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Polyunsaturated fatty acids supplementation impairs anti-oxidant high-density lipoprotein function in heart failure.
Wurm, Raphael; Schrutka, Lore; Hammer, Alexandra; Moertl, Deddo; Berger, Rudolf; Pavo, Noemi; Lang, Irene M; Goliasch, Georg; Huelsmann, Martin; Distelmaier, Klaus.
Afiliação
  • Wurm R; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Schrutka L; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Hammer A; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Moertl D; Clinical Department of Internal Medicine III, University Hospital St. Poelten, St. Poelten, Austria.
  • Berger R; Department of Cardiology, KH Barmherzige Brueder, Eisenstadt, Austria.
  • Pavo N; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Lang IM; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Goliasch G; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Huelsmann M; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
  • Distelmaier K; Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Eur J Clin Invest ; 48(9): e12998, 2018 Sep.
Article em En | MEDLINE | ID: mdl-30004123
ABSTRACT

BACKGROUND:

The underlying reasons for the highly inconsistent clinical outcome data for omega-3-polyunsaturated fatty acids (n3-PUFAs) supplementation in patients with cardiac disease have not been understood yet. The aim of this prospective, randomized, double-blind, placebo controlled study was to determine the effects of oral treatment with n3-PUFAs on the anti-oxidant capacity of HDL in heart failure (HF) patients.

METHODS:

A total of 40 patients with advanced HF of nonischaemic origin, defined by NT-proBNP levels of >2000 pg/mL, NYHA class III or IV and a LVEF <35% who were on stable optimized medical therapy for ≥3 months, were consecutively enrolled into this prospective, double-blind, placebo-controlled trial and randomized in a 111 fashion to receive 1 g/day or 4 g/day of n3-PUFA, or placebo, respectively, for 12 weeks.

RESULTS:

After 12 weeks of treatment, the anti-oxidant function of HDL, measured by the HDL inflammatory index, was found significantly impaired in the treatment group in a dose-dependent fashion with 0.67 [IQR 0.49-1.04] for placebo vs 0.71 [IQR 0.55-1.01] for 1 g/day n3-PUFA vs 0.98 [IQR 0.73-1.16] for 4 g/day n3-PUFA (P for trend = 0.018).

CONCLUSION:

We provide evidence for an adverse effect of n3-PUFA supplementation on anti-oxidant function of HDL in nonischaemic heart failure patients, establishing a potential mechanistic link for the controversial outcome data on n3-PUFA supplementation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Graxos Ômega-3 / Suplementos Nutricionais / Insuficiência Cardíaca / Lipoproteínas HDL / Antioxidantes Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácidos Graxos Ômega-3 / Suplementos Nutricionais / Insuficiência Cardíaca / Lipoproteínas HDL / Antioxidantes Idioma: En Ano de publicação: 2018 Tipo de documento: Article