4.6 Article

Sinus node dysfunction in atrial fibrillation patients: the evidence of regional atrial substrate remodelling

期刊

EUROPACE
卷 15, 期 2, 页码 205-211

出版社

OXFORD UNIV PRESS
DOI: 10.1093/europace/eus219

关键词

Atrial fibrillation; Catheter ablation; Mapping; Sinus node

资金

  1. National Science Council (NSC) [99-2628-B-075-007-MY3, 99-2627-B-008-003, 100-2221-E-008-008-MY2]
  2. VGH [VGHUST100-G 1-4-3]
  3. NSC Center for Dynamical Biomarkers and Translational Medicine, National Central University, Taiwan [NSC 99-2911-I-008-100, NSC100-2911-I-008-001]
  4. NCU [VGHUST100-G 1-4-3]

向作者/读者索取更多资源

It remains unclear as to whether regional atrial substrates of certain areas of the atrium in patients with atrial fibrillation (AF) can be related to sinoatrial node dysfunction. We investigated the relationship between the biatrial substrate characteristics and sinus node function in these patients. The study enrolled 34 patients (aged 57 11 years old; 20 males) who underwent catheter ablation for symptomatic paroxysmal AF. Sinus node dysfunction was defined as having corrected sinus node recovery time longer than 550 ms. Atrial substrate analyses of both atria and atrial conductive properties were investigated in patients with (Group 1) and without sinus node dysfunction (Group 2). The mean global bipolar voltage of both atria and the atrial refractory period were similar between the two groups. Regional analysis showed that the mean bipolar voltage for patients in Group 1 was lower than in Group 2 (1.0 0.3 vs. 2.1 0.7 mV, P 0.001) only in the sinus node region, while the electrophysiological properties were similar for both groups in other anatomic regions of both atria. The right atrial total activation time was significantly longer (97 9 vs. 89 10 ms, P 0.023) and the conduction velocity along the crista terminalis was significantly slower (1.0 0.2 vs. 1.2 0.3 m/s, P 0.019) in Group 1 patients than in Group 2 patients. In patients with AF, regional atrial remodelling near the sinus node area was associated with sinus node dysfunction.

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