Abstract
Inflammatory bowel disease (IBD), which includes ulcerative colitis (UC) and Crohn’s disease (CD), is an idiopathic condition related to a dysregulated immune response to commensal intestinal microflora in a genetically susceptible host. As a global disease, the morbidity of IBD reached a rate of 84.3 per 100,000 persons and reflected a continued gradual upward trajectory. The medical cost of IBD is also notably extremely high. For example, in Europe, it has €3,500 in CD and €2,000 in UC per patient per year, respectively. In addition, taking into account the work productivity loss and the reduced quality of life, the indirect costs are incalculable. In modern times, the diagnosis of IBD is still a subjective judgment based on laboratory tests and medical images. Its early diagnosis and intervention is therefore a challenging goal and also the key to control its progression. Artificial intelligence (AI)-assisted diagnosis and prognosis prediction has proven effective in many fields including gastroenterology. In this study, support vector machines were utilized to distinguish the significant features in IBD. As a result, the reliability of IBD diagnosis due to its impressive performance in classifying and addressing region problems was improved. Convolutional neural networks are advanced image processing algorithms that are currently in existence. Digestive endoscopic images can therefore be better understood by automatically detecting and classifying lesions. This study aims to summarize AI application in the area of IBD, objectively evaluate the performance of these methods, and ultimately understand the algorithm–dataset combination in the studies.
Introduction
Inflammatory bowel disease (IBD) is a chronic inflammatory disorder with soaring incidences recorded worldwide in recent years. For example, in Western countries, the prevalence of IBD has exceeded 0.3% and is expected to continue rising steadily over the next decade. In the same light, several studies have drawn attention to the similarity between the current prevalence of IBD in newly industrialized countries, with anterior patterns observed in the Western world. The global burden on the healthcare system caused by IBD is also currently increasingly becoming a high-priority matter (). It is important to note that the complete etiology of IBD is still uncertain. However, the two major manifestations of IBD, namely, ulcerative colitis (UC) and Crohn’s disease (CD), are recognized as a result of complex interactions between genetic and environmental factors. A recent genetic association study identified 163 susceptibility loci for IBD. In this case, the impact of host–microbe interactions in pathogenesis was scrutinized due to the link between these susceptibility loci and the microbial response (). The intestinal microecology has also been a focal point for recent studies (; ).
Currently, there is no clearly defined criterion for diagnosing IBD (; ). Laboratory tests that include blood, stool, serum markers, and gene examination can be supportive in estimating the severity of IBD but are unable to confirm the diagnosis. As a fundamental process in the diagnosis of suspected patients with IBD, an endoscopic examination improves the accuracy of the diagnosis. On the other hand, biopsies of selected bowel segments can further confirm the diagnosis and make a valid assessment of the state of the IBD and its progression. However, it has been observed that endoscopic images and histological changes are evident only when the appropriate sampling sites are selected, and the images are of good quality. The undifferentiated results were obtained in some of the patients, which in turn resulted in the delayed diagnosis or reclassification over time, proving that the definite diagnosis of IBD is still a challenging endeavor ().
The goal of treatment of IBD has evolved from traditional clinical remission to a more specific, integrated, and complete deep remission or mucosal healing (; ; ). And the advent of biological agents, such as anti-adhesion molecules, anti-cytokine molecules, blockage of downstream signaling, and anti-trafficking molecules promoted the achievement of goal in the treatment of IBD. Intestinal microbiome manipulation and stem cell transplantation are also the treatment option for certain patients with IBD (). Considering the development of research about IBD, its combination with artificial intelligence (AI) technology is not simply a result of interdisciplinary thinking but an inevitable merging of the two treatments. Digital images and medical records require advanced technology as this would lead to a great extent to significant strides being made in the studies of IBD (Figure 1).
FIGURE 1
Artificial Intelligence
Artificial intelligence, in particular, the deep-learning subtype has emerged as a breakthrough in computer technology enabled by the application of labeled big data across all the sectors (). AI allows computers to identify, quantify, and interpret relationships among variables by algorithmically learning the efficient data representations, which is a formidable task for physicians (). As a technique being initially confined as “the science and engineering of making intelligent machines,” AI was considered in medical research when its ability to learn complex patterns and make predictions was noticed. From the 1950s to present, machine learning (ML) has become the most common approach of AI mostly owing to the ML models with the function of prediction or making decisions including support vector machines (SVMs), neural network, Naïve Bayes (NB), and random forest (RF).
Artificial neural network (ANN), a remarkable one of these AI approaches, was structured with an input, hidden connection, and output layer. The basic computing units of ANN are the simulation of neurons and synapses in the human brain and are responsible for outputting a decision signal based on the weighted sum of evidence. Deep learning (DL) was developed based on ANN with extra hidden layers between the input and output layers to overcome its shortcomings such as overfitting, vanishing gradient, and decreasing in the local minimum during optimization. It impressed the researchers due to the excellent performance of convolutional neural networks (CNNs) in the computer vision field. The outstanding performance depended on the preprocessing operation named convolution that applied specific filters to draw specific features and created numerous feature maps. Then, the feature maps were handled by the pooling layers to smaller sizes, and this process of convolutional and pooling layers was duplicated. The fully connected layers were the last step to produce the combination of all features and make an overall classification (Figure 2).
FIGURE 2
Artificial Intelligence in the Etiology of IBD
In recent years, the etiology of IBD has expanded from a focus on abnormal gene expression to more complex factors such as the environmental and intestinal microflora (). However, genetic susceptibility continues to seek breakthroughs, and many results are available (). AI facilitates the data analysis used to determine suspicious risk genes, which are then verified experimentally. However, AI does not seem to be widely used in intestinal microecology due to the current lack of adequate and uniform data records. Considering the novel perspectives on the pathogenesis of IBD in the study of intestinal microecology and the demand for a large amount of data processing, AI technology will be applied to the study of IBD pathogenesis by intestinal flora.
Seeking IBD-Associated Susceptibility Loci and Genes
In the past, genome-wide association studies (GWAS) were used to analyze the genome of patients for identifying possible disease-related sequence variations (; ). The principle of GWAS was to compare the allele frequencies of a specific variant between unrelated cases and controls to test significant differences that are expected to be disease-related (). So far, around 200 genes implicated in the etiology of IBD have been found through GWAS and differential gene expression analysis (). Although more genes are expected to participate in the pathophysiological process (), the existing study methods are incompetent to mine the massive and complex genomic data utilizing only visual investigation of pairwise correlations. Moreover, the effectiveness of GWAS was limited by its nature as a non-candidate-gene approach leading to a high occurrence of false-positive results. The associated single nucleotide polymorphisms (SNPs) identified by GWAS are not usually the direct causal ones with disease because of the case-control designed only to reveal associations but not causation (). Instead, analytical tools are in demand to support the discovery of unforeseen relationships, to develop new hypotheses or models, and to forecast. The design of ML algorithms automatically detects patterns in data and accordingly fits the data-driven sciences especially genomics (). As overcoming the deficiency of causal relationship explanation when only applying GWAS, a framework based on DL was certified to success in identifying causal variants by computing the causal variants in trait-associated loci (). Another study was conducted to prioritize the IBD-risk genes for detecting a new candidate in IBD-associated genes using an ML-based method. This method used numerical expression data (microarray and RNA-seq) and categorical terms from several databases to categorize genes as risk-conferring or not conferring risk to IBD. It is noteworthy that positive gene instances were collected from GWAS (). Finally, 67 genes that had never been mentioned in other publications of IBD were identified as a novel candidate in IBD-risk genes. These genes can be used as targets in the future. This study shows that ML can remedy some inherent limitations of GWAS and can analyze the GWAS data.
In another study, investigators attempted to find genes that differentiate patients with IBD from normal individuals and identify their subtypes. After selecting IBD-related genes using the method of minimum redundancy, maximum relevance (mRMR), and incremental feature selection (IFS), the investigators applied protein–protein interaction to establish a network and then applied the shortest path method to obtain other related genes (). The mRMR is a method for identifying SNPs that provide an mRMR feature list to inform the evaluation of relevance between feature and sample class labels and the redundancies between it and the features listed before it (). Then, the IFS method selects the optimal combination as biomarkers applying the mRMR feature list and the sequential minimal optimization prediction engine (). In the future, phenotypic and clinical data may be used as the basis for selecting an optimal combination, thereby linking genes to more intuitive information and improving the interpretability of data to some extent.
Relevance Between Extra-Intestinal Manifestations and Genetic Factors
In addition to common digestive symptoms of IBD, extra-intestinal manifestations are also a significant factor affecting the health and quality of life of the patient (). In recent years, studies have predicted the possibility of extra-intestinal symptoms in patients with IBD to intervene as early as possible and reduce patient suffering (). After ML emerged as an efficient approach, these data-based studies were reconsidered. Two studies based on the same data of 152 patients were observed and compared for the efficiencies of NB, Bayesian Additive Regression Trees (BART), and Bayesian Networks (BNs) (; ).
Naïve Bayes is a classifier based on Bayes’ theorem, assuming that there is no interaction between the features except the independent given class that shows outstanding performance in automatic medical diagnosis (). BART is a method using a sum of many regressions or classification trees plus a random component to specify the relationship between the outcome and a set of covariates (). BNs can also give the probability of event occurrence through computing the conditional probabilities of the parameters in models given the values of variables ().
In 2016, the identification ability of three Bayesian machine-learning technologies (BMLTs) was compared based on disease characteristics, risk factors, and genetic polymers of the NOD2, CD14, TNF-α, IL12B, and IL1RN genes. Finally, BNs were confirmed to make an identification without a large sample, with 82% (considering only clinical factors) and 89% (considering genetic information as well) accuracies (). They also built an interpretable graphical model that displayed the links between variables and can be modified according to medical knowledge; thus, interdisciplinary research in IBD has its advantages ().
The objective of this study in 2019 was to compare these three BMLTs with logistic regression, generalized additive model, projection pursuit regression (PPR), linear discriminant analysis (LDA), quadratic discriminant analysis, and ANNs taken from the study of . In this study, BMLTs did not show superiority over the traditional method as expected. Three BMLTs ameliorated the function after considering genetic variables. However, the best performance of three BMLTs was made by BART with 0.76 area under the receiver operating characteristic curve (AUC), which was still worse than PPR (AUC = 0.94). This outcome was caused not only by the method itself but also by the different results of 10-fold cross-validation by evaluation under the premise of selecting different features and folds (). This reminds us that the data-based approach to ML has a characteristic similar to statistical methods and that the existence of an outlier may introduce a gap in the results.
Influence of Environmental Factors on IBD Flares
At present, many researchers consider that the imbalance between proinflammatory and anti-inflammatory forces that lead to an occurrence of IBD is a response to genetic and environmental factors (). Several ML models such as ANN and SVM are sufficient for working with complex datasets to compensate for the deficiency of traditional linear statistics (). A study of the association between seasonal changes and onset and recurrence of IBD revealed a high incidence of CD in July and August (). This study used an ANN model to predict the frequency of onset, relapse, and severity of IBD and achieved a high accuracy in predicting the frequency of the relapse of IBD (mean square error = 0.009 and mean absolute percentage error = 17.1%). The previous studies applying multiple logistic regression or multiple LDA models came to conflicting conclusions about the relationship between IBD flares and season variation due to inadequate statistical stability (). Thus, this study confirmed the feasibility of applying ANN methods to verify the correlation between certain factors and disease incidence (; Table 1). Epidemiological studies that directly link risk factors to the incidence of IBD are still instrumental. In addition to suggesting that the association between the two factors provides advice for public health management, the studies may suggest a non-immune, directly related IBD etiological mechanism, including smoking, obesity, and dietary factors such as high-fat or low-fiber diets ().
TABLE 1
| References | Published year | Aim of study | Type of AI | Number of subjects | Input variables (number/type) | Outcomes |
| 2017 | Prioritization of IBD risk genes to detect candidate novel IBD-associated genes | Four different machine-learning classification models: rf, svmPoly, xgbTree, and glmnet | 180 CD, 149 UC, 94 colorectal neoplasms, and 90 normal tissue | 309/expression data from both array and RNA-seq data sets, GO, KEGG, and the Pathway Interactions Database terms | 67 novel candidate IBD-risk genes | |
| 2017 | Screening for differential expressing genes among different clusters based on an IBD database to identify genes related to IBD | SMO | 59 CD, 26 UC, and 42 normal samples | 12,754/expression levels of 12,754 genes | 21 candidate genes related to IBD | |
| 2016 | Assessment of the predictive power of three BMLTs as classifiers for EIM in CD patients | 3 BMLTs: NB, BART, and BN | 152 patients with CD | 12/disease characteristics, risk factors, and genetic variables | Accuracy: 89% (BN achieved the best performance) | |
| 2019 | Determination of whether BMLT could improve EIM prediction | 3 BMLTs: NB, BART, and BN | 152 patients with CD | 12/disease characteristics, risk factors, and genetic variables | Sensitivity: 66.0%, specificity: 69.0% (BART achieved the best performance) | |
| 2015 | Prediction of IBD onset and relapse frequency with meteorological data | ANN | 569 UC and 332 CD patients | 5/meteorological data | Accuracy in predicting the frequency of IBD relapse (mean square error = 0.009, mean absolute percentage error = 17.1%) |
Summary of studies using artificial intelligence in IBD etiology.
IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; GO, gene ontology; KEGG, Kyoto encyclopedia of genes and genomes; rf, random forest; svmPoly, support vector machine with polynomial kernel; xgbTree, extreme gradient boosting; glmnet, elastic net regularized generalized linear model; SMO, sequential minimal optimization; BMLTs, Bayesian Machine Learning Techniques; EIM, extra-intestinal manifestations; NB, Naïve Bayes; BART: Bayesian Additive Regression Trees; BN, Bayesian Networks; ANN, artificial neural network.
Artificial Intelligence in Diagnosis of IBD
In recent years, with the increasing incidence of IBD, seeking more accurate diagnostic tools for IBD has become a hot topic. Currently, there is no gold standard for diagnosing IBD (; ). A comprehensive analysis combining clinical presentation, laboratory examination, imaging, endoscopy, and histopathology and exclusion of a range of infectious diseases and intestinal TB is required to provide further treatment plans (; ). However, integration of information is influenced by the subjective factors of investigators (; ). A survey involving 58 gastroenterologists, using the Mayo endoscopic subscale to evaluate the mucosal healing of patients with UC and Rutgeerts score to evaluate the postoperative scores of patients with CD, showed that the inter-judgment consistency was only 0.47 and 0.33, respectively (). This study did not aim to reveal differences between diagnoses in order to emphasize the requirements of the expertise of physicians. Instead, it expressed the need for a more effective IBD scoring system and suggested the feasibility of a “training program” for diagnosis (). Based on the characteristics that the diagnosis of IBD relies on the personal experience of physicians and consideration of the defect of personal subjective factors (; ), the application of the diagnosis of ML-assisted IBD shows great potential.
Image Analysis and Automatic Preprocessing of Images
Some computer-aided diagnosis (CAD) programs combine computers and new image acquisition devices such as endocytoscopes to collect images with higher resolution and then analyze the images using AI, facilitating more accurate and faster diagnoses ().
Convolutional neural networks show excellent performance in image recognition (). Good results were also demonstrated when applying CAD systems for intestinal diseases based on CNNs (). However, there are many deficiencies in this new method, including differences in evaluation caused by the location of image selection and the difficulty in scoring caused by local treatment. These problems are still challenging to eliminate as in traditional imaging studies (; ), and the multifactor analysis function of ML technology itself is not fully played.
A study to improve the diagnosis of IBD by improving a CAD system to analyze the endoscopic images revealed that in addition to achieving higher sensitivity, specificity, and accuracy, the CAD systems have some advantages over traditional imaging such as providing more comprehensive imaging information, implementing an automatic selection of the region of interest, and better reproducibility. Based on the data from 187 patients with UC, a study collected 525 validation sets from 100 patients and utilized the 12,900 endoscopic images of the remaining 87 patients to develop the CAD system. All endoscopic images were marked with their histological assessment according to the biopsy samples. Finally, this CAD system constructed by 312 features on the endoscopic image showed its potential to fully automated the identification of histological inflammation related to UC with 74% diagnostic sensitivity, 97% specificity, and 91% accuracy (Figure 3; ).
FIGURE 3
Moreover, one study concentrated on the evaluation of endoscopic images in UC, which uses the red density (RD) algorithm refined by integrating computerized vessel pattern recognition and multiple regression analysis. The endoscopic images and biopsy samples from 29 consecutive patients with UC and 6 healthy controls were used to build the algorithm. This algorithm was developed based on automatic computer-aided assessment of redness on a pixel level and was further refined through recalibrating and expanding the RD score with the information of clinical, endoscopic, and histological scorings. Its stable and reproducible outcome conforms with the requirement of objectivity for the diagnosis. The strong correlation between the way how the entire image is digitized and histology suggests its potential for predicting the prognosis (
After more ML structural frameworks have been published, the cross-discipline boom has resulted in the broader use of image recognition for the diagnosis of IBD. The future value of CAD and the use of images for data extraction and analysis are very compelling (
Machine Learning Enhancing Non-invasive Test for IBD With miRNA Signatures
In addition to the progress made in the diagnosis of IBD imaging and by the influence of technology and other published results, some new methods of assisted diagnosis have been applied. A study uses penalized SVMs and RF for analyzing peripheral blood miRNAs in subjects to achieve a differential diagnosis of CD and UC. It established a sparse model based on the expression levels of certain miRNAs from 76 patients with IBD and 38 healthy controls and then selected 16 distinct miRNAs to be the markers for diagnostic application. Then, the classification was achieved by penalized SVMs and used RF to validate the SVM-based miRNA signatures (
There are also studies directly analyzing the genes of subjects, trying to classify healthy people and patients with CD according to their genomic information. These studies are different from those simply looking for risk genes, and their purpose is to diagnose patients with clinical signs. In one study, three ML methods, namely, penalized logistic regression, gradient boosted trees, and ANNs, were used to reanalyze the Immunochip dataset genotyped by the International Inflammatory Bowel Disease Genetics Consortium (IIBDGC). This study included 18,227 patients with CD and 34,050 healthy controls, finally resulting in a maximum AUC of 0.80 achieved by LR methods (
Determining IBD Subtype and Evaluation of Disease Status
Some studies have made new claims in addition to the diagnosis of IBD. They have tried to classify and stage IBD using ML technology, which is vital for the choice of follow-up therapy.
FIGURE 4

Model construction and data processing. The whole project was composed of model construction, validation, and inflammatory bowel disease unclassified reclassification. The study recruited 239 pediatric patients from the Genetics of Pediatric Inflammatory Bowel Disease study at Southampton Children’s Hospital. The clinical data were used to search the best parameters for classification and train the model. The linear SVM was applied to construct the optimal model, allowing for assessing the relevance with the disease of the selected variable. Then, the optimal penalty parameter (C) tuning and fivefold cross-validation scheme (RFE-CV) help maximizing the classification accuracy by avoiding overfitting. Adapted with permission from
One study attempted to use intestinal microecology to diagnose IBD, with combined human genetic data and 16S and metagenomic (MGS) intestinal biopsy data, to classify patients with CD according to disease status and treatment response (
TABLE 2
| References | Published year | Aim of study | Type of AI | Number of subjects | Outcomes |
| 2019 | Prediction of persistent histologic inflammation associated with UC | SVM | Training set: 12,900 images from 87 patients. Test set: 9935 images from 100 patients | Sensitivity: 74%, specificity: 97%, accuracy: 91% | |
| 2016 | Segmentation of CD from abdominal MRI | Active learning framework combined with semi-supervised learning | 70 patients (fivefold cross validation) | Dice Metric: 92.4%, Hausdorff distance: 7.0 mm | |
| 2015 | Diagnostics of IBD | SVM | 114 patients | AUROC: 0.75–1.00 | |
| 2017 | Classification of Pediatric Inflammatory Bowel Disease | SVM | 239 patients | Accuracy: 82.7% (model utilizing combined endoscopic/histological data achieved the best performance) | |
| 2018 | Classification of disease state and treatment outcome in pediatric Crohn’s disease | RF | Intestinal biopsies of 20 treatment-naïve CD and 20 control pediatric patients | Accuracy: 84.2% (model utilizing 16S taxonomic datasets achieved the best performance) |
Summary of studies using artificial intelligence in IBD diagnosis.
IBD, inflammatory bowel disease; UC, ulcerative colitis; SVM, support vector machine; CD, Crohn’s disease; MRI, magnetic resonance images; AUROC, area under receiver operating characteristic; RF, random forest.
Artificial Intelligence in Treatment of IBD
Currently, the goal of treatment of IBD has changed from the traditional clinical remission to a more specific, integrated, and complete deep remission or mucosal healing (
Machine Learning Supporting the Prediction of IBD Progression
One study applied RF algorithms for predicting the likelihood of patients with IBD experiencing disease flares over a certain period. Corticosteroid use and hospitalizations were considered as a surrogate for IBD flares in this study. This study initially limited the predictors, including age, sex, and five other features, for the diagnosis of IBD and used these finite factors to establish models for predicting the IBD flares. Finally, the best prediction performance was achieved by the RF longitudinal model anticipated with previous hospitalization or steroid use, and its AUC reached 0.87 (
Forecasting the Efficacy After Clinical Intervention
In addition to predicting the likelihood of IBD flare emergence, prediction of the possible efficacy of some treatments is also a major direction of further research. A retrospective study analyzed some known patients with a good response to steroids, cyclosporine, or infliximab and selected nine miRNAs plus five clinical factors as predictors of first-line and second-line treatment effects with the help of a deep network-based classifier. The classification accuracy of this panel to discriminate responders to steroids from non-responders reached 93%. Interestingly, a linear program is the most effective way when the number of parameters is increased (
TABLE 3
| References | Published year | Aim of study | Type of AI | Number of subjects | Input variables (number/type) | Outcomes |
| 2017 | Prediction of IBD flares | RF | 20,368 patients | 6/demographic data, lab data, and clinical variables | AUROC: 0.87 (RF longitudinal model utilizing previous hospitalization or steroid use achieved the best performance) | |
| 2019 | Prediction and explanation of inflammation in CD | Gradient boosting machines | 82 patients | 40/demographic data, lab data, and clinical variables | AUROC: 0.93 | |
| 2020 | Detection of intestinal strictures in CD patients | Two-class decision forest algorithm | 67 patients | 15/serum elafin level and 14 clinical variables | AUROC: 0.92 (model utilizing serum elafin levels and commonly available clinical data achieved the best performance) | |
| 2019 | Prediction of responses to therapy of patients with Acute Severe UC | Neural networks | 47 patients | 14/9 microRNAs and five clinical variables | Accuracy: 93%, AUROC: 0.91 | |
| 2019 | Identification of CD patients likely to be durable responders to ustekinumab | RF | 401 patients | 12/5 demographic data and seven laboratory test results | AUROC: 0.78 (model utilizing data through week 8 achieved the best performance) | |
| 2019 | Prediction of CD recurrence risk after ileocolic resection | RF | 60 patients (five patients with extreme variability on whole transcriptome analysis had been excluded) | 30/expression levels of 30 transcripts | Accuracy: 91.67% (in anti-TNFα-naïve patients), 92.86% (in patients receiving anti-TNFα therapy) | |
| 2020 | Prediction of sustained remission after exclusive enteral nutrition in pediatric CD | RF | 22 patients | 34/demographic data, clinical variables, and 27 microbial data | AUROC: 0.9 (model utilizing microbial abundances, species richness, and Paris disease classification achieved the best performance) |
Summary of studies using artificial intelligence in IBD treatment.
IBD, inflammatory bowel disease; CD, Crohn’s disease; UC, ulcerative colitis; AUROC, area under receiver operating characteristic; RF, random forest.
The ileocolic resection is an essential treatment for a large number of patients with CD after a long disease progression, and the rate of the second or third surgeries gets to 23–43% (
To date, with a better understanding of how gut microbiota participates in IBD pathogenesis, there are more and more studies focusing on its predictive value. Casey et al. studied the gut microbiome taxonomy and functional capacity in 139 fecal samples of 22 patients (8–15 years of age) with CD who underwent treatment with exclusive enteral nutrition (EEN). The RF model was employed to classify treatment response and successfully made a distinction between sustained remission and those who neither achieved remission nor relapsed by 24 weeks with clinical metadata and baseline microbiome. The microbiome data and Paris classification of disease behavior and location were confirmed as the best feature for prediction, which may imply the clinical application indicator of EEN (
Machine Learning Facilitating Personalized Therapeutic Intervention
A study on the use of ML technology to achieve precision medicine is also underway. The multifactor analysis capabilities of ML facilitate the provision of personalized therapies (
Discussion
In the entire field of gastroenterology, AI is mainly used in image recognition and statistical analysis of diagnosis or prediction of prognosis (
At present, natural language processing as the important area of AI could bring another peak of AI application in IBD research based on clinical data due to its ability to extract information from plain text (
In addition to the advantages of AI technology, there are still some problems that cannot be ignored. AI technology has inherent pitfalls, such as overfitting, selection bias, and spectrum bias (class imbalance), which may lead to overestimation of accuracy or inappropriate generalization of results (
Search Strategy and Selection Criteria
Articles for this study were identified using PubMed, and references from relevant articles using the following search terms: “Inflammatory bowel disease” OR “Crohn’s disease” OR “Ulcerative colitis,” AND “Artificial intelligence” OR “Machine learning” OR “Artificial neural network” OR “Convolutional neural network.” Only the most impactful papers were considered.
Conclusion
Artificial intelligence can boost studies on IBD by identifying the susceptibility loci and other IBD etiological factors. For the diagnosis of IBD, the images and miRNA signatures can be analyzed by AI, and predicting flares are effective for treatment.
Statements
Author contributions
GC collected the papers and data, analyzed the conclusions, and drafted the manuscript. JS presented the idea of this manuscript, supported the funding, analyzed the conclusions, and drafted and revised the manuscript. Both authors contributed to the article and approved the submitted version.
Funding
This study was supported by grants from the National Natural Science Foundation of China (No. 81770545) and MDT Project of Clinical Research Innovation Foundation, Renji Hospital, School of Medicine, Shanghai Jiao Tong University (PYI-17-003).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
AbadiM.AgarwalA.BarhamP.BrevdoE.ZhengX. (2016). TensorFlow: Large-Scale Machine Learning on Heterogeneous Distributed Systems. arXiv [Preprint]. Available online at: https://arxiv.org/abs/1603.04467∗accq.
2
AnneseV.DapernoM.RutterM. D.AmiotA.BossuytP.EastJ.et al (2013). European evidence based consensus for endoscopy in inflammatory bowel disease.J. Crohns Colitis7982–1018.
3
AshtonJ. J.BeattieR. M. J. L. (2019). Personalised therapy for inflammatory bowel disease.Lancet3931672–1674. 10.1016/s0140-6736(18)33125-8
4
AtreyaR.NeurathM. F. (2018). Mechanisms of molecular resistance and predictors of response to biological therapy in inflammatory bowel disease.Lancet Gastroenterol. Hepatol.3790–802. 10.1016/s2468-1253(18)30265-6
5
BernsteinC. N.BenchimolE. I.BittonA.MurthyS. K.NguyenG. C.LeeK.et al (2019). The impact of inflammatory bowel disease in Canada 2018: extra-intestinal diseases in IBD.J. Can. Assoc. Gastroenterol.2S73–S80.
6
BossuytP.NakaseH.VermeireS.De HertoghG.EelbodeT.FerranteM.et al (2020). Automatic, computer-aided determination of endoscopic and histological inflammation in patients with mild to moderate ulcerative colitis based on red density.Gut691778–1786. 10.1136/gutjnl-2019-320056
7
BossuytP.NakaseH.VermeireS.WillekensH.IkemotoY.MakinoT.et al (2018). 436 - Automated digital calculation of endoscopic inflammation in ulcerative colitis: results of the red density study.Gastroenterology154S–98–S–99. 10.1136/gutjnl-2019-320056
8
BottigliengoD.BerchiallaP.LaneraC.AzzolinaD.LorenzoniG.MartinatoM.et al (2019). The role of genetic factors in characterizing extra-intestinal manifestations in crohn’s disease patients: are bayesian machine learning methods improving outcome predictions?J. Clin. Med.8:865. 10.3390/jcm8060865
9
ChenL.ChuC.FengK. (2016). Predicting the types of metabolic pathway of compounds using molecular fragments and sequential minimal optimization.Comb. Chem. High Throughput Screen.19136–143. 10.2174/1386207319666151110122453
10
CoganT.CoganM.TamilL. (2019). MAPGI: accurate identification of anatomical landmarks and diseased tissue in gastrointestinal tract using deep learning.Comput. Biol. Med.111:103351. 10.1016/j.compbiomed.2019.103351
11
CushingK. C.McleanR.McdonaldK. G.GustafssonJ. K.KnoopK. A.KulkarniD. H.et al (2019). Predicting risk of postoperative disease recurrence in crohn’s disease: patients with indolent crohn’s disease have distinct whole transcriptome profiles at the time of first surgery.Inflamm. Bowel Dis.25180–193. 10.1093/ibd/izy228
12
DapernoM.ComberlatoM.BossaF.ArmuzziA.BianconeL.BonanomiA. G.et al (2017). Training programs on endoscopic scoring systems for inflammatory bowel disease lead to a significant increase in interobserver agreement among community gastroenterologists.J. Crohns Colitis11556–561.
13
DouglasG. M.HansenR.JonesC. M. A.DunnK. A.ComeauA. M.BielawskiJ. P.et al (2018). Multi-omics differentially classify disease state and treatment outcome in pediatric Crohn’s disease.Microbiome6:13.
14
DuY.XieJ.ChangW.HanY.CaoG. (2012). Genome-wide association studies: inherent limitations and future challenges.Front. Med.6:444–450. 10.1007/s11684-012-0225-3
15
EnglandJ. R.ChengP. M. (2019). Artificial intelligence for medical image analysis: a guide for authors and reviewers.AJR. Am. J. Roentgenol.212513–519. 10.2214/ajr.18.20490
16
EraslanG.AvsecŽGagneurJ.TheisF. J. (2019). Deep learning: new computational modelling techniques for genomics.Nat. Rev. Genet.20389–403. 10.1038/s41576-019-0122-6
17
FernandesS. R.PintoJ.Marques Da CostaP.CorreiaL. (2018). Disagreement among gastroenterologists using the mayo and rutgeerts endoscopic scores.Inflamm. Bowel Dis.24254–260. 10.1093/ibd/izx066
18
GeversD.KugathasanS.DensonL. A.Vázquez-BaezaY.Van TreurenW.RenB.et al (2014). Microbe the treatment-naive microbiome in new-onset crohn’s disease.Cell Host Microbe15382–392.
19
GiachinoD. F.RegazzoniS.BardessonoM.MarchiM. D.GregoriD. J. (2007). Modeling the role of genetic factors in characterizing extra-intestinal manifestations in Crohn’s disease patients: does this improve outcome predictions?Curr. Med. Res. Opin.231657–1665. 10.1185/030079907x210471
20
HerzogD.FournierN.BuehrP.RuegerV.KollerR.HeylandK.et al (2018). Age at disease onset of inflammatory bowel disease is associated with later extraintestinal manifestations and complications.Eur. J. Gastroenterol. Hepatol.30598–607. 10.1097/meg.0000000000001072
21
HubenthalM.Hemmrich-StanisakG.DegenhardtF.SzymczakS.DuZ.ElsharawyA.et al (2015). Sparse modeling reveals miRNA signatures for diagnostics of inflammatory bowel disease.PLoS One10:e0140155. 10.1371/journal.pone.0140155
22
IsakovO.DotanI.Ben-ShacharS. (2017). Machine learning-based gene prioritization identifies novel candidate risk genes for inflammatory bowel disease.Inflamm. Bowel Dis.231516–1523. 10.1097/mib.0000000000001222
23
JeongC.-S.KimD. (2016). Inferring crohn’s disease association from exome sequences by integrating biological knowledge.BMC Med. Genomics9(Suppl. 1):35. 10.1186/s12920-016-0189-2
24
JohnsonK. W.Torres SotoJ.GlicksbergB. S.ShameerK.MiottoR.AliM.et al (2018). Artificial intelligence in cardiology.J. Am. Coll. Cardiol.712668–2679.
25
JonesC. M. A.ConnorsJ.DunnK. A.BielawskiJ. P.ComeauA. M.LangilleM. G. I.et al (2020). Bacterial taxa and functions are predictive of sustained remission following exclusive enteral nutrition in pediatric crohn’s disease.Inflamm. Bowel Dis.261026–1037. 10.1093/ibd/izaa001
26
JostinsL.RipkeS.WeersmaR. K.DuerrR. H.McgovernD. P.HuiK. Y.et al (2012). Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.Nature491119–124.
27
KhorB.GardetA.XavierR. J. (2011). Genetics and pathogenesis of inflammatory bowel disease.Nature474307–317.
28
KlenskeE.BojarskiC.WaldnerM.RathT.NeurathM. F.AtreyaR. (2019). Targeting mucosal healing in Crohn’s disease: what the clinician needs to know.Therap. Adv. Gastroenterol.12:1756284819856865.
29
LeggettC. L.WangK. K. (2016). Computer-aided diagnosis in GI endoscopy: looking into the future.Gastrointest. Endosc.84842–844. 10.1016/j.gie.2016.07.045
30
LiuJ. Z.Van SommerenS.HuangH.NgS. C.AlbertsR.TakahashiA.et al (2015). Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.Nat. Genet.47979–986. 10.1038/ng.3359
31
LiuX.LiN.-S.LvL.-S.HuangJ.-H.TangH.ChenJ.-X.et al (2013). A comparison of the performances of an artificial neural network and a regression model for GFR estimation.Am. J. Kidney Dis.621109–1115. 10.1053/j.ajkd.2013.07.010
32
LuoY.De LangeK. M.JostinsL.MoutsianasL.RandallJ.KennedyN. A.et al (2017). Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.Nat. Genet.49186–192. 10.1038/ng.3761
33
MaedaY.KudoS. E.MoriY.MisawaM.OgataN.SasanumaS.et al (2019). Fully automated diagnostic system with artificial intelligence using endocytoscopy to identify the presence of histologic inflammation associated with ulcerative colitis (with video).Gastrointest. Endosc.89408–415. 10.1016/j.gie.2018.09.024
34
MagroF.LangnerC.DriessenA.EnsariA.GeboesK.MantzarisG. J.et al (2013). European consensus on the histopathology of inflammatory bowel disease.J. Crohns Colitis7827–851.
35
MahapatraD.VosF. M.BuhmannJ. M. (2016). Active learning based segmentation of Crohns disease from abdominal MRI.Comput. Methods Programs Biomed.12875–85. 10.1016/j.cmpb.2016.01.014
36
MentiE.LaneraC.LorenzoniG.GiachinoD. F.MarchiM.GregoriD.et al (2016). Bayesian machine learning techniques for revealing complex interactions among genetic and clinical factors in association with extra-intestinal manifestations in IBD patients.AMIA Annu. Symp. Proc.2016884–893.
37
MomozawaY.DmitrievaJ.TheatreE.DeffontaineV.RahmouniS.CharloteauxB.et al (2018). IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.Nat. Commun.9:2427.
38
MoriY.KudoS. E.BerzinT. M.MisawaM.TakedaK. (2017). Computer-aided diagnosis for colonoscopy.Endoscopy49813–819. 10.1055/s-0043-109430
39
MorillaI.UzzanM.LaharieD.Cazals-HatemD.DenostQ.DanielF.et al (2019). Colonic MicroRNA profiles, identified by a deep learning algorithm, that predict responses to therapy of patients with acute severe ulcerative colitis.Clin. Gastroenterol. Hepatol.17905–913. 10.1016/j.cgh.2018.08.068
40
MossottoE.AshtonJ. J.CoelhoT.BeattieR. M.MacarthurB. D.EnnisS. (2017). Classification of paediatric inflammatory bowel disease using machine learning.Sci. Rep.7:2427.
41
NaS.-Y.MoonW. (2019). Perspectives on current and novel treatments for inflammatory bowel disease.Gut Liver13604–616. 10.5009/gnl19019
42
NadeemS.TahirM. A.NaqviS. S. A.ZaidM. (2018). “Ensemble of texture and deep learning features for finding abnormalities in the gastro-intestinal tract,” inComputational Collective Intelligence. ICCCI 2018. Lecture Notes in Computer Science, Vol. 11056edsNguyenN.PimenidisE.KhanZ.TrawińskiB. (Cham: Springer International Publishing), 469–478. *editmade.10.1007/978-3-319-98446-9_44
43
NegreanuL.VoiosuT.StateM.VoiosuA.BengusA.MateescuB. R. (2019). Endoscopy in inflammatory bowel disease: from guidelines to real life.Therap. Adv. Gastroenterol.12:1756284819865153.
44
NishidaA.InoueR.InatomiO.BambaS.NaitoY.AndohA. (2018). Gut microbiota in the pathogenesis of inflammatory bowel disease.Clin. J. Gastroenterol.111–10.
45
PanaccioneR.ColombelJ. F.LouisE.Peyrin-BirouletL.SandbornW. J. (2013). Evolving definitions of remission in Crohn’s disease.Inflamm. Bowel Dis.191645–1653.
46
PengH.LongF.DingC. (2005). Feature selection based on mutual information: criteria of max-dependency, max-relevance, and min-redundancy.IEEE Trans. Pattern Anal. Mach. Intell.271226–1238. 10.1109/tpami.2005.159
47
PengJ. C.RanZ. H.ShenJ. (2015). Seasonal variation in onset and relapse of IBD and a model to predict the frequency of onset, relapse, and severity of IBD based on artificial neural network.Int. J. Colorectal Dis.301267–1273. 10.1007/s00384-015-2250-6
48
PiovaniD.DaneseS.Peyrin-BirouletL.NikolopoulosG. K.LytrasT.BonovasS. (2019). Environmental risk factors for inflammatory bowel diseases: an umbrella review of meta-analyses.Gastroenterology157647–659.e4.
49
PlevyS.SilverbergM. S.LocktonS.StockfischT.CronerL.StachelskiJ.et al (2013). Combined serological, genetic, and inflammatory markers differentiate non-IBD, Crohn’s disease, and ulcerative colitis patients.Inflamm. Bowel Dis.191139–1148. 10.1097/mib.0b013e318280b19e
50
RathT.TontiniG. E.NeurathM. F.NeumannH. (2015). From the surface to the single cell: novel endoscopic approaches in inflammatory bowel disease.World J. Gastroenterol.2111260–11272. 10.3748/wjg.v21.i40.11260
51
ReddyB. K.DelenD.AgrawalR. K. (2019). Predicting and explaining inflammation in Crohn’s disease patients using predictive analytics methods and electronic medical record data.Health Informatics J.251201–1218. 10.1177/1460458217751015
52
RomagnoniA.JegouS.Van SteenK.WainribG.HugotJ. P. (2019). Comparative performances of machine learning methods for classifying crohn disease patients using genome-wide genotyping data.Sci. Rep.9:10351.
53
SandbornW. J.HanauerS.Van AsscheG.PanesJ.WilsonS.PeterssonJ.et al (2014). Treating beyond symptoms with a view to improving patient outcomes in inflammatory bowel diseases.J. Crohns Colitis8927–935. 10.1016/j.crohns.2014.02.021
54
SearsM. R.JohnstonN. W. (2007). Understanding the september asthma epidemic.J. Allergy Clin. Immunol.120526–529. 10.1016/j.jaci.2007.05.047
55
SinghS.DulaiP. S.ZarrinparA.RamamoorthyS.SandbornW. J. (2017). Obesity in IBD: epidemiology, pathogenesis, disease course and treatment outcomes.Nat. Rev. Gastroenterol. Hepatol.14110–121. 10.1038/nrgastro.2016.181
56
SokolH.SeksikP. (2010). The intestinal microbiota in inflammatory bowel diseases: time to connect with the host.Curr. Opin. Gastroenterol.26327–331. 10.1097/mog.0b013e328339536b
57
TopolE. J. (2019). High-performance medicine: the convergence of human and artificial intelligence.Nat. Med.2544–56. 10.1038/s41591-018-0300-7
58
Upstill-GoddardR.EcclesD.EnnisS.RafiqS.TapperW.FliegeJ.et al (2013). Support vector machine classifier for estrogen receptor positive and negative early-onset breast cancer.PLoS One8:e68606. 10.1371/journal.pone.0068606
59
VerstocktB.FerranteM.VermeireS.Van AsscheG. (2018). New treatment options for inflammatory bowel diseases.J. Gastroenterol.53585–590.
60
WaljeeA. K.LipsonR.WiitalaW. L.ZhangY.LiuB.ZhuJ.et al (2017). Predicting hospitalization and outpatient corticosteroid use in inflammatory bowel disease patients using machine learning.Inflamm. Bowel Dis.2445–53. 10.1093/ibd/izx007
61
WaljeeA. K.WallaceB. I.Cohen-MekelburgS.LiuY.LiuB.SauderK.et al (2019). Development and validation of machine learning models in prediction of remission in patients with moderate to severe crohn disease.JAMA Netw. Open2:e193721. 10.1001/jamanetworkopen.2019.3721
62
WangJ.OrtizC.FontenotL.XieY.HoW.MattaiS. A.et al (2020). High circulating elafin levels are associated with Crohn’s disease-associated intestinal strictures.PLoS One15:e0231796. 10.1371/journal.pone.0231796
63
WilliamsA. M.LiuY.RegnerK. R.JotterandF.LiuP.LiangM. (2018). Artificial intelligence, physiological genomics, and precision medicine.Physiol. Genomics50237–243. 10.1152/physiolgenomics.00119.2017
64
WimmerG.GadermayrM.WolkersdorferG.KwittR.TamakiT.TischendorfJ.et al (2019). Quest for the best endoscopic imaging modality for computer-assisted colonic polyp staging.World J. Gastroenterol.251197–1209. 10.3748/wjg.v25.i10.1197
65
WindsorJ. W.KaplanG. G. (2019). Evolving epidemiology of IBD.Curr. Gastroenterol. Rep.21:40.
66
WuS.RobertsK.DattaS.DuJ.JiZ.SiY.et al (2020). Deep learning in clinical natural language processing: a methodical review.J. Am. Med. Inform. Assoc.27457–470.
67
YangY. J.BangC. S. (2019). Application of artificial intelligence in gastroenterology.World J. Gastroenterol.251666–1683. 10.3748/wjg.v25.i14.1666
68
YeB. D.McGovernD. P. B. (2016). Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.Exp. Rev. Clin. Immunol.121091–1107. 10.1080/1744666x.2016.1184972
69
YuanF.ZhangY. H.KongX. Y.CaiY. D. (2017). Identification of candidate genes related to inflammatory bowel disease using minimum redundancy maximum relevance, incremental feature selection, and the shortest-path approach.Biomed. Res. Int.2017:5741948.
70
YueB.LuoX.YuZ.ManiS.WangZ.DouW. (2019). Inflammatory bowel disease: a potential result from the collusion between gut microbiota and mucosal immune system.Microorganisms7:440. 10.3390/microorganisms7100440
71
ZhouJ.TheesfeldC. L.YaoK.ChenK. M.WongA. K.TroyanskayaO. G. (2018). Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk.Nat. Genet.501171–1179. 10.1038/s41588-018-0160-6
72
ZouJ.HussM.AbidA.MohammadiP.TorkamaniA.TelentiA. (2019). A primer on deep learning in genomics.Nat. Genet.5112–18. 10.1038/s41588-018-0295-5
Summary
Keywords
inflammatory bowel disease, artificial intelligence, Crohn’s disease, ulcerative colitis, machine learning
Citation
Chen G and Shen J (2021) Artificial Intelligence Enhances Studies on Inflammatory Bowel Disease. Front. Bioeng. Biotechnol. 9:635764. doi: 10.3389/fbioe.2021.635764
Received
18 January 2021
Accepted
09 June 2021
Published
08 July 2021
Volume
9 - 2021
Edited by
Maria Gazouli, National and Kapodistrian University of Athens, Greece
Reviewed by
Stefan G. Stanciu, Politehnica University of Bucharest, Romania; Shobna Bhatia, Sir H. N. Reliance Foundation Hospital and Research Centre, India
Updates

Check for updates
Copyright
© 2021 Chen and Shen.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jun Shen, shenjun_med2000@163.com
This article was submitted to Nanobiotechnology, a section of the journal Frontiers in Bioengineering and Biotechnology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.