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Establishing a machine learning model based on dual-energy CT enterography to evaluate Crohn’s disease activity

Abstract

Objectives

The simplified endoscopic score of Crohn’s disease (SES-CD) is the gold standard for quantitatively evaluating Crohn’s disease (CD) activity but is invasive. This study aimed to develop and validate a machine learning (ML) model based on dual-energy CT enterography (DECTE) to noninvasively evaluate CD activity.

Methods

We evaluated the activity in 202 bowel segments of 46 CD patients according to the SES-CD score and divided the segments randomly into training set and testing set at a ratio of 7:3. Least absolute shrinkage and selection operator (LASSO) was used for feature selection, and three models based on significant parameters were established based on logistic regression. Model performance was evaluated using receiver operating characteristic (ROC), calibration, and clinical decision curves.

Results

There were 110 active and 92 inactive bowel segments. In univariate analysis, the slope of spectral curve in the venous phases (λHU-V) has the best diagnostic performance, with an area under the ROC curve (AUC) of 0.81 and an optimal threshold of 1.975. In the testing set, the AUC of the three models established by the 7 variables to differentiate CD activity was 0.81–0.87 (DeLong test p value was 0.071–0.766, p > 0.05), and the combined model had the highest AUC of 0.87 (95% confidence interval (CI): 0.779–0.959).

Conclusions

The ML model based the DECTE can feasibly evaluate CD activity, and DECTE parameters provide a quantitative analysis basis for evaluating specific bowel activities in CD patients.

Critical relevance statement

The machine learning model based on dual-energy computed tomography enterography can be used for evaluating Crohn’s disease activity noninvasively and quantitatively.

Key Points

  • Dual-energy CT parameters are related to Crohn’s disease activity.

  • Three machine learning models effectively evaluated Crohn’s disease activity.

  • Combined models based on conventional and dual-energy CT have the best performance.

Graphical Abstract

Introduction

Crohn’s disease (CD) is a chronic, recurrent inflammatory bowel disease (IBD), and its global incidence rate has been increasing, resulting in an extreme economic burden [1, 2]. Progressive inflammation-based stimulation may result in serious complications such as strictures, perforation, or fistulas that require surgery [3]. It is important to monitor the treatment response continuously to adjust medication and guide clinical treatment decisions [4].

The simplified endoscopic score of Crohn’s disease (SES-CD) is the most mature and quantitative scoring system for CD activity; it is limited by its invasiveness, with a risk of serious complications and difficulty in evaluating segments with severe strictures [5, 6]. CT, MR, and intestinal ultrasound have successfully become noninvasive assessment methods for CD due to their ability to visualise the full intestine [7,8,9]. Some quantitative scoring systems have been developed based on these cross-sectional imaging methods, such as the magnetic resonance activity index, Clermont score, and London score, which mainly reference qualitative parameters [10,11,12]. However, their clinical practicality has been limited by poor observer consistency and complex calculation methods.

Dual-energy CT enterography (DECTE) is an imaging technique based on two different energy settings for data acquisition that has been widely used in vascular imaging, tumour differentiation, and prognosis in recent years and is now gradually being applied to IBD [13,14,15]. The Dane team assessed inflammation activity with the iodine concentration (IC) from DECTE and compared it with the results of pathological analysis, indicating that the IC can serve as a radiological marker of CD activity [16]. In addition, some studies have found that the IC, normalised iodine concentration (NIC), and slope of the energy spectrum curve (λHU) are related to CD activity [17,18,19]. Forty kiloelectron-volt (keV) DECTE contributes to distinguishing wall enhancement between normal and diseased intestinal segments and can improve image quality [20]. Currently, most studies use DECTE to evaluate activity by comparing it with the Crohn’s disease activity index (CDAI) or pathological analysis, with only a few studies comparing it with SES-CD score and finding that NIC and λHU help differentiate CD activity [21, 22]. This study aimed to analyse and establish an ML model based on DECTE to noninvasively evaluate CD activity with the SES-CD score as the gold standard.

Materials and methods

Ethics

This retrospective study was approved by the Ethics Committee of Chongqing General Hospital and exempted from the requirement for written informed consent from patients.

Patients

Patients suspected as CD at Chongqing General Hospital from July 2021 to 2023 were included, and all subjects underwent DECTE scans. The inclusion criteria for candidate patient selection were as follows: (1) age 18–65 years old, (2) confirmed Crohn’s disease, and (3) endoscopy segmented score obtained within ± 14 days of DECTE scan. The exclusion criteria were as follows: (1) no DECTE image at the postprocessing workstation, (2) poor image quality, such as an intestinal wall that was too thin or had poor fullness, and (3) incomplete clinical data. Clinical data included patient age, sex, course of the disease, disease behavior, drug treatment method (traditional or biological therapy), C-reactive protein (CRP), albumin (ALB), and erythrocyte sedimentation rate (ESR). Finally, 46 CD patients were included, and a total of 202 segments were evaluated. According to the principle of hierarchical randomisation, the data were divided into a training set (N = 141) and a testing set (N = 61) at a 7:3 ratio. The flow chart of the study population is shown in Fig. 1.

Fig. 1
figure 1

Follow diagram of the study population

Endoscopic evaluation

One gastroenterologist who was blinded to the clinical data of each patient performed the endoscopy, divided the whole intestinal segment into five segments (the ileum, right colon, transverse colon, left colon, and rectum), and then assessed inflammation with the SES-CD criteria [23]. Next, they calculated the total score for each bowel, with a score of 0–12 points for each segment. SES-CD < 3 was considered to indicate inactive disease, and SES-CD ≥ 3 was considered to indicate active disease.

CT scanning

All patients fasted for 8 h before intestinal CTE examination and took 2000 mL 2.5% mannitol solution orally 1 h before examination. All patients were scanned with a dual-energy CT scanner (IQon spectral CT, Philips Healthcare, China). The tube voltage was fixed at 120 kVp, tube current 145 mAs, pitch 1.2, rotation speed 0.5 s, and reconstruction layer thickness 1.00 mm. The contrast agent (Ioversol, 350 mg(I)/mL, Jiangsu Hengrui medicine CO., LTD, China) was administered via a peripheral vein at 1.5 mL/kg and a rate of 3.0 mL/s with a high-pressure syringe. The scanning time was monitored using a monitoring method. The abdominal aorta was detected 10 s after injection of contrast agent, and the threshold was automatically triggered when it reached 150 HU. The arterial and venous phases of DECTE were collected approximately 30 s and 80 s after injection of contrast agent, respectively. We reconstructed dual-energy images at a Philips postprocessing workstation, obtained conventional images at 120 keV, examined decomposed images of water and iodine based on the materials, and obtained monochromatic images within the energy range of 40 to 120 keV.

Image processing and evaluation

Two radiologists with more than 5 years of expertise in diagnostic abdominal imaging, and who were blinded to the patient information reviewed the traditional CT and DECTE images. The images were evaluated and analysed using the Philips postprocessing workstation. A circular area of interest (ROI) was ideally defined to capture as much of the highly enhanced part of the lesion in the intestinal wall as possible, with a minimum value set at 5 mm2 (range: 5 mm2–10 mm2), and the IC in an artery in the same layer was measured (abdominal aorta or iliac artery). Then, the NIC was calculated as IC in the affected intestinal segment/IC in the artery in the same layer, and the λ HU was calculated as (HU40 keV–HU100 keV)/60 [24]. The thickness of the intestinal wall, segmental mural hyperenhancement, strictures, upstream dilation, comb sign, fibrofatty proliferation, inflammation, and regional lymph node size were assessed on conventional CT images. To ensure consistency in the results, all measurements were taken three times at different locations on the same layer, and the average value was calculated. Quantitative parameters are ultimately displayed as the arithmetic mean of the value obtained by two radiologists. When qualitative parameters were inconsistent, disagreements were resolved by consensus [25]. The consistency analysis between observers is shown in Supplementary Tables 1 and 2.

Model construction

The model was constructed with the training set to compare and analyse the clinical, routine imaging, and quantitative parameters of DECTE representing active and inactive intestinal segments. Features with p < 0.05 were screened using LASSO regression combined with 10-fold cross validation. We developed three ML models based on conventional image features (model 1), DECTE parameters (model 2), and all significant parameters (model 3) by a logistic regression algorithm and performed parameter tuning by using 5-fold cross validation. Finally, model performance was tested in the testing set.

Statistical analysis

Python software 3.8 and SPSS 23.0 statistical software were applied to analyse the data. p < 0.05 was considered statistically significant. Continuous variables conforming to a normal distribution are expressed as the mean ± standard deviation (SD), and the groups were compared using Student’s t test. Continuous variables that did not conform to a normal distribution are presented as medians and interquartile ranges based on their distribution and were compared by the Mann‒Whitney U test. Classification data are represented as frequencies (percentages) and were compared using the chi-square test or Fisher’s exact test. Receiver operating characteristic curves, calibration curves and decision curves were used to evaluate model performance.

Results

Clinical findings

The demographic and clinical characteristics of the participants are shown in Table 1. This study included 46 CD patients, including 19 males and 27 females, with an average age of 27.50 years [23.00, 33.00]. A total of 202 segments of the intestine were included: 110 segments were active, and 92 segments were inactive. Table 2 shows the distribution of variables in the training and testing sets, indicating that there were no significant differences between the two groups (p > 0.05).

Table 1 Patient characteristic
Table 2 Comparison of baseline characteristic between train set and test set

Diagnostic performance of DECTE parameters

Comparing the DECTE parameters of the active and inactive segments in the total sample, it was found that all parameters of the active intestinal segments were higher than those of the inactive intestinal segments (p < 0.001). As demonstrated in Table 3, all DECTE parameters performed well in evaluating CD activity (AUC value > 0.75). λ HU in the venous phase (λ HU-V) had the greatest performance in evaluating the activity of CD, with an AUC value of 0.81. When λ HU-V ≥ 1.975, its sensitivity and specificity in diagnosing active intestinal segments were 0.800 and 0.783, respectively. According to this result, the ROC curves were plotted in Fig. 2a. Examples of typical images of active and inactive patients are shown in Figs. 3 and 4.

Table 3 Evaluation performance of all spectral parameters
Fig. 2
figure 2

The performance of single DECTE parameters and machine learning models. Receiver operating characteristic curves of single parameters in all sample (a). Receiver operating characteristic curves of machine learning models in the test set (b). Calibration curves for the three model in testing sets (c). Decision curve analysis for the three model in testing sets (d)

Fig. 3
figure 3

Dual energy CT examination in a 40-years-old female patient with rectum SES-CD score 0. Endoscope, rectum (a), iodine centration in the arterial phase (b), iodine concentration in the vein phase (c), Z-Effective in the arterial phase (d), Z-effective in the vein phase (e), Slope of the energy spectrum curve in the arterial phase (f), Slope of the energy spectrum curve in the vein phase (g)

Fig. 4
figure 4

Dual energy CT examination in a 20-years-old female patient with left colon SES-CD score 6. Endoscope, Left colon (a), iodine centration in the arterial phase (b), iodine concentration in the vein phase (c), Z-effective in the arterial phase (d), Z-effective in the vein phase (e), Slope of the energy spectrum curve in the arterial phase (f), Slope of the energy spectrum curve in the vein phase (g)

Model variable selection

A comparison between the active and inactive bowels groups in the training set is shown in Table 4, and the results show significant differences (p < 0.05) except for age, sex, upstream dilation, and engorged vasa recta. The LASSO algorithm combined with 10-fold cross validation was used to further screen the characteristics when the minimum mean square error (λ was 0.032). Finally, three DECTE parameters and four radiographic features were significant difference: λ HU in the arterial phase, λ HU-V, and NIC in the arterial phase, wall thickness, stricture, segmental mural hyperenhancement, and regional lymph node size (Fig. 5).

Table 4 Difference between active and inactive segment in training set
Fig. 5
figure 5

LASSO feature screening pattern diagram. LASSO coefficients for machine learning features (a). A coefficient profile plot was generated at the selected log λ value using a tenfold cross-validation, seven machine learning features with the best coefficients were selected. Standard parameters (λ) selection in LASSO model used tenfold cross-validation with a minimum criterion (b). The optimal λ values are indicated by the vertical black lines, and a λ value of 0.032 was selected

Diagnostic performance of the machine learning model

The performance indicators of each model in the test set are shown in Table 5, among which model 2 and model 3 had a more balanced overall performance. The three ML models performed well in evaluating CD activity (AUC > 0.80), with the combined model having the highest AUC of 0.87(95% confidence interval (CI): 0.779–0.959) (Fig. 2b). However, the DeLong test showed no statistically significant difference in the AUC among the three models in the test set (the p value range of the three models was approximately 0.071 to 0.766, p value > 0.05), as detailed in Supplementary Table 3. The calibration curves showed that the fitting curves of the three models almost coincided with the diagonal, indicating a good fit with the actual data (Fig. 2c). Decision curve analysis showed that within the range of approximately 10% to 90%, the clinical net benefits of three models were higher than those of all and none, indicating that all three models had clinical net benefits within a certain threshold probability. Among them, the net benefits of model 2 and model 3 were higher than that of model 1 in the probability range of approximately 38% to 82% (Fig. 2d).

Table 5 The performance of three models in testing set

Discussion

This study explored the value of DECTE quantitative parameters in evaluating CD activity and developed ML models for evaluating inflammation in CD patients, including a conventional CT model, a DECTE model, and a combined model. Although there was no significant difference in the AUC among the three models, the DECTE model and the combined model were more balanced in overall performance than the conventional CT model and exhibited better diagnostic performance than individual DECTE quantitative parameters alone.

Among the identified variables, wall thickness and segmental mural hyperenhancement had been previously identified as characteristic parameters in the traditional CT evaluation of CD activity [26, 27]. Literature reports that strictures can also distinguish CD activity [28], and our research confirms these results. Previous studies have shown that lymph node enlargement (length ≥ 1 cm) can be considered a sign of the active stage of CD, but it is more prominent in severely active intestinal segments [27, 29]. We found that there was statistical significance in the size of regional lymph nodes between active and inactive intestinal segments, which could be reactive hyperplasia of mesentery lymph nodes caused by CD activity. This result is contrary to the conclusion of Amir [30], who found that there was no significant difference in the size of regional lymph nodes (diameter > 3 mm) between the active and inactive groups. We believe that this may be firstly due to different reference standards for defining activity–clinical activity scores are nonspecific and cannot represent a certain inflammatory segment or clarify the contribution of the affected segment. Secondly, the included lymph nodes were too small, resulting in statistical insignificance. Although ulceration is an important parameter for CD activity, this study did not evaluate it due to the lower soft tissue resolution of CT compared to MRE.

Zhu et al [21] and Dane et al [16] suggested that NIC is a radiological marker for differentiating active and inactive bowels with SES-CD, which is consistent with the results of our study. We assumed that the outcome may be caused by inflammatory congestion, inflammatory cell infiltration, and noncaseous granulomas in CD patients. λHU represents the attenuation changes within the lesion during the passage of contrast agent. We found that λ HU-V and λ HU-A were significantly correlated with CD activity, consistent with previous studies [22, 31], indicating that the amount of contrast agent increases as the blood vessels increase when CD is in the active phase. Our results show that λ HU-V had better diagnostic efficacy (AUC 0.81 vs 0.79) than λ HU-A, which is consistent with previous research results [31, 32]. This may be because when active inflammation occurs, although the vasa recta expands and increases, the arterial imaging is too early and the contrast agent does not fully enter the lesion. During the venous phase, the contrast agent is fully filled. In addition, when the contrast agent seeps into the extravascular space, the interstitial fibrous tissue can reduce the outflow rate of the contrast agent.

Machine learning is a subset of artificial intelligence. Using feature selection to reduce the dimensions of the data and adjust the hyperparameters can produce a more powerful and generalizable ML model. In recent years, ML in IBD has mainly been used for phenotype diagnosis, gene classification of gut microbiota, and prediction of postoperative recurrence [33,34,35]. A few studies have constructed ML models to evaluate CD activity and severity. Recently, all ML models constructed by Cai et al [36] performed well in predicting activity in CD test sets. Their study used the CDAI score as the assessment criterion for grouping, while we used the SES-CD as the standard, which displayed the activity of the affected intestinal segment more intuitively compared to CDAI. The Guez [37] team established a multimodal ML model to evaluate CD endoscopic activity by integrating MR information and biochemical indicators. The results showed that the length of diseased intestinal segments and the biochemical indicators were the most informative parameters. In summary, previous research results indicate the potential of ML to accurately and noninvasively assess intestinal activity. Our research also confirms this result. The use of DECTE to establish a ML model provides a new method for non-invasive quantitative evaluation of CD activity, which does not require complex calculations, and the parameters are intuitive and easily acquired. In addition, DECTE scans can reduce scan duration and radiation exposure because of their unique hardware design [38]. The model in this study follows the approach of gastroenterologists in evaluating diseases and specific intestinal segments, revealing the role of different features on the activity of diseased intestinal segments and providing an effective tool for precise clinical diagnosis and treatment decision-making. In addition, compared to traditional statistical methods, machine learning models can usually be rigorously validated.

There are a few limitations that should be noted in this study. First, we used manual ROIs to measure DECTE parameters; in the future, semiautomatic or fully automated methods should be developed to ensure measurement accuracy. Second, our study did not evaluate the correlation between biochemical biomarkers and CD activity, as the relative contribution of each inflammatory segment to the overall biochemical biomarker (such as CRP and ESR, etc.) is unknown. Third, false positive results are a concern in the model. Increasing sample size and using multiple algorithms may be a key factor in reducing false positive rates and improving diagnostic accuracy in the future. Fourth, deep learning is a branch of machine learning and the mainstream trend of future artificial intelligence development. Due to sample size and time constraints, we will further explore the application value of deep learning in Crohn’s disease in the future. Finally, this was a single-centre study whose conclusions require additional validation with multi-centre data before future clinical applications.

Conclusion

Our machine learning model based on DECTE can feasibly evaluate intestinal segment activity in CD patients, and the DECT parameters provide a quantitative analysis for the evaluation of specific intestinal segment activity in CD patients.

Data availability

The datasets generated and/or analysed during the current study are not publicly available due to patient privacy regulations but are available from the corresponding author on reasonable request.

Abbreviations

AUC:

Area under the curve

CD:

Crohn’s disease

CDAI:

Crohn’s disease activity index

CI:

Confidence interval

CRP:

C-reactive protein

DECTE:

Dual-energy CT Enterography

ESR:

Erythrocyte sedimentation rate

HU:

Hounsfield unit

IBD:

Inflammatory bowel disease

IC:

Iodine concentration

keV:

Kiloelectron volt

LASSO:

Least absolute shrinkage and selection operator

NIC:

Normalised iodine concentration

ROC:

Receiver operating characteristic

ROI:

Region of interest

SES-CD:

Simplified endoscopic scoring of Crohn’s disease

Zeff:

Effective atomic number

λ HU :

Slope of energy spectrum curve

References

  1. Ma T, Wan M, Liu G, Zuo X, Yang X, Yang X (2023) Temporal trends of inflammatory bowel disease burden in China from 1990 to 2030 with comparisons to Japan, South Korea, the European Union, the United States of America, and the World. Clin Epidemiol 15:583–599

    Article  PubMed  PubMed Central  Google Scholar 

  2. Yu Q, Zhu C, Feng S et al (2021) Economic burden and health care access for patients with inflammatory bowel diseases in China: web-based survey study. J Med Internet Res 23:e20629

    Article  PubMed  PubMed Central  Google Scholar 

  3. Adamina M, Bonovas S, Raine T et al (2020) ECCO guidelines on therapeutics in Crohn’s disease: surgical treatment. J Crohns Colitis 14:155–168

    Article  PubMed  Google Scholar 

  4. Torres J, Bonovas S, Doherty G et al (2020) ECCO guidelines on therapeutics in Crohn’s disease: medical treatment. J Crohns Colitis 14:4–22

    Article  PubMed  Google Scholar 

  5. Buisson A, Gonzalez F, Poullenot F et al (2017) Comparative acceptability and perceived clinical utility of monitoring tools: a nationwide survey of patients with inflammatory bowel disease. Inflamm Bowel Dis 23:1425–1433

    Article  PubMed  Google Scholar 

  6. Turner D, Ricciuto A, Lewis A et al (2021) STRIDE-II: an update on the selecting therapeutic targets in inflammatory bowel disease (STRIDE) initiative of the international organization for the study of IBD (IOIBD): determining therapeutic goals for treat-to-target strategies in IBD. Gastroenterology 160:1570–1583

    Article  CAS  PubMed  Google Scholar 

  7. Deepak P, Fowler KJ, Fletcher JG, Bruining DH (2019) Novel imaging approaches in inflammatory bowel diseases. Inflamm Bowel Dis 25:248–260

    Article  PubMed  Google Scholar 

  8. Shenoy-Bhangle AS, Gee MS (2023) CT versus MR enterography: counterpoint-MR enterography is the primary imaging modality for assessing activity and therapeutic response in pediatric and adult Crohn disease. AJR Am J Roentgenol 220:789–790

    Article  PubMed  Google Scholar 

  9. Guglielmo FF, Anupindi SA, Fletcher JG et al (2020) Small bowel Crohn disease at CT and MR enterography: imaging atlas and glossary of terms. Radiographics 40:354–375

    Article  PubMed  Google Scholar 

  10. Rimola J, Ordás I, Rodriguez S et al (2011) Magnetic resonance imaging for evaluation of Crohn’s disease: validation of parameters of severity and quantitative index of activity. Inflamm Bowel Dis 17:1759–1768

    Article  PubMed  Google Scholar 

  11. Buisson A, Pereira B, Goutte M et al (2017) Magnetic resonance index of activity (MaRIA) and Clermont score are highly and equally effective MRI indices in detecting mucosal healing in Crohn’s disease. Digest Liver Dis 49:1211–1217

    Article  Google Scholar 

  12. Sparrow MP (2021) Quantification of digestive disease damage in Crohn’s disease, are we there yet with the Lémann index? Gastroenterology 161:800–802

    Article  PubMed  Google Scholar 

  13. Dai Y, Xu H, Fang X et al (2023) Dual-energy CT in assessment of thrombus perviousness and its application in predicting outcomes after intravenous thrombolysis in acute ischemic stroke. Eur J Radiol 164:110861

    Article  PubMed  Google Scholar 

  14. Arico FM, Trimarchi R, Portaluri A et al (2023) Virtual monoenergetic dual-layer dual-energy CT images in colorectal cancer: CT diagnosis could be improved? Radiol Med 128:891–899

    Article  PubMed  Google Scholar 

  15. Singh R, Rai R, Mroueh N, Kambadakone A (2022) Role of dual energy computed tomography in inflammatory bowel disease. Semin Ultrasound ct 43:320–332

    Article  Google Scholar 

  16. Dane B, Sarkar S, Nazarian M et al (2021) Crohn disease active inflammation assessment with iodine density from dual-energy CT enterography: comparison with histopathologic analysis. Radiology 301:144–151

    Article  PubMed  Google Scholar 

  17. De Kock I, Delrue L, Lecluyse C, Hindryckx P, De Vos M, Villeirs G (2019) Feasibility study using iodine quantification on dual-energy CT enterography to distinguish normal small bowel from active inflammatory Crohn’s disease. Acta Radiol 60:679–686

    Article  PubMed  Google Scholar 

  18. Dane B, Duenas S, Han J et al (2020) Crohn’s disease activity quantified by iodine density obtained from dual-energy computed tomography enterography. J Comput Assist Tomogr 44:242–247

    Article  PubMed  Google Scholar 

  19. Dane B, O’Donnell T, Ream J, Chang S, Megibow A (2020) Novel dual-energy computed tomography enterography iodine density maps provide unique depiction of Crohn disease activity. J Comput Assist Tomogr 44:772–779

    Article  PubMed  Google Scholar 

  20. Guler E, Unal NG, Hekimsoy I et al (2021) Dual-energy CT enterography in evaluation of Crohn’s disease: the role of virtual monochromatic images. Jpn J Radiol 39:341–348

    Article  PubMed  Google Scholar 

  21. Zhu C, Hu J, Rong C et al (2023) Mucosal healing assessment in Crohn’s disease with normalized iodine concentration from dual-energy CT enterography: comparison with endoscopy. Insights Imaging 14:63

    Article  PubMed  PubMed Central  Google Scholar 

  22. Peng JC, Feng Q, Zhu J et al (2016) Usefulness of spectral computed tomography for evaluation of intestinal activity and severity in ileocolonic Crohn’s disease. Therap Adv Gastroenterol 9:795–805

    Article  PubMed  PubMed Central  Google Scholar 

  23. Daperno M, D’Haens G, Van Assche G et al (2004) Development and validation of a new, simplified endoscopic activity score for Crohn’s disease: the SES-CD. Gastrointest Endosc 60:505–512

    Article  PubMed  Google Scholar 

  24. Wu LM, Li YL, Yin YH et al (2014) Usefulness of dual-energy computed tomography imaging in the differential diagnosis of sellar meningiomas and pituitary adenomas: preliminary report. PLoS One 9:e90658

    Article  PubMed  PubMed Central  Google Scholar 

  25. Magalhães FCB, Lima EM, Carpentieri-Primo P, Barreto MM, Rodrigues RS, Parente DB (2023) Crohn’s disease: review and standardization of nomenclature. Radiol Bras 56:95–101

    PubMed  PubMed Central  Google Scholar 

  26. Tong J, Feng Q, Zhang C, Xu X, Ran Z (2022) CT enterography for evaluation of disease activity in patients with ileocolonic Crohn’s disease. BMC Gastroenterol 22:324

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Cantarelli BCF, de Oliveira RS, Alves AMA, Ribeiro BJ, Velloni F, D’Ippolito G (2020) Evaluating inflammatory activity in Crohn’s disease by cross-sectional imaging techniques. Radiol Bras 53:38–46

    Article  PubMed  PubMed Central  Google Scholar 

  28. Qiu Y, Mao R, Chen BL et al (2014) Systematic review with meta-analysis: magnetic resonance enterography vs. computed tomography enterography for evaluating disease activity in small bowel Crohn’s disease. Aliment Pharm Therap 40:134–146

    Article  CAS  Google Scholar 

  29. Ma L, Shen X, Chen YJ, Zhang Q, Li B, Zhang W (2021) Computed tomography enterography for crohn’s disease: correlation between the imaging findings and histopathologic scoring system. Abdom Radiol (NY) 46:4121–4129

    Article  PubMed  Google Scholar 

  30. Radmard AR, Eftekhar Vaghefi R, Montazeri SA et al (2018) Mesenteric lymph nodes in MR enterography: are they reliable followers of bowel in active Crohn’s disease? Eur Radiol 28:4429–4437

    Article  PubMed  Google Scholar 

  31. Xiao WX, Zhu YT, Zhang ZC, Luo M, Ma MP (2021) A preliminary study on the feasibility of the quantitative parameters of dual-energy computed tomography enterography in the assessment of the activity of intestinal Crohn’s disease. Int J Gen Med 14:7051–7058

    Article  PubMed  PubMed Central  Google Scholar 

  32. Yang X, Yu Y, Guo Y, Wu S (2018) Efficiency of CT enterography and energy spectral imaging in evaluation on activity of Crohn’s disease. Chin J Med Imaging Technol 34:1228–1232

    Google Scholar 

  33. Safra M, Werner L, Peres A et al (2023) A somatic hypermutation-based machine learning model stratifies individuals with Crohn’s disease and controls. Genome Res 33:71–79

    Article  PubMed  PubMed Central  Google Scholar 

  34. Yao J, Zhou J, Zhong Y et al (2023) Computed tomography-based radiomics nomogram using machine learning for predicting 1-year surgical risk after diagnosis of Crohn’s disease. Med Phys 50:3862–3872

    Article  CAS  PubMed  Google Scholar 

  35. Stafford IS, Gosink MM, Mossotto E, Ennis S, Hauben M (2022) A systematic review of artificial intelligence and machine learning applications to inflammatory bowel disease, with practical guidelines for interpretation. Inflamm Bowel Dis 28:1573–1583

    Article  PubMed  PubMed Central  Google Scholar 

  36. Cai W, Xu J, Chen Y, Wu X, Zeng Y, Yu F (2023) Performance of machine learning algorithms for predicting disease activity in inflammatory bowel disease. Inflammation 46:1561–1574

    Article  PubMed  Google Scholar 

  37. Guez I, Focht G, Greer MC et al (2022) Development of a multimodal machine-learning fusion model to non-invasively assess ileal Crohn’s disease endoscopic activity. Comput Meth Prog Bio 227:107207

    Article  Google Scholar 

  38. Kim YS, Kim SH, Ryu HS, Han JK (2018) Iodine quantification on spectral detector-based dual-energy CT enterography: correlation with Crohn’s disease activity index and external validation. Korean J Radiol 19:1077–1088

    Article  PubMed  PubMed Central  Google Scholar 

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Funding

This work was supported by the Chongqing’s technological innovation and application development (cstc2020jscx-sbqwX0015).

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Contributions

JL designed the research study and edited the manuscript; GX analysed the data; WT and LZ collected data; DW, YZ and LZ progressed image, KL revised the important intellectual content. All authors contributed to the review of the manuscript and approved the final version for submission.

Corresponding author

Correspondence to Kang Li.

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Institutional Review Board approval was obtained by the Ethics Committee of Chongqing General Hospital, and written informed consent was waived due to the retrospective nature (Ethical code: KY S2022-102-01).

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Li, J., Xie, G., Tang, W. et al. Establishing a machine learning model based on dual-energy CT enterography to evaluate Crohn’s disease activity. Insights Imaging 15, 115 (2024). https://doi.org/10.1186/s13244-024-01703-x

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