Advances and prospects in deuterium metabolic imaging (DMI): a systematic review of in vivo studies.

IF 3.7 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Radiology Experimental Pub Date : 2024-06-03 DOI:10.1186/s41747-024-00464-y
Feng Pan, Xinjie Liu, Jiayu Wan, Yusheng Guo, Peng Sun, Xiaoxiao Zhang, Jiazheng Wang, Qingjia Bao, Lian Yang
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Abstract

Background: Deuterium metabolic imaging (DMI) has emerged as a promising non-invasive technique for studying metabolism in vivo. This review aims to summarize the current developments and discuss the futures in DMI technique in vivo.

Methods: A systematic literature review was conducted based on the PRISMA 2020 statement by two authors. Specific technical details and potential applications of DMI in vivo were summarized, including strategies of deuterated metabolites detection, deuterium-labeled tracers and corresponding metabolic pathways in vivo, potential clinical applications, routes of tracer administration, quantitative evaluations of metabolisms, and spatial resolution.

Results: Of the 2,248 articles initially retrieved, 34 were finally included, highlighting 2 strategies for detecting deuterated metabolites: direct and indirect DMI. Various deuterated tracers (e.g., [6,6'-2H2]glucose, [2,2,2'-2H3]acetate) were utilized in DMI to detect and quantify different metabolic pathways such as glycolysis, tricarboxylic acid cycle, and fatty acid oxidation. The quantifications (e.g., lactate level, lactate/glutamine and glutamate ratio) hold promise for diagnosing malignancies and assessing early anti-tumor treatment responses. Tracers can be administered orally, intravenously, or intraperitoneally, either through bolus administration or continuous infusion. For metabolic quantification, both serial time point methods (including kinetic analysis and calculation of area under the curves) and single time point quantifications are viable. However, insufficient spatial resolution remains a major challenge in DMI (e.g., 3.3-mL spatial resolution with 10-min acquisition at 3 T).

Conclusions: Enhancing spatial resolution can facilitate the clinical translation of DMI. Furthermore, optimizing tracer synthesis, administration protocols, and quantification methodologies will further enhance their clinical applicability.

Relevance statement: Deuterium metabolic imaging, a promising non-invasive technique, is systematically discussed in this review for its current progression, limitations, and future directions in studying in vivo energetic metabolism, displaying a relevant clinical potential.

Key points: • Deuterium metabolic imaging (DMI) shows promise for studying in vivo energetic metabolism. • This review explores DMI's current state, limits, and future research directions comprehensively. • The clinical translation of DMI is mainly impeded by limitations in spatial resolution.

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氘代谢成像(DMI)的进展与前景:体内研究系统回顾。
背景:氘代谢成像(DMI)已成为研究体内代谢的一种前景广阔的非侵入性技术。本综述旨在总结氘代谢成像技术的发展现状,并探讨其在体内应用的前景:方法:两位作者根据 PRISMA 2020 声明进行了系统的文献综述。方法:两位作者根据 PRISMA 2020 声明进行了系统的文献综述,总结了 DMI 在体内的具体技术细节和潜在应用,包括氘代代谢物检测策略、氘标记示踪剂和体内相应的代谢途径、潜在的临床应用、示踪剂给药途径、代谢的定量评估和空间分辨率:在最初检索到的 2,248 篇文章中,有 34 篇最终被收录,其中突出了两种检测氘代代谢物的策略:直接和间接 DMI。在 DMI 中使用了各种氘化示踪剂(如[6,6'-2H2]葡萄糖、[2,2,2'-2H3]乙酸酯)来检测和量化不同的代谢途径,如糖酵解、三羧酸循环和脂肪酸氧化。这些量化指标(如乳酸水平、乳酸/谷氨酰胺和谷氨酸比率)有望用于诊断恶性肿瘤和评估早期抗肿瘤治疗反应。示踪剂可通过口服、静脉注射或腹腔注射给药,也可通过栓剂给药或持续输注给药。在代谢定量方面,连续时间点方法(包括动力学分析和曲线下面积计算)和单个时间点定量都是可行的。然而,空间分辨率不足仍是 DMI 面临的主要挑战(例如,在 3 T 下 10 分钟采集的空间分辨率为 3.3 毫升):结论:提高空间分辨率可促进 DMI 的临床转化。此外,优化示踪剂合成、给药方案和定量方法将进一步提高其临床适用性:氘代谢成像是一种前景广阔的非侵入性技术,本综述系统地讨论了它在研究体内能量代谢方面的当前进展、局限性和未来方向,并展示了相关的临床潜力:- 氘代谢成像(DMI)有望用于研究体内能量代谢。- 这篇综述全面探讨了 DMI 的现状、局限性和未来研究方向。- 氘代谢成像的临床应用主要受到空间分辨率的限制。
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来源期刊
European Radiology Experimental
European Radiology Experimental Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
6.70
自引率
2.60%
发文量
56
审稿时长
18 weeks
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