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Inflammatory activity of Crohn's disease: Evaluation by MR T2*mapping without intravenous enhancement
Si yun Huang1, Xue hua Li1, Zhong wei Zhang2, Jin jiang Lin1, Li Huang1, Zhuang nian Fang1, Meng chen Zhang1, Meng jie Jiang3, Hua song Cai1, Margaret H. Pui4, Shi ting Feng1, Can hui Sun3, and Zi ping Li3

1Department of Radiology, The First Affiliated Hospital of Sun Yat-Sen University,Guangzhou, China, Guangzhou, People's Republic of China, 2Department of Biomedical Engineering, Cancer Biology and Radiology, Wake Forest School of Medicine, 3Department of Radiology, Hospital of Stomatology, Guanghua School of Stomatology, Sun Yat-Sen University, Guangdong Provincial Key Laboratory of Stomatology, 4Department of Radiology, Conde de S. Januario Central Hospital, Macau

Synopsis

Crohn's disease (CD) is a chronic relapsing inflammatory bowel disease leading to structurally irreversible bowel damage. The incidence of CD had been increasing in the past century epidemiologically . Accurate evaluation of CD activity is crucial for new therapeutic goals of mucosal healing, preventing bowel damage, limiting disability, and improving quality of life . Although colonoscopy remains the gold standard for assessing CD activity, it is invasive, limited to assessment of the small bowel, and not suitable for continuing monitoring of CD activity . Thus, seeking for alternative noninvasive and accurate approaches to assess CD activity is necessary.

Purpose

Crohn's disease (CD), a chronic relapsing inflammatory bowel disease, often results in structurally irreversible bowel damage. Accurate evaluation of CD activity is crucial for new therapeutic goals of mucosal healing, preventing bowel damage, limiting disability, and improving quality of life.Magnetic resonance enterography (MRE) is a technique that involves the use of MR imaging (MRI) to assess especially the small bowel.MR T2* mapping has the potential for reflecting tiny change on biochemical components of the counterpart without contrast medium injection. It remains unclear whether T2* mapping could differentiate grades of inflammation activity in Crohn’s disease (CD). In this study, we aim to assess the efficacy of T2* mapping for evaluating CD activity compared to conventional magnetic resonance enterography (MRE).

Method

We performed an observational study conducted from August 2014 to December 2015of a single-center cohort which inclusive criteria were established CD diagnosis by conventional clinical, endoscopic and histologic criteria for all patients. 98 adults diagnosed of CD underwent MRE and T2*-weighted MR imaging. The disease activity was scored by Magnetic Resonance Index of Activity (MaRIA) as inactive (<7), mild (≥7 and <11) or moderate-severe (≥11). T2* values of thickened bowel wall were measured on T2* mapping, compared to conventional MRE and correlated with MaRIA.

Result

All of the bowel segments in the enrolled 98 patients presented acceptable image quality on MR were evaluated. The difference in T2* values of 160 bowel segments among inactive (26), mild (23) and moderate-severe (111) CD was significant (all P<.001). T2* value correlated significantly with MaRIA (r=0.743) better than mural thickness (r=0.611), relative contrast enhancement (r=0.473) and ulceration (r=0.309). T2* value was accurate with good inter-observer agreement for distinguishing inactive from active CD (AUC=0.877) and differentiating inactive-mild from moderate-severe CD (AUC=0.848). The threshold T2* value of 15.94 ms was 93.3% sensitive and 72% specific for distinguishing active from inactive CD whereas T2* value of 20.00 ms was 74.5% sensitive and 84.0% specific for differentiating inactive-mild from moderate-severe CD.

Discussion

Assessing CD activity is extremely important for treatment plan. Researchers have been searching for a brief, noninvasive and accurate method to evaluate inflammatory activity of CD without complicated calculation. MaRIA was with cockamamie calculations and was not convenient for routine clinical application. Despite above limitation, it can be considered as the most validated mean for assessing inflammation by MRI in CD. The efficacy of conventional MRE has been widely introduced in CD but little attention has been paid to the interest of T2*WI. According to our knowledge, our study is the first observational study to assess the accuracy of T2*WI in evaluating bowel inflammation in CD by comparing findings of T2* mapping and conventional MRE.

Conclusion

T2* values correlated well with CD activity and T2* mapping is a promising novel imaging tool for evaluating activity of CD and monitoring therapeutic effect.
Conclusions: T2* values correlated well with CD activity and T2* mapping is a promising novel imaging tool for evaluating activity of CD and monitoring therapeutic effect.
Conclusions: T2* values correlated well with CD activity and T2* mapping is a promising novel imaging tool for evaluating activity of CD and monitoring therapeutic effect.

Acknowledgements

The first draft of the article was written by Si-yun Huang. All authors reviewed and approved the final manuscript. No writing assistance was used.

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Figures

A 19 year-old girl with moderate-severe Crohn’s disease activity in the ascending colon and MaRIA score of 37.24. (a) Axial T2-weighted image shows 10.1 mm ascending colon wall thickening and hyperintensity with marked relative contrast enhancement of 354.56 on (b) axial T1-weighted image. Axial T2*WI (c) shows light grey intestinal wall with white lumen. On T2* mapping (d), ROI (white circle) was placed on the thickened bowel wall to measure the T2* value (34.33 ms). Pseudo color map of T2 * mapping is shown in (e) for observation of the T2* signal variation with naked eye.

A 32 year-old woman with inactive Crohn’s disease of ascending colon and MaRIA score of 6.87. (a) Axial T2-weighted image shows ascending colon wall thickening (5.7 mm) and mild hyperintensity with mild relative contrast enhancement of 63.86 on (b) axial T1-weighted image (arrows). Axial T2*WI (c) shows dark grey intestinal wall with white lumen. On T2* mapping (d), ROI (white circle) was placed on the thickened bowel wall to measure the T2* value (16.81 ms). Pseudo color map of T2* mapping (e) allows qualitative assessment of the T2* signal variation.

Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
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