TY - JOUR
T1 - Glucose and insulin variations in patients during the time course of a FDG-PET study and implications for the "glucose-corrected" SUV
AU - Hadi, Mohiuddin
AU - Bacharach, Stephen L.
AU - Whatley, Millie
AU - Libutti, Steven K.
AU - Straus, Stephen E.
AU - Rao, V. Koneti
AU - Wesley, Robert
AU - Carrasquillo, Jorge A.
N1 - Funding Information:
This work was supported by the National Institute of Allergy and Infectious Diseases Intramural Program.
PY - 2008/5
Y1 - 2008/5
N2 - Introduction: 2-Deoxy-2[18F]fluoro-d-glucose (FDG) positron emission tomography (PET) has an established role in the evaluation of cancer. Generally, tumor uptake and response to treatment are evaluated using the standardized uptake value (SUV). Some authors have proposed correcting SUV for glucose levels. Insulin is also thought to influence tumor uptake by changing uptake in other tissues. However, little attention has been paid to understanding the variability of glucose or insulin during a single PET study. Method: We studied the biological and instrumental variability of glucose and insulin measurements in 71 nondiabetic patients undergoing FDG-PET studies. Multiple glucose measurements were obtained in all 71 subjects, and in 69 of these 71 subjects, multiple serum insulin measurements were made. We determined the coefficient of observed variation (CVow) and the coefficient of variation attributable to biological variability (CVbv) for both glucose and insulin. Results: The mean glucose concentration was 78.9±13.5 mg/dl. The mean insulin value was 6.49±5.92 μU/ml. The weighted mean CVow and CVbv was 5.0% and 3.6%, respectively, for glucose and 14.2% and 8.3%, respectively, for insulin. Conclusions: Variations in the range of 3.6% are observed in glucose measurements during the time course of an FDG scan even after accounting for analytical error; larger variations of 8.3% are observed in insulin levels. Therefore, corrections of SUV for blood glucose, especially if obtained from single measurements, can introduce additional errors of at least this much.
AB - Introduction: 2-Deoxy-2[18F]fluoro-d-glucose (FDG) positron emission tomography (PET) has an established role in the evaluation of cancer. Generally, tumor uptake and response to treatment are evaluated using the standardized uptake value (SUV). Some authors have proposed correcting SUV for glucose levels. Insulin is also thought to influence tumor uptake by changing uptake in other tissues. However, little attention has been paid to understanding the variability of glucose or insulin during a single PET study. Method: We studied the biological and instrumental variability of glucose and insulin measurements in 71 nondiabetic patients undergoing FDG-PET studies. Multiple glucose measurements were obtained in all 71 subjects, and in 69 of these 71 subjects, multiple serum insulin measurements were made. We determined the coefficient of observed variation (CVow) and the coefficient of variation attributable to biological variability (CVbv) for both glucose and insulin. Results: The mean glucose concentration was 78.9±13.5 mg/dl. The mean insulin value was 6.49±5.92 μU/ml. The weighted mean CVow and CVbv was 5.0% and 3.6%, respectively, for glucose and 14.2% and 8.3%, respectively, for insulin. Conclusions: Variations in the range of 3.6% are observed in glucose measurements during the time course of an FDG scan even after accounting for analytical error; larger variations of 8.3% are observed in insulin levels. Therefore, corrections of SUV for blood glucose, especially if obtained from single measurements, can introduce additional errors of at least this much.
KW - FDG-PET
KW - Glucose
KW - Insulin
KW - PET
KW - PET/CT
KW - Variability
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U2 - 10.1016/j.nucmedbio.2008.02.007
DO - 10.1016/j.nucmedbio.2008.02.007
M3 - Article
C2 - 18482681
AN - SCOPUS:43049171680
SN - 0969-8051
VL - 35
SP - 441
EP - 445
JO - International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology
JF - International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology
IS - 4
ER -