TY - JOUR
T1 - Polyunsaturated fatty acids supplementation impairs anti-oxidant high-density lipoprotein function in heart failure
AU - Wurm, Raphael
AU - Schrutka, Lore
AU - Hammer, Alexandra
AU - Moertl, Deddo
AU - Berger, Rudolf
AU - Pavo, Noemi
AU - Lang, Irene M
AU - Goliasch, Georg
AU - Huelsmann, Martin
AU - Distelmaier, Klaus
N1 - Funding Information:
This project has been funded by the Medical Scientific Fund of the Mayor of the City of Vienna (2015; to KD).
Publisher Copyright:
© 2018 The Authors. European Journal of Clinical Investigation published by John Wiley & Sons Ltd on behalf of Stichting European Society for Clinical Investigation Journal Foundation
PY - 2018/9
Y1 - 2018/9
N2 - 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 1:1:1 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.
AB - 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 1:1:1 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.
KW - Aged
KW - Antioxidants/metabolism
KW - Dietary Supplements
KW - Double-Blind Method
KW - Fatty Acids, Omega-3/therapeutic use
KW - Fatty Acids, Unsaturated
KW - Female
KW - Heart Failure/metabolism
KW - Humans
KW - Lipoproteins, HDL/metabolism
KW - Lipoproteins, LDL/metabolism
KW - Male
KW - Middle Aged
KW - Natriuretic Peptide, Brain/blood
KW - Peptide Fragments/blood
KW - Severity of Illness Index
KW - Stroke Volume
KW - heart failure
KW - high-density lipoprotein
KW - n3-PUFA
UR - http://www.scopus.com/inward/record.url?scp=85052401115&partnerID=8YFLogxK
U2 - 10.1111/eci.12998
DO - 10.1111/eci.12998
M3 - Journal article
C2 - 30004123
SN - 0014-2972
VL - 48
SP - e12998
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 9
M1 - e12998
ER -