General cardiovascular risk profile for use in primary care: the Framingham Heart Study
Ralph B D'Agostino1, Ramachandran S Vasan, Michael J Pencina
1Boston University, Department of Mathematics and Statistics, 111 Cummington St, Boston, MA 02215, USA.
Insights
A new sex-specific algorithm predicts overall atherosclerotic cardiovascular disease (CVD) risk and individual event risks. This tool aids in quantifying risk and guiding preventive care for better cardiovascular health.
Area of Science:
- Cardiology
- Preventive Medicine
- Epidemiology
Background:
- Current practice uses separate risk algorithms for distinct atherosclerotic cardiovascular disease (CVD) events.
- A unified approach is needed to assess overall CVD risk and its components.
Purpose of the Study:
- To develop and validate a single, sex-specific multivariable risk algorithm for predicting general CVD risk.
- To assess the algorithm's ability to predict individual CVD events, including coronary heart disease, stroke, peripheral artery disease, and heart failure.
Main Methods:
- Cox proportional-hazards regression analysis of 8491 Framingham study participants.
- Inclusion of traditional risk factors: age, cholesterol, blood pressure, hypertension treatment, smoking, and diabetes status.
- Validation of sex-specific algorithms for predicting general and specific CVD events over 12 years.
Main Results:
- The developed "general CVD" algorithm demonstrated good predictive performance (C-statistics: 0.763 for men, 0.793 for women).
- All evaluated traditional risk factors significantly predicted CVD risk (P<0.0001).
- Simple adjustments allowed estimation of risks for individual CVD components.
Conclusions:
- A sex-specific multivariable algorithm effectively assesses general CVD risk and individual event risks.
- This tool can quantify absolute CVD event rates to guide preventive strategies.
- The algorithm offers a convenient method for risk assessment in clinical practice.
Background:
Separate multivariable risk algorithms are commonly used to assess risk of specific atherosclerotic cardiovascular disease (CVD) events, ie, coronary heart disease, cerebrovascular disease, peripheral vascular disease, and heart failure. The present report presents a single multivariable risk function that predicts risk of developing all CVD and of its constituents.
Methods And Results:
We used Cox proportional-hazards regression to evaluate the risk of developing a first CVD event in 8491 Framingham study participants (mean age, 49 years; 4522 women) who attended a routine examination between 30 and 74 years of age and were free of CVD. Sex-specific multivariable risk functions ("general CVD" algorithms) were derived that incorporated age, total and high-density lipoprotein cholesterol, systolic blood pressure, treatment for hypertension, smoking, and diabetes status. We assessed the performance of the general CVD algorithms for predicting individual CVD events (coronary heart disease, stroke, peripheral artery disease, or heart failure). Over 12 years of follow-up, 1174 participants (456 women) developed a first CVD event. All traditional risk factors evaluated predicted CVD risk (multivariable-adjusted P<0.0001). The general CVD algorithm demonstrated good discrimination (C statistic, 0.763 [men] and 0.793 [women]) and calibration. Simple adjustments to the general CVD risk algorithms allowed estimation of the risks of each CVD component. Two simple risk scores are presented, 1 based on all traditional risk factors and the other based on non-laboratory-based predictors.
Conclusions:
A sex-specific multivariable risk factor algorithm can be conveniently used to assess general CVD risk and risk of individual CVD events (coronary, cerebrovascular, and peripheral arterial disease and heart failure). The estimated absolute CVD event rates can be used to quantify risk and to guide preventive care.
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