Key result
Left atrial deformation in patients with atrial fibrillation did not correlate significantly with platelet aggregability or inflammation markers.
Cross-Sectional (n=17)
In patients with atrial fibrillation, the thrombogenic risk associated with left atrial stasis appears independent of systemic platelet aggregability or inflammation.
LA deformation uncorrelated with platelet/inflammatory markers in AF; leaves open independent mechanisms of LA stasis-related thromboembolism.
It has been documented recently that left atrial (LA) deformation in AF patients (while in AF) is predictive of subsequent stroke risk. Additionally, diminished LA deformation during AF correlates with the presence of LA blood stasis. Given that endothelial function is dependent on laminar blood flow, the present study sought to investigate the effect of diminished LA deformation (during AF) on platelet reactivity and inflammation in AF patients. Patients (n = 17) hospitalised with AF underwent echocardiography (while in AF) for determination of peak positive LA strain (LASp). Whole blood impedance aggregometry was used to measure extent of ADP-induced aggregation and subsequent inhibitory response to the nitric oxide (NO) donor, sodium nitroprusside. Platelet thioredoxin-interacting protein (Txnip) content was determined by immunohistochemistry. LASp tended (p = 0.078) to vary inversely with CHA2DS2VASc scores. However, mediators of inflammation (C-reactive protein, Txnip) did not correlate significantly with LASp nor did extent of ADP-induced platelet aggregation or platelet NO response. These results suggest that the thrombogenic risk associated with LA stasis is independent of secondary effects on platelet aggregability or inflammation.
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Procter et al. (2016) conducted a cross-sectional in Atrial Fibrillation (n=17). Left atrial deformation (peak positive LA strain) was evaluated on Correlation of peak positive LA strain with platelet reactivity and inflammation. Left atrial deformation in patients with atrial fibrillation did not correlate significantly with platelet aggregability or inflammation markers.
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