From the Departments of Radiology (R.J.M., J.S.M., D.D., D.S., R.K., L.J.E., D.F.K.), Laboratory Medicine and Pathology (M.E.J., D.L.M.), and Neurosurgery (D.F.K.), College of Medicine, Mayo Clinic, 200 1st St SW, Rochester, MN 55905.
Radiology. 2017 Nov;285(2):536-545. doi: 10.1148/radiol.2017161594. Epub 2017 Jun 19.
Purpose To compare gadolinium tissue concentrations of multiple linear and macrocyclic chelates in a rat model to better understand the scope and extent of tissue deposition following multiple intravenous doses of gadolinium-based contrast agent (GBCA). Materials and Methods In this Institutional Animal Care and Use Committee-approved study, healthy rats received 20 intravenous injections of 2.5 mmol gadolinium per kilogram (gadolinium-exposed group) or saline (control group) over a 26-day period. Unenhanced T1 signal intensities of the dentate nucleus were measured from magnetic resonance (MR) images obtained prior to GBCA injection and 3 days after final injection. Rat brain and renal, hepatic, and splenic tissues were harvested 7 days after final injection and subjected to inductively coupled plasma mass spectrometry and transmission electron microscopy for quantification and characterization of gadolinium deposits. Results Gadolinium deposition in brain tissue significantly varied with GBCA type (F = 31.2; P < .0001), with median concentrations of 0 μg gadolinium per gram of tissue (95% confidence interval [CI]: 0, 0.2) in gadoteridol-injected rats, 1.6 μg gadolinium per gram of tissue (95% CI: 0.9, 4.7) in gadobutrol-injected rats, 4.7 μg gadolinium per gram of tissue (95% CI: 3.5, 6.1) in gadobenate dimeglumine-injected rats, and 6.9 μg gadolinium per gram of tissue (95% CI: 6.2, 7.0) in gadodiamide-injected rats; a significant positive dose-signal intensity correlation was identified (ρ = 0.93; P < .0001). No detectable neural tissue deposition or MR imaging signal was observed in control rats (n = 6). Similar relative differences in gadolinium deposition were observed in renal, hepatic, and splenic tissues at much higher tissue concentrations (P < .0001). Gadolinium deposits were visualized directly in the endothelial capillary walls and neural interstitium in GBCA-injected rats, but not in control rats. Conclusion Tissue deposition of gadolinium was two- to fourfold higher following administration of the linear agents gadodiamide and gadobenate dimeglumine compared with the macrocyclic agents gadobutrol and gadoteridol. These findings suggest that organ tissue deposition is reduced but not eliminated following administration of macrocyclic GBCA chelates in lieu of linear chelates. RSNA, 2017 Online supplemental material is available for this article.
目的 比较大鼠模型中多种线性和大环螯合物的钆组织浓度,以更好地了解多次静脉注射钆基对比剂(GBCA)后组织沉积的范围和程度。
材料与方法 在这项获得机构动物护理和使用委员会批准的研究中,健康大鼠在 26 天内接受 20 次 2.5mmol 每千克体重的钆(钆暴露组)或生理盐水(对照组)静脉注射。在 GBCA 注射前和最后一次注射后 3 天,从磁共振(MR)图像中测量齿状核的未增强 T1 信号强度。最后一次注射后 7 天,收获大鼠脑和肾、肝、脾组织,并用电感耦合等离子体质谱法和透射电子显微镜定量和表征钆沉积物。
结果 脑组织中钆的沉积量随 GBCA 类型的不同而显著变化(F = 31.2;P <.0001),在注射加德西醇的大鼠中,组织中每克钆的浓度中位数为 0μg(95%置信区间[CI]:0,0.2),注射钆布醇的大鼠为 1.6μg(95%CI:0.9,4.7),注射钆贝葡胺的大鼠为 4.7μg(95%CI:3.5,6.1),注射钆喷酸葡胺的大鼠为 6.9μg(95%CI:6.2,7.0);鉴定出与剂量信号强度呈显著正相关(ρ=0.93;P <.0001)。在对照组大鼠(n=6)中未观察到神经组织沉积或 MR 成像信号。在肾、肝和脾组织中也观察到类似的相对差异较大的钆沉积,但其组织浓度更高(P <.0001)。在 GBCA 注射大鼠的内皮毛细血管壁和神经间质中直接观察到钆沉积,但在对照组大鼠中未观察到。
结论 与大环螯合物加德西醇和钆贝葡胺相比,线性螯合物钆喷酸葡胺和钆贝醇给药后,钆的组织沉积增加了两到四倍。这些发现表明,在使用大环 GBCA 螯合物代替线性螯合物后,器官组织沉积减少但并未消除。
RSNA,2017 在线补充材料可用于本文。