knitr::opts_chunk$set( collapse = TRUE, comment = "#>" )
The CVrisk package now includes support for the American Heart Association's PREVENT (Predicting Risk of cardiovascular disease EVENTs) equations, published in 2024. These equations provide improved cardiovascular risk prediction compared to legacy models like the Pooled Cohort Equations (PCE).
Implementation Note: The PREVENT risk calculations in CVrisk are powered by the preventr package, which provides a comprehensive implementation of the AHA PREVENT equations. While the PREVENT equations can predict multiple cardiovascular outcomes (total CVD, ASCVD, heart failure, CHD, and stroke), CVrisk focuses specifically on ASCVD (atherosclerotic cardiovascular disease) risk to maintain consistency with legacy risk scores for research applications.
This vignette demonstrates how to:
compute_CVrisk()The package provides two main functions:
ascvd_10y_prevent() - Calculate 10-year ASCVD riskascvd_30y_prevent() - Calculate 30-year ASCVD riskBoth functions support multiple model variants through the model parameter, with model = "auto" as the default, which automatically selects the best model based on available data.
The PREVENT equations support several model variants through the preventr package:
When model = "auto" (the default), the preventr package automatically selects the most appropriate model variant based on which optional predictors you provide in your data:
This intelligent selection ensures you always get the most accurate risk estimate based on your available data, without needing to manually specify which model variant to use. The auto-selection examines the data for each patient individually, so different patients in the same dataset can use different model variants based on their available data.
The base model requires these parameters:
library(CVrisk) # Calculate 10-year risk for a 50-year-old female risk_10y <- ascvd_10y_prevent( gender = "female", age = 50, sbp = 160, # Systolic blood pressure (mm Hg) bp_med = 1, # On BP medication (1=Yes, 0=No) totchol = 200, # Total cholesterol (mg/dL) hdl = 45, # HDL cholesterol (mg/dL) statin = 0, # On statin (1=Yes, 0=No) diabetes = 1, # Has diabetes (1=Yes, 0=No) smoker = 0, # Current smoker (1=Yes, 0=No) egfr = 90, # Estimated GFR (mL/min/1.73m²) bmi = 35 # Body mass index (kg/m²) ) print(risk_10y) # Returns risk as percentage
For younger patients, 30-year risk provides better long-term perspective:
# Calculate 30-year risk for a 45-year-old male risk_30y <- ascvd_30y_prevent( gender = "male", age = 45, sbp = 130, bp_med = 0, totchol = 200, hdl = 50, statin = 0, diabetes = 0, smoker = 1, # Current smoker egfr = 95, bmi = 28 ) print(risk_30y)
When HbA1c data is available, the model automatically uses the enhanced equation:
# With HbA1c - model will automatically select "hba1c" variant risk_with_hba1c <- ascvd_10y_prevent( gender = "male", age = 55, sbp = 140, bp_med = 0, totchol = 213, hdl = 50, statin = 0, diabetes = 1, smoker = 0, egfr = 90, bmi = 30, hba1c = 7.5, # Glycated hemoglobin (%) model = "auto" # Automatically uses hba1c model )
UACR (urine albumin-to-creatinine ratio) provides additional kidney function information:
# With UACR risk_with_uacr <- ascvd_10y_prevent( gender = "female", age = 60, sbp = 150, bp_med = 1, totchol = 220, hdl = 55, statin = 1, diabetes = 1, smoker = 0, egfr = 75, bmi = 32, uacr = 150 # UACR in mg/g )
SDI captures socioeconomic factors using ZIP code:
# With ZIP code for SDI risk_with_sdi <- ascvd_10y_prevent( gender = "male", age = 52, sbp = 135, bp_med = 0, totchol = 195, hdl = 48, statin = 0, diabetes = 0, smoker = 0, egfr = 88, bmi = 29, zip = "02114" # Boston, MA )
When multiple optional predictors are available:
# Full model with all optional predictors risk_full <- ascvd_10y_prevent( gender = "female", age = 58, sbp = 145, bp_med = 1, totchol = 210, hdl = 52, statin = 1, diabetes = 1, smoker = 0, egfr = 80, bmi = 31, hba1c = 7.2, uacr = 100, zip = "10001", model = "auto" # Will use full model )
You can explicitly specify which model to use instead of "auto":
# Force base model even with optional predictors available risk_base_only <- ascvd_10y_prevent( gender = "male", age = 55, sbp = 140, bp_med = 0, totchol = 213, hdl = 50, statin = 0, diabetes = 1, smoker = 0, egfr = 90, bmi = 30, hba1c = 7.5, # Available but will be ignored model = "base" # Explicitly use base model )
The compute_CVrisk() function allows you to calculate multiple risk scores simultaneously and compare PREVENT with legacy scores.
# Create sample patient data patient_data <- data.frame( age = c(50, 55, 60), gender = c("female", "male", "female"), race = c("white", "aa", "white"), sbp = c(160, 140, 150), bp_med = c(1, 0, 1), totchol = c(200, 213, 220), hdl = c(45, 50, 55), statin = c(0, 0, 1), diabetes = c(1, 0, 1), smoker = c(0, 0, 0), egfr = c(90, 90, 75), bmi = c(35, 30, 32) ) # Compare PREVENT 10-year with ACC/AHA 2013 results <- compute_CVrisk( patient_data, scores = c("ascvd_10y_accaha", "ascvd_10y_prevent"), age = "age", gender = "gender", race = "race", sbp = "sbp", bp_med = "bp_med", totchol = "totchol", hdl = "hdl", statin = "statin", diabetes = "diabetes", smoker = "smoker", egfr = "egfr", bmi = "bmi" ) # View results print(results[, c("age", "gender", "ascvd_10y_accaha", "ascvd_10y_prevent")])
# Compare PREVENT with Framingham Risk Score results_frs <- compute_CVrisk( patient_data, scores = c("ascvd_10y_frs", "ascvd_10y_prevent"), age = "age", gender = "gender", sbp = "sbp", bp_med = "bp_med", totchol = "totchol", hdl = "hdl", diabetes = "diabetes", smoker = "smoker", egfr = "egfr", bmi = "bmi" ) print(results_frs)
# Calculate multiple scores including 30-year risk comprehensive_results <- compute_CVrisk( patient_data, scores = c("ascvd_10y_accaha", "ascvd_10y_frs", "ascvd_10y_prevent", "ascvd_30y_prevent"), age = "age", gender = "gender", race = "race", sbp = "sbp", bp_med = "bp_med", totchol = "totchol", hdl = "hdl", statin = "statin", diabetes = "diabetes", smoker = "smoker", egfr = "egfr", bmi = "bmi" ) # View side-by-side comparison print(comprehensive_results[, c("age", "gender", "ascvd_10y_accaha", "ascvd_10y_frs", "ascvd_10y_prevent", "ascvd_30y_prevent")])
You can specify the PREVENT model variant when using compute_CVrisk():
# Force base model for all PREVENT calculations results_base <- compute_CVrisk( patient_data, scores = c("ascvd_10y_prevent", "ascvd_30y_prevent"), age = "age", gender = "gender", sbp = "sbp", bp_med = "bp_med", totchol = "totchol", hdl = "hdl", statin = "statin", diabetes = "diabetes", smoker = "smoker", egfr = "egfr", bmi = "bmi", model = "base" # Pass model parameter )
The PREVENT functions return NA for patients with missing required predictors:
# Patient with missing eGFR risk_missing <- ascvd_10y_prevent( gender = "male", age = 55, sbp = 140, bp_med = 0, totchol = 213, hdl = 50, statin = 0, diabetes = 0, smoker = 0, egfr = NA, # Missing bmi = 30 ) print(risk_missing) # Returns NA
Both PREVENT functions are vectorized and work efficiently with data frames:
# Calculate risks for multiple patients at once ages <- c(45, 50, 55, 60) genders <- c("male", "female", "male", "female") sbps <- c(130, 140, 150, 160) risks <- ascvd_10y_prevent( gender = genders, age = ages, sbp = sbps, bp_med = c(0, 0, 1, 1), totchol = c(200, 210, 220, 230), hdl = c(50, 45, 55, 48), statin = c(0, 0, 0, 1), diabetes = c(0, 0, 1, 1), smoker = c(0, 1, 0, 0), egfr = c(95, 90, 85, 80), bmi = c(28, 30, 32, 34) ) print(risks) # Returns vector of risks
PREVENT equations typically provide more accurate risk estimates because they:
The table below compares all clinical parameters across the available risk scores in CVrisk:
| Clinical Parameter | PREVENT (2024) | ACC/AHA (2013) | Framingham (2008) | MESA (2015) | |-------------------|---------|--------------|-----------------|-------------| | Age range | 30-79 years | 40-79 years | 30-74 years | 45-85 years | | Gender | Required | Required | Required | Required | | Race | Not used | Required (White/AA/Other) | Not used | Required (White/AA/Chinese/Hispanic) | | Systolic BP | Required | Required | Required | Required | | BP medication | Required | Required | Required | Required | | Total cholesterol | Required | Required | Required | Required | | HDL cholesterol | Required | Required | Required | Required | | Diabetes status | Required | Required | Required | Required | | Smoking status | Required | Required | Required | Required | | Lipid medication | Required (statin) | Not used | Not used | Required (lipid meds) | | BMI | Required | Not used | Optional | Not used | | eGFR | Required | Not used | Not used | Not used | | Family history | Not used | Not used | Not used | Optional | | CAC score | Not used | Not used | Not used | Optional | | HbA1c | Optional | Not used | Not used | Not used | | UACR | Optional | Not used | Not used | Not used | | ZIP code (SDI) | Optional | Not used | Not used | Not used | | 30-year risk | Yes | No | No | No | | Risk outcome | ASCVD | ASCVD | CVD (broader) | CHD |
Key advantages of PREVENT: - Most comprehensive risk factor assessment (includes kidney function via eGFR) - Does not require race (reduces potential for bias) - Accounts for statin therapy - Offers optional predictors for enhanced accuracy (HbA1c, UACR, socioeconomic factors) - Provides both 10-year and 30-year risk estimates
Khan SS, Matsushita K, Sang Y, et al. Development and Validation of the American Heart Association's PREVENT Equations. Circulation. 2024;149(6):430-449. doi:10.1161/CIRCULATIONAHA.123.067626
Mayer MG. preventr: R Implementation of the AHA PREVENT Equations. R package. https://github.com/martingmayer/preventr
McClelland RL, Jorgensen NW, Budoff M, et al. 10-Year Coronary Heart Disease Risk Prediction Using Coronary Artery Calcium and Traditional Risk Factors: Derivation in the MESA (Multi-Ethnic Study of Atherosclerosis) With Validation in the HNR (Heinz Nixdorf Recall) Study and the DHS (Dallas Heart Study). J Am Coll Cardiol. 2015;66(15):1643-1653. doi:10.1016/j.jacc.2015.08.035
D’agostino, RB, Vasan, RS, Pencina, et al. General cardiovascular risk profile for use in primary care: the Framingham Heart Study. Circulation. 2008;117(6), pp.743-753.
Goff, DC, et al. 2013 ACC/AHA guideline on the assessment of cardiovascular risk: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Journal of the American College of Cardiology. 2014;63.25 Part B: 2935-2959.
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