4.7 Article

Evaluation of amide proton transfer-weighted imaging for endometrial carcinoma histological features: a comparative study with diffusion kurtosis imaging

期刊

EUROPEAN RADIOLOGY
卷 31, 期 11, 页码 8388-8398

出版社

SPRINGER
DOI: 10.1007/s00330-021-07966-y

关键词

Diffusion magnetic resonance imaging; Magnetization transfer contrast imaging; Endometrial neoplasms

资金

  1. National Key R&D Program of China [2017YFE0103600]
  2. Henan Medical Science and Technology Research Program [2018020357, 2018020367]
  3. National Natural Science Foundation of China [81720108021, 31470047]
  4. Zhongyuan Thousand Talents Plan Project-Basic Research Leader Talent [ZYQR201810117]
  5. Zhengzhou Collaborative Innovation Major Project [20XTZX05015]

向作者/读者索取更多资源

Both DKI- and APTWI-related parameters have potential as imaging markers in estimating the histological features of EC, while DKI shows better performance than APTWI in this study.
Objectives To investigate whether amide proton transfer-weighted imaging (APTWI) and diffusion kurtosis imaging (DKI) can be used to evaluate endometrial carcinoma (EC) in terms of clinical type, histological grade, subtype, and Ki-67 index. Methods Eighty-eight patients with EC underwent pelvic DKI and APTWI. The non-Gaussian diffusion coefficient (D-app), apparent kurtosis coefficient (K-app), and magnetization transfer ratio asymmetry (MTRasym (3.5 ppm)) were calculated and compared based on the clinical type (type I, II), histological grade (high- and low-grade), and subtype (endometrioid adenocarcinoma (EA) and non-EA). Correlation coefficients were calculated for each parameter with histological grades and the Ki-67 index. Results The MTRasym (3.5 ppm) and K-app values were higher in the type II group and high-grade group than in the type I and low-grade groups, respectively, while the D-app values were lower in the type I and low-grade groups, respectively (all p < 0.05). The K-app value was higher in the EA group than in the non-EA group (p = 0.022). The K-app value was the only independent predictor for the histological grade of EA and the clinical type of EC. The AUC (DKI) was higher than the AUC (APTWI) in the identification of type I and II EC and high- and low-grade EA (Z = 2.042, 2.013, p = 0.041, 0.044), while in the identification of EA and non-EA, only the difference in K-app was statistically significant. Moreover, the K-app and MTRasym (3.5 ppm) values and D-app values correlated positively and negatively, respectively, with histological grade (r = 0.759, 0.555, 0.624, and 0.462, all p < 0.05) and Ki-67 index (r = -0.704, -0.507, all p < 0.05). Conclusion Both DKI- and APTWI-related parameters have potential as imaging markers in estimating the histological features of EC, while DKI shows better performance than APTWI in this study.

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