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Some studies suggest that 10-year cardiovascular risk prediction models are effective for certain populations and conditions, while other studies indicate that they may overestimate risk or be less accurate compared to lifetime risk assessments, especially in younger and middle-aged individuals.
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The 10-year cardiovascular risk metric is a widely used tool to estimate the likelihood of developing cardiovascular disease (CVD) within a decade. This metric helps healthcare professionals identify individuals at high risk and implement preventive measures. Various models and algorithms have been developed to predict this risk, each with its own strengths and limitations.
The Framingham risk models and pooled cohort equations (PCE) are among the most commonly used tools for predicting 10-year risk of coronary heart disease (CHD) and CVD. These models consider factors such as age, sex, blood pressure, cholesterol levels, smoking status, and diabetes. However, studies have shown that these models often overestimate the risk, especially in high-risk populations and European cohorts, necessitating local recalibration for accurate predictions.
SCORE2 is a recently developed algorithm designed to estimate the 10-year risk of first-onset CVD in European populations. It includes factors like age, sex, smoking status, systolic blood pressure, and cholesterol levels, and is recalibrated for different European regions to improve accuracy. SCORE2-Diabetes extends this model to individuals with type 2 diabetes, incorporating diabetes-specific variables such as HbA1c and estimated glomerular filtration rate (eGFR) to enhance risk prediction.
Globorisk provides both laboratory-based and office-based risk scores to predict 10-year CVD risk in 182 countries. The laboratory-based model includes traditional risk factors, while the office-based model substitutes BMI for cholesterol and diabetes, making it useful in settings without laboratory access. Both models have been recalibrated for country-specific risk factors and CVD rates, although the office-based model may underestimate risk in diabetic patients.
The EPOCH-JAPAN study developed risk prediction models for the Japanese population, focusing on the absolute 10-year risk of death from CHD, stroke, and CVD. The models demonstrated high discrimination and adequate calibration, making them effective tools for primary prevention in Japan.
In China, the Guangzhou Biobank Cohort Study developed a 10-year CVD risk prediction model tailored to contemporary Chinese populations. This model showed better discrimination and closer alignment with actual risk compared to the Framingham and China-PAR models, highlighting the importance of population-specific risk assessments.
The 10-year risk metric often underestimates the risk in younger individuals and women, as it is heavily influenced by age and sex. This limitation can lead to insufficient preventive measures for these groups, despite their high lifetime risk of CVD.
Recent studies suggest that lifetime risk estimates may provide a more comprehensive assessment of future CVD burden, especially for younger patients with risk factors. Communicating lifetime risk can enhance patient perception and willingness to engage in preventive therapies .
The 10-year cardiovascular risk metric remains a valuable tool for predicting CVD risk and guiding preventive strategies. However, its limitations necessitate the use of region-specific models and consideration of lifetime risk, particularly for younger and female populations. By integrating these insights, healthcare professionals can better identify high-risk individuals and implement effective prevention programs.
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