TY - JOUR
T1 - Effects of trimetazidine in nonischemic heart failure
T2 - A randomized study
AU - Winter, José Luis
AU - Castro, Pablo F.
AU - Quintana, Juan Carlos
AU - Altamirano, Rodrigo
AU - Enriquez, Andres
AU - Verdejo, Hugo E.
AU - Jalil, Jorge E.
AU - Mellado, Rosemarie
AU - Concepción, Roberto
AU - Sepúlveda, Pablo
AU - Rossel, Victor
AU - Sepúlveda, Luis
AU - Chiong, Mario
AU - García, Lorena
AU - Lavandero, Sergio
N1 - Funding Information:
Funding: Fondo Nacional de Desarrollo Científico y Tecnologico grants 1050768 (to P.F.C.) and 1120212 to (S.L.), Anillo ACT 1111 (to P.F.C., M.C., L.G., and S.L.), and FONDAP 15130011 (to P.F.C., H.E.V., M.C., L.G., and S.L.).
PY - 2014/3
Y1 - 2014/3
N2 - Objectives Heart failure (HF) is associated with changes in myocardial metabolism that lead to impairment of contractile function. Trimetazidine (TMZ) modulates cardiac energetic efficiency and improves outcomes in ischemic heart disease. We evaluated the effects of TMZ on left ventricular ejection fraction (LVEF), cardiac metabolism, exercise capacity, O2 uptake, and quality of life in patients with nonischemic HF. Methods and Results Sixty patients with stable nonischemic HF under optimal medical therapy were included in this randomized double-blind study. Patients were randomized to TMZ (35 mg orally twice a day) or placebo for 6 months. LVEF, 6-minute walk test (6MWT), maximum O2 uptake in cardiopulmonary exercise test, different markers of metabolism, oxidative stress, and endothelial function, and quality of life were assessed at baseline and after TMZ treatment. Left ventricular peak glucose uptake was evaluated with the use of the maximum standardized uptake value (SUV) by 18-fluorodeoxyglucose positron emission tomography (18FDG-PET). Etiology was idiopathic in 85% and hypertensive in 15%. Both groups were similar in age, functional class, LVEF, and levels of N-terminal pro-B-type natriuretic peptide at baseline. After 6 months of TMZ treatment, no changes were observed in LVEF (31 ± 10% vs 34 ± 8%; P =.8), 6MWT (443 ± 25 m vs 506 ± 79 m; P =.03), maximum O2 uptake (19.1 ± 5.0 mL kg-1 min-1 vs 23.0 ± 7.2 mL kg-1 min-1; P =.11), functional class (percentages of patients in functional classes I/II/III/IV 10/3753/0 vs 7/40/50/3; P =.14), or quality of life (32 ± 26 points vs 24 ± 18 points; P =.25) in TMZ versus placebo, respectively. In the subgroup of patients evaluated with 18FDG-PET, no significant differences were observed in SUV between both groups (7.0 ± 3.6 vs 8.2 ± 3.4 respectively; P =.47). Conclusions In patients with nonischemic HF, the addition of TMZ to optimal medical treatment does not result in significant changes of LVEF, exercise capacity, O2 uptake, or quality of life.
AB - Objectives Heart failure (HF) is associated with changes in myocardial metabolism that lead to impairment of contractile function. Trimetazidine (TMZ) modulates cardiac energetic efficiency and improves outcomes in ischemic heart disease. We evaluated the effects of TMZ on left ventricular ejection fraction (LVEF), cardiac metabolism, exercise capacity, O2 uptake, and quality of life in patients with nonischemic HF. Methods and Results Sixty patients with stable nonischemic HF under optimal medical therapy were included in this randomized double-blind study. Patients were randomized to TMZ (35 mg orally twice a day) or placebo for 6 months. LVEF, 6-minute walk test (6MWT), maximum O2 uptake in cardiopulmonary exercise test, different markers of metabolism, oxidative stress, and endothelial function, and quality of life were assessed at baseline and after TMZ treatment. Left ventricular peak glucose uptake was evaluated with the use of the maximum standardized uptake value (SUV) by 18-fluorodeoxyglucose positron emission tomography (18FDG-PET). Etiology was idiopathic in 85% and hypertensive in 15%. Both groups were similar in age, functional class, LVEF, and levels of N-terminal pro-B-type natriuretic peptide at baseline. After 6 months of TMZ treatment, no changes were observed in LVEF (31 ± 10% vs 34 ± 8%; P =.8), 6MWT (443 ± 25 m vs 506 ± 79 m; P =.03), maximum O2 uptake (19.1 ± 5.0 mL kg-1 min-1 vs 23.0 ± 7.2 mL kg-1 min-1; P =.11), functional class (percentages of patients in functional classes I/II/III/IV 10/3753/0 vs 7/40/50/3; P =.14), or quality of life (32 ± 26 points vs 24 ± 18 points; P =.25) in TMZ versus placebo, respectively. In the subgroup of patients evaluated with 18FDG-PET, no significant differences were observed in SUV between both groups (7.0 ± 3.6 vs 8.2 ± 3.4 respectively; P =.47). Conclusions In patients with nonischemic HF, the addition of TMZ to optimal medical treatment does not result in significant changes of LVEF, exercise capacity, O2 uptake, or quality of life.
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U2 - 10.1016/j.cardfail.2014.01.004
DO - 10.1016/j.cardfail.2014.01.004
M3 - Article
C2 - 24412523
AN - SCOPUS:84896075851
SN - 1071-9164
VL - 20
SP - 149
EP - 154
JO - Journal of Cardiac Failure
JF - Journal of Cardiac Failure
IS - 3
ER -