Key result
Elevated serum FGF-23 linked to marked increase in LAA thrombosis risk in low-risk AF.
Why the study?
The study was conducted to evaluate the role of FGF-23 as a predictor of LAA thrombosis in patients with non-valvular AF across different risk levels of thromboembolic complications based on the CHA2DS2-VASc score.
Does elevated FGF-23 predict left atrial appendage thrombosis in patients with non-valvular atrial fibrillation?
Cross-Sectional (n=250)
No
Does elevated FGF-23 predict left atrial appendage thrombosis in patients with non-valvular atrial fibrillation?
FGF-23 is a novel biomarker that can help predict left atrial appendage thrombosis in patients with non-valvular atrial fibrillation, particularly in those with low CHA2DS2-VASc scores.
Answers are grounded in this paper and cite their sources.
May support FGF-23 for LAA thrombosis risk in low-CHA2DS2-VASc AF; hypothesis-generating and should not yet change practice.
Aim. To study the role of fibroblast growth factor 23 (FGF-23) as a predictor of left atrial appendage (LAA) thrombosis in patients (pts) with non-valvular atrial fibrillation (AF) and different risk levels of thromboembolic complications (TEC) according to the CHA 2 DS 2 -VASc score. Methods. The study included 250 pts with non-valvular AF hospitalized for radiofrequency ablation, divided into 2 groups: group (gr.) 1 - with 0-1 points (n=79) and gr.2 - with ≥2 points on the CHA2DS2-VASc scale (n=171). According to the results of transesophageal echocardiography, pts of each group were divided into subgroups depending on the presence of LAA thrombosis, which was found in 19 pts of gr.1 and 72 of gr.2. Patients underwent transthoracic echocardiography, determination of blood biomarkers: NT-proBNP (pg/ml), GDF-15 (pg/ml), FGF-23 (pmol/l), highly sensitive C-reactive protein (mg/l), cystatin C (mg/l). Results. Pts with LAA thrombosis in both groups had in common: a longer history of arterial hypertension, a greater proportion of coronary artery disease and persistent AF, lower GFR, higher values of atrial volume indices, left ventricle myocardial mass, systolic pressure in the pulmonary artery, median NT-proBNP, FGF-23 and GDF-15. Logistic regression analysis performed separately in the groups revealed the same independent predictors of LAA thrombosis in both groups: LA volume index (LAVI) and the level of FGF-23 in the blood. At the same time, the threshold value of FGF-23, separating pts by the presence of LAA thrombosis, was higher in gr.1 (≥0.85 and ≥0.5 pmol/l, respectively), and the area under the AUC curve for FGF-23 in gr.1 was greater: 0.964 vs 0.865 in gr.2 (p=0.026). Conclusion. The serum level of FGF-23, along with the LAVI, is an independent predictor of LAA thrombosis in pts with AF and various risk of TEC according to CHA 2 DS 2 -VASc; the threshold level of FGF-23 for pts at low risk of TEC is significantly higher than for high risk pts, and allows more accurate prediction of the presence of LAA thrombosis.
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Гизатулина et al. (2022) conducted a cross-sectional in Non-valvular atrial fibrillation (n=250). Fibroblast growth factor 23 (FGF-23) vs. Lower FGF-23 levels was evaluated on Left atrial appendage (LAA) thrombosis (OR 75.914, 95% CI 6.925-432.2, p=0.001). Elevated serum FGF-23 (≥0.85 pmol/l) independently predicted left atrial appendage thrombosis in low-risk atrial fibrillation patients (OR 75.914).
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