PMID- 30835327 OWN - NLM STAT- MEDLINE DCOM- 20200310 LR - 20210511 IS - 1898-018X (Electronic) IS - 1897-5593 (Print) IS - 1898-018X (Linking) VI - 26 IP - 2 DP - 2019 TI - Effect of coenzyme Q10 in Europeans with chronic heart failure: A sub-group analysis of the Q-SYMBIO randomized double-blind trial. PG - 147-156 LID - 10.5603/CJ.a2019.0022 [doi] AB - BACKGROUND: Geographical differences in patient characteristics, management and outcomes in heart failure (HF) trials are well recognized. The aim of this study was to assess the consistency of the treat- ment effect of coenzyme Q10 (CoQ10) in the European sub-population of Q-SYMBIO, a randomized double-blind multinational trial of treatment with CoQ10, in addition to standard therapy in chronic HF. METHODS: Patients with moderate to severe HF were randomized to CoQ10 300 mg daily or placebo in addition to standard therapy. At 3 months the primary short-term endpoints were changes in New York Heart Association (NYHA) functional classification, 6-min walk test, and levels of N-terminal pro-B type natriuretic peptide. At 2 years the primary long-term endpoint was major adverse cardiovascular events (MACE). RESULTS: There were no significant changes in short-term endpoints. The primary long-term endpoint of MACE was reached by significantly fewer patients in the CoQ10 group (n = 10, 9%) compared to the placebo group (n = 33, 27%, p = 0.001). The following secondary endpoints were significantly improved in the CoQ10 group compared with the placebo group: all-cause and cardiovascular mortality, NYHA classification and left ventricular ejection fraction (LVEF). In the European sub-population, when compared to the whole group, there was greater adherence to guideline directed therapy and similar results for short- and long-term endpoints. A new finding revealed a significant improvement in LVEF. CONCLUSIONS: The therapeutic efficacy of CoQ10 demonstrated in the Q-SYMBIO study was confirmed in the European sub-population in terms of safely reducing MACE, all-cause mortality, cardiovascular mortality, hospitalization and improvement of symptoms. FAU - Mortensen, Anne Louise AU - Mortensen AL AD - annelou.mortensen@gmail.com. FAU - Rosenfeldt, Franklin AU - Rosenfeldt F AD - Faculty of Health, Arts and Design, Swinburne University of Technology, Melbourne, Australia. AD - Baker Heart and Diabetes Institute, Melbourne, Australia. FAU - Filipiak, Krzysztof J AU - Filipiak KJ AD - 1st Department of Cardiology, Medical University of Warsaw, Poland. LA - eng PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial DEP - 20190305 PL - Poland TA - Cardiol J JT - Cardiology journal JID - 101392712 RN - 0 (Biomarkers) RN - 0 (Peptide Fragments) RN - 0 (Vitamins) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) RN - 1339-63-5 (Ubiquinone) RN - EJ27X76M46 (coenzyme Q10) SB - IM MH - Aged MH - Biomarkers/blood MH - Chromatography, High Pressure Liquid MH - Dose-Response Relationship, Drug MH - Double-Blind Method MH - Europe/epidemiology MH - Female MH - Follow-Up Studies MH - Heart Failure/blood/*drug therapy/mortality MH - Humans MH - Male MH - Middle Aged MH - Natriuretic Peptide, Brain/blood MH - Peptide Fragments/blood MH - Prospective Studies MH - Stroke Volume/*physiology MH - Survival Rate/trends MH - Treatment Outcome MH - Ubiquinone/administration & dosage/*analogs & derivatives/pharmacokinetics MH - Ventricular Function, Left/physiology MH - Vitamins/administration & dosage/pharmacokinetics PMC - PMC8086660 OTO - NOTNLM OT - chronic heart failure OT - coenzyme CoQ10 OT - hospitalization OT - major adverse cardiovascular events OT - mortality OT - randomized controlled trial OT - ubiquinone COIS- Conflict of interest: None declared EDAT- 2019/03/06 06:00 MHDA- 2020/03/11 06:00 PMCR- 2019/04/26 CRDT- 2019/03/06 06:00 PHST- 2019/01/31 00:00 [received] PHST- 2019/02/05 00:00 [accepted] PHST- 2019/03/06 06:00 [pubmed] PHST- 2020/03/11 06:00 [medline] PHST- 2019/03/06 06:00 [entrez] PHST- 2019/04/26 00:00 [pmc-release] AID - VM/OJS/J/62920 [pii] AID - cardj-26-2-147 [pii] AID - 10.5603/CJ.a2019.0022 [doi] PST - ppublish SO - Cardiol J. 2019;26(2):147-156. doi: 10.5603/CJ.a2019.0022. Epub 2019 Mar 5.