T1 Mapping 在检测印度重型地中海贫血患者铁超载方面的诊断价值:与 T2* Mapping 的比较。

Q4 Arts and Humanities
Echa Przeszlosci Pub Date : 2023-09-04 eCollection Date: 2024-01-01 DOI:10.1055/s-0043-1772467
Surya Pratap Singh, Priya Jagia, Vineeta Ojha, Tulika Seth, Nitish Naik, Kartik P Ganga, Sanjeev Kumar
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引用次数: 0

摘要

目的 T2*是肝脏和心肌铁定量的金标准。在这项研究中,我们评估了在重型地中海贫血(TM)患者中评估心肌铁负荷过重(MIO)的心肌 T1 图谱与 T2* 图谱的诊断准确性。方法 前瞻性地招募了在地中海贫血诊所就诊的连续重型地中海贫血患者。磁共振成像在 1.5 T 扫描仪(德国西门子 Healthineers 公司)上进行,使用梯度回波 T2* 和 T1 映射(MOLLI)序列在左心室中轴短轴单个 8 毫米切片上进行。通过在中隔手动绘制感兴趣区来分析数值。以 T2* 小于 20ms 作为明显 MIO 的临界值。结果 103名患者(58名男性,平均年龄:17 ± 7.8岁,平均铁蛋白:2009.5 µg/L)接受了心血管磁共振检查。心肌中位 T2* 为 33.45ms。19 名患者(18.4%)的 T2* 小于 20 毫秒。T1 值偏低(P 结论 T1 和 T2* 相互关系良好,正常的 T1 值可排除 MIO 的存在。T1 映射可作为 MIO 的额外成像标记,在没有 T2* 或 T2* 经验有限的中心可能会有所帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic Value of T1 Mapping in Detecting Iron Overload in Indian Patients with Thalassemia Major: A Comparison with T2* Mapping.

Purpose  T2* is the gold standard for iron quantification in liver as well as myocardium. In this study, we evaluated the diagnostic accuracy of myocardial T1 mapping for the assessment of myocardial iron overload (MIO) as compared to the T2* mapping in patients with thalassemia major (TM). Methods  Consecutive TM patients attending the thalassemia clinic were prospectively enrolled. Magnetic resonance imaging was performed on a 1.5 T scanner (Siemens Healthineers, Germany) using a gradient echo T2* as well as a T1 mapping (MOLLI) sequence done at a mid-ventricular short-axis single 8 mm slice of the left ventricle. Values were analyzed by manually drawing a region of interest in the mid-septum. T2*less than 20ms was used as the cutoff for significant MIO. Results  One-hundred three patients (58 males, mean age: 17 ± 7.8 years, mean ferritin: 2009.5 µg/L) underwent cardiovascular magnetic resonance. Median T2* of myocardium was 33.45ms. Nineteen patients (18.4%) had T2*less than 20ms. T1 value was low (<850ms) in all the patients with T2* less than 20 ms. Receiver operating characteristic curve analysis revealed the best cutoff of native T1 mapping value as 850 ms which had high specificity (95.2%), sensitivity (94.2%) and negative predictive value (98.8%) for T2* less than 20ms. There was excellent agreement between T1 and T2* for diagnosis of MIO (Kappa-0.848, p <0.001). We did not find any patient who had normal T1 mapping values but had MIO on T2*. Conclusion  T1 and T2* correlate well and normal T1 values may rule out presence of MIO. T1 mapping can act as additional imaging marker for MIO and may be helpful in centers with nonavailability or limited experience of T2*.

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Echa Przeszlosci
Echa Przeszlosci Arts and Humanities-History
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