Deuterium metabolic imaging of the human abdomen at clinical field strength

Pascal Wodtke, Mary A McLean, Ines Horvat-Menih, Jonathan R Birchall, Maria J Zamora-Morales, Ashley Grimmer, Elizabeth Latimer, Marta Wylot, Rolf F Schulte, Ferdia A Gallagher
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Abstract

Background The Warburg effect is a hallmark of cancer and is characterized by increased glucose consumption and lactate formation. Deuterium metabolic imaging (DMI) is an emerging non-invasive MRI method for probing this metabolic reprogramming in the field of neuroimaging. Here we show the feasibility of the technique for abdominal imaging using a routine 3 T MRI system, which has previously presented significant technical challenges. Purpose This study aimed to translate abdominal DMI to clinical field strength by optimizing the radiofrequency coil setup, the administered dose of deuterium (2H)-labelled glucose, and the data processing pipeline for quantitative characterization of DMI signals over time in the kidney and liver, establishing a basis for routine clinical studies in the future. Materials and Methods Five healthy volunteers were recruited and imaged on 2 or 3 occasions, with different 2H-glucose doses (totalling 13 DMI scan sessions). DMI was performed at 3 T using a flexible 20 x 30 cm2 2H-tuned transmit-receive surface coil. We have defined three novel quantitative parameters as metrics of metabolism and compared these between doses and organs. Results The careful positioning of a dedicated surface coil minimized unwanted gastric signals while maintaining excellent hepatic and renal measurements. The timecourses derived from the liver and kidney were reproducible and comparable across different doses, with a trend towards lower quantitative measurements with decreasing dose. An increase in the 2H-water signal over time particularly in the liver, could be used as an indirect measure of metabolism. Conclusion DMI of the human abdomen is feasible using a routine MRI system and the metabolism measured in the kidney and liver can serve as a reference for future clinical studies. The 2H-glucose dose can be reduced from 0.75 to 0.25 g/kg to minimize gastric signal without substantially affecting the reliability of organ quantification.
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临床场强下的人体腹部氘代谢成像
背景沃伯格效应是癌症的特征之一,其特点是葡萄糖消耗和乳酸盐形成增加。氘代谢成像(DMI)是一种新兴的无创磁共振成像方法,用于探测神经成像领域的代谢重编程。在这里,我们展示了使用常规 3 T 核磁共振成像系统进行腹部成像的可行性。目的本研究旨在通过优化射频线圈设置、氘(2H)标记葡萄糖的给药剂量以及数据处理管道,将腹部 DMI 转化为临床场强,从而定量表征肾脏和肝脏随时间变化的 DMI 信号,为将来的常规临床研究奠定基础。材料与方法招募五名健康志愿者,用不同剂量的 2H 葡萄糖进行 2 或 3 次成像(共 13 次 DMI 扫描)。DMI 在 3 T 下使用灵活的 20 x 30 平方厘米 2H 调谐发射接收表面线圈进行。我们定义了三个新的定量参数作为代谢指标,并在不同剂量和器官之间进行了比较。结果专用表面线圈的精心定位最大限度地减少了不必要的胃信号,同时保持了出色的肝脏和肾脏测量结果。从肝脏和肾脏得出的时间历程具有可重复性,并且在不同剂量下具有可比性,随着剂量的减少,定量测量值呈下降趋势。随着时间的推移,尤其是在肝脏中,2H-水信号的增加可用作新陈代谢的间接测量。结论 使用常规磁共振成像系统对人体腹部进行 DMI 是可行的,在肾脏和肝脏测量到的新陈代谢情况可作为未来临床研究的参考。2H-葡萄糖剂量可从 0.75 克/千克减少到 0.25 克/千克,以尽量减少胃信号,而不会对器官定量的可靠性产生重大影响。
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