Min Zhou, Zhuang Nie, Jie Zhao, Yao Xiao, Xiaohua Hong, Yuhui Wang, Chengjun Dong, Alexander P Lin, Ziqiao Lei
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The optimized and 97 ms TE PRESS were then applied to 84 prospectively enrolled patients suspected of glioma or glioma recurrence to examine the influence of aspartate on cystathionine quantification by fitting the spectra with and without aspartate. The diagnostic performance of PRESS for 1p/19q-codeleted gliomas were assessed.</p><p><strong>Results: </strong>The TE of PRESS was optimized as (TE1, TE2) = (17 ms, 28 ms). The spectral pattern of cystathionine and aspartate were consistent between calculation and phantom. The mean concentrations of cystathionine in vivo fitting without aspartate were significantly higher than those fitting with full basis-set for 97 ms TE PRESS (1.97 ± 2.01 mM vs. 1.55 ± 1.95 mM, p < 0.01), but not significantly different for 45 ms method (0.801 ± 1.217 mM and 0.796 ± 1.217 mM, p = 0.494). The cystathionine concentrations of 45 ms approach was better correlated with those of edited MRS than 97 ms counterparts (r = 0.68 vs. 0.49, both p < 0.01). 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引用次数: 0
摘要
背景:胱硫醚会在1p/19q编码缺失的胶质瘤中选择性蓄积,可作为一种可能的无创生物标记物。本研究旨在优化点分辨光谱法(PRESS)检测胶质瘤中胱硫醚的回波时间(TE),并评估PRESS对1p/19q编码缺失识别的诊断准确性:通过数值分析和模型分析对 PRESS 的 TE 进行了优化,以更好地从重叠的天冬氨酸多信号中分辨出胱硫醚。然后将优化后的和 97 ms TE 的 PRESS 应用于 84 例前瞻性入组的疑似胶质瘤或胶质瘤复发患者,通过拟合含天冬氨酸和不含天冬氨酸的光谱,研究天冬氨酸对胱硫醚定量的影响。评估了 PRESS 对 1p/19q 缺失编码胶质瘤的诊断性能:结果:PRESS 的 TE 优化为 (TE1, TE2) = (17 ms, 28 ms)。胱硫醚和天门冬氨酸的光谱模式在计算和模型中保持一致。在 97 ms TE PRESS 条件下,不含天冬氨酸的体内拟合胱硫醚平均浓度明显高于全基集拟合(1.97 ± 2.01 mM vs. 1.55 ± 1.95 mM,p 结论):45 毫秒 TE PRESS 比 97 毫秒方法能得出更精确的胱硫醚估计值,预计将有助于对 1p/19q 缺失编码胶质瘤进行无创诊断,并监测这些患者的治疗反应。据观察,PRESS 对 1p/19q 缺失编码胶质瘤的诊断效果中等,值得进一步研究。
Optimization and validation of echo times of point-resolved spectroscopy for cystathionine detection in gliomas.
Background: Cystathionine accumulates selectively in 1p/19q-codeleted gliomas, and can serve as a possible noninvasive biomarker. This study aims to optimize the echo time (TE) of point-resolved spectroscopy (PRESS) for cystathionine detection in gliomas, and evaluate the diagnostic accuracy of PRESS for 1p/19q-codeletion identification.
Methods: The TE of PRESS was optimized with numerical and phantom analysis to better resolve cystathionine from the overlapping aspartate multiplets. The optimized and 97 ms TE PRESS were then applied to 84 prospectively enrolled patients suspected of glioma or glioma recurrence to examine the influence of aspartate on cystathionine quantification by fitting the spectra with and without aspartate. The diagnostic performance of PRESS for 1p/19q-codeleted gliomas were assessed.
Results: The TE of PRESS was optimized as (TE1, TE2) = (17 ms, 28 ms). The spectral pattern of cystathionine and aspartate were consistent between calculation and phantom. The mean concentrations of cystathionine in vivo fitting without aspartate were significantly higher than those fitting with full basis-set for 97 ms TE PRESS (1.97 ± 2.01 mM vs. 1.55 ± 1.95 mM, p < 0.01), but not significantly different for 45 ms method (0.801 ± 1.217 mM and 0.796 ± 1.217 mM, p = 0.494). The cystathionine concentrations of 45 ms approach was better correlated with those of edited MRS than 97 ms counterparts (r = 0.68 vs. 0.49, both p < 0.01). The sensitivity and specificity for discriminating 1p/19q-codeleted gliomas were 66.7% and 73.7% for 45 ms method, and 44.4% and 52.5% for 97 ms method, respectively.
Conclusion: The 45 ms TE PRESS yields more precise cystathionine estimates than the 97 ms method, and is anticipated to facilitate noninvasive diagnosis of 1p/19q-codeleted gliomas, and treatment response monitoring in those patients. Medium diagnostic performance of PRESS for 1p/19q-codeleted gliomas were observed, and warrants further investigations.
Cancer ImagingONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
7.00
自引率
0.00%
发文量
66
审稿时长
>12 weeks
期刊介绍:
Cancer Imaging is an open access, peer-reviewed journal publishing original articles, reviews and editorials written by expert international radiologists working in oncology.
The journal encompasses CT, MR, PET, ultrasound, radionuclide and multimodal imaging in all kinds of malignant tumours, plus new developments, techniques and innovations. Topics of interest include:
Breast Imaging
Chest
Complications of treatment
Ear, Nose & Throat
Gastrointestinal
Hepatobiliary & Pancreatic
Imaging biomarkers
Interventional
Lymphoma
Measurement of tumour response
Molecular functional imaging
Musculoskeletal
Neuro oncology
Nuclear Medicine
Paediatric.