A novel method in myocardial injury risk stratification using intravenous fat emulsion as sole rapid preparation for unfasted patients to suppress myocardial 18F-fluorodeoxyglucose uptake for optimal cardiac PET imaging: a proof-of-concept randomized-crossover trial.

Michael H-G Li, Raef R Boktor, Christopher Rowe, Laurence Weinberg, Bernhard Riedel
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Abstract

Objectives: Optimal imaging of ischemic or inflammed myocardium via 18F-FDG PET imaging requires suppression of background carbohydrate metabolism in normal myocardium. Sole administration of intravenous lipid emulsion has not previously been used to rapidly prepare unfasted patients, such as in emergent clinical situations. In this proof-of-concept pilot, we posited that intravenous fat emulsion suppresses physiological metabolic uptake of in non-ischemic, non-inflammatory myocardium in unprepared and unfasted setting for enhanced cardiac positron emission tomography (PET) imaging.

Methods: We conducted an ethics-approved, single-blind, prospective randomized crossover trial of 10 healthy volunteers from January 2020 to June 2021. Participants were unfasted and rendered hyperglycemic before being administered either high dose intravenous lipid emulsion-1.5 ml kg of 20% lipid emulsion, followed by 15 ml/kg/hr for 30mins-or saline prior to 18F-FDG injection and subsequent cardiac PET imaging. Assessors undertook image analysis for maximum standard uptake value (SUVmax), minimum standard uptake value (SUVmin) and qualitative assessment, and groups were compared using univariate analysis.

Results: The study population age was 44.5 years [IQR 32.5-56.5], with 50% male and a median BMI of 22.75 [IQR 25.0-28.5] kg/m2. The study was feasible and there were no adverse side effects from the interventions. In these participants with normal myocardium, 18F-FDG uptake was reduced by intravenous lipid emulsion as assessed by SUVmax and qualitative assessment (p = 0.042, r = 0.454 and p = 0.009, r = -0.581, respectively).

Conclusions: Intravenous lipid emulsion suppresses background metabolic uptake of 18F-FDG even in unprepared and unfasted patients. Our findings prove and expand the possible applications for cardiac 18F-FDG PET in various settings, including in emergent settings as a means of rapid preparation in place of current more time-consuming standard protocols, allowing time-critical management to be effected.

一种新的心肌损伤风险分层方法,使用静脉注射脂肪乳剂作为未禁食患者的唯一快速制剂,抑制心肌18F-氟脱氧葡萄糖摄取,以优化心脏正电子发射计算机断层成像:概念验证随机交叉试验。
目的:通过 18F-FDG PET 成像对缺血或发炎心肌进行最佳成像需要抑制正常心肌中碳水化合物的背景代谢。在临床急诊等情况下,单独静脉注射脂质乳剂还未被用于快速准备未禁食的患者。在这项概念验证试验中,我们假设静脉注射脂肪乳剂可抑制非缺血、非炎症心肌在无准备、无空腹情况下的生理性代谢摄取,从而增强心脏正电子发射断层扫描(PET)成像:我们于 2020 年 1 月至 2021 年 6 月对 10 名健康志愿者进行了一项伦理批准的单盲前瞻性随机交叉试验。在注射 18F-FDG 和随后进行心脏 PET 成像之前,参加者均未禁食,并先进行高血糖治疗,然后静脉注射大剂量脂质乳剂--1.5 毫升/千克 20% 脂质乳剂,然后 15 毫升/千克/小时,持续 30 分钟--或生理盐水。评估人员对最大标准摄取值(SUVmax)、最小标准摄取值(SUVmin)和定性评估进行图像分析,并通过单变量分析对各组进行比较:研究对象年龄为 44.5 岁 [IQR 32.5-56.5],50% 为男性,体重指数中位数为 22.75 [IQR 25.0-28.5] kg/m2。这项研究是可行的,而且干预措施没有不良副作用。在这些心肌正常的参与者中,通过SUVmax和定性评估(分别为p = 0.042,r = 0.454和p = 0.009,r = -0.581),静脉注射脂质乳剂降低了18F-FDG摄取量:结论:静脉注射脂质乳剂可抑制 18F-FDG 的本底代谢摄取,即使是在无准备和未空腹的患者中也是如此。我们的研究结果证明并拓展了心脏 18F-FDG PET 在各种情况下的可能应用,包括在紧急情况下作为一种快速准备手段,取代目前耗时较长的标准方案,使时间紧迫的管理得以实施。
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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