From the Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN.
Invest Radiol. 2017 Nov;52(11):686-692. doi: 10.1097/RLI.0000000000000390.
Renal fibrosis is a useful biomarker for diagnosis and evaluation of therapeutic interventions of renal diseases but often requires invasive testing. Magnetization transfer magnetic resonance imaging (MT-MRI), which evaluates the presence of macromolecules, offers a noninvasive tool to probe renal fibrosis in murine renal artery stenosis (RAS) at 16.4 T. In this study, we aimed to identify appropriate imaging parameters for collagen detection at 3.0 T MRI and to test the utility of MT-MRI in measuring renal fibrosis in a swine model of atherosclerotic RAS (ARAS).
To select the appropriate offset frequency, an MT-MRI study was performed on a phantom containing 0% to 40% collagen I and III with offset frequencies from -1600 to +1600 Hz and other MT parameters empirically set as pulse width at 16 milliseconds and flip angle at 800 degrees. Then selected MT parameters were used in vivo on pigs 12 weeks after sham (n = 8) or RAS (n = 10) surgeries. The ARAS pigs were fed with high-cholesterol diet to induce atherosclerosis. The MT ratio (MTR) was compared with ex vivo renal fibrosis measured using Sirius-red staining.
Offset frequencies at 600 and 1000 Hz were selected for collagen detection without direct saturation of free water signal, and subsequently applied in vivo. The ARAS kidneys showed mild cortical and medullary fibrosis by Sirius-red staining. The cortical and medullary MTRs at 600 and 1000 Hz were both increased. Renal fibrosis measured ex vivo showed good linear correlations with MTR at 600 (cortex: Pearson correlation coefficient r = 0.87, P < 0.001; medulla: r = 0.70, P = 0.001) and 1000 Hz (cortex: r = 0.75, P < 0.001; medulla: r = 0.83, P < 0.001).
Magnetization transfer magnetic resonance imaging can noninvasively detect renal fibrosis in the stenotic swine kidney at 3.0 T. Therefore, MT-MRI may potentially be clinically applicable and useful for detection and monitoring of renal pathology in subjects with RAS.
肾纤维化是诊断和评估肾脏疾病治疗干预的有用生物标志物,但通常需要进行有创性检测。磁化转移磁共振成像(MT-MRI)评估大分子的存在,为在 16.4T 下探测鼠肾动脉狭窄(RAS)中的肾纤维化提供了一种非侵入性工具。在这项研究中,我们旨在确定在 3.0T MRI 上检测胶原的合适成像参数,并在动脉粥样硬化性 RAS(ARAS)猪模型中测试 MT-MRI 测量肾纤维化的效用。
为了选择合适的偏移频率,我们在一个含有 0%至 40%I 型和 III 型胶原的体模上进行了 MT-MRI 研究,偏移频率范围为-1600 至+1600Hz,其他 MT 参数根据经验设置为脉宽 16 毫秒,翻转角 800 度。然后在 12 周后接受假手术(n=8)或 RAS 手术(n=10)的猪体内使用选定的 MT 参数。ARAS 猪用高胆固醇饮食喂养以诱导动脉粥样硬化。MT 比(MTR)与天狼星红染色测量的离体肾纤维化进行比较。
选择 600 和 1000Hz 的偏移频率用于胶原检测,而不会直接饱和游离水信号,随后在体内应用。ARAS 肾脏通过天狼星红染色显示轻度皮质和髓质纤维化。600 和 1000Hz 的皮质和髓质 MTR 均升高。离体纤维化测量与 600Hz(皮质:皮尔逊相关系数 r=0.87,P<0.001;髓质:r=0.70,P=0.001)和 1000Hz(皮质:r=0.75,P<0.001;髓质:r=0.83,P<0.001)的 MTR 均呈良好的线性相关。
3.0T 下磁化转移磁共振成像可无创探测狭窄猪肾脏的纤维化。因此,MT-MRI 可能具有临床应用潜力,有助于检测和监测 RAS 患者的肾脏病理。