Polyunsaturated Fatty Acids Improved Long Term Prognosis by Reducing Oxidative Stress, Inflammation, and Endothelial

Alexandru Covaciu1,2, Theodora Benedek1, Elena Bobescu2,3

  • 1M3 Department-Clinical and Medical-Surgical Disciplines, "George Emil Palade" University of Medicine, Pharmacy, Sciences and Technology from Târgu Mureș, 540139 Târgu Mureș, Romania.

Marine Drugs
|April 25, 2025
PubMed

Insights

Omega-3 fatty acids therapy significantly reduced oxidative stress, inflammation, and endothelial dysfunction in acute coronary syndromes (ACS). This improved long-term prognosis, lowering risks of cardiovascular events and death.

Area of Science:

  • Cardiovascular Medicine
  • Nutritional Science
  • Biochemistry

Background:

  • Oxidative stress, inflammation, and endothelial dysfunction are key drivers of atherosclerosis and acute coronary syndromes (ACS).
  • Omega-3 polyunsaturated fatty acids (Omega-3 PUFAs), found in marine sources, possess properties that can mitigate these pathological processes.
  • Supplementation with Omega-3 PUFAs may offer a therapeutic strategy to reduce atherosclerosis progression and ACS incidence.

Purpose of the Study:

  • To investigate the impact of Omega-3 PUFAs therapy on oxidative stress, inflammatory markers, and endothelial function in ACS patients.
  • To assess the long-term clinical outcomes and prognosis associated with Omega-3 PUFAs supplementation in ACS.

Main Methods:

  • A prospective study involving 1140 ACS patients, divided into four groups receiving Omega-3 PUFAs plus optimal medical therapy (OMT) or OMT alone.
  • Evaluated changes in oxidative stress (TAS, Ab anti-ox-LDL, IgG anti-MPO), inflammatory markers (CRP, fibrinogen), and endothelial function (FMD, vWf activity) over 6 months.
  • Monitored 5-year clinical events, including cardiovascular death, ACS recurrence, stroke, and heart failure readmissions.

Main Results:

  • Omega-3 PUFAs, when added to OMT, significantly reduced markers of oxidative stress, inflammation, and endothelial dysfunction at 6 months.
  • Patients treated with Omega-3 PUFAs showed a significant reduction in the risk of cardiovascular death and sudden death.
  • A decreased incidence of recurrent ACS, in-stent restenosis, stroke, and heart failure readmissions was observed in the Omega-3 PUFA-treated groups.

Conclusions:

  • Therapy with Omega-3 PUFAs, as an adjunct to OMT, effectively improves biochemical parameters related to cardiovascular risk in ACS patients.
  • Omega-3 PUFAs supplementation leads to a significant enhancement of long-term prognosis in individuals with acute coronary syndromes.
  • The findings support the use of Omega-3 PUFAs in managing ACS to reduce both subclinical disease markers and major adverse cardiovascular events.
Abstract

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