Does Mediterranean Diet Reduce Cardiovascular Events and Oxidative Stress in Atrial Fibrillation?

Daniele Pastori1, Roberto Carnevale1,2, Simona Bartimoccia1

  • 11 I Clinica Medica, Department of Internal Medicine and Medical Specialties, Atherothrombosis Centre, Sapienza University of Rome , Rome, Italy .

Insights

The Mediterranean diet (Med-Diet) may reduce cardiovascular events in atrial fibrillation (AF) patients by lowering oxidative stress. Higher adherence to Med-Diet correlated with lower levels of oxidative stress markers and fewer cardiovascular events.

Area of Science:

  • Cardiology
  • Nutritional Science
  • Oxidative Stress Research

Background:

  • Atrial fibrillation (AF) is linked to increased oxidative stress and cardiovascular events (CVEs), inadequately managed by anticoagulation alone.
  • The Mediterranean diet (Med-Diet) shows promise in mitigating atherosclerotic progression.

Purpose of the Study:

  • To investigate if adherence to the Med-Diet can reduce CVEs in anticoagulated AF patients.
  • To explore the potential role of the Med-Diet in lowering oxidative stress as a mechanism for CVE reduction.

Main Methods:

  • A prospective cohort study of 709 anticoagulated AF patients.
  • Assessment of Med-Diet adherence using a scoring system (0-9 points).
  • Follow-up for CVEs over a mean of 39.9 months, with analysis of oxidative stress markers (sNOX2-dp, F2-isoprostanes) and time in therapeutic range.

Main Results:

  • A significant reduction in CVEs was observed with increasing Med-Diet adherence (23.4% low, 8.4% intermediate, 5.3% high adherence; p<0.001).
  • Med-Diet score was inversely correlated with oxidative stress markers sNOX2-dp (Rs: -0.297) and F2-isoprostanes (Rs: -0.411), with progressively lower median values across adherence groups (p<0.001).
  • Cox regression identified Med-Diet score (HR: 0.771) and F2-isoprostanes (HR: 1.002) as predictors of CVEs.

Conclusions:

  • Adherence to the Med-Diet may be associated with a reduced risk of CVEs in AF patients.
  • This protective effect might be mediated by an antioxidant mechanism, evidenced by reduced oxidative stress markers (Nox2, F2-isoprostanes).

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