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These studies suggest that the 10-year ASCVD risk is useful for predicting cardiovascular events, especially in specific populations and conditions, but may be less accurate for younger patients and can be complemented by other tools and factors for better risk assessment.
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The 10-year risk models for atherosclerotic cardiovascular disease (ASCVD) are widely used to predict the likelihood of cardiovascular events within a decade. These models, such as the Pooled Cohort Equations (PCE), are essential tools for guiding preventive measures and treatment plans . The PCE, for instance, is a well-established model that stratifies patients into low, intermediate, and high-risk categories based on their 10-year risk of major adverse cardiovascular events (MACE).
While 10-year risk estimates are standard, recent studies suggest that lifetime risk estimates may provide a more comprehensive understanding of future ASCVD burden, especially in younger patients. For instance, a study comparing 10-year and lifetime risk in Dutch patients found significant discrepancies, particularly in younger age groups, where lifetime risk was substantially higher. This suggests that lifetime risk estimates could be more effective in identifying patients who might benefit from intensified preventive treatments.
Risk prediction models developed for specific populations can enhance the accuracy of ASCVD risk assessments. The China-PAR project, for example, developed and validated 10-year risk prediction equations tailored to the Chinese population. These equations demonstrated good performance and calibration, outperforming the Pooled Cohort Equations in this demographic. Similarly, a study in Shanghai compared the PCE and China-PAR models, finding that the latter provided lower and potentially more accurate risk estimates for the local population.
Cancer survivors are at a higher risk of developing ASCVD compared to the general population. A study using data from the National Health and Nutrition Examination Survey found that individuals with a history of cancer had significantly higher odds of elevated 10-year ASCVD risk, particularly those with specific types of cancer such as bladder, kidney, and lung cancer. This highlights the importance of cardiovascular health surveillance in cancer survivors to reduce the disease burden and prolong survival.
There is a notable correlation between 10-year ASCVD risk and depressive symptoms. A study conducted in Liaoning Province, China, found that higher 10-year ASCVD risk was associated with increased depressive symptoms, with the correlation being more pronounced in females. This suggests that mental health considerations should be integrated into cardiovascular risk assessments and management strategies.
The ASCVD-10 risk score has also been shown to predict the presence of true resistant hypertension (TRH) in high-risk overweight and obese individuals. A study found that a higher ASCVD-10 score was associated with an increased likelihood of TRH, indicating that this risk score could be useful in identifying patients who may require more aggressive hypertension management.
Emerging research suggests that proteomic and metabolomic profiling can enhance the prediction of ASCVD risk. For instance, the CV Risk SomaSignal® Test (SST) provides a 4-year risk probability of MACE and can be scaled to a 10-year risk, offering improved risk stratification compared to traditional models. Additionally, metabolomic profiling has identified several metabolites associated with 10-year ASCVD risk, which could serve as early indicators for preventive interventions.
Incorporating genetic information into risk assessments can further refine predictions. A study on individuals with type 2 diabetes found that adding a polygenic risk score (PRS) to the 10-year ASCVD risk model improved the prediction of incident ASCVD, particularly in those at borderline or intermediate risk. This approach could help identify patients who might benefit from more intensive statin therapy.
The 10-year ASCVD risk models remain a cornerstone in cardiovascular risk assessment, guiding preventive and therapeutic strategies. However, integrating lifetime risk estimates, population-specific models, mental health considerations, and advanced biomarkers can enhance the accuracy and effectiveness of these predictions. As research continues to evolve, these enhancements will likely play a crucial role in personalized cardiovascular care.
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