Studies of Therapeutic Strategies for Atrial Fibrillation Based on a Biophysical Model of the Human Atria

Author(s):  
Laurent Uldry ◽  
Nathalie Virag ◽  
Jean-Marc Vesin ◽  
Lukas Kappenberger
Cells ◽  
2020 ◽  
Vol 9 (7) ◽  
pp. 1729 ◽  
Author(s):  
Roeliene Starreveld ◽  
Kennedy S. Ramos ◽  
Agnes J. Q. M. Muskens ◽  
Bianca J. J. M. Brundel ◽  
Natasja M. S. de Groot

Pharmaco-therapeutic strategies of atrial fibrillation (AF) are moderately effective and do not prevent AF onset and progression. Therefore, there is an urgent need to develop novel therapies. Previous studies revealed heat shock protein (HSP)-inducing compounds to mitigate AF onset and progression. Such an HSP inducing compound is L-glutamine. In the current study we investigate the effect of L-glutamine supplementation on serum HSP27 and HSP70 levels and metabolite levels in patients with AF patients (n = 21). Hereto, HSP27 and HSP70 levels were determined by ELISAs and metabolites with LC-mass spectrometry. HSP27 levels significantly decreased after 3-months of L-glutamine supplementation [540.39 (250.97–1315.63) to 380.69 (185.68–915.03), p = 0.004] and normalized to baseline levels after 6-months of L-glutamine supplementation [634.96 (139.57–3103.61), p < 0.001]. For HSP70, levels decreased after 3-months of L-glutamine supplementation [548.86 (31.50–1564.51) to 353.65 (110.58–752.50), p = 0.045] and remained low after 6-months of L-glutamine supplementation [309.30 (118.29–1744.19), p = 0.517]. Patients with high HSP27 levels at baseline showed normalization of several metabolites related to the carbohydrates, nucleotides, amino acids, vitamins and cofactors metabolic pathways after 3-months L-glutamine supplementation. In conclusion, L-glutamine supplementation reduces the serum levels of HSP27 and HSP70 within 3-months and normalizes metabolite levels. This knowledge may fuel future clinical studies on L-glutamine to improve cardioprotective effects that may attenuate AF episodes.


2007 ◽  
Vol 31 (1) ◽  
pp. 65-69 ◽  
Author(s):  
Patrick Ruchat ◽  
Lam Dang ◽  
Nathalie Virag ◽  
Jürg Schlaepfer ◽  
Ludwig Karl von Segesser ◽  
...  

EP Europace ◽  
2012 ◽  
Vol 14 (suppl 5) ◽  
pp. v112-v120 ◽  
Author(s):  
L. Uldry ◽  
N. Virag ◽  
F. Lindemans ◽  
J.-M. Vesin ◽  
L. Kappenberger

2007 ◽  
Vol 96 (5) ◽  
pp. 1014-1019
Author(s):  
Gaku Sekita ◽  
Hiroyuki Daida

PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0258285
Author(s):  
Matthias Lange ◽  
Annie M. Hirahara ◽  
Ravi Ranjan ◽  
Gregory J. Stoddard ◽  
Derek J. Dosdall

Slow conduction areas and conduction block in the atria are considered pro-arrhythmic conditions. Studies examining the size and distribution of slow conduction regions in the context of persistent atrial fibrillation (AF) may help to develop improved therapeutic strategies for patients with AF. In this work, we studied the differences of size and number in slow conduction areas between control and persistent AF goats and the influence of propagation direction on the development of these pathological conduction areas. Epicardial atrial electrical activations from the left atrial roof were optically mapped with physiological pacing cycle lengths and for the shortest captured cycle lengths. The recordings were converted to local activation times and conduction velocity measures. Regions with slow conduction velocity (less than 0 . 2 m s) were identified. The size of the connected regions and the number of non-connected regions were counted for propagation from different orthogonal directions. We found that regions of slow conduction significantly increases in our 15 persistent AF goat recordings in response to premature stimulation (24.4±4.3% increase to 36.6±4.4%, p < 0.001). This increase is driven by an increase of size from (3.70±0.89[mm2] to 6.36±0.91[mm2], p = 0.014) for already existing regions and not by generation of new slow conduction regions (11.6±1.8 vs. 13±1.9, p = 0.242). In 12 control goat recordings, no increase from baseline pacing to premature pacing was found. Similarly, size of the slow conduction areas and the count did not change significantly in control animals.


2007 ◽  
Vol 32 (1) ◽  
pp. 90-95 ◽  
Author(s):  
Patrick Ruchat ◽  
Lam Dang ◽  
Jürg Schlaepfer ◽  
Nathalie Virag ◽  
Ludwig Karl von Segesser ◽  
...  

ABOUTOPEN ◽  
2018 ◽  
Vol 4 (1) ◽  
pp. 116-121
Author(s):  
Gianluca Campo ◽  
Giulia Bugani

The management of antithrombotic therapy in patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) is a challenge cardiologists face daily. The main difficulty is represented by finding the right balance between the prevention of thrombotic risk and the inevitable increase in bleeding. Most guidelines recommend the use of both oral anticoagulants and dual antiplatelet therapy in combination (triple therapy) in patients with FA undergoing PCI, suggesting however immediate use of dual antithrombotic therapy in patients with prevalent bleeding risk. Many studies show that triple therapy is associated with high frequency of major bleeding, thus stimulating the research for new therapeutic strategies. We report the case of a patient suffering from hypertension, dyslipidemia and epistaxis, hospitalized for the onset of angina associated with moderate efforts. Despite scientific evidence to support the use of dual therapy with dabigatran, the patient's detailed clinical history shows that this type of approach has not yet entered into current clinical practice, although the final therapeutic choice is in line with the results of the RE-DUAL PC study (Cardiology).


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