定量钠-MRI 检测良性与恶性肿瘤性肾肿瘤中不同的钠含量

Ines Horvat-Menih, Jonathan R Birchall, Maria J Zamora-Morales, Alice Bebb, Joshua Kaggie, Frank Riemer, Andrew B Gill, Andrew N Priest, Marta Wylot, Iosif A Mendichovszky, Anne Y Warren, James O Jones, James N Armitage, Thomas J Mitchell, Grant D Stewart, Mary A McLean, Ferdia A Gallagher
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Purpose: Here we used non-invasive sodium MRI (23Na-MRI) to quantify sodium concentration and relaxation dynamics across a range of different kidney tumour subtypes and have correlated these findings with imaging surrogates for perfusion, hypoxia, and cellularity. Materials and Methods: Between January and April 2023, patients with localised renal masses were prospectively recruited and underwent 23Na and proton (1H) MRI at 3T to acquire 3D maps of B1, total sodium concentration (TSC), proton and sodium relaxation rates (R2*), and diffusion weighted imaging (DWI). Statistical analysis included comparison and correlation of quantified imaging parameters across kidney tumour subtypes. Results: Ten patients were included in the final analysis (mean age ± S.D. = 64 ± 8 years; 7:3 male:female ratio) encompassing seven ROs, two chRCCs, two clear cell RCCs (ccRCC), and one papillary RCC (pRCC). 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引用次数: 0

摘要

背景:对局部肾脏肿瘤进行准确的非侵入性亚型鉴定是泌尿肿瘤学尚未解决的临床问题。良性肾肿瘤细胞瘤(RO)与恶性嗜色性肾细胞癌(chRCC)的鉴别无法通过传统成像技术实现。尽管肾功能对钠的调节非常重要,但人们对肾肿瘤中钠的处理却知之甚少。目的:在此,我们使用无创钠核磁共振成像(23Na-MRI)来量化一系列不同肾脏肿瘤亚型的钠浓度和弛豫动态,并将这些发现与灌注、缺氧和细胞性的成像替代物相关联。材料和方法:在 2023 年 1 月至 4 月期间,前瞻性地招募了局部肾肿块患者,并在 3T 下进行了 23Na 和质子(1H)磁共振成像,以获取 B1、总钠浓度 (TSC)、质子和钠弛豫率 (R2*) 以及弥散加权成像 (DWI) 的三维图。统计分析包括不同肾脏肿瘤亚型的量化成像参数的比较和相关性。结果:最终分析包括10名患者(平均年龄±S.D. = 64 ± 8岁;男女比例为7:3),其中包括7例RO、2例chRCC、2例透明细胞RCC(ccRCC)和1例乳头状RCC(pRCC)。与chRCC相比,RO的TSC明显更高:162 ± 58 mM vs. 71 ± 2 mM(P <0.05)。ccRCC的平均TSC为135 ± 59 mM,pRCC为81 mM。23Na 导出的 R2* 值和 1H 导出的 R2* 值显示出微弱的相关性(Spearman r = 0.17;P = 0.50)。TSC与1H-R2*之间存在明显的反相关性(Spearman r = -0.39,P <0.05),但TSC与DWI衍生成像参数无关。结论:23Na-MRI 在良性 RO 和恶性 chRCC 中检测到明显不同的钠浓度。此外,钠信号与作为缺氧代用指标的 1H-R2* 呈反相关。因此,我们证明了 23Na-MRI 在未来肾肿瘤研究中的可行性和潜力。
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Quantitative sodium-MRI detects differential sodium content in benign vs. malignant oncocytic renal tumours
Background: Accurate non-invasive subtyping of localised kidney tumours is an unmet clinical question in uro-oncology. Differentiation of benign renal oncocytomas (RO) from malignant chromophobe renal cell carcinomas (chRCC) is not possible using conventional imaging. Despite the importance of renal function for sodium regulation, little is known about sodium handling in kidney tumours. Purpose: Here we used non-invasive sodium MRI (23Na-MRI) to quantify sodium concentration and relaxation dynamics across a range of different kidney tumour subtypes and have correlated these findings with imaging surrogates for perfusion, hypoxia, and cellularity. Materials and Methods: Between January and April 2023, patients with localised renal masses were prospectively recruited and underwent 23Na and proton (1H) MRI at 3T to acquire 3D maps of B1, total sodium concentration (TSC), proton and sodium relaxation rates (R2*), and diffusion weighted imaging (DWI). Statistical analysis included comparison and correlation of quantified imaging parameters across kidney tumour subtypes. Results: Ten patients were included in the final analysis (mean age ± S.D. = 64 ± 8 years; 7:3 male:female ratio) encompassing seven ROs, two chRCCs, two clear cell RCCs (ccRCC), and one papillary RCC (pRCC). The TSC was significantly higher in the ROs compared to the chRCCs: 162 ± 58 mM vs. 71 ± 2 mM (P < 0.05). The mean TSC in ccRCC was 135 ± 59 mM, and 81 mM in pRCC. The 23Na-derived and 1H-derived R2* values showed a weak correlation (Spearman r = 0.17; P = 0.50). There was a significant inverse correlation between TSC and 1H-R2* (Spearman r = -0.39, P < 0.05), but TSC was independent of the DWI-derived imaging parameters. Conclusion: 23Na-MRI detected markedly different sodium concentrations within benign ROs and malignant chRCCs. In addition, the sodium signal inversely correlated with 1H-R2* as a surrogate for hypoxia. Therefore we have shown the feasibility and potential of 23Na-MRI for future research in renal tumours.
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