在 7T 下利用交错三核 MRS 对人体肝脏的碳水化合物和脂质代谢进行单次研究。

IF 2.7 4区 医学 Q2 BIOPHYSICS NMR in Biomedicine Pub Date : 2024-08-01 Epub Date: 2024-02-29 DOI:10.1002/nbm.5123
Simone Poli, Ahmed F Emara, Naomi F Lange, Edona Ballabani, Angeline Buser, Michele Schiavon, David Herzig, Chiara Dalla Man, Lia Bally, Roland Kreis
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引用次数: 0

摘要

肝脏在新陈代谢平衡中发挥着核心作用,各种肝脏和全身代谢紊乱的临床疾病就是例证。尤其令人感兴趣的是,在肥胖、糖尿病和脂肪肝等高发疾病中,脂质和碳水化合物代谢之间存在复杂的相互作用。对人体进行直接研究面临着可及性有限和需要侵入性程序的挑战。因此,对糖酵解通量的无创动态评估以及对脂质水平和组成的稳态评估对基本了解至关重要,并可能为新的治疗目标开辟新的途径。在此,我们对在 7T 磁共振扫描仪的一次交错检查中结合使用的三种不同磁共振光谱(MRS)技术进行了评估。1 H-MRS 和 13 C-MRS 对内源性代谢物进行探测,而氘代谢成像(DMI)则依靠施用氘化示踪剂(目前是 2 H 标记的葡萄糖)来绘制代谢命运的空间和时间演变图。所有这三种技术都经过了优化,可用于单次临床调查,并已应用于对健康受试者的初步研究。使用三通道 1 H/2 H/13 C 射频线圈可进行交错检查,无需重新定位。短回波时间 STEAM 光谱法可提供分辨率较高的光谱,用于量化脂质含量和组成。评估了使用水饱和度与代谢物循环和呼吸同步类型的相对优势。口服 2 H 葡萄糖后,2 H-MR 光谱成像可对时间和空间分辨的葡萄糖水平进行登记,而糖原的天然丰度 13 C-MRS 可对肝脏葡萄糖储存进行动态测量。就 DMI 和 13 C-MRS 而言,在 5 分钟扫描周期内,该方法的测量精度分别约为 0.2 毫摩尔和 16 毫摩尔。用 DMI 测定葡萄糖的动态吸收和用 1 H-MRS 测定脂质概况的结果都非常好,而用 13 C-MRS 测定糖原水平的变化也是可行的,但受信噪比的限制较大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Interleaved trinuclear MRS for single-session investigation of carbohydrate and lipid metabolism in human liver at 7T.

The liver plays a central role in metabolic homeostasis, as exemplified by a variety of clinical disorders with hepatic and systemic metabolic disarrays. Of particular interest are the complex interactions between lipid and carbohydrate metabolism in highly prevalent conditions such as obesity, diabetes, and fatty liver disease. Limited accessibility and the need for invasive procedures challenge direct investigations in humans. Hence, noninvasive dynamic evaluations of glycolytic flux and steady-state assessments of lipid levels and composition are crucial for basic understanding and may open new avenues toward novel therapeutic targets. Here, three different MR spectroscopy (MRS) techniques that have been combined in a single interleaved examination in a 7T MR scanner are evaluated. 1H-MRS and 13C-MRS probe endogenous metabolites, while deuterium metabolic imaging (DMI) relies on administration of deuterated tracers, currently 2H-labelled glucose, to map the spatial and temporal evolution of their metabolic fate. All three techniques have been optimized for a robust single-session clinical investigation and applied in a preliminary study of healthy subjects. The use of a triple-channel 1H/2H/13C RF coil enables interleaved examinations with no need for repositioning. Short-echo-time STEAM spectroscopy provides well resolved spectra to quantify lipid content and composition. The relative benefits of using water saturation versus metabolite cycling and types of respiratory synchronization were evaluated. 2H-MR spectroscopic imaging allowed for registration of time- and space-resolved glucose levels following oral ingestion of 2H-glucose, while natural abundance 13C-MRS of glycogen provides a dynamic measure of hepatic glucose storage. For DMI and 13C-MRS, the measurement precision of the method was estimated to be about 0.2 and about 16 mM, respectively, for 5 min scanning periods. Excellent results were shown for the determination of dynamic uptake of glucose with DMI and lipid profiles with 1H-MRS, while the determination of changes in glycogen levels by 13C-MRS is also feasible but somewhat more limited by signal-to-noise ratio.

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来源期刊
NMR in Biomedicine
NMR in Biomedicine 医学-光谱学
CiteScore
6.00
自引率
10.30%
发文量
209
审稿时长
3-8 weeks
期刊介绍: NMR in Biomedicine is a journal devoted to the publication of original full-length papers, rapid communications and review articles describing the development of magnetic resonance spectroscopy or imaging methods or their use to investigate physiological, biochemical, biophysical or medical problems. Topics for submitted papers should be in one of the following general categories: (a) development of methods and instrumentation for MR of biological systems; (b) studies of normal or diseased organs, tissues or cells; (c) diagnosis or treatment of disease. Reports may cover work on patients or healthy human subjects, in vivo animal experiments, studies of isolated organs or cultured cells, analysis of tissue extracts, NMR theory, experimental techniques, or instrumentation.
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