کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3298618 1209909 2007 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Quantification of Liver Glucose Metabolism by Positron Emission Tomography: Validation Study in Pigs
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی بیماری‌های گوارشی
پیش نمایش صفحه اول مقاله
Quantification of Liver Glucose Metabolism by Positron Emission Tomography: Validation Study in Pigs
چکیده انگلیسی

Background & Aims: The liver is inaccessible to organ balance measurements in humans. To validate [18F]fluorodeoxyglucose ([18F]FDG) positron emission tomography (PET) in the quantification of hepatic glucose uptake (HGU), we determined [18F]FDG modeling parameters, lumped constant (LC), and input functions (single arterial versus dual). Methods: Anesthetized pigs were studied during fasting (n = 6), physiologic (n = 4), and supraphysiologic (n = 4) hyperinsulinemia. PET was performed with C15O (blood pool) and [18F]FDG (glucose uptake). 6,6-Deuterated glucose ([2H]G) was coinjected with [18F]FDG and blood collected from the carotid artery and portal and hepatic veins to compute LC as ratio between tracers fractional extraction. HGU was estimated from PET images and ex vivo from high-performance liquid chromatography measurements of liver [18F]FDG versus [18F]FDG-6-phosphate and [18F]-glycogen. Endogenous glucose production was measured with [2H]G and hepatic blood flow by flowmeters. Results: HGU was increased in hyperinsulinemia versus fasting (P < .05). Fractional extraction of [18F]FDG and [2H]G was similar (not significant), intercorrelated (r = 0.98, P < .0001), and equally higher during hyperinsulinemia than fasting (P ≤ .05), with an LC of 0.98 ± 0.10 and 1.18 ± 0.26, respectively. [18F]FDG-PET modeling provided HGU values that did not differ from, and were correlated with, those from ex vivo measurements (r = 0.61, P ≤ .02); proportional estimates of liver perfusion and endogenous glucose production were also obtained. Single and dual input functions produced strongly intercorrelated results (r > 0.95, P < .0001), with a modest underestimation of HGU by the former. Conclusions: [18F]FDG-PET–derived parameters provide accurate quantification of HGU and estimates of liver perfusion and glucose production. In the liver, LC of [18F]FDG is nearly unitary. Using a single arterial input introduces only a small error in estimation of HGU.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gastroenterology - Volume 132, Issue 2, February 2007, Pages 531–542
نویسندگان
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