From the Departments of General Medicine.
Viapath Analytics, King's College Hospital NHS Foundation Trust, London, United Kingdom.
Invest Radiol. 2020 Jul;55(7):405-411. doi: 10.1097/RLI.0000000000000657.
Over the recent years, there have been increasing concerns that exposure to gadolinium-based contrast agents (GBCAs) may be associated with retention of Gd within the skin, bones, and solid organs in patients with normal renal function, although the clinical implications of this deposition remain to be established. There are no published data available to guide the development of reference intervals for Gd concentrations in biological samples from healthy people. The aims of this study were to (1) determine whether healthy individuals who have not received GBCAs have detectable concentrations of Gd in their blood and urine, and (2) to develop a reference range for Gd concentrations in blood and spot urine samples for healthy individuals.
Whole blood, plasma, and spot urine samples were taken from 120 healthy volunteers with estimated glomerular filtration rate 70 mL/min per 1.73 m or greater. Gd concentrations were measured in these samples using inductively coupled plasma mass-spectrometry. The reference intervals for Gd concentrations in whole blood, plasma, and urine were estimated as the 2.5th percentile and the upper reference limit as the 97.5th percentile.
Ten (8.33%) of the 120 subjects had detectable concentrations of Gd in their whole blood (n = 5) or spot urine (n = 5) samples; no subjects had detectable concentrations of Gd in their plasma samples. Our proposed reference intervals for Gd are as follows: whole blood, <0.008 ng/mL or <0.050 nmol/L; plasma, <0.009 ng/mL or <0.057 nmol/L; spot urine, <0.036 μg/g or <0.0250 nmol/mmol.
The results of this study provide reference intervals for whole blood, plasma, and urine Gd concentrations in healthy subjects who have not previously received GBCAs and will assist clinicians in assessing patients who have concerns regarding potential Gd retention postexposure and help guide further clinical studies to explore the pharmacokinetics of GBCAs in patients with normal renal function.
近年来,人们越来越担心,在肾功能正常的患者中,接触钆基造影剂(GBCA)可能会导致 Gd 在皮肤、骨骼和实体器官中蓄积,尽管这种蓄积的临床意义尚未确定。目前尚无发表的数据可用于指导健康人群生物样本中 Gd 浓度的参考区间的制定。本研究旨在:(1)确定是否未接受 GBCA 治疗的健康个体的血液和尿液中可检测到 Gd 浓度;(2)建立健康个体血液和尿样中 Gd 浓度的参考范围。
从估计肾小球滤过率(eGFR)≥70mL/min/1.73m2 的 120 名健康志愿者中采集全血、血浆和尿样。使用电感耦合等离子体质谱法(ICP-MS)测定这些样本中的 Gd 浓度。全血、血浆和尿液中 Gd 浓度的参考区间采用第 2.5 百分位数和第 97.5 百分位数上限估计。
在 120 名受试者中,有 10 名(8.33%)的全血(n=5)或尿样(n=5)中可检测到 Gd 浓度;没有受试者的血浆样本中可检测到 Gd 浓度。我们提出的 Gd 参考区间如下:全血,<0.008ng/mL 或<0.050nmol/L;血浆,<0.009ng/mL 或<0.057nmol/L;尿样,<0.036μg/g 或<0.0250nmol/mmol。
本研究结果为未接受 GBCA 治疗的健康受试者的全血、血浆和尿液中 Gd 浓度提供了参考区间,这将有助于临床医生评估接触 GBCA 后潜在 Gd 蓄积的患者,并有助于指导进一步的临床研究,以探索肾功能正常患者 GBCA 的药代动力学。