Sep 2026· Cardiology in Review· 0 citations· 51 references
Medicine
TL;DR
Evidence on all 3 LA strain phases in ESUS through July 2026 supports subclinical atrial cardiomyopathy as an embolic substrate independent of atrial fibrillation.
Abstract
Embolic stroke of undetermined source (ESUS) accounts for approximately one-third of all ischemic strokes. Atrial cardiomyopathy, independent of paroxysmal atrial fibrillation, is an increasingly recognized embolic substrate. Left atrial (LA) strain assessed by speckle-tracking echocardiography or cardiac magnetic resonance provides a sensitive, noninvasive measure of subclinical atrial mechanical dysfunction that precedes chamber enlargement. This systematic review and meta-analysis synthesizes evidence on all 3 LA strain phases in ESUS through July 2026. Seven studies met the inclusion criteria; 5 provided extractable quantitative data for meta-analysis (n = 656, n = 40, n = 56, n = 82, and n = 459; total N = 1293). ESUS patients demonstrated significantly reduced LA reservoir strain [mean difference (MD) = -4.43%, 95% confidence interval (CI), -6.77 to -2.09; I2 = 82.25%; P = 0.0002], LA conduit strain (LAScd) (MD = -1.69%, 95% CI, -2.20 to -1.18; I2 = 0.00%; P < 0.0001), and LA contractile strain (MD = -2.24%, 95% CI, -3.34 to -1.14; I2 = 69.92%; P < 0.0001). LAScd I2 = 0.00% indicates remarkably consistent conduit impairment across all 5 studies. All 5 meta-analytic studies achieved a Newcastle-Ottawa Scale score of ≥7. All 3 LA strain phases are consistently and significantly impaired in ESUS patients versus controls. Near-zero LAScd heterogeneity identifies conduit strain as the most reproducible marker of atrial cardiomyopathy in ESUS. These findings support subclinical atrial cardiomyopathy as an embolic substrate independent of atrial fibrillation. Large, prospective, standardized multicenter studies are required before clinical translation.
Background/Objectives: Embolic Stroke of Undetermined Source (ESUS) refers to non-lacunar ischemic stroke without an identified cause and is presumed to be related to a cardioembolic mechanism. A potential etiological factor is atrial fibrosis leading to left atrial (LA) dysfunction, also known as atrial cardiomyopathy...
U. Gancarczyk, A. Stefanini, Paweł Prochownik et al.· Journal of Clinical Medicine· 0 citations
This study aims to evaluate left atrial (LA) strain as an imaging biomarker for predicting subclinical atrial fibrillation (AF) in embolic stroke of undetermined source (ESUS) patients undergoing long-term rhythm monitoring with implantable loop recorders (ILR).
Retrospectively study of 67 ESUS patients wh...
Traditional CHA₂DS₂-VASc scoring has well-recognized limitations in thromboembolic risk assessment for atrial fibrillation (AF), particularly in low-score patients who nevertheless thrombose, high-score event-free individuals, cancer patients, and post-ablation cohorts. The left atrial appendage (LAA) is the source...
Bing-Xin Liu, Xian-Yong Liu, Chang-Lin Zhang et al.· Frontiers in Cardiovascular...· 0 citations
BACKGROUND
Electrical left atrial appendage isolation (LAAI) may be accompanied by impaired appendage function and thromboembolic complications. We evaluated the association between LAAI and clinical stroke or transient ischemic attack (TIA), while separately examining imaging-detected left atrial appendage (LAA) throm...
The left atrial appendage (LAA) is nowadays recognized as both an arrhythmogenic substrate and the dominant source of thromboembolism in atrial fibrillation (AF). In this review we tried to summarize recent data on the anatomy, physiology, and imaging of the LAA, and examine how these findings help guide rhythm-control...
A. Sârb, Csilla-Andrea Eötvös, T. Avram et al.· Current Cardiology Reports· 0 citations
Extending the CT stroke protocol to the LAA was technically feasible and did not significantly increase radiation dose, but added little diagnostic yield, and on current evidence should complement rather than replace echocardiography.
Kaitlyn E. Heintzelman, Enrique M. Carrera, Katherine Burkhardt et al.· Hearts· 0 citations
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