TY - JOUR
T1 - Blood-Based Biomarkers to Search for Atrial Fibrillation in High-Risk Asymptomatic Individuals and Cryptogenic Stroke Patients
AU - Palà, Elena
AU - Bustamante, Alejandro
AU - Pagola, Jorge
AU - Juega, Jesus
AU - Francisco-Pascual, Jaume
AU - Penalba, Anna
AU - Rodriguez, Maite
AU - De Lera Alfonso, Mercedes
AU - Arenillas, Juan F.
AU - Cabezas, Juan Antonio
AU - Pérez-Sánchez, Soledad
AU - Moniche, Francisco
AU - de Torres, Reyes
AU - González-Alujas, Teresa
AU - Clúa-Espuny, Josep Lluís
AU - Ballesta-Ors, Juan
AU - Ribas, Domingo
AU - Acosta, Juan
AU - Pedrote, Alonso
AU - Gonzalez-Loyola, Felipe
AU - Gentile Lorente, Delicia
AU - Ángel Muñoz, Miguel
AU - Molina, Carlos A.
AU - Montaner, Joan
N1 - Publisher Copyright:
Copyright © 2022 Palà, Bustamante, Pagola, Juega, Francisco-Pascual, Penalba, Rodriguez, De Lera Alfonso, Arenillas, Cabezas, Pérez-Sánchez, Moniche, de Torres, González-Alujas, Clúa-Espuny, Ballesta-Ors, Ribas, Acosta, Pedrote, Gonzalez-Loyola, Gentile Lorente, Ángel Muñoz, Molina and Montaner.
PY - 2022/7/4
Y1 - 2022/7/4
N2 - Background: Atrial fibrillation (AF) increases the risk of ischemic stroke in asymptomatic individuals and may be the underlying cause of many cryptogenic strokes. We aimed to test the usefulness of candidate blood-biomarkers related to AF pathophysiology in two prospective cohorts representative of those populations. Methods: Two hundred seventy-four subjects aged 65–75 years with hypertension and diabetes from the AFRICAT cohort, and 218 cryptogenic stroke patients aged >55 years from the CRYPTO-AF cohort were analyzed. AF was assessed by 4 weeks of monitoring with a wearable Holter device (NuuboTM™). Blood was collected immediately before monitoring started. 10 candidate biomarkers were measured by automated immunoassays (Roche, Penzberg) in the plasma of all patients. Univariate and logistic regression analyses were performed in each cohort separately. Results: Atrial fibrillation detection rate was 12.4% (AFRICAT cohort) and 22.9% (CRYPTO-AF cohort). 4 biomarkers were significantly increased in asymptomatic individuals with AF [Troponin-T, Angiopoietin-2 (Ang-2), Endocan, and total N-terminal pro-B type natriuretic peptide (NT-proBNP)] and 7 biomarkers showed significantly higher concentrations in cryptogenic stroke patients with AF detection [growth differentiation factor 15, interleukin 6, Troponin-T, Ang-2, Bone morphogenic protein 10, Dickkopf-related protein 3 (DKK-3), and total NT-proBNP]. The models including Ang-2 and total NT-proBNP [AUC 0.764 (0.665–0.863)], and Ang-2 and DKK-3 [AUC = 0.733 (0.654–0.813)], together with age and sex, showed the best performance to detect AF in high-risk asymptomatic individuals, and in cryptogenic stroke patients, respectively. Conclusion: Blood-biomarkers, in particular, total NT-proBNP, DKK-3, and Ang-2, were associated with AF reflecting two mechanistically different pathways involved in AF pathophysiology (AF stretch and vascular changes). The combination of these biomarkers could be useful in AF screening strategies in the primary care setting and also for searching AF after cryptogenic stroke.
AB - Background: Atrial fibrillation (AF) increases the risk of ischemic stroke in asymptomatic individuals and may be the underlying cause of many cryptogenic strokes. We aimed to test the usefulness of candidate blood-biomarkers related to AF pathophysiology in two prospective cohorts representative of those populations. Methods: Two hundred seventy-four subjects aged 65–75 years with hypertension and diabetes from the AFRICAT cohort, and 218 cryptogenic stroke patients aged >55 years from the CRYPTO-AF cohort were analyzed. AF was assessed by 4 weeks of monitoring with a wearable Holter device (NuuboTM™). Blood was collected immediately before monitoring started. 10 candidate biomarkers were measured by automated immunoassays (Roche, Penzberg) in the plasma of all patients. Univariate and logistic regression analyses were performed in each cohort separately. Results: Atrial fibrillation detection rate was 12.4% (AFRICAT cohort) and 22.9% (CRYPTO-AF cohort). 4 biomarkers were significantly increased in asymptomatic individuals with AF [Troponin-T, Angiopoietin-2 (Ang-2), Endocan, and total N-terminal pro-B type natriuretic peptide (NT-proBNP)] and 7 biomarkers showed significantly higher concentrations in cryptogenic stroke patients with AF detection [growth differentiation factor 15, interleukin 6, Troponin-T, Ang-2, Bone morphogenic protein 10, Dickkopf-related protein 3 (DKK-3), and total NT-proBNP]. The models including Ang-2 and total NT-proBNP [AUC 0.764 (0.665–0.863)], and Ang-2 and DKK-3 [AUC = 0.733 (0.654–0.813)], together with age and sex, showed the best performance to detect AF in high-risk asymptomatic individuals, and in cryptogenic stroke patients, respectively. Conclusion: Blood-biomarkers, in particular, total NT-proBNP, DKK-3, and Ang-2, were associated with AF reflecting two mechanistically different pathways involved in AF pathophysiology (AF stretch and vascular changes). The combination of these biomarkers could be useful in AF screening strategies in the primary care setting and also for searching AF after cryptogenic stroke.
KW - Atrial fibrillation
KW - Biomarkers
KW - Cryptogenic stroke
KW - Screening
KW - Stroke
KW - Atrial fibrillation
KW - Biomarkers
KW - Cryptogenic stroke
KW - Screening
KW - Stroke
KW - Atrial fibrillation
KW - Biomarkers
KW - Cryptogenic stroke
KW - Screening
KW - Stroke
UR - http://www.scopus.com/inward/record.url?scp=85134404431&partnerID=8YFLogxK
U2 - 10.3389/fcvm.2022.908053
DO - 10.3389/fcvm.2022.908053
M3 - Article
AN - SCOPUS:85134404431
VL - 9
JO - Frontiers in Cardiovascular Medicine
JF - Frontiers in Cardiovascular Medicine
M1 - 908053
ER -