From the Sections of Radiology (E.J., K.H., H.A., J.K.) and Nuclear Medicine (M.L.), Department of Surgical Sciences, and Department of Medical Sciences (J.W.E.), Uppsala University, Akademiska Sjukhuset, SE-75185 Uppsala, Sweden; Centre for Clinical Research Sörmland, Uppsala University, Eskilstuna, Sweden (E.J.); Uppsala-Örebro Regional Research Council, Uppsala, Sweden (E.J.); Department of Medical Physics, Uppsala University Hospital, Uppsala, Sweden (M.L.); AstraZeneca R&D, Gothenburg, Sweden (S.S.); Department of Medicine, Sahlgrenska Academy at Gothenburg University, Gothenburg, Sweden (S.S.); and Antaros Medical, Mölndal, Sweden (H.A., J.K.).
Radiology. 2018 Jan;286(1):271-278. doi: 10.1148/radiol.2017162949. Epub 2017 Aug 25.
Purpose To develop, evaluate, and demonstrate the feasibility of a whole-body protocol for simultaneous assessment of tissue-specific insulin-mediated fluorine 18 (F) fluorodeoxyglucose (FDG) influx rates, tissue depots, and whole-body insulin sensitivity (referred to as the M value). Materials and Methods An integrated positron emission tomography (PET)/magnetic resonance (MR) imaging system combined with hyperinsulinemic euglycemic clamp (HEC) was used. Dynamic whole-body PET imaging was used to determine the insulin-mediated F-FDG tissue influx rate (K) in the whole-body region by using the Patlak method. M value was determined with the HEC method at PET imaging. Tissue depots were quantified by using water-fat separated MR imaging and manual segmentations. Feasibility of the imaging protocol was demonstrated by using five healthy control participants and five patients with type 2 diabetes. Associations between M value and K were studied in multiple tissues by using the Pearson correlation. Results Positive correlations were found between M value and K in multiple tissues: the gluteus muscle (r = 0.875; P = .001), thigh muscle (r = 0.903; P , .001), calf muscle (r = 0.825; P = .003), and abdominal visceral adipose tissue (r = 0.820; P = .004). A negative correlation was found in the brain (r = 20.798; P = .006). The MR imaging-based method for quantification of tissue depots was feasible for determining adipose tissue volumes and fat fractions. Conclusion This PET/MR imaging protocol may be feasible for simultaneous assessment of tissue-specific insulin-mediated F-FDG influx rates, tissue depots, and M value. RSNA, 2017 Online supplemental material is available for this article.
目的 开发、评估并验证一种全身方案的可行性,该方案可同时评估组织特异性胰岛素介导的氟 18(F)氟脱氧葡萄糖(FDG)流入率、组织储量和全身胰岛素敏感性(称为 M 值)。
材料与方法 使用集成正电子发射断层扫描(PET)/磁共振(MR)成像系统结合高胰岛素正葡萄糖钳夹(HEC)。采用动态全身 PET 成像,使用 Patlak 方法确定全身区域的胰岛素介导的 F-FDG 组织流入率(K)。采用 HEC 法在 PET 成像时确定 M 值。通过水脂分离的 MR 成像和手动分割来量化组织储量。通过对 5 名健康对照者和 5 名 2 型糖尿病患者进行成像方案的可行性验证。使用 Pearson 相关性研究了 M 值和 K 在多个组织之间的相关性。
结果 在多个组织中,M 值与 K 之间存在正相关关系:臀肌(r = 0.875;P =.001)、大腿肌肉(r = 0.903;P ,.001)、小腿肌肉(r = 0.825;P =.003)和腹部内脏脂肪组织(r = 0.820;P =.004)。在大脑中发现了负相关(r = 20.798;P =.006)。基于 MR 成像的组织储量定量方法可用于确定脂肪组织体积和脂肪分数。
结论 这种 PET/MR 成像方案可能可用于同时评估组织特异性胰岛素介导的 F-FDG 流入率、组织储量和 M 值。
RSNA,2017 年
在线补充材料可在本文中获取。