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Published on: July 20, 2022
Biomarker Assays for Personalised Stroke Risk Assessment in Atrial Fibrillation
Angela Hall1, Rupert F G Simpson1, Andrew R J Mitchell2
1Department of Cardiology, Jersey General Hospital, Jersey, United Kingdom.
Insights
For atrial fibrillation patients at intermediate stroke risk, cardiac biomarkers like troponin and BNP can improve personalized risk assessment. These markers aid in deciding whether to start anticoagulation therapy.
Area of Science:
- Cardiology
- Neurology
- Biomarker Research
Background:
- Atrial fibrillation is a significant stroke risk factor.
- Current guidelines lack consensus on anticoagulation for intermediate-risk patients (CHA2DS2-VASc score 1).
- Need for enhanced stroke risk stratification beyond conventional tools.
Purpose of the Study:
- To explore the use of cardiac biomarkers for personalized thromboembolism risk assessment in atrial fibrillation.
- To aid clinicians in managing intermediate-risk atrial fibrillation patients.
- To assist in the decision-making process for initiating anticoagulation.
Main Methods:
- Utilizing advanced cardiac biomarkers: highly sensitive troponins, B-type natriuretic peptide (BNP), and D-dimers.
- Integrating biomarker data with conventional stroke risk stratification tools.
- Focusing on patients with atrial fibrillation and an intermediate stroke risk score.
Main Results:
- Cardiac biomarkers offer incremental enhancements for personalized risk assessment.
- These markers provide prognostic data for cardiovascular morbidities.
- Biomarkers add specificity to assessing stroke and thromboembolic risk in atrial fibrillation.
Conclusions:
- Cardiac biomarkers can improve stroke risk assessment in intermediate-risk atrial fibrillation patients.
- Personalized risk assessment using biomarkers aids anticoagulation decisions.
- Biomarker assays enhance risk prognosis alongside existing tools.
Background:
Atrial fibrillation is a well-known independent risk factor for stroke yet there is no international consensus on guidelines regarding the introduction of anticoagulation in patients deemed at intermediate risk (e.g. CHA2DS2-VASc of 1). The evolution of cardiac biomarkers such as highly sensitive troponins and B-type natriuretic peptide as well as data on D-dimers, may offer incremental enhancements for personalized thromboembolism risk assessment. These markers provide prognostic data for risk of cardiovascular morbidities associated with atrial fibrillation and offer additional specificity for assessing stroke and thromboembolic risk. These assays may therefore enhance risk prognosis in atrial fibrillation alongside conventional stroke risk stratification tool patients. We seek to explore the application of personalised risk assessment using the biomarkers to aid the clinician treating the patient with atrial fibrillation deemed to be at intermediate risk of stroke.
Conclusion:
The stroke risk assessment of a patient with an intermediate risk of stroke (CHA2DS2- VASc score 1) may be improved by using cardiac biomarkers such as highly sensitive troponin, BNP and D-dimers. We explore the application of these biomarkers to provide personalised risk assessment to help a patient with AF decide on whether to commence anticoagulation.
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