Related Experiment Video
Updated: Apr 28, 2026

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies
Published on: January 28, 2014
Cardiac risk factors: biomarkers and genetic tests to determine cardiovascular risk
David Anthony1, Paul George2, Charles B Eaton3
1Memorial Hospital of Rhode Island, 111 Brewster St, Pawtucket, RI 02903, david_anthony@brown.edu.
Insights
Assessing coronary heart disease (CHD) risk involves multiple tools, including Framingham Risk Score and newer Pooled Cohort Equations. Biomarkers like C-reactive protein and lipoprotein (a) can refine CHD risk prediction.
Area of Science:
- Cardiology
- Biomarkers
- Risk Assessment
Background:
- Current guidelines emphasize global risk assessment for coronary heart disease (CHD).
- Established tools include the Framingham Risk Score (FRS) and Pooled Cohort Equations for 10-year risk prediction.
- Emerging biomarkers offer potential for enhanced risk stratification.
Observation:
- High-sensitivity C-reactive protein and family history improve CHD risk prediction when integrated into the Reynolds Risk Score.
- Elevated urinary albumin correlates with higher CHD event rates, though its incremental predictive value is modest.
- Lipoprotein (a) [Lp(a)] elevation predicts increased CHD risk, particularly in those with a family history of premature disease.
- Platelet-activating factor acetylhydrolase (Lp-PLA2) is another biomarker indicating elevated risk.
Findings:
- The Reynolds Risk Score refines 10-year CHD risk by incorporating inflammation biomarkers and family history into the FRS.
- Urinary albumin and Lp(a) show predictive value for CHD events, with Lp(a) testing recommended in specific clinical scenarios.
- Lp-PLA2 levels may influence treatment goals, such as low-density lipoprotein targets during statin therapy.
Implications:
- Integrating multiple biomarkers and clinical factors provides a more comprehensive assessment of individual CHD risk.
- Further research into genetic risk factors may lead to more personalized CHD prevention strategies in the future.
- Refined risk assessment can guide more targeted and effective preventive interventions for coronary heart disease.
Abstract:
Current guidelines recommend global risk assessment instruments as the primary approach for determining risk of coronary heart disease (CHD). The Framingham Risk Score (FRS) yields a 10-year risk of CHD, whereas the newer Pooled Cohort Equations yield a 10-year risk of stroke or CHD. High-sensitivity C-reactive protein, a biomarker for inflammation, along with family history of CHD, can be added to the parameters of the FRS in the Reynolds Risk Score to yield a more refined 10-year CHD risk. Various other biomarkers also can be used. Patients with elevated urinary albumin have higher rates of CHD events, though the incremental yield of adding urinary albumin provides only minor improvements in risk assessment compared with the FRS. Elevated levels of lipoprotein (a) [Lp(a)] also predict increased risk of CHD, and some guidelines recommend Lp(a) testing for patients with strong family histories of premature CHD. Another biomarker is platelet-activating factor acetylhydrolase (Lp-PLA2). Elevated levels indicate increased risk, and some recommendations suggest a lower goal level for low-density lipoprotein with statin therapy when Lp-PLA2 levels are high. Finally, genome-wide association studies for genetic risk of CHD currently are not recommended, but such tests likely will be useful within the next few years.
Related Concept Videos
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Blood Studies for Cardiovascular System I: Cardiac Biomarkers
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
Coronary Artery Disease I: Introduction
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenomics: Identification of New Drug Targets
Coronary Artery Disease IV: Preventive Measures

