ASSESSMENT OF MYOCARDIAL OXIDATIVE-METABOLISM IN AORTIC-VALVE DISEASE USING POSITRON EMISSION TOMOGRAPHY WITH C-11 ACETATE

被引:16
作者
HICKS, RJ [1 ]
SAVAS, V [1 ]
CURRIE, PJ [1 ]
KALFF, V [1 ]
STARLING, M [1 ]
BERGIN, P [1 ]
KIRSCH, M [1 ]
SCHWAIGER, M [1 ]
机构
[1] UNIV MICHIGAN HOSP,DEPT INTERNAL MED,DIV NUCL MED,B1G412,ANN ARBOR,MI 48105
关键词
D O I
10.1016/0002-8703(92)90503-N
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
C-11 acetate has recently been introduced as a tracer of myocardial oxidative metabolism with the use of positron emission tomography. To evaluate this approach in the pressure- or volume-loaded heart, C-11 acetate clearance rate constants were determined in 22 patients with chronic aortic valve disease and in nine normal subjects. Global myocardial C-11 clearance was significantly higher in patients with predominant aortic stenosis (n = 11) or aortic regurgitation (n = 11) than in normal subjects (0.069 +/- 0.017 min-1 and 0.072 +/- 0.010 min-1 compared with 0.050 +/- 0.004 min-1, p < 0.05) and correlated significantly with the rate-pressure product corrected for mean aortic valve gradient (r = 0.73, p = 0.0001) for all studies. However, analysis of patient subgroups demonstrated that this correlation held only aortic stenosis (r = 0.79, p < 0.005 for gradient-corrected rate-pressure product). Additionally, C-11 clearance was strongly correlated with the product of heart rate and mean wall stress in patients with aortic stenosis (r = 0.89, p < 0.005) but not in patients with aortic regurgitation. Normalization of C-11 acetate clearance rate constants for gradient-corrected rate-pressure product were significantly lower in patients with loaded ventricles, particularly in the presence of a low ejection fraction, compared to normal subjects. Possible mechanisms include myocardial adaptation through hypertrophy or depressed contractility, which would both tend to reduce oxygen consumption under any given load. Serial comparison of C-11 acetate kinetics and noninvasive indexes of oxygen demand may provide assessment of disease progression in pathologic ventricular loading.
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页码:653 / 664
页数:12
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