-C levels as low as 100 mg/dL (Hazard Ratio: 1.75).

    • At LDL-C levels of 130-160 mg/dL, risk increased more than twofold (HR: 2.1).

    • The combination of a high PRS and LDL-C of 190 mg/dL or higher was associated with a greater than 3.5-fold increase in CHD risk, comparable to the risk observed in patients with heterozygous familial hypercholesterolemia (FH).

    Clinical and Preventive Implications

    The study underscores the critical role that integrating genetic data with clinical assessments can play in revolutionising cardiovascular risk stratification and prevention and guide earlier intervention in at-risk populations. Individuals with high genetic risk may benefit from more proactive lipid management and lifestyle or therapeutic intervention, even at LDL-C levels traditionally considered low or moderate.

    By integrating PRS assessment into existing clinical pathways, healthcare providers can more accurately identify individuals at heightened lifetime risk of CHD and personalise prevention strategies. This can reduce the incidence of severe cardiovascular events, such as heart attacks and stroke and mitigate the economic costs associated with long-term heart disease care. The findings represent a significant step toward improving public health outcomes, particularly in addressing the global burden of cardiovascular disease.

    Dr. Richard Kovacs, Q.E. and Sally Russell Professor of Cardiology at IUSOM and Chief Medical Officer of the ACC and Past President of the ACC said:These results provide further compelling clinical evidence for the inclusion of polygenic risk scores (PRS) in conjunction with clinical risk for improved risk assessment of CHD. The polygenic risk score is especially important in relation to patients clinically classified at borderline/intermediate risk and younger patients with a family history of CHD. The recent scientific statements and acknowledgment of the value of PRS by the American College of Cardiology and American Heart Association is also welcome.

    Contact Information

    Matthew Walls
    CEO
    mwalls@genincode.com
    00447887501998

    .

    SOURCE: GENinCode US inc

    View the original press release on ACCESS Newswire