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Effects of hyperglycemia on fluorine-18-fluorodeoxyglucose biodistribution in a large oncology clinical practice

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Aim Suggested cutoff points of blood glucose levels (BGL) before 18F-FDG PET/CT scanning vary between 120 and 200 mg/dl in current guidelines. This study’s purpose was to compare the frequency of… Click to show full abstract

Aim Suggested cutoff points of blood glucose levels (BGL) before 18F-FDG PET/CT scanning vary between 120 and 200 mg/dl in current guidelines. This study’s purpose was to compare the frequency of abnormal fluorine-18-fluorodeoxyglucose (18F-FDG) biodistribution on PET/CT scans of patients with various ranges of abnormal BGL and to determine the effect of BGL greater than 200 mg/dl on 18F-FDG uptake in various organs. Patients and methods 18F-FDG PET/CT scans were retrospectively reviewed for 325 patients with BGL greater than 120 mg/dl at the time of scan and 112 with BGL less than or equal to 120 mg/dl. 18F-FDG biodistribution was categorized as normal, mildly abnormal, or abnormal by visual analysis of brain, background soft tissue, and muscle. Mean standardized uptake values (SUVmean) in brain, liver, fat (flank), gluteal muscle, and blood pool (aorta) were recorded. 18F-FDG biodistribution frequencies were assessed using a nonparametric &khgr;2-test for trend. Normal organ SUVs were compared using Kruskal–Wallis tests using the following BGL groupings: ⩽120, 121–150, 151–200, and ≥201 mg/dl. Results Although higher BGL were significantly associated with an increased proportion of abnormal biodistribution (P<0.001), most patients with BGL less than or equal to 200 mg/dl had normal or mildly abnormal biodistribution. Average brain SUVmean significantly decreased with higher BGL groupings (P<0.001). Average aorta, gluteal muscle, and liver SUVmean did not significantly differ among groups with BGL greater than 120 mg/dl (P=0.66, 0.84, and 0.39, respectively), but were significantly lower in those with BGL less than or equal to 120 mg/dl (P⩽0.001). Flank fat SUVmean was not significantly different among BGL groups (P=0.67). Conclusion Abnormal 18F-FDG biodistribution is associated with higher BGL at the time of scan, but the effects are negligible or mild in most patients with BGL less than 200 mg/dl. Although mildly increased soft tissue uptake is seen with BGL greater than 120 mg/dl, decline in brain metabolic activity correlated the most with various BGL.

Keywords: bgl; biodistribution; fdg biodistribution; fluorine fluorodeoxyglucose; 18f fdg; oncology

Journal Title: Nuclear Medicine Communications
Year Published: 2018

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