ArticleFrontiers in physiology2026
ECG-derived Poincaré plot graphical metrics for differentiating axillary lymph node metastasis in breast cancer.
Article in Frontiers in physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Axillary lymph node metastasis (ALNM) status serves as a cornerstone for clinical decision-making in personalized breast cancer (BC) management. Although autonomic nervous system (ANS) dysfunction correlates with tumor progression, its applicability for capturing BC-ALNM-specific ANS signatures remains exploratory. This proof-of-concept study aimed to investigate whether Poincaré plot analysis of short-duration electrocardiograms could potentially identify ANS signals associated with ALNM more effectively than conventional heart rate variability (HRV) metrics. Methods: Resting electrocardiograph data were collected from 218 pathologically confirmed BC patients at the First Affiliated Hospital of Bengbu Medical University (142 ALNM-positive, 76 ALNM-negative). Conventional HRV metrics and Poincaré plot-derived spatial metrics were compared using raw and detrended data. Beyond univariable comparisons evaluated by Cohen's d effect sizes with 95% confidence intervals (CIs), multivariable Analysis of Covariance (ANCOVA) adjusting for clinicopathological confounders were employed to ensure model robustness. Discriminative performance was evaluated using Receiver Operating Characteristic (ROC) analysis. To assess the potential for overfitting, a 10-fold cross-validation procedure was implemented for the ROC analysis. Results: Conventional metrics showed no significant intergroup differences or predictive value (AUC = 0.532). Univariable analysis revealed differences in the detrended Area Index (AI) ( Conclusions: In this exploratory study, Poincaré plot analysis, specifically the detrended AI, suggests a potential methodological advantage for characterizing ALNM-associated autonomic spatial asymmetry independent of general tumor burden. However, given the modest discriminative ability and single-center design, these findings must be interpreted with caution. These non-invasive metrics may offer a novel pathophysiological perspective but require future large-scale, multi-center prospective studies to overcome current limitations and validate their clinical utility.
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