肾移植患者使用超极化[1-13C]丙酮酸核磁共振成像进行代谢成像的初步经验

Xiaoxi Liu, Ying-Chieh Lai., Di Cui, Shiang-Cheng Kung, Meyeon Park, Laszik Zoltan, Peder E. Z. Larson, Zhen J. Wang
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摘要

背景:肾移植是治疗晚期肾病患者的首选方法。早期发现异体移植损伤对于延缓或预防不可逆转的损伤非常重要。目的:研究超极化(HP)[1-13C]丙酮酸核磁共振成像评估肾脏异体移植代谢的可行性。受试者:6 名计划进行肾移植活检的受试者(平均年龄 45.2 +- 12.4 岁,2 名女性)和 5 名肾细胞癌(RCC)患者(平均年龄 59.6 +- 10.4 岁,2 名女性)。评估:六名肾脏异体移植参与者中有五人在接受核磁共振成像后进行了活组织检查。在核磁共振成像后 4 周内收集估计肾小球滤过率 (eGFR) 和尿蛋白肌酐比值 (uPCR)。通过 HP[1-13C]pyruvate MRI,利用异体移植肾和 RCC 患者非肿瘤携带肾的乳酸与丙酮酸比率,对肾脏代谢进行量化。结果:活检平均在 HP [1-13C] 丙酮酸 MRI 后 9 天(5-19 天)进行。三例活检结果正常,一例显示低度纤维化,一例显示中度微血管炎症。所有受试者的异体移植物功能稳定,eGFR >60 mL/min/1.73 m2,uPCR 正常。一名未进行活组织检查的参与者的 eGFR 降低至 49 mL/min/1.73 m2,uPCR 升高。检查结果正常者(3 人)的乳酸丙酮酸比值平均为 0.373,检查结果异常者(2 人)的乳酸丙酮酸比值平均为 0.552。在 eGFR 降低和 uPRC 升高的参与者中,乳酸与丙酮酸的比率最高(0.847)。原生无肿瘤肾脏的乳酸丙酮酸比值平均为 0.309。数据结论:活检结果正常的稳定异体移植肾的乳酸丙酮酸比值与原生无肿瘤肾相似,而活检结果异常的异体移植肾的乳酸丙酮酸比值更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Initial Experience of Metabolic Imaging with Hyperpolarized [1-13C]pyruvate MRI in Kidney Transplant Patients
BACKGROUND: Kidney transplant is the treatment of choice for patients with end-stage renal disease. Early detection of allograft injury is important to delay or prevent irreversible damage. PURPOSE: To investigate the feasibility of hyperpolarized (HP) [1-13C]pyruvate MRI for assessing kidney allograft metabolism. SUBJECTS: 6 participants (mean age, 45.2 +- 12.4 years, 2 females) scheduled for kidney allograft biopsy and 5 patients (mean age, 59.6 +- 10.4 years, 2 females) with renal cell carcinoma (RCC). ASSESSMENT: Five of the six kidney allograft participants underwent biopsy after MRI. Estimated glomerular filtration rate (eGFR) and urine protein-to-creatine ratio (uPCR) were collected within 4 weeks of MRI. Kidney metabolism was quantified from HP [1-13C]pyruvate MRI using the lactate-to-pyruvate ratio in allograft kidneys and non-tumor bearing kidneys from RCC patients. RESULTS: Biopsy was performed a mean of 9 days (range 5-19 days) after HP [1-13C]pyruvate MRI. Three biopsies were normal, one showed low-grade fibrosis and one showed moderate microvascular inflammation. All had stable functioning allografts with eGFR > 60 mL/min/1.73 m2 and normal uPCR. One participant who did not undergo biopsy had reduced eGFR of 49 mL/min/1.73 m2 and elevated uPCR. The mean lactate-to-pyruvate ratio was 0.373 in participants with normal findings (n = 3) and 0.552 in participants with abnormal findings (n = 2). The lactate-to-pyruvate ratio was highest (0.847) in the participant with reduced eGFR and elevated uPRC. Native non-tumor bearing kidneys had a mean lactate-to-pyruvate ratio of 0.309. DATA CONCLUSION: Stable allografts with normal findings at biopsy showed lactate-to-pyruvate ratios similar to native non-tumor bearing kidneys, whereas allografts with abnormal findings showed higher lactate-to-pyruvate ratios.
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