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Associations between cardiac fibrosis and permanent atrial fibrillation in advanced heart failure
B Aldhoon1, T Kučera, N Smorodinová
1Department of Cardiology, Institute for Clinical and Experimental Medicine - IKEM, Prague, Czech Republic. bashar.aldhoon@ikem.cz
Insights
In advanced heart failure (HF), atrial fibrosis is common regardless of atrial fibrillation (AF). However, increased atrial wall stress may contribute to AF development in these patients.
Area of Science:
- Cardiology
- Pathology
Background:
- Atrial fibrosis is a known precursor to long-standing atrial fibrillation (AF).
- The role of fibrosis in AF development is unclear in advanced heart failure (HF) due to concurrent atrial scarring from HF itself.
Purpose of the Study:
- To differentiate between patients with and without AF within a cohort of advanced HF patients.
- To investigate the independent contribution of atrial fibrosis to AF in advanced HF.
Main Methods:
- Myocardial samples from 21 advanced HF patients undergoing heart transplantation were analyzed.
- Collagen volume fraction (CVF), TGF-beta, and CTGF expression were assessed histologically and immunohistochemically.
- Echocardiographic and hemodynamic data were collected pre-transplantation.
Main Results:
- No significant differences in atrial CVF, TGF-beta, or CTGF expression were found between AF and sinus rhythm groups.
- Patients with AF exhibited higher right atrial pressure, larger left atrium diameter, and increased left atrial wall stress.
- The AF group also had a longer duration of HF compared to the control group.
Conclusions:
- Atrial fibrosis (measured by CVF) is consistently present in advanced HF, irrespective of AF occurrence.
- Increased atrial wall stress, in addition to existing fibrosis, may play a role in AF development in advanced HF patients.
Abstract:
Atrial fibrosis is considered as the basis in the development of long-standing atrial fibrillation (AF). However, in advanced heart failure (HF), the independent role of fibrosis for AF development is less clear since HF itself leads to atrial scarring. Our study aimed to differentiate patients with AF from patients without AF in a population consisting of patients with advanced HF. Myocardial samples from the right atrial and the left ventricular wall were obtained during heart transplantation from the explanted hearts of 21 male patients with advanced HF. Long-standing AF was present in 10 of them and the remaining 11 patients served as sinus rhythm controls. Echocardiographic and hemodynamic measurements were recorded prior to heart transplantation. Collagen volume fraction (CVF), transforming growth factor-beta (TGF-beta), and connective tissue growth factor (CTGF) expression in myocardial specimens were assessed histologically and immunohistochemically. The groups were well matched according to age (51.9+/-8.8 vs. 51.3+/-9.3 y) and co-morbidities. The AF group had higher blood pressure in the right atrium (13.6+/-7.7 vs. 6.0+/-5.0 mmHg; p=0.02), larger left atrium diameter (56.1+/-7.7 vs. 50+/-5.1 mm; p=0.043), higher left atrium wall stress (18.1+/-2.1 vs. 16.1+/-1.7 kdynes/m(2); p=0.04), and longer duration of HF (5.0+/-2.9 vs. 2.0+/-1.6 y, p=0.008). There were no significant differences in CVF (p=0.12), in CTGF (p=0.60), and in TGF-beta expression (p=0.66) in the atrial myocardium between the two study groups. In conclusions, in advanced HF, atrial fibrosis expressed by CVF is invariably present regardless of occurrence of AF. In addition to atrial wall fibrosis, increased wall stress might contribute to AF development in long-standing AF.
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