Delayed Calf Muscle Phosphocreatine Recovery After Exercise Identifies Peripheral Arterial Disease
David C. Isbell, MD*,
Stuart S. Berr, PhD , ,
Alicia Y. Toledano, ScD||,
Frederick H. Epstein, PhD , ,
Craig H. Meyer, PhD ,
Walter J. Rogers, PhD*, ,
Nancy L. Harthun, MD ,
Klaus D. Hagspiel, MD ,
Arthur Weltman, PhD* and
Christopher M. Kramer, MD*, ,*
* Medicine
Radiology
Biomedical Engineering
Surgery, University of Virginia Health System, University of Virginia, Charlottesville, Virginia
|| Center for Statistical Sciences, Brown University, Providence, Rhode Island

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Figure 1 Sequential phosphorous-31 spectra acquired after exercise in a subject with peripheral arterial disease. In this example the first three spectra (45 s) after exercise are shown. Note the incremental increase in phosphocreatine (PCr) and simultaneous decrease in inorganic phosphate reflecting PCr regeneration in the skeletal muscle tissue. ATP = adenosine triphosphate; PDE = phosphodiester; Pi = inorganic phosphate; PME = phosphomonester.
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Figure 2 Representative phosphocreatine (PCr) recovery plots in control (top) and peripheral arterial disease (bottom) subjects. Note the steeper recovery curve in the control subject. The PCr recovery time constant was 34.4 s in the control subject and 121.1 s in the peripheral arterial disease patient.
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Figure 3 In this graph of phosphocreatine (PCr) recovery time constants, the boxes extend from the 25th to the 75th percentile, and the horizontal lines depict the medians. The median PCr recovery time constant is longer in peripheral arterial disease (PAD) patients.
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Figure 4 Receiver-operating characteristic curve for phosphocreatine (PCr) recovery kinetics. The points shown are the observed data.
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Figure 5 Reproducibility analyzed using the method of Bland and Altman.
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