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Prof. C. Moro, Madrid

Non antiarrhythmic drugs for AF. Prof. C. Moro, Madrid. AF Treatment. Therapy Objectives for AF. Symptomatic Improvement Quality of life Improvement Thromboembolism Prevention Remodelling Prevention Heart Failure Prevention Mortality Reduction. Therapy Options in AF .

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Prof. C. Moro, Madrid

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  1. Non antiarrhythmic drugs for AF Prof. C. Moro, Madrid

  2. AF Treatment

  3. Therapy Objectives for AF Symptomatic Improvement Quality of life Improvement Thromboembolism Prevention Remodelling Prevention Heart Failure Prevention Mortality Reduction

  4. Therapy Options in AF Type and Duration of AF Type y Severity of Symptoms Associated Cardiac Diseases Age Systemic Associated Diseases Long or Short Term Follow up Pharmacologic or Non Pharmacologic

  5. Upstream Therapy in AF Renin Angiotensin Inhibitors Drugs ACE`s ARB`s Statins Steroids PUFA

  6. Experimental Data • Blockade of Ang II prevents electrical remodeling induced by rapid atrial pacing. Nakashima, 2000. • ACE–dependent Ekr1/Ekr2 responsible of atrial fibrosis. Goette, 2000 • Candesartan prevents development of structural remodeling in the atria. Kumagai, 2003

  7. Nakashima et al . 2000 Effect of Candesartan/ Captopril preventing electrical remodeling with rapid atrial pacing in the animal model

  8. Genetic Determinants of AF Potasium and Sodium Channels

  9. Experimental AF. Electro/Anatomic Changes with Candesartan Candesartan Control Kumagai K et al. JACC 2003

  10. ACEI´s and ARB´s Hemodynamic Effects • Decrease Peripheral Vascular Resistance • Improve Cardiac Distensibility • Reduce Arterial Pressure in Hypertension • In HF patients • Venous and Arterial Dilatation • Reduce Preload and Afterload • Reduce PWP and Pulmonary Congestion • Increase Cardiac Output

  11. ACEI´s and ARB´s Neurohormonal Effects • Decrease Angiotensin II. • Decrease Aldosterone. • Increase in Renin and Angiotensin I. • Reduce Epinephrine and Norepinephrine. • ACEI´s increase Bradikinin.

  12. ACEI`s or ARB`s for IHD Prevention • Plaque Stabilization • Improvement of Endothelial Dysfunction • Improvement of Fibrinolysis • Modulation of Arterial Vasoconstriction • Blood Pressure Reduction

  13. ACEI´s and ARB´s Antiproliferative Effects • Reduction of Vascular Hypertrophy. • Reduction of Ventricular Hypertrophy. • Reduce Extracellular Proliferation. • Reduction of Fibrosis.

  14. Atrial Remodeling: Mechanisms of Efficacy for ARB´s Hemodynamic effect: Decreased atrial stretch Lowering end-diastolic left ventricular pressure Prevention of electrical remodeling: Direct action on ionic currents at the atrial level Modifying the sympathetic tone Preventing structural remodeling Reduction of atrial fibrosis Reduction of atrial dilatation and apoptosis Madrid A , Moro C. Circulation 2002;106:331–6

  15. Electrophysiological Effect of Irbesartan 1. Irbesartán does not modify IKr or IKs: Should not alter APD at VENTRICULAR level 2. Irbesartán blocks moderately IKur and Ito currents: it should prolong APD at ATRIAL level IKur: hKv1.5 ITo: Kv4.3 Moreno et al., J Pharmacol Exp Ther 2003;304:862

  16. Maintenance of Sinus Rhythm after Conversion from Persistent AF 1.0 0.9 Amiodarone + Irbesartan 0.8 Amiodarone 0.7 0.6 % Event-free patients 0.5 0.4 2-month lower recurrence rate of atrial fibrillation Longer time to first arrhythmia recurrence 0.3 0.2 Log Rank = 0.007 0.1 0.0 0 30 60 90 120 150 180 210 240 270 300 330 360 390 Follow-up (days) Madrid AH, Moro C et al. Circulation 2002;106:331-6.

  17. Prevention of Atrial Fibrillation Metaanalysis with ACEI’s ARB’s Madrid AH, Moro C. PACE 2004

  18. Irbesartan in Lone AFDose Response : 150-300 mg Madrid AH, Moro C. JRAAS 2004; 5 :114-120

  19. RAS Inhibitors in Lone AF

  20. RAS Inhibitors in Lone AF

  21. RAS Inhibitors in Lone AF

  22. Ramipril in Lone AF • Preventing histological remodeling such as Inflammation, myocarditis-like changes,Fibrosis and atrial dilatation. • Preventing electrical remodeling induced by Angiotensin II. • Reducing atrial stretch and intraatrial pressure. • Reduction of sympathetic tone. • Reduction of blood pressure. Belluzi et al JACC 2009;53:24

  23. Randomized clinical trials of RAS I in AF Primary Prevention

  24. Randomized clinical trials of RAS I in AF Secondary Prevention

  25. SR AF Inflammation and AF Reduced AERP Loss of AERP adaptation to rate SR AF ACTION POTENTIAL APD Fybrosis Hypertrophy Inflammation EEF ANATOMICAL EEF

  26. Statins for AF

  27. Statins for AF

  28. Statins for AF

  29. Review of randomized clinical trials of Statins to prevent Post Thoracic Surgery AF

  30. Steroids for AF Prevention Double blind study with 104 patients Persistent AF. After Cardioversion. High PCR levels. Profafenone + 16mg-4 mg Methylprednisolone vs Placebo. Follow-up mean 23 months. Recurrent AF was reduced from 50-9,6% Permanent AF was reduced from 29-2%. Significant reduction also of PCR levels. • Dernellis et al Eur H J 2004; 25:1100-07

  31. Steroids for AF Prevention

  32. Clinical Trials with PUFA Mozaffarian/04 4815 12 years ++ Calo/05 160 days ++ Frost/05 47949 5,7 years -- Brouwer/06 5284 6,4 years -- Author/Year Publication Patients Follow up Results

  33. Conclusions ACE`s and ARB´s are equipotent tools to fight against AF in primary and secondary prevention . Lone AF may also be treated with them. (Not recognized yet in Guidelines). The RR for AF prevention with those drugs is higher in patients with high arryhthmogenic risk. Steroids should not be used in AF prevention due to its plural and potent adverse effects. Statins are useful to prevent post surgical AF. PUFA effects for AF prevention show controversial results.

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