Dujardin Martine, Luypaert Rob, Vandenbroucke F, Van der Niepen Patricia, Sourbron Steven, Verbeelen Dierik, Stadnik T, de Mey Johan
Department of Radiology/BEFY, UZ Brussel, Vrije Universiteit Brussel, Laarbeeklaan 101, 1090 Brussels, Belgium.
Eur J Radiol. 2009 Mar;69(3):542-9. doi: 10.1016/j.ejrad.2007.11.033. Epub 2008 Mar 4.
To investigate the feasibility of implementing quantitative T1-perfusion in the routine MRA-protocol and to obtain a first experience in normals and pathology.
For perfusion imaging, IR-prepared FLASH (one 4 mm slice at mid-renal level, TR 4.4 ms, TE 2.2 ms, TI 180 ms, FA 50 degrees , matrix 128 x 256, bandwidth per pixel 300, 400 dynamics, temporal resolution 0.3 s, total measurement time 2 min) was applied during the injection of 10 ml of standard 0.5 mmol/ml Gadolinium-DTPA solution at 2 ml/s, followed by 3DCE-MRA with bolus tracking (TR 5.4, TE 1.4, FA 40 degrees , matrix 192 x 512, NSA 1, slice thickness 1.5 mm), using a second dose of 0.1 mmol Gadolinium-DTPA per kg body weight with a maximum of 20 ml. The T1-weighted signals (perfusion data) were converted to tissue tracer concentrations and deconvolved with an inflow corrected AIF; blood flow, distribution volume, mean transit time and blood flow heterogeneity were derived.
MRA quality was uncompromised by the first bolus administered for perfusion purposes. In the normals, average cortical RBF, RVD and MTT were 1.2 ml/min/ml (S.D. 0.3 ml/min/ml), 0.4 ml/ml (S.D. 0.1 ml/ml) and 21s (S.D. 4s). These RBF values are lower than those found in the literature, probably due to residual AIF inflow effects. The sensitivity of the technique was sufficient to demonstrate altered perfusion in the examples of pathology.
Combined quantitative T1-perfusion and MRA have a potential for noninvasive renovascular screening and may provide an anatomical and physiological evaluation of renal status.
研究在常规MRA协议中实施定量T1灌注的可行性,并在正常人和病变患者中获得初步经验。
对于灌注成像,在以2ml/s的速度注射10ml标准0.5mmol/ml钆喷酸葡胺溶液期间,应用IR预脉冲快速小角度激发序列(肾中水平一个4mm层面,TR 4.4ms,TE 2.2ms,TI 180ms,翻转角50°,矩阵128×256,每像素带宽300,400个动态时相,时间分辨率0.3s,总测量时间2分钟),随后采用团注追踪法进行三维对比增强MRA(TR 5.4,TE 1.4,翻转角40°,矩阵192×512,采集次数1,层厚1.5mm),使用每千克体重0.1mmol钆喷酸葡胺,最大剂量20ml。将T1加权信号(灌注数据)转换为组织示踪剂浓度,并与流入校正后的动脉输入函数进行去卷积;得出血流量、分布容积、平均通过时间和血流异质性。
用于灌注目的的首次团注未损害MRA质量。在正常人群中,平均皮质肾血流量、分布容积和平均通过时间分别为1.2ml/min/ml(标准差0.3ml/min/ml)、0.4ml/ml(标准差0.1ml/ml)和21秒(标准差4秒)。这些肾血流量值低于文献报道的值,可能是由于动脉输入函数残留流入效应。该技术的敏感性足以在病变实例中显示灌注改变。
联合定量T1灌注和MRA在无创性肾血管筛查方面具有潜力,可能为肾脏状况提供解剖学和生理学评估。