(Circulation. 1995;91:2299-2301.)
© 1995 American Heart Association, Inc.
Articles |
From the Department of Biochemistry (K.C.), University of Oxford, Oxford, UK; and LMMB (R.L.V.), NIAAA, Rockville, Md.
Correspondence to Dr Richard L. Veech, LMMB, NIAAA, 12501 Washington Ave, Rockville, MD 20852.
Key Words: imaging editorials metabolism
| Introduction |
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Modeling of FDG as a glucose analogue for glycolysis in the heart comes in large part from work in brain metabolism,2 where glucose is the major metabolic fuel and glycogen synthesis from glucose is essentially nil. In contrast, the heart is omnivorous in its choice of metabolic fuels, with a preference for fatty acids and with considerable glycogen synthesis and degradation.3 4 Consequently, expressions such as "myocardial glucose metabolism" and "myocardial glucose utilization" were coined in part out of recognition that FDG flux rates are unable to distinguish glycogen synthesis from glycolysis. In the heart, therefore, a measure of the rate of FDG accumulation may be just thata measure of FDG accumulation and not a measure of metabolic rate.
If one is to interpret the
meaning of a change in FDG accumulation
over time,
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