The Effect of Coenzyme Q10 on Morbidity and Mortality in Chronic Heart Failure Results From Q-SYMBIO: A Randomized Double-Blind Trial

被引:304
作者
Mortensen, Svend A. [1 ]
Rosenfeldt, Franklin [2 ]
Kumar, Adarsh [3 ]
Dolliner, Peter [4 ]
Filipiak, Krzysztof J. [5 ]
Pella, Daniel [6 ]
Alehagen, Urban [7 ]
Steurer, Guenter [4 ]
Littarru, Gian P. [8 ]
机构
[1] Copenhagen Univ Hosp, Dept Cardiol, Ctr Heart, DK-2100 Copenhagen O, Denmark
[2] Monash Univ, Alfred Hosp, Cardiac Surg Res Unit, Melbourne, Vic 3181, Australia
[3] GND Hosp, Govt Med Coll, Dept Cardiol, Amritsar, Punjab, India
[4] Med Univ Vienna, Dept Internal Med 2, Vienna, Austria
[5] Med Univ Warsaw, Dept Cardiol 1, Warsaw, Poland
[6] Safarik Univ, Fac Med, Kosice, Slovakia
[7] Linkoping Univ Hosp, S-58185 Linkoping, Sweden
[8] Polytech Univ Marche, Biochem Sect, Clin & Dent Sci, Ancona, Italy
关键词
chronic heart failure; coenzyme Q(10); metabolic therapy; randomized controlled trial; ubiquinone; THERAPY; SUPPLEMENTATION; BIOAVAILABILITY; DEFICIENCY; INHIBITORS; RATIONALE; EXERCISE; PLASMA; ASSAY;
D O I
10.1016/j.jchf.2014.06.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This randomized controlled multicenter trial evaluated coenzyme Q(10) (CoQ(10)) as adjunctive treatment in chronic heart failure (HF). BACKGROUND CoQ(10) is an essential cofactor for energy production and is also a powerful antioxidant. A low level of myocardial CoQ(10) is related to the severity of HF. Previous randomized controlled trials of CoQ(10) in HF were underpowered to address major clinical endpoints. METHODS Patients with moderate to severe HF were randomly assigned in a 2-year prospective trial to either CoQ(10) 100 mg 3 times daily or placebo, in addition to standard therapy. The primary short-term endpoints at 16 weeks were changes in New York Heart Association (NYHA) functional classification, 6-min walk test, and levels of N-terminal pro-B type natriuretic peptide. The primary long-term endpoint at 2 years was composite major adverse cardiovascular events as determined by a time to first event analysis. RESULTS A total of 420 patients were enrolled. There were no significant changes in short-term endpoints. The primary long-term endpoint was reached by 15% of the patients in the CoQ(10) group versus 26% in the placebo group (hazard ratio: 0.50; 95% confidence interval: 0.32 to 0.80; p = 0.003) by intention-to-treat analysis. The following secondary endpoints were significantly lower in the CoQ(10) group compared with the placebo group: cardiovascular mortality (9% vs. 16%, p = 0.026), all-cause mortality (10% vs. 18%, p = 0.018), and incidence of hospital stays for HF (p = 0.033). In addition, a significant improvement of NYHA class was found in the CoQ(10) group after 2 years (p = 0.028). CONCLUSIONS Long-term CoQ(10) treatment of patients with chronic HF is safe, improves symptoms, and reduces major adverse cardiovascular events. (Coenzyme Q(10) as adjunctive treatment of chronic heart failure: a randomised, double-blind, multicentre trial with focus on SYMptoms, BIomarker status [Brain-Natriuretic Peptide (BNP)], and long-term Outcome [hospitalisations/mortality]; ISRCTN94506234) (C) 2014 by the American College of Cardiology Foundation.
引用
收藏
页码:641 / 649
页数:9
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