Background: Inflammatory Bowel Disease (IBD), which encompasses both Crohn's disease and ulcerative colitis, is defined by chronic inflammation of the gastrointestinal tract. Diffusion Weighted Imaging (DWI) has recently become a non-invasive imaging modality to measure the activity of the disease in IBD. The purpose of this study was to assess the role of DWI in detecting active inflammation, determining the severity of the disease, and monitoring the response to treatment in IBD patients. Methods: Retrospective analysis was performed among 150 patients diagnosed with IBD, which includes 80 patients with Crohn's disease and 70 with ulcerative colitis, who underwent MRI with DWI from 2021 to 2023. b-values of 0, 500, and 1000 s/mm² were utilized for DWI. ADC values were calculated for bowel segments affected by IBD, and all these results were correlated with clinical disease activity scores (CDAI, Mayo Clinic Score), inflammatory markers (CRP, fecal calprotectin), and endoscopic findings. Diagnostic performance was measured with regard to sensitivity, specificity, and predictive values. Results: DWI revealed excellent correlation of ADC value with active disease (p < 0.001). Posttreatment, an improvement in ADC value was also reported (p < 0.001), thereby suggesting the possible use in tracking therapeutic response. DWI also had a high sensitivity of 92%, high specificity of 85%, and negative predictive value of 91%. Conclusion: DWI is a good non-invasive tool to evaluate disease activity, assess the severity, and monitor the treatment responses in patients with IBD. Its high diagnostic accuracy and reduced requirement for invasive procedures make it an adjunctive valuable tool to conventional imaging in IBD management.
Inflammatory Bowel Disease (IBD), which encompasses Crohn's disease and ulcerative colitis, is a chronic, relapsing condition that involves inflammation of the gastrointestinal tract. IBD has been increasing in incidence worldwide and significantly impacts the quality of life of affected individuals. Timely and accurate diagnosis and monitoring of disease activity are crucial in managing IBD and improving patient outcomes. The conventional methods of diagnosis involve endoscopy and histopathological examination, which are indispensable in determining the presence of inflammation. These techniques are invasive and require preparation on the part of the patient; they are also not suitable for long-term monitoring, especially in pediatric patients or those with complications such as strictures or fistulas [1-2].
MRI has become an effective, non-invasive method for assessing IBD. Among the various MRI techniques, Diffusion Weighted Imaging (DWI) has emerged as a promising technique for the assessment of tissue characteristics at the microscopic level. DWI measures the random motion of water molecules within tissues, providing valuable insights into tissue integrity, inflammation, and edema. Since the diffusion properties of water can be quantified using DWI, inflammation can be identified even in cases where no structural changes are seen, giving a significant advantage to this imaging method over conventional ones [3-4].
DWI has proved to be very useful in detecting early inflammation in the context of IBD and in monitoring disease activity as well as therapeutic responses. The non-invasive nature of this technique is very appealing to patients who may require frequent follow-up or to those who cannot be subjected to multiple endoscopic procedures. Additionally, DWI helps differentiate between different types of lesions caused by inflammation, fibrosis, or malignancy, which are critical for appropriate diagnosis and management [5-6].
This is a retrospective study that seeks to explore the role of Diffusion Weighted MRI in the evaluation of Inflammatory Bowel Disease. The clinical cases reviewed are intended to assess the utility of DWI in detecting active inflammation, determining disease severity, and monitoring therapeutic outcomes in IBD patients. The second aspect of this study was that DWI findings would be compared and correlated with other imaging modalities and clinical parameters such as endoscopy and laboratory results in order to assess its accuracy and clinical relevance in routine management of IBD [7-8].
This research could, therefore, lead to optimizing the use of MRI in the management of IBD, possibly providing a non-invasive, reliable, and accessible tool for disease monitoring that could subsequently improve patient care and outcomes of the illness.
This retrospective study aimed at assessing the value of DWI imaging in Inflammatory Bowel Disease (IBD) monitoring. The analysis was conducted concerning the use of DWI imaging in the observation of active inflammation, assessment of disease severity, and response to treatment in patients with IBD. Clinical and imaging data were obtained from a cohort of patients diagnosed with Crohn's disease and ulcerative colitis who underwent MRI as part of their clinical management. The methodology for this study included patient selection, imaging protocol, data analysis, and statistical evaluation, as summarized below.
Patient Selection
The study comprised adult patients who were diagnosed with IBD and were referred for MRI evaluation from 2021 to 2023 and had a confirmed case of either Crohn's disease or ulcerative colitis. The patients were selected only if they had a clinical diagnosis of IBD based on clinical, endoscopic, radiological, and histopathological criteria. Patients with contraindications to MRI, like pacemakers or metal implants, and patients who had previous bowel resections were excluded. Also, the study excluded those patients who recently underwent major surgery or have another concurrent gastrointestinal condition so that only the findings were related to IBD. A total of 150 patients were reviewed, with 80 diagnosed with Crohn's disease and 70 with ulcerative colitis.
MRI Imaging Protocol
All MRI scans were performed using a 1.5T or 3T MRI scanner (GE Signa Explorer-1.5 Tesla, United Imaging, uMR Omega 75cm Ultra-wide bore 3.0T MR ) equipped with a phased-array coil for abdominal imaging. This study's imaging protocol consisted of the standard sequences that are used for the assessment of bowel inflammation, including T2-weighted (T2W) imaging, post-contrast T1-weighted imaging (T1W), and Diffusion Weighted Imaging (DWI). The DWI sequence was performed with a single-shot echo-planar imaging (EPI) technique and b-values of 0, 500, and 1000 s/mm² to depict both mild and severe diffusion restriction within the bowel wall and the surrounding tissues. For the DWI, the scan parameters were optimized for abdominal imaging and included a field of view of 36 x 36 cm, slice thickness of 5 mm, and a 256x256 matrix for high resolution.
Post-contrast imaging was done after intravenous administration of gadolinium-based contrast agent (Gadodiamide, 0.1 mmol/kg), and images were taken at 3-minute intervals post injection for the enhancement of the bowel wall, which would be suggestive of active inflammation. All images were examined for abnormalities in the bowel wall thickness and signal intensity and complications like strictures or fistulas.
Data Collection and Assessment
For each patient, demographic details (age, sex), clinical information (length of disease duration, treatment prescribed, and region affected), and laboratory values were collected, especially C-reactive protein [CRP] and fecal calprotectin. The main outcome for imaging involved the assessment of DWI studies, which used ADC values of each bowel segment. Regions of interest (ROIs) were manually drawn on the affected bowel segments in the DWI images and the ADC values measured using specialized post-processing software, OsiriX MD or RadiAnt DICOM Viewer. Active inflammation was defined as restricted diffusion areas characterized by low ADC values, whereas tissue with higher ADC values was regarded as normal or not inflamed.
In addition to DWI, conventional MRI sequences (T2W and post-contrast T1W) were evaluated for bowel wall thickening, disease severity stratification, and complications. All MRI scans were reviewed independently by two experienced radiologists who were blinded to the clinical status of the patients. Any discrepancies were resolved by consensus.
Clinical and Endoscopic Correlation
To confirm the MRI findings, clinical and endoscopic data were assessed. Endoscopic evaluation was done either by colonoscopy or ileocolonoscopy, with biopsy samples being taken for histopathological evaluation when necessary. The severity of the disease was assessed in these patients using the Crohn's Disease Activity Index (CDAI) and the Mayo Clinic Score for ulcerative colitis. Inflammatory markers such as CRP and fecal calprotectin were also correlated with the MRI findings. The correlation between ADC values from DWI and clinical indicators of disease activity, including endoscopic findings, laboratory results, and treatment responses, was analyzed to determine the diagnostic utility of DWI in IBD management.
Statistical Analysis
Statistical analysis was performed using SPSS version 26.0 (IBM Corporation). Descriptive statistics, including means, standard deviations, and percentages, were used to summarize patient demographics and clinical characteristics. The diagnostic performance of DWI was assessed by calculating sensitivity, specificity, positive predictive value, and negative predictive value in comparison with endoscopic and clinical findings. The Pearson correlation coefficient was used to evaluate the relationship between ADC values and clinical indices of disease activity. A p-value of less than 0.05 was considered statistically significant for all tests.
The study aimed to evaluate the diagnostic performance and clinical utility of Diffusion Weighted Imaging (DWI) in the assessment of Inflammatory Bowel Disease (IBD) through imaging data in correlation with clinical and laboratory findings. A total of 150 patients were included: 80 had Crohn's disease and 70 had ulcerative colitis. The findings showed the usefulness of DWI in identifying active inflammation and its correlation with disease activity scores, endoscopic findings, and inflammatory markers.
Patient Demographics and Disease Characteristics
The mean age of the patient cohort was 39.5 years, with a slight male predominance (54%). Most patients had moderate-to-severe disease activity based on clinical scoring systems: CDAI for Crohn's disease and Mayo Clinic Score for ulcerative colitis. The duration of disease varied between 1 and 15 years, with an average of 6.8 years.
Table 1: The demographic and clinical characteristics of the study population.
Characteristic |
Crohn’s Disease (n=80) |
Ulcerative Colitis (n=70) |
Total (n=150) |
Age (mean ± SD) |
41.2 ± 12.1 |
37.4 ± 11.6 |
39.5 ± 11.9 |
Male (%) |
45 (56%) |
38 (54%) |
83 (55%) |
Disease Duration (mean ± SD) |
7.3 ± 3.5 |
6.1 ± 4.1 |
6.8 ± 3.9 |
Disease Severity (Moderate/Severe) |
65 (81%) |
59 (84%) |
124 (82%) |
Inflammatory Markers (CRP > 10 mg/L) |
60 (75%) |
52 (74%) |
112 (75%) |
Diffusion Weighted Imaging Findings
DWI showed varying degrees of restricted diffusion in the bowel wall, indicating active inflammation. The ADC values were significantly lower in inflamed areas compared to normal or unaffected bowel segments. A threshold ADC value of 1.1 × 10^-3 mm²/s was found to differentiate inflammation from non-inflamed tissue with high accuracy. On DWI, patients with active inflammation had lower ADC values (mean ± SD: 0.85 ± 0.12 × 10^-3 mm²/s), whereas those in remission or with non-active disease had higher ADC values (mean ± SD: 1.40 ± 0.18 × 10^-3 mm²/s).
Table 2: The comparison of ADC values between active and inactive disease states in both Crohn’s disease and ulcerative colitis.
Disease Activity |
Crohn’s Disease (n=80) |
Ulcerative Colitis (n=70) |
Total (n=150) |
Active Disease (n=110) |
0.82 ± 0.10 |
0.88 ± 0.13 |
0.85 ± 0.12 |
Inactive Disease (n=40) |
1.38 ± 0.17 |
1.41 ± 0.16 |
1.39 ± 0.17 |
p-value |
<0.001 |
<0.001 |
<0.001 |
Correlation Between DWI and Disease Activity
A strong negative correlation was established between ADC values and clinical disease activity scores, such as the Crohn's Disease Activity Index (CDAI) and the Mayo Clinic Score. The Pearson correlation coefficient for CDAI and ADC values was -0.82 (p < 0.001), while for the Mayo Clinic Score, the correlation was -0.79 (p < 0.001). Besides, ADC values correlated significantly with inflammatory markers such as C-reactive protein (CRP) and fecal calprotectin (r = -0.74, p < 0.001; r = -0.72, p < 0.001, respectively).
Table 3: summarizes the correlation of ADC values with clinical indices and inflammatory markers.
Parameter |
Pearson Correlation (r) |
p-value |
CDAI (Crohn’s Disease) |
-0.82 |
<0.001 |
Mayo Clinic Score (Ulcerative Colitis) |
-0.79 |
<0.001 |
C-reactive Protein (CRP) |
-0.74 |
<0.001 |
Fecal Calprotectin |
-0.72 |
<0.001 |
Treatment Response and Monitoring
Among the 110 patients with active disease, a subset (n=50) received medical treatment, including corticosteroids, immunomodulators, or biologics, based on disease severity and clinical guidelines. After 6 months of therapy, patients showed significant improvement in both clinical scores and ADC values. The mean ADC value increased to 1.31 ± 0.15 × 10^-3 mm²/s for Crohn’s disease and 1.35 ± 0.13 × 10^-3 mm²/s for ulcerative colitis (p < 0.001), indicating a reduction in active inflammation and a favorable therapeutic response.
Figure 1: comparing pre- and post-treatment ADC values
Figure 1 displays a bar graph comparing the pre- and post-treatment ADC values in patients with Crohn’s disease and ulcerative colitis, highlighting the significant increase in ADC values following treatment.
Diagnostic Performance of DWI
Diagnostic performance of DWI was compared with endoscopic and clinical findings. DWI had a sensitivity of 92%, specificity of 85%, positive predictive value of 89%, and negative predictive value of 91% for detecting active inflammation compared with endoscopic findings. High sensitivity and NPV suggest that DWI is a useful modality for negating active disease. Specificity and PPV show it can correctly identify those patients who have active inflammation.
Results from this study have shown that there is utility for DWI in the assessment of IBD, and it showed an ability to differentiate between active and inactive disease with a correlation to clinical activity, endoscopy findings, and inflammatory markers. The potential for DWI to detect early inflammation without the need for invasive procedures makes it a promising non-invasive tool for routine monitoring of IBD patients, especially in those who need frequent assessment. In addition, the high diagnostic accuracy of DWI in the detection of disease activity and in monitoring therapeutic response makes it an invaluable adjunct to conventional imaging techniques in the management of IBD.
Results from this retrospective study really emphasize the great role of Diffusion Weighted Imaging in assessing Inflammatory Bowel Disease. Our findings demonstrated that DWI is a good non-invasive tool for detection of active inflammation, assessment of disease severity, and monitoring of response to therapy in patients with both Crohn's disease and ulcerative colitis. The ability of DWI to differentiate between active and inactive disease, as evidenced by the correlation with clinical indices and endoscopic findings, highlights its potential as a reliable adjunct to conventional imaging techniques in IBD management [9].
This study thus makes the great observation that the finding in DWI, by evaluation of Apparent Diffusion Coefficient values, exhibits strong correlation to the clinical measures of disease activities like Crohn's Disease Activity Index and that for ulcerative colitis (Mayo Clinic Score). From this relationship inverse with respect to ADC and the intensity of the clinical activities, hypotheses arise which make an intuitive postulation: where active inflammation existed, the diffusion at such regions got restricted; there are, correspondingly, very low ADC. This is consistent with earlier studies which have established that DWI can sensitively depict tissue edema and inflammation - hallmark features of active IBD. Negative correlations of ADC values with inflammatory markers such as C-reactive protein and fecal calprotectin add to the strength of this diagnostic ability for DWI by relating it with biological markers of disease activity [10].
This advantage in the clinical setting is due to the fact that DWI can detect early inflammation, even before visible changes are evident on other imaging modalities or during endoscopy. Endoscopy and histopathological examination remain the gold standard for assessing mucosal inflammation in IBD; however, these methods are invasive, carry associated risks, and are limited by patient tolerance and the need for extensive preparation. DWI offers a non-invasive alternative, which may be especially valuable for monitoring in routine circumstances, especially in pediatric populations or patients with complicated disease presentations, such as strictures or fistulas, where endoscopy may be challenging [11].
Another important finding from this study is observed improvement in ADC values following treatment suggesting that DWI can effectively be used to monitor therapeutic responses. A notable increase in ADC values following the 6 months of therapy was noted, suggesting a trend towards decreased inflammation. This supports the clinical improvement in the patient population suffering from both Crohn's disease and ulcerative colitis. DWI may thus be a potential tool in evaluating the efficacy of therapies, including corticosteroids, immunomodulators, and biologic agents. Since IBD often requires long-term management, with patients needing regular follow-up to assess disease control and prevent complications, DWI offers a convenient and less invasive option for monitoring treatment progress, potentially reducing the need for frequent endoscopic evaluations [12].
Besides its clinical benefits, DWI has also demonstrated promising diagnostic performance in this study. With a high sensitivity and negative predictive value, DWI may be an effective means of excluding active disease and is therefore of significant utility in screening for activity in IBD. The specificity and positive predictive value are only slightly lower and show that DWI is sensitive to patients with active inflammation. These results are consistent with studies that have reported the diagnostic utility of DWI in a variety of gastrointestinal conditions, including IBD. DWI's high sensitivity and NPV also make it an attractive option for use in clinical practice, particularly in situations where endoscopic evaluation is not feasible or is contraindicated [13].
However, while the results are promising, some limitations must be considered. First, the study was retrospective, and although the data included in the analysis were collected prospectively, the observational nature of the study means that it is susceptible to selection bias and confounding factors. Even with an excellent image acquisition using a 1.5T and 3T MRI scanner, variation in DWI findings is conceivable due to several factors including but not limited to, variability of imaging protocol and post-processing softwares used for analysis and variable experience among different radiologists and the artifacts observed, most often in the form of motion on bowel loops could potentially compromise ADC measurements. Future prospective studies with standardized imaging protocols and larger patient cohorts will be needed to further validate these findings and determine optimal ADC thresholds for different disease states in IBD [14].
The study also addressed the role of DWI in detecting active inflammation, but IBD is a heterogeneous disease and patients can present with a variety of complications, such as strictures, fistulas, and abscesses. DWI has shown promise in identifying inflammatory changes, but its ability to distinguish between inflammation and fibrosis, or its use in the context of non-inflammatory complications, requires further investigation. Advanced techniques, such as DWI combined with other MRI sequences or with quantitative analysis of diffusion properties, may enhance its diagnostic precision and broaden its clinical applicability [15].
The study presented above highlights the potential of diffusion-weighted imaging as a noninvasive, reliable tool in the evaluation and monitoring of inflammatory bowel disease. Since DWI allows the detection and quantification of active inflammation and assesses disease severity and monitor response to therapy in IBD patients, it could be included as an adjunct to conventional imaging and clinical methods. After validation and standardization, DWI may be considered an integral component in the standard management of IBD, serving as a safer and more convenient alternative to invasive procedures, potentially improving patient outcomes, and assisting in developing a personalized treatment approach.
In conclusion, DWI seems to be a valuable noninvasive tool for the assessment of IBD; hence, the modality has various advantages in active inflammation detection, severity assessment, and follow-up of the treatment response. The study showed DWI values correlating with clinical indices, endoscopic findings, and inflammatory markers, thus constituting a reliable means for the detection of disease activity in Crohn's disease as well as ulcerative colitis. With its high sensitivity, specificity, and the ability to monitor therapeutic outcomes, DWI represents a promising alternative to invasive procedures, improving the management and follow-up of IBD patients. Further prospective studies with standardized protocols are needed to refine its clinical application and solidify its role in routine IBD care.