Current management of Crohn?s disease (CD) relies on monitoring objective endpoints of mucosal inflammation. While structural bowel damage drives surgery in more than half of patients with CD, assessments of structural bowel damage are challenging to quantify and incorporate into treatment decision- making. Cross-sectional imaging can survey deep bowel damage and fibrostenotic changes, but the time and expertise needed, and the susceptibility of qualitative features to interobserver variation, pose challenges in the broader use of imaging data to personalize care. The long-term goal of this research is to develop methods to objectively measure structural bowel damage and individualize predictions of clinical outcomes in CD. The overall objectives in this application are to test (i) the ability of computational image analysis methods to collect traditional and novel characterizations of bowel damage using common enterography imaging studies and (ii) to evaluate these measures? ability to improve predictions of CD outcomes. The central hypothesis is that bowel damage features collected by computational image analysis methods will improve the accuracy of models predicting therapeutic and clinical outcomes in CD. This central hypothesis will be tested through three specific aims: (1) Determine the performance of computational analysis of enterography studies capturing bowel damage measurements for predicting CD clinical outcomes in the regular course of care, (2) Prospectively compare the performance of enterography image analysis for predicting therapeutic response to existing laboratory and endoscopic measures, and (3) Evaluate image analysis capacity to determine underlying tissue histology in CD using conventional imaging. In the first aim, enterography studies in a national prospective CD natural history dataset will undergo image analysis to extract measurements used to model surgical, hospitalization, and steroid use outcomes. Further work in this aim will test the agreement between expert radiologists and computer-derived bowel measurements. In the second aim, subjects starting new biologic therapies will undergo scheduled enterography to compare the prognostic capabilities of computationally derived bowel features to inflammatory biomarkers and endoscopy for predicting therapeutic response. Finally, in the third aim, patients undergoing elective surgical resection of intestine for CD will have pre-operative enterography. High dimensional image features will be used to model histologic grading of inflammation and fibrosis. The proposed research is innovative in approaching structural bowel damage as a related, but independent and equally important, companion assessment to inflammation in the prognosis and treatment of CD. Further, computational image analysis opens new horizons not only in objectivity and reproducibility, but also concepts of how to measure CD burden. The proposed research is significant because it will demonstrate the indispensable importance of structural intestinal damage features for the most accurate predictions of CD course and therapeutic responsiveness in both clinical care and therapeutic trials.

Public Health Relevance

The proposed research is relevant to public health because it will develop new methods and concepts for measuring fibrostenotic and structural intestinal damage in patients with Crohn?s disease. Quantitative assessment of bowel damage in Crohn?s disease using techniques that are readily incorporated into routine clinical practice will fundamentally change how we characterize Crohn?s disease, while improving the precision and individualization of care. This proposal is relevant to the mission of the NIH by improving the health and quality of life of patients, specifically in those with digestive diseases, though development of new imaging biomarkers to improve risk stratification, monitor treatment response, and guide care in Crohn?s disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK124779-01
Application #
9942718
Study Section
Clinical Translational Imaging Science Study Section (CTIS)
Program Officer
Hamilton, Frank A
Project Start
2020-07-01
Project End
2024-04-30
Budget Start
2020-07-01
Budget End
2021-04-30
Support Year
1
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109