Copyright
©The Author(s) 2016.
World J Cardiol. Feb 26, 2016; 8(2): 114-119
Published online Feb 26, 2016. doi: 10.4330/wjc.v8.i2.114
Published online Feb 26, 2016. doi: 10.4330/wjc.v8.i2.114
Table 4 Clinical studies investigating the effect of n-3 poly-unsaturated fatty acids on secondary prevention for atrial fibrillation
Study design | Population | PUFA administration | PUFA quantification | AF diagnosis | Results |
Double blind-RCT[30] | 109 pts, age: 70 yr; Italy; heart structural abnormality: 90%; Amiodarone + ACE-i/ARBs: 100% | N-3 PUFA (EPA/DHA 1.2:1) 2 g/d, 1 mo before and 12 after ECV vs olive oil | No PUFA dosage | Weekly ECG for the first 3 wk after ECV and ECG + Holter ECG after 1, 3, 6, 12 mo and at symptoms occurrence | Less AF relapses with PUFA |
Open-label randomized[31] | 178 pts, Australia. Concomitant amiodarone, sotalol, ACE-i/ARBs | N-3 PUFA (EPA/DHA 1.3:1) 1.8 g/d for approximately 56 d before ECV and 1 year thereafter vs not | Serum dosage of EPA, DHA basally, before ECV | ECG at week 2 and 6 and every 3 mo. AF: ≥ 1 wk | Less AF relapses at 90 d and 1 yr with PUFA, P < 0.001; higher serum EPA, DHA |
Double blind-RCT[33] | 663 pts; paroxysmal AF: 18%; age: 60.5 yr; United States. No heart abnormality. Amiodarone: 0%, antiarrhythmic drugs: 13%; ACE-i/ARBs: 39% | N-3 PUFA (EPA/DHA 4.6:3.7; load: 8 g/d for 1 wk) 4 g/d for 24 wk vs oil | Serum DHA, EPA dosage basally, after 4 and 24 wk | Biweekly transtelephonic monitoring | No lower symptomatic AF recurrence in the paroxysmal and persistent |
Prospective[35] | 50 pts; ≥ 2 previous AF episodes; age: 54 yr, Japan. IC antiarrhythmic drugs: 100% | Observational period: no PUFA for 6 mo. Interventional period: EPA 1.8 g/d for 6 mo | Serum EPA, DHA dosage basally and at study end | Daily ECG monitoring and at symptoms occurrence | No lower AF burden and time to first relapse |
Double blind-RCT[32] | 204 pts, age: 69.3 yr; Italy. LAs 45 mm. First ECV: 59%; IC antiarrhythmic drugs: 29.5%, sotalol: 12.6%, amiodarone: 27.4% | N-3 PUFA (EPA/DHA 1.2:1) 3 g/d ≥ 1 wk before and 2 g/d after ECV for 6 mo vs olive oil | N-3 PUFA serum dosage basally, 6 mo after ECV | Transtelephonic monitoring: 2/first week after ECV and 3/wk for 3 mo + clinical visits after 7 d, 1, 3, 6 mo | No difference in ECV success, AF incidence, time to first relapse. Increase of EPA and DHA |
Double blind RCT[36] | 337 pts; symptomatic paroxysmal or persistent AF within 6 mo of enrollment | Fish oil (4 g/d) or placebo | Followed, on average, for 271 ± 129 d | Trans-telephonic event recorder, 12-lead ECG or Holter | No lower AF with PUFA |
Double blind-RCT[37] | 190 pts with paroxysmal or persistent AF | N-3 PUFAs (4 g/d; n = 126) or placebo (n = 64) in a 2:1 ratio | No PUFA dosage | Not specified | No reduction of AF recurrence and inflammation markers |
Double blind-RCT[34] | 586 pts with symptomatic paroxysmal AF requiring ECV (n = 428), at least 2 episodes of AF in the 6 mo before (n = 55), or both (103) | N-3 PUFA (1 g/d) or placebo for 12 mo | No PUFA dosage | Not specified | No lower AF with PUFA |
- Citation: Martino A, Pezzi L, Magnano R, Salustri E, Penco M, Calo’ L. Omega 3 and atrial fibrillation: Where are we? World J Cardiol 2016; 8(2): 114-119
- URL: https://www.wjgnet.com//full/v8/i2/114.htm
- DOI: https://dx.doi.org/10.4330/wjc.v8.i2.114