THE EFFECT OF CAPTOPRIL ON TL-201 MYOCARDIAL PERFUSION IN SYSTEMIC-SCLEROSIS

被引:43
作者
KAHAN, A
DEVAUX, JY
AMOR, B
MENKES, CJ
WEBER, S
VENOT, A
STRAUCH, G
机构
[1] UNIV PARIS 05,SCH MED,INST RECH THERAPEUT,F-75270 PARIS 06,FRANCE
[2] UNIV PARIS 05,SCH MED,DEPT RHEUMATOL,F-75270 PARIS 06,FRANCE
[3] UNIV PARIS 05,SCH MED,DEPT CARDIOL,F-75270 PARIS 06,FRANCE
[4] UNIV PARIS 05,SCH MED,DEPT NUCL MED,F-75270 PARIS 06,FRANCE
关键词
D O I
10.1038/clpt.1990.61
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In systemic sclerosis, abnormalities of myocardial perfusion are common and may be caused by a disturbance of the coronary microcirculation. We evaluated the long-term effect of captopril (75 to 150 mg per day) on thallium 201 myocardial perfusion in 12 normotensive patients with systemic sclerosis. Captopril significantly decreased the mean (±SD) number of segments with thallium 201 myocardial perfusion defects (6.5 ± 1.9 at baseline and 4.4 ± 2.7 after 1 year of treatment with captopril; p < 0.02) and increased the mean global thallium score (9.6 ± 1.7 at baseline and 11.4 ± 2.1 after captopril; p < 0.05). In a control group of eight normotensive patients with systemic sclerosis who did not receive captopril, no significant modification in thallium results occurred. Side effects with captopril included hypotension (six patients), taste disturbances (one patient), and skin rash (one patient). These side effects subsided when the dosage was reduced. These findings demonstrate that captopril improves thallium 201 myocardial perfusion in patients with systemic sclerosis and may therefore have a beneficial effect on scleroderma myocardial disease. © 1990.
引用
收藏
页码:483 / 489
页数:7
相关论文
共 30 条
[1]   REVERSIBLE COLD-INDUCED ABNORMALITIES IN MYOCARDIAL PERFUSION AND FUNCTION IN SYSTEMIC-SCLEROSIS [J].
ALEXANDER, EL ;
FIRESTEIN, GS ;
WEISS, JL ;
HEUSER, RR ;
LEITL, G ;
WAGNER, HN ;
BRINKER, JA ;
CIUFFO, AA ;
BECKER, LC .
ANNALS OF INTERNAL MEDICINE, 1986, 105 (05) :661-668
[2]   PRIMARY HEART-DISEASE IN SYSTEMIC-SCLEROSIS (SCLERODERMA) - ADVANCES IN CLINICAL AND PATHOLOGIC FEATURES, PATHOGENESIS, AND NEW THERAPEUTIC APPROACHES [J].
BOTSTEIN, GR ;
LEROY, EC .
AMERICAN HEART JOURNAL, 1981, 102 (05) :913-919
[3]  
BULKLEY B H, 1979, Clinics in Rheumatic Diseases, V5, P131
[4]   MYOCARDIAL LESIONS OF PROGRESSIVE SYSTEMIC-SCLEROSIS - CAUSE OF CARDIAC DYSFUNCTION [J].
BULKLEY, BH ;
RIDOLFI, RL ;
SALYER, WR ;
HUTCHINS, GM .
CIRCULATION, 1976, 53 (03) :483-490
[5]  
COHEN ML, 1982, J PHARMACOL EXP THER, V220, P63
[6]   PATHOLOGIC OBSERVATIONS IN SYSTEMIC SCLEROSIS (SCLERODERMA) - A STUDY OF 58 AUTOPSY CASES AND 58 MATCHED CONTROLS [J].
DANGELO, WA ;
FRIES, JF ;
MASI, AT ;
SHULMAN, LE .
AMERICAN JOURNAL OF MEDICINE, 1969, 46 (03) :428-+
[7]  
DIXON WJ, 1981, BMDP STATISTICAL SOF
[9]   LARGE CONDUIT ARTERIES IN HYPERTENSION - ROLE OF THE VASCULAR RENIN-ANGIOTENSIN SYSTEM [J].
DZAU, VJ ;
SAFAR, ME .
CIRCULATION, 1988, 77 (05) :947-954
[10]  
DZAU VJ, 1988, CIRCULATION S1, V77, P13