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Multiparametric assessment of atrial cardiopathy in cryptogenic stroke patients: Implications for personalized
Iria López-Dequidt1, Sonia Eiras-Penas2,3, Adrián González-Maestro2,3
1Neurology Department, University Clinical Hospital of A Coruña, A Coruña, Galicia, Spain.
Insights
A new model combining N-terminal pro-brain natriuretic peptide (NT-proBNP) and left atrial strain (LAS) accurately identifies atrial cardiopathy (AC) in cryptogenic stroke (CS) patients. This aids in distinguishing cardioembolic from non-cardioembolic stroke causes.
Area of Science:
- Cardiology
- Neurology
- Medical Diagnostics
Background:
- Cryptogenic stroke (CS) has heterogeneous causes, with atrial cardiopathy (AC) increasingly recognized as a significant factor.
- Current diagnostic tools for early and accurate AC identification in CS patients are lacking.
- Atrial cardiopathy is a key substrate for both stroke and atrial fibrillation (AF).
Purpose of the Study:
- To develop and validate a diagnostic model for identifying atrial cardiopathy (AC) in patients with cryptogenic stroke (CS).
- To differentiate between cardioembolic and non-cardioembolic etiologies of stroke using biomarkers.
- To assess the clinical utility of a multiparametric model in guiding personalized patient management.
Main Methods:
- Prospective study involving patients with cardioembolic stroke due to AF (CES-AF), non-cardioembolic stroke (NCES), and CS.
- Evaluation of left atrial strain (LAS) via speckle-tracking echocardiography and serum AC markers.
- Development of a logistic regression model using ROC analysis to predict AC probability in CS patients.
Main Results:
- The combination of NT-proBNP levels (≥469 pg/mL) and biplanar LAS during contraction (LASct) (≥-10.2%) showed high accuracy (AUC=0.995) for AC detection.
- Approximately 30% of CS patients exhibited a predicted AC probability >0.5.
- CS patients with high predicted AC probability were older, had more severe strokes, and a higher incidence of AF during follow-up.
Conclusions:
- The combined NT-proBNP and biplanar LASct model provides highly sensitive and specific biomarkers for AC.
- This multiparametric approach enables individualized AC probability estimation in CS patients.
- The model shows potential utility in differentiating stroke etiologies and informing personalized clinical strategies.
Introduction:
Cryptogenic stroke (CS) represents a heterogeneous group in terms of etiology. Atrial cardiopathy (AC) has emerged as a relevant underlying substrate for both stroke and atrial fibrillation (AF) in these patients. However, no reliable tools are currently available for the early and accurate identification of AC.
Material And Methods:
We conducted a prospective study including consecutive patients with cardioembolic stroke due to AF (CES-AF), non-cardioembolic stroke (NCES) and cryptogenic stroke (CS). Left atrial strain (LAS) assessed by speckle-tracking echocardiography, and serum markers of AC were evaluated in CES-AF versus NCES patients using ROC curve analysis. Based on these results, we developed a logistic regression model to calculate the probability of AC in CS patients, aiming to discriminate between cardioembolic and non-cardioembolic etiology. Clinical characteristics were compared between CS patients with high (>0.5) and low (<0.5) predicted probability of AC.
Results:
A total of 136 patients were included: 44 with CES-AF, 52 with NCES, and 40 with CS. The combination of N-terminal pro-brain natriuretic peptide (NT-proBNP) levels ⩾ 469 pg/mL and biplanar LAS during the contraction phase (LASct) ⩾ -10.2% demonstrated the best-performing AC biomarker combination among those evaluated for identifying cardioembolic etiology (AUC = 0.995). Based on this combination, 30% of CS patients had a predicted probability > 0.5 for AC. These patients were older (77.3 ± 8 vs 68.8 ± 10 years; p = 0.011), had more severe strokes (NIHSS score 10.1 ± 7.5 vs 4.6 ± 5.2; p = 0.024) and showed a higher incidence of AF during follow-up (6 vs 0 cases; p = 0.029).
Conclusions:
The combination of NT-proBNP levels and biplanar LASct provides highly sensitive and specific biomarkers of AC. This multiparametric model allows for individualized estimation of AC probability in CS patients, supporting its potential utility in discriminating cardioembolic from non-cardioembolic etiologies and guiding personalized clinical management.
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