Nishino Kotaro, Temma Taro, Natsui Hiroyuki, Watanabe Masaya, Nakao Motoki, Kawasaki Masahiro, Shimano Kintaro, Kawakami Kei, Saito Shota, Koya Jiro, Tatsuta Daishiro, Koizumi Takuya, Kadosaka Takahide, Koya Taro, Tsuneta Satonori, Kamiya Kiwamu, Nagai Toshiyuki, Anzai Toshihisa
Department of Cardiovascular Medicine, Faculty of Medicine and Graduate School of Medicine Hokkaido University Sapporo Japan.
Department of Cardiovascular Medicine Otaru Kyokai Hospital Otaru Japan.
J Am Heart Assoc. 2025 Apr;14(7):e039192. doi: 10.1161/JAHA.124.039192. Epub 2025 Mar 21.
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.
This prospective, cross-sectional study was conducted at Hokkaido University Hospital between August 2021 and September 2023. We included 108 patients with atrial fibrillation scheduled for catheter ablation. Blood samples were collected during ablation to measure VIP using an ELISA. Electroanatomical mapping identified LVAs, defined as regions with bipolar voltage ≤0.5 mV and occupying >5% of the left atrial surface. Statistical analyses evaluated the relationship between VIP and LVAs. Fifty-one patients (47%) had LVAs, with significantly higher serum VIP levels than those without (335.1 versus 247.7 pg/mL, <0.001). VIP levels and female sex were statistically significant factors of LVAs. Adding VIP to the existing score significantly improved its discrimination (area under the curve: 0.784 versus 0.707, <0.001).
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.
左心房低电压区域可预测导管消融术后房颤复发,并与死亡、心力衰竭和中风等不良结局相关。检测低电压区域(LVA)通常需要侵入性操作,这凸显了对一种简单、微创标志物的需求。血管活性肠肽(VIP)是在副交感神经刺激时释放的一种神经肽,会影响房颤中的电生理重塑。我们假设血清VIP可作为检测这些患者LVA的生物标志物。
这项前瞻性横断面研究于2021年8月至2023年9月在北海道大学医院进行。我们纳入了108例计划进行导管消融的房颤患者。在消融过程中采集血样,使用酶联免疫吸附测定法测量VIP。电解剖标测确定LVA,定义为双极电压≤0.5 mV且占左心房表面积>5%的区域。统计分析评估了VIP与LVA之间的关系。51例患者(47%)存在LVA,其血清VIP水平显著高于无LVA的患者(335.1对247.7 pg/mL,<0.001)。VIP水平和女性性别是LVA的统计学显著因素。将VIP添加到现有评分中可显著提高其辨别能力(曲线下面积:0.784对0.707,<0.001)。
存在LVA的房颤患者血清VIP水平较高,表明其有潜力作为检测这些区域的无创生物标志物并改善临床管理。