Key result
Elevated serum VIP levels correlate with low-voltage areas in AF, suggesting noninvasive biomarker potential.
Why the study?
Detecting left atrial low-voltage areas typically requires invasive procedures, creating a need for a simple, minimally invasive marker to identify patients with atrial fibrillation at risk of adverse outcomes.
Can serum Vasoactive Intestinal Peptide (VIP) serve as a biomarker for detecting low-voltage areas in patients with atrial fibrillation?
Observational
Can serum Vasoactive Intestinal Peptide (VIP) serve as a biomarker for detecting low-voltage areas in patients with atrial fibrillation?
Answers are grounded in this paper and cite their sources.
Serum VIP may serve as a novel, noninvasive biomarker to detect left atrial low-voltage areas in patients with atrial fibrillation, potentially aiding in risk stratification and ablation planning.
BACKGROUND: Low-voltage areas in the left atrium predict atrial fibrillation recurrence after catheter ablation and are associated with adverse outcomes like death, heart failure, and stroke. Detecting low-voltage areas (LVAs) typically requires invasive procedures, highlighting the need for a simple, minimally invasive marker. Vasoactive intestinal peptide (VIP), a neuropeptide released during parasympathetic stimulation, affects electrophysiological remodeling in atrial fibrillation. We hypothesized that serum VIP could serve as a biomarker for detecting LVAs in these patients. METHODS AND CONCLUSIONS: Serum VIP levels are higher in patients with atrial fibrillation with LVAs, suggesting its potential as a noninvasive biomarker for detecting these areas and improving clinical management.
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Nishino et al. (2025) conducted an observational in Atrial Fibrillation. Serum Vasoactive Intestinal Peptide (VIP) was evaluated on Low-voltage areas (LVAs) (p=<0.001). Serum VIP levels are significantly higher in patients with atrial fibrillation who have low-voltage areas (P<0.001), suggesting its potential as a noninvasive biomarker.
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