Diffusion-Weighted MRI as a Non-Invasive Diagnostic Tool for Ascites Characterization: A Comparative Analysis of Mean and Minimum ADC Values Against the Serum-Ascites Albumin Gradient

扩散加权磁共振成像作为一种无创诊断工具在腹水表征中的应用:平均和最小ADC值与血清-腹水白蛋白梯度的比较分析

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Abstract

Background/Objectives: This study aimed to evaluate the diagnostic accuracy of Apparent Diffusion Coefficient (ADC) values, derived from Diffusion-Weighted Imaging (DWI), in differentiating benign and malignant ascites. Methods: This retrospective study included 150 patients (85 benign, 65 malignant) who underwent abdominal MRI. All patients were scanned on a DWI sequence (b-values: 0, 500, and 1000 s/mm(2)). Two experienced radiologists, blinded to clinical and cytological outcomes, measured the mean ADC (ADCmean) from three distinct ROIs and the minimum ADC (ADCmin) from the area of lowest signal intensity on the ADC map. The diagnostic performance of ADC parameters and the Serum-Ascites Albumin Gradient (SAAG) was assessed using Receiver Operating Characteristic (ROC) curve analysis. Results: The mean values of ADCmean (3162 ± 204 × 10(-6) mm(2)/s) and ADCmin (2885 ± 148 × 10(-6) mm(2)/s) in the malignant group were significantly lower than those in the benign group (3596 ± 239 and 3322 ± 218 × 10(-6) mm(2)/s; p = 0.006 and p = 0.0016, respectively). Inter-observer agreement was good for both ADCmean (ICC = 0.844) and ADCmin (ICC = 0.879). In the ROC analysis, ADCmin demonstrated the highest diagnostic performance (AUC: 0.930). An optimal cut-off value for ADCmin of ≤ 2983 × 10(-6) mm(2)/s yielded 81.5% sensitivity and 85.8% specificity. The diagnostic performance of ADCmin was found to be superior to that of ADCmean (AUC: 0.877) and SAAG (AUC: 0.919). Conclusions: ADC values derived from DWI, particularly ADCmin, represent a highly accurate, non-invasive, and reproducible biomarker for differentiating benign from malignant ascites. The identified ADCmin threshold provides quantitative parameter that can aid in patient triage, especially when cytology is inconclusive, potential surrogate for fluid characterization.

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