Proposed antiischemic effects of trimetazidine in coronary diabetic patients. A substudy from TRIMPOL-1

被引:55
作者
Szwed, H
Sadowski, Z
Pachocki, R
Domzat-Bochenska, M
Szymczak, K
Szydlowski, Z
Paradowski, A
Gajos, G
Kaluza, G
Kulon, I
Wator-Brzezinska, A
Elikowski, W
Kuzniak, M
机构
[1] Natl Inst Cardiol, PL-02637 Warsaw, Poland
[2] Serv Polska, Warsaw, Poland
[3] Voivodeship Cardiol Ctr, Lomza, Poland
[4] PCK, City Hosp, Bialystok, Poland
[5] Jagiellonian Univ, Coll Med, Dept Ischaem Heart Dis, Krakow, Poland
[6] Jagiellonian Univ, Coll Med, Dept Cardiol, Krakow, Poland
[7] Voivodeship Specialist Hosp, G Narutowicza, Krakow, Poland
[8] Voivideship Cardiol Ctr, Krakow, Poland
[9] Strusia Hosp, Poznan, Poland
[10] Dist Hosp, Olesno, Poland
关键词
trimetazidine; diabetes mellitus; coronary heart disease; ischemia; tolerability;
D O I
10.1023/A:1007744109064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus, a disease with a wide prevalence, has major cardiovascular effects, being a risk factor for the development of ischemic heart disease and congestive heart failure. The aim of this open, multicenter study was to assess the antiischemic efficacy and tolerability of trimetazidine, a metabolic agent acting at the myocardial mitochondrial level, in diabetic patients with stable effort angina treated previously with a single conventional antianginal drug. Fifty diabetic patients (mean age 58 years) with proven coronary artery disease, stable effort angina for at least 3 months, and positive, comparable results of two initial treadmill exercise tests separated by a 1-week interval were included in the study. They continued their conventional antianginal monotherapy with a long-acting nitrate, beta-blocker, or calcium channel blocker. After stabilization, 4-week therapy with trimetazidine, three times daily, 20 mg was initiated in combination with previous treatment. The results showed a significant improvement in exercise tolerance (440.2 vs. 383.2 s; P < 0.01), time to 1-mm ST-segment depression (358.3 vs. 301.6 s; P < 0.01), time to onset of anginal pain (400.0 vs. 238.3 s; P < 0.01), and total work (9.39 vs. 8.67 metabolic equivalents, P < 0.01). Maximal ST-segment depression was attenuated compared with baseline (1.82 vs. 1.91 mm). Other findings included a significant decrease in the mean frequency of anginal episodes (3.06 vs. 4.79 per week; P < 0.01) and in mean nitrate consumption (2.29 vs. 4.2 doses/week). These results suggest that trimetazidine may be effective and is well tolerated as combination therapy for diabetic coronary artery disease patients uncontrolled with a single hemodynamic agent.
引用
收藏
页码:217 / 222
页数:6
相关论文
共 31 条
[1]  
Alderman EL, 1996, NEW ENGL J MED, V335, P217
[2]   ANGIOGRAPHIC PROGRESSION OF CORONARY-ARTERY DISEASE AND THE DEVELOPMENT OF MYOCARDIAL-INFARCTION [J].
AMBROSE, JA ;
TANNENBAUM, MA ;
ALEXOPOULOS, D ;
HJEMDAHLMONSEN, CE ;
LEAVY, J ;
WEISS, M ;
BORRICO, S ;
GORLIN, R ;
FUSTER, V .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1988, 12 (01) :56-62
[3]   IMPROVEMENT OF LONG-TERM PRESERVATION OF ISOLATED ARRESTED RAT-HEART - BENEFICIAL EFFECT OF THE ANTIISCHEMIC AGENT TRIMETAZIDINE [J].
AUSSEDAT, J ;
RAY, A ;
KAY, L ;
VERDYS, M ;
HARPEY, C ;
ROSSI, A .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1993, 21 (01) :128-135
[4]   REGULATION BY INSULIN OF MYOCARDIAL GLUCOSE AND FATTY-ACID METABOLISM IN THE CONSCIOUS DOG [J].
BARRETT, EJ ;
SCHWARTZ, RG ;
FRANCIS, CK ;
ZARET, BL .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (03) :1073-1079
[5]   NEW ANTI-ISCHAEMIC DRUGS - CYTOPROTECTIVE ACTION WITH NO PRIMARY HEMODYNAMIC-EFFECTS [J].
BODDEKE, E ;
HUGTENBURG, J ;
JAP, W ;
HEYNIS, J ;
VANZWIETEN, P .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1989, 10 (10) :397-400
[6]   COMPARISON OF TRIMETAZIDINE WITH NIFEDIPINE IN EFFORT ANGINA - A DOUBLE-BLIND, CROSSOVER STUDY [J].
DALLAVOLTA, S ;
MARAGLINO, G ;
DELLAVALENTINA, P ;
VIENA, P ;
DESIDERI, A .
CARDIOVASCULAR DRUGS AND THERAPY, 1990, 4 :853-860
[7]  
DESIDERI A, 1995, RES CLIN FORUMS, V17, P43
[8]   TRIMETAZIDINE - A NEW CONCEPT IN THE TREATMENT OF ANGINA - COMPARISON WITH PROPRANOLOL IN PATIENTS WITH STABLE ANGINA [J].
DETRY, JM ;
SELLIER, P ;
PENNAFORTE, S ;
COKKINOS, D ;
DARGIE, H ;
MATHES, P .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1994, 37 (03) :279-288
[9]   GLYCOLYSIS AND GLUCOSE-OXIDATION DURING REPERFUSION OF ISCHEMIC HEARTS FROM DIABETIC RATS [J].
GAMBLE, J ;
LOPASCHUK, GD .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1994, 1225 (02) :191-199
[10]   RELATION OF THE SITE OF ACUTE MYOCARDIAL-INFARCTION TO THE MOST SEVERE CORONARY ARTERIAL-STENOSIS AT PRIOR ANGIOGRAPHY [J].
GIROUD, D ;
LI, JM ;
URBAN, P ;
MEIER, B ;
RUTISHAUSER, W .
AMERICAN JOURNAL OF CARDIOLOGY, 1992, 69 (08) :729-732