Your browser doesn't support javascript.
loading
Association Between Achieved ω-3 Fatty Acid Levels and Major Adverse Cardiovascular Outcomes in Patients With High Cardiovascular Risk: A Secondary Analysis of the STRENGTH Trial.
Nissen, Steven E; Lincoff, A Michael; Wolski, Kathy; Ballantyne, Christie M; Kastelein, John J P; Ridker, Paul M; Ray, Kausik K; McGuire, Darren K; Mozaffarian, Dariush; Koenig, Wolfgang; Davidson, Michael H; Garcia, Michelle; Katona, Brian G; Himmelmann, Anders; Loss, Larrye E; Poole, Matthew; Menon, Venu; Nicholls, Stephen J.
Afiliação
  • Nissen SE; Cleveland Clinic Coordinating Center for Clinical Research, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
  • Lincoff AM; Cleveland Clinic Coordinating Center for Clinical Research, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
  • Wolski K; Cleveland Clinic Coordinating Center for Clinical Research, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
  • Ballantyne CM; Baylor College of Medicine, Houston, Texas.
  • Kastelein JJP; Academic Medical Center, Amsterdam, the Netherlands.
  • Ridker PM; Center for Cardiovascular Disease Prevention, Harvard Medical School, Boston, Massachusetts.
  • Ray KK; Imperial College of London, London, England.
  • McGuire DK; University of Texas Southwestern Medical Center, Dallas.
  • Mozaffarian D; Friedman School of Nutrition Science and Policy, Tufts University, Boston, Massachusetts.
  • Koenig W; Deutsches Herzzentrum München, Technische Universität München, DZHK (German Centre for Cardiovascular Research) Munich Heart Alliance, Munich, Germany.
  • Davidson MH; Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany.
  • Garcia M; University of Chicago, Chicago, Illinois.
  • Katona BG; Cleveland Clinic Coordinating Center for Clinical Research, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
  • Himmelmann A; AstraZeneca BioPharmaceuticals R&D, Late-stage Development, Cardiovascular, Renal and Metabolic, Gaithersburg, Maryland.
  • Loss LE; AstraZeneca BioPharmaceuticals R&D, Late-stage Development, Cardiovascular, Renal and Metabolic, Gothenburg, Sweden.
  • Poole M; AstraZeneca BioPharmaceuticals R&D, Late-stage Development, Cardiovascular, Renal and Metabolic, Gaithersburg, Maryland.
  • Menon V; AstraZeneca BioPharmaceuticals R&D, Late-stage Development, Cardiovascular, Renal and Metabolic, Gothenburg, Sweden.
  • Nicholls SJ; Cleveland Clinic Coordinating Center for Clinical Research, Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
JAMA Cardiol ; 2021 May 16.
Article em En | MEDLINE | ID: mdl-33993205
ABSTRACT
IMPORTANCE In patients treated with ω-3 fatty acids, it remains uncertain whether achieved levels of eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA) are associated with cardiovascular outcomes.

OBJECTIVE:

To determine the association between plasma levels of EPA and DHA and cardiovascular outcomes in a trial of ω-3 fatty acids compared with corn oil placebo. DESIGN, SETTING, AND

PARTICIPANTS:

A double-blind, multicenter trial enrolled patients at high cardiovascular risk with elevated triglyceride levels and low levels of high-density lipoprotein cholesterol at 675 centers (enrollment from October 30, 2014, to June 14, 2017; study termination January 8, 2020; last visit May 14, 2020).

INTERVENTIONS:

Participants were randomized to receive 4 g daily of ω-3 carboxylic acid (CA) or an inert comparator, corn oil. MAIN OUTCOMES AND

MEASURES:

The primary prespecified end point was a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina requiring hospitalization. The primary outcome measure was the hazard ratio, adjusted for baseline characteristics, for patients treated with the ω-3 CA compared with corn oil for the top tertile of achieved EPA and DHA plasma levels 12 months after randomization.

RESULTS:

Of the 13 078 total participants, 6539 (50%) were randomized to receive ω-3 CA and 6539 (50%) randomized to corn oil. ω-3 Fatty acid levels were available at both baseline and 12 months after randomization in 10 382 participants (5175 ω-3 CA patients [49.8%] and 5207 corn oil-treated patients [50.2%]; mean [SD] age, 62.5 [8.9] years, 3588 [34.6%] were women, 9025 [86.9%] were White, and 7285 [70.2%] had type 2 diabetes). The median plasma levels at 12 months in ω-3 CA patients were 89 µg/mL (interquartile range [IQR], 46-131 µg/mL) for EPA and 91 µg/mL (IQR, 71-114 µg/mL) for DHA with top tertile levels of 151 µg/mL (IQR, 132-181 µg/mL) and 118 µg/mL (IQR, 102-143 µg/mL), respectively. Compared with corn oil, the adjusted hazard ratios for the highest tertile of achieved plasma levels were 0.98 (95% CI, 0.83-1.16; P = .81) for EPA, and 1.02 (95% CI, 0.86-1.20; P = .85 for DHA. Sensitivity analyses based on changes in plasma and red blood cell levels of EPA and DHA and primary and secondary prevention subgroups showed similar results. CONCLUSIONS AND RELEVANCE Among patients treated with ω-3 CA, the highest achieved tertiles of EPA and DHA were associated with neither benefit nor harm in patients at high cardiovascular risk. TRIAL REGISTRATION ClinicalTrials.gov Identifier NCT02104817.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JAMA Cardiol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JAMA Cardiol Ano de publicação: 2021 Tipo de documento: Article