The Role of Artificial Intelligence in the Diagnosis and Treatment of Ulcerative Colitis
Abstract
:1. Introduction
2. Methods
3. An Overview of Ulcerative Colitis with Modern Diagnostic Approaches
4. The Scope of Artificial Intelligence and Its Subdivisional Networks
5. Artificial Intelligence in the Diagnosis of Ulcerative Colitis
6. Artificial Intelligence in the Treatment of Ulcerative Colitis
7. The Post-Operative Role of Artificial Intelligence
8. Prematurity in the Advancement and Utilization of Artificial Intelligence in Ulcerative Colitis
9. Discussion
10. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
- Ordás, I.; Eckmann, L.; Talamini, M.; Baumgart, D.C.; Sandborn, W.J. Ulcerative colitis. Lancet 2012, 380, 1606–1619. [Google Scholar] [CrossRef]
- Conrad, K.; Roggenbuck, D.; Laass, M.W. Diagnosis and classification of ulcerative colitis. Autoimmun. Rev. 2014, 13, 463–466. [Google Scholar] [CrossRef] [PubMed]
- Da Rio, L.; Spadaccini, M.; Parigi, T.L.; Gabbiadini, R.; Buono, A.D.; Busacca, A.; Maselli, R.; Fugazza, A.; Colombo, M.; Carrara, S.; et al. Artificial intelligence and inflammatory bowel disease: Where are we going? World J. Gastroenterol. 2023, 29, 508–520. [Google Scholar] [CrossRef]
- Diaconu, C.; State, M.; Birligea, M.; Ifrim, M.; Bajdechi, G.; Georgescu, T.; Mateescu, B.; Voiosu, T. The Role of Artificial Intelligence in Monitoring Inflammatory Bowel Disease-The Future Is Now. Diagnostics 2023, 13, 735. [Google Scholar] [CrossRef] [PubMed]
- Yu, Y.R.; Rodriguez, J.R. Clinical presentation of Crohn’s, ulcerative colitis, and indeterminate colitis: Symptoms, extraintestinal manifestations, and disease phenotypes. Semin. Pediatr. Surg. 2017, 26, 349–355. [Google Scholar] [CrossRef]
- Jiang, X.; Luo, X.; Nan, Q.; Ye, Y.; Miao, Y.; Miao, J. Application of deep learning in the diagnosis and evaluation of ulcerative colitis disease severity. Ther. Adv. Gastroenterol. 2023, 16, 17562848231215579. [Google Scholar] [CrossRef]
- Chen, X.; Jiang, L.; Han, W.; Bai, X.; Ruan, G.; Guo, M.; Zhou, R.; Liang, H.; Yang, H.; Qian, J. Artificial Neural Network Analysis-Based Immune-Related Signatures of Primary Non-Response to Infliximab in Patients With Ulcerative Colitis. Front. Immunol. 2021, 12, 742080. [Google Scholar] [CrossRef]
- Cheng, J.Y.; Abel, J.T.; Balis, U.G.J.; McClintock, D.S.; Pantanowitz, L. Challenges in the Development, Deployment, and Regulation of Artificial Intelligence in Anatomic Pathology. Am. J. Pathol. 2021, 191, 1684–1692. [Google Scholar] [CrossRef] [PubMed]
- Sarwar, S.; Dent, A.; Faust, K.; Richer, M.; Djuric, U.; Van Ommeren, R.; Diamandis, P. Physician perspectives on integration of artificial intelligence into diagnostic pathology. NPJ Digit. Med. 2019, 2, 28. [Google Scholar] [CrossRef]
- Rex, D.K. Making a resect-and-discard strategy work for diminutive colorectal polyps: Let’s get real. Endoscopy 2022, 54, 364–366. [Google Scholar] [CrossRef]
- Le Berre, C.; Honap, S.; Peyrin-Biroulet, L. Ulcerative colitis. Lancet 2023, 402, 571–584. [Google Scholar] [CrossRef] [PubMed]
- Stein, P. Ulcerative colitis—Diagnosis and surgical treatment. AORN J. 2004, 80, 243–266. [Google Scholar] [CrossRef] [PubMed]
- Ahmad, H.A.; East, J.E.; Panaccione, R.; Travis, S.; Canavan, J.B.; Usiskin, K.; Byrne, M.F. Artificial intelligence in inflammatory bowel disease: Implications for clinical practice and future directions. Intest. Res. 2023, 21, 283–294. [Google Scholar] [CrossRef]
- Sundaram, S.; Choden, T.; Mattar, M.C.; Desai, S.; Desai, M. Artificial intelligence in inflammatory bowel disease endoscopy: Current landscape and the road ahead. Ther. Adv. Gastrointest. Endosc. 2021, 14, 26317745211017809. [Google Scholar] [CrossRef]
- Ahmad, H.A.; East, J.E.; Panaccione, R.; Travis, S.; Canavan, J.B.; Usiskin, K.; Byrne, M.F. Artificial Intelligence in Inflammatory Bowel Disease Endoscopy: Implications for Clinical Trials. J. Crohns Colitis 2023, 17, 1342–1353. [Google Scholar] [CrossRef]
- Chang, Y.; Wang, Z.; Sun, H.B.; Li, Y.Q.; Tang, T.Y. Artificial Intelligence in Inflammatory Bowel Disease Endoscopy: Advanced Development and New Horizons. Gastroenterol. Res. Pract. 2023, 2023, 3228832. [Google Scholar] [CrossRef]
- Chen, G.; Shen, J. Artificial Intelligence Enhances Studies on Inflammatory Bowel Disease. Front. Bioeng. Biotechnol. 2021, 9, 635764. [Google Scholar] [CrossRef]
- Okagawa, Y.; Abe, S.; Yamada, M.; Oda, I.; Saito, Y. Artificial Intelligence in Endoscopy. Dig. Dis. Sci. 2022, 67, 1553–1572. [Google Scholar] [CrossRef] [PubMed]
- Park, S.K.; Kim, S.; Lee, G.Y.; Kim, S.Y.; Kim, W.; Lee, C.W.; Park, J.L.; Choi, C.H.; Kang, S.B.; Kim, T.O.; et al. Development of a Machine Learning Model to Distinguish between Ulcerative Colitis and Crohn’s Disease Using RNA Sequencing Data. Diagnostics 2021, 11, 2365. [Google Scholar] [CrossRef]
- Iacucci, M.; Parigi, T.L.; Del Amor, R.; Meseguer, P.; Mandelli, G.; Bozzola, A.; Bazarova, A.; Bhandari, P.; Bisschops, R.; Danese, S.; et al. Artificial Intelligence Enabled Histological Prediction of Remission or Activity and Clinical Outcomes in Ulcerative Colitis. Gastroenterology 2023, 164, 1180–1188.e2. [Google Scholar] [CrossRef]
- Gutierrez Becker, B.; Arcadu, F.; Thalhammer, A.; Serna, C.G.; Feehan, O.; Drawnel, F.; Oh, Y.S.; Prunotto, M. Training and deploying a deep learning model for endoscopic severity grading in ulcerative colitis using multicenter clinical trial data. Ther. Adv. Gastrointest. Endosc. 2021, 14, 2631774521990623. [Google Scholar] [CrossRef] [PubMed]
- Huang, T.Y.; Zhan, S.Q.; Chen, P.J.; Yang, C.W.; Lu, H.H. Accurate diagnosis of endoscopic mucosal healing in ulcerative colitis using deep learning and machine learning. J. Chin. Med. Assoc. 2021, 84, 678–681. [Google Scholar] [CrossRef] [PubMed]
- Najdawi, F.; Sucipto, K.; Mistry, P.; Hennek, S.; Jayson, C.K.B.; Lin, M.; Fahy, D.; Kinsey, S.; Wapinski, I.; Beck, A.H.; et al. Artificial Intelligence Enables Quantitative Assessment of Ulcerative Colitis Histology. Mod. Pathol. 2023, 36, 100124. [Google Scholar] [CrossRef] [PubMed]
- Bhambhvani, H.P.; Zamora, A. Deep learning enabled classification of Mayo endoscopic subscore in patients with ulcerative colitis. Eur. J. Gastroenterol. Hepatol. 2021, 33, 645–649. [Google Scholar] [CrossRef]
- Takenaka, K.; Kawamoto, A.; Okamoto, R.; Watanabe, M.; Ohtsuka, K. Artificial intelligence for endoscopy in inflammatory bowel disease. Intest. Res. 2022, 20, 165–170. [Google Scholar] [CrossRef]
- Sutton, R.T.; Zai Ane, O.R.; Goebel, R.; Baumgart, D.C. Artificial intelligence enabled automated diagnosis and grading of ulcerative colitis endoscopy images. Sci. Rep. 2022, 12, 2748. [Google Scholar] [CrossRef] [PubMed]
- Iacucci, M.; Cannatelli, R.; Parigi, T.L.; Nardone, O.M.; Tontini, G.E.; Labarile, N.; Buda, A.; Rimondi, A.; Bazarova, A.; Bisschops, R.; et al. A virtual chromoendoscopy artificial intelligence system to detect endoscopic and histologic activity/remission and predict clinical outcomes in ulcerative colitis. Endoscopy 2023, 55, 332–341. [Google Scholar] [PubMed]
- Hamamoto, Y.; Kawamura, M.; Uchida, H.; Hiramatsu, K.; Katori, C.; Asai, H.; Shimizu, S.; Egawa, S.; Yoshida, K. The Histological Detection of Ulcerative Colitis Using a No-Code Artificial Intelligence Model. Int. J. Surg. Pathol. 2023. [Google Scholar] [CrossRef] [PubMed]
- Yang, Y.; Hua, Y.; Zheng, H.; Jia, R.; Ye, Z.; Su, G.; Gu, Y.; Zhan, K.; Tang, K.; Qi, S.; et al. Biomarkers prediction and immune landscape in ulcerative colitis: Findings based on bioinformatics and machine learning. Comput. Biol. Med. 2024, 168, 107778. [Google Scholar] [CrossRef]
- Wang, Y.; Huang, J.; Zhang, J.; Wang, F.; Tang, X. Identifying biomarkers associated with the diagnosis of ulcerative colitis via bioinformatics and machine learning. Math. Biosci. Eng. 2023, 20, 10741–10756. [Google Scholar] [CrossRef]
- Li, Y.; Tang, M.; Zhang, F.J.; Huang, Y.; Zhang, J.; Li, J.; Wang, Y.; Yang, J.; Zhu, S. Screening of ulcerative colitis biomarkers and potential pathways based on weighted gene co-expression network, machine learning and ceRNA hypothesis. Hereditas 2022, 159, 42. [Google Scholar] [CrossRef] [PubMed]
- Khorasani, H.M.; Usefi, H.; Peña-Castillo, L. Detecting ulcerative colitis from colon samples using efficient feature selection and machine learning. Sci. Rep. 2020, 10, 13744. [Google Scholar] [CrossRef] [PubMed]
- Lu, J.; Wang, Z.; Maimaiti, M.; Hui, W.; Abudourexiti, A.; Gao, F. Identification of diagnostic signatures in ulcerative colitis patients via bioinformatic analysis integrated with machine learning. Hum. Cell 2022, 35, 179–188. [Google Scholar] [CrossRef]
- Moriichi, K.; Fujiya, M.; Okumura, T. The endoscopic diagnosis of mucosal healing and deep remission in inflammatory bowel disease. Dig. Endosc. 2021, 33, 1008–1023. [Google Scholar] [CrossRef] [PubMed]
- Colombel, J.F.; Rutgeerts, P.; Reinisch, W.; Esser, D.; Wang, Y.; Lang, Y.; Marano, C.W.; Strauss, R.; Oddens, B.J.; Feagan, B.G.; et al. Early mucosal healing with infliximab is associated with improved long-term clinical outcomes in ulcerative colitis. Gastroenterology 2011, 141, 1194–1201. [Google Scholar] [CrossRef] [PubMed]
- Hota, S.; Parascandola, S.; Smith, S.; Tampo, M.M.; Amdur, R.; Obias, V. Robotic and laparoscopic surgical techniques in patients with Crohn’s disease. Surg. Endosc. 2021, 35, 4602–4608. [Google Scholar] [CrossRef] [PubMed]
- Liu, X.Y.; Tang, H.; Zhou, Q.Y.; Zeng, Y.L.; Chen, D.; Xu, H.; Li, Y.; Tan, B.; Qian, J.M. Advancing the precision management of inflammatory bowel disease in the era of omics approaches and new technology. World J. Gastroenterol. 2023, 29, 272–285. [Google Scholar] [CrossRef] [PubMed]
- Liu, X.; Prasath, S.; Siddiqui, I.; Walters, T.D.; Denson, L.A.; Hyams, J.S.; Kugathasan, S.; Griffiths, A.M.; Collins, M.H.; Baldassano, R.N.; et al. Machine Learning—Based Prediction of Pediatric Ulcerative Colitis Treatment Response Using Diagnostic Histopathology. Gastroenterology 2024, 166, 921–924.e4. [Google Scholar] [CrossRef] [PubMed]
- Iacucci, M.; Maeda, Y.; Ghosh, S. A Baby Step or a Real Giant Stride: Histomic Enabled by Artificial Intelligence to Predict Treatment Response in Pediatric Patients with Ulcerative Colitis. Gastroenterology 2024, 166, 730–732. [Google Scholar] [CrossRef]
- Singh, S.; Fumery, M.; Sandborn, W.J.; Murad, M.H. Systematic review with network meta-analysis: First- and second-line pharmacotherapy for moderate-severe ulcerative colitis. Aliment. Pharmacol. Ther. 2018, 47, 162–175. [Google Scholar] [CrossRef]
- Danese, S.; Fiorino, G.; Peyrin-Biroulet, L.; Lucenteforte, E.; Virgili, G.; Moja, L.; Bonovas, S. Biological agents for moderately to severely active ulcerative colitis: A systematic review and network meta-analysis. Ann. Intern. Med. 2014, 160, 704–711. [Google Scholar] [CrossRef] [PubMed]
- Favale, A.; Onali, S.; Caprioli, F.; Pugliese, D.; Armuzzi, A.; Macaluso, F.S.; Orlando, A.; Viola, A.; Fries, W.; Rispo, A.; et al. Comparative Efficacy of Vedolizumab and Adalimumab in Ulcerative Colitis Patients Previously Treated With Infliximab. Inflamm. Bowel Dis. 2019, 25, 1805–1812. [Google Scholar] [CrossRef]
- Popa, I.V.; Burlacu, A.; Mihai, C.; Prelipcean, C.C. A Machine Learning Model Accurately Predicts Ulcerative Colitis Activity at One Year in Patients Treated with Anti-Tumour Necrosis Factor α Agents. Medicina 2020, 56, 628. [Google Scholar] [CrossRef]
- Miyoshi, J.; Maeda, T.; Matsuoka, K.; Saito, D.; Miyoshi, S.; Matsuura, M.; Okamoto, S.; Tamura, S.; Hisamatsu, T. Machine learning using clinical data at baseline predicts the efficacy of vedolizumab at week 22 in patients with ulcerative colitis. Sci. Rep. 2021, 11, 16440. [Google Scholar] [CrossRef] [PubMed]
- Chen, Y.; Guzauskas, G.F.; Gu, C.; Wang, B.C.M.; Furnback, W.E.; Xie, G.; Dong, P.; Garrison, L.P. Precision Health Economics and Outcomes Research to Support Precision Medicine: Big Data Meets Patient Heterogeneity on the Road to Value. J. Pers. Med. 2016, 6, 20. [Google Scholar] [CrossRef]
- Gardiner, L.J.; Carrieri, A.P.; Bingham, K.; Macluskie, G.; Bunton, D.; McNeil, M.; Pyzer-Knapp, E.O. Combining explainable machine learning, demographic and multi-omic data to inform precision medicine strategies for inflammatory bowel disease. PLoS ONE 2022, 17, e0263248. [Google Scholar] [CrossRef] [PubMed]
- Øresland, T.; Bemelman, W.A.; Sampietro, G.M.; Spinelli, A.; Windsor, A.; Ferrante, M.; Marteau, P.; Zmora, O.; Kotze, P.G.; Espin-Basany, E.; et al. European evidence based consensus on surgery for ulcerative colitis. J. Crohns Colitis 2015, 9, 4–25, Erratum in J. Crohns Colitis 2023, 17, 149. [Google Scholar] [CrossRef] [PubMed]
- Sofo, L.; Caprino, P.; Schena, C.A.; Sacchetti, F.; Potenza, A.E.; Ciociola, A. New perspectives in the prediction of postoperative complications for high-risk ulcerative colitis patients: Machine learning preliminary approach. Eur. Rev. Med. Pharmacol. Sci. 2020, 24, 12781–12787. [Google Scholar] [PubMed]
- Mizuno, S.; Okabayashi, K.; Ikebata, A.; Matsui, S.; Seishima, R.; Shigeta, K.; Kitagawa, Y. Prediction of pouchitis after ileal pouch-anal anastomosis in patients with ulcerative colitis using artificial intelligence and deep learning. Tech. Coloproctol. 2022, 26, 471–478. [Google Scholar] [CrossRef]
- Le Berre, C.; Sandborn, W.J.; Aridhi, S.; Devignes, M.-D.; Fournier, L.; Smaïl-Tabbone, M.; Danese, S.; Peyrin-Biroulet, L. Application of Artificial Intelligence to Gastroenterology and Hepatology. Gastroenterology 2020, 158, 76–94.e2. [Google Scholar] [CrossRef]
Study | Publication Year | Diagnostics or Therapeutics | Dataset Utilized | AI Model | Results | Conclusion |
---|---|---|---|---|---|---|
Becker et al. [21] | 2021 | Diagnostic | 1672 endoscopic videos | End-to-end computer-assisted diagnosis system based on deep learning | AUC = 0.84 for Mayo Clinic Endoscopic Subscore ≥1, 0.85 for ≥2, and 0.85 for ≥3), with reduced manual annotation required. | The evaluation on 1672 endoscopic videos from the etrolizumab Phase II Eucalyptus and Phase III Hickory and Laurel trials demonstrates high accuracy and robustness, which provides an increase in efficiency and standardization in the diagnosis of UC within a clinical setting. |
Bhambhvani HP et al. [24] | 2021 | Diagnostics | 777 Still images of endoscopies | 101-layer convolutional neural network model | The model achieved AUCs of 0.96 for MES 3, 0.86 for MES 2, and 0.89 for MES 1 classifications, with an overall accuracy of 77.2%. Across the MES categories, it showed an average specificity of 85.7%, a sensitivity of 72.4%, a PPV of 77.7%, and an NPV of 87.0%. | They have illustrated the robust capability of a deep learning model to effectively classify different grades of endoscopic disease severity in ulcerative colitis patients. |
Sutton et al. [26] | 2022 | Diagnostics | 8000 labelled endoscopic still images derived from HyperKvasir |
| The DenseNet121 architecture achieved the highest accuracy (87.50%) and Area Under the Curve (AUC) (0.90), surpassing the majority class prediction (‘no skill’ model), which attained 72.02% accuracy and 0.50 AUC. | They achieved moderate-to-good performance, distinguishing between mild and moderate-to-severe ulcerative colitis (UC), using a relatively small public dataset of endoscopy images. This achievement is notable, considering that images with global labels, such as Mayo endoscopic subscores, typically necessitate larger datasets to achieve satisfactory performance. |
Iacucci et al. [20] | 2023 | Diagnostic | 535 digitalized biopsies | VGG16 CNN | The system effectively distinguished between histological activity and remission, achieving sensitivities and specificities of 89% and 85% (PHRI), 94% and 76% (Robarts Histological Index), and 89% and 79% (Nancy Histological Index), respectively. Moreover, it accurately predicted endoscopic remission/activity with 79% and 82% accuracy for UC endoscopic index of severity and Paddington International virtual ChromoendoScopy ScOre, respectively. The hazard ratios for disease flare-up between histological activity and remission groups were 3.56 for PHRI assessed by pathologists and 4.64 for AI-assessed PHRI. | The CAD system accurately differentiated between disease remission and activity, as defined by the PHRI, RHI, and NHI, in real-time. Additionally, it effectively predicted corresponding endoscopic activity and assessed the risk of flare-up. |
Iacucci et al. [27] | 2023 | Diagnostic | 1090 endoscopic videos | ResNet50 CNN | The AI system detected endoscopic remission (UCEIS ≤ 1) in WLE videos with 72% sensitivity, 87% specificity, and an AUROC of 0.85. For VCE videos (PICaSSO ≤ 3), sensitivity was 79%, specificity 95%, and AUROC 0.94. | The system effectively differentiated between endoscopic remission/activity and predicted HR and clinical outcomes from colonoscopy videos. It represents the inaugural computer model designed to detect inflammation/healing on VCE using PICaSSO and the pioneering computer tool offering comprehensive clinical, endoscopic and histologic assessments. |
Yang et al. [29] | 2023 | Diagnostics | The gene expression profiles were obtained from the GEO database and subsequently received preprocessing and normalization using R software. |
| Through the intersection of LASSO, RF, and WGCNA results, 8 signature genes were discerned: TCN1, S100A8, DUOX2, CXCL1, IL-1B, SLC6A14, GREM1, and MMP10. | Credible potential biomarkers for the diagnosis and therapy of UC were identified through the discovery of 8 signature genes. These biomarkers are integral to the immune response underlying the onset and progression of UC, facilitated by reciprocal interactions between the signature biomarkers and immune-infiltrated cells. |
Wang et al. [30] | 2023 | Diagnostic | Two datasets were merged to obtain 193 UC samples and 42 normal samples. |
| In our analysis, 102 differentially expressed genes (DEGs) were identified, with 64 showing significant upregulation and 38 exhibiting significant downregulation. Machine learning methods and ROC tests validated DUOX2, DMBT1, CYP2B7P, PITX2, and DEFB1 as pivotal diagnostic genes for UC. | Prospective biomarkers for UC, including DUOX2, DMBT1, CYP2B7P, PITX2, and DEFB1, were identified. These biomarkers, along with their associations with immune cell infiltration, may offer a novel perspective on understanding the progression of UC. |
Li et al. [31] | 2022 | Diagnostic | The GEO database was used to obtain gene data sets. |
| A total of 107 differentially expressed genes were identified, predominantly linked to biological functions like humoral immune response and inflammatory response. From this set, five marker genes were meticulously screened, revealing associations with M0 macrophages, quiescent mast cells, M2 macrophages, and activated NK cells in terms of immune cell infiltration. | The study identified five biomarkers—IRAK3, HMGCS2, APOBEC3B, SLC6A14, and TIMP1—as potential aids in the diagnosis and treatment of UC. It verified their involvement in the onset and advancement of UC through immune infiltration analysis and proposed a potential RNA regulatory pathway governing UC progression. |
Khorasani et al. [32] | 2020 | Diagnostic | The NCBI Gene Expression Omnibus database (GEO) was utilised for expression profiling studies using colonic samples from UC subjects |
| Achieving flawless detection of all active cases, the model exhibited an average precision of 0.62 in identifying inactive cases. This performance was benchmarked against results from prior studies and a machine learning-based biomarker discovery tool, BioDiscML, recently introduced into the scientific field. | In terms of average precision, the final model for detecting UC demonstrates superior performance. |
Jiang et a [6] | 2023 | Diagnostics | 12,257 endoscopic images | Inception-ResNet-v2 | The MES-CNN model attained an accuracy of 97.04% in diagnosing endoscopic remission in UC cases. Additionally, the MES-CNN and UCEIS-CNN models demonstrated accuracies of 90.15% and 85.29%, respectively, in evaluating the endoscopic severity of UC. In predicting histological remission, CNN models achieved accuracy and kappa values of 91.28% and 0.826, respectively, surpassing the accuracy achieved by human endoscopists (87.69%). | Based on evaluations of MES and UCEIS by expert gastroenterologists, the proposed artificial intelligence model provides accurate assessments of inflammation in UC endoscopic images. Furthermore, it demonstrates reliable predictive capability for histological remission |
Chen et al. [7] | 2021 | Therapeutics | Independent GEO dataset. | ANN | The study suggests that a combination of six genes—CDX2, CHP2, HSD11B2, RANK, NOX4, and VDR—accurately predicts patients’ response to IFX therapy, with a repeated overall AUC ranging from 0.850 ± 0.103. The validation using an independent GEO dataset confirms the predictive value of these genes, with an overall AUC range of 0.759 ± 0.065 for forecasting patient non-response (PNR) to IFX. | The study established a correlation between RNA and protein models, with both being accessible. However, the composite signature of VDR and RANK proves more favourable for clinical application. This composite signature could potentially guide the pre-selection of patients likely to benefit from pharmacological treatment in the future. |
Popa et al. [43] | 2020 | Therapeutics | 55 UC Patients | Multi-layered Perceptron Neural Network Model | The classifier demonstrated outstanding performance in predicting disease activity at one year. On the test set, it achieved an accuracy of 90% and an AUC of 0.92. Meanwhile, on the validation set, it attained a perfect accuracy of 100% and an AUC of 1. | After validation on independent external patient cohorts, the ML solution could serve as a valuable tool for clinicians, aiding them in decisions regarding dosage adjustments or transitions to alternative biologic agents. |
Gardiner et al. [46] | 2022 | Therapeutics | 25 patient organoculture assay data sets |
| The top-performing model accurately predicted TNFα levels using demographic, medicinal and genomic features, achieving a remarkably low error rate of only 4.98% on unseen patients. Additionally, the findings revealed differences in drug effectiveness, as measured by ex vivo assays, among patients based on gender, age or condition. Moreover, new genetic polymorphisms were identified, highlighting their role in influencing variations in patient response to the anti-inflammatory treatment BIRB796 (Doramapimod). | They showcased the promise of merging preclinical functional assessments of drug effectiveness and inter-patient variability in drug response. By integrating cutting-edge omics, bioinformatics and ML/AI methodologies, they introduced a novel approach to crafting precision medicine strategies during the initial phases of drug development. |
Miyoshi et al. [44] | 2021 | Therapeutics | 34 Patients | RF | During validation with external Cohort 2, the prediction model exhibited positive and negative predictive values of 54.5% and 92.3%, respectively. This tool proved valuable in identifying UC patients unlikely to achieve SFCR at week 22 while undergoing VDZ therapy. | This study demonstrates the feasibility of personalized treatment for UC through machine learning with real-world data, serving as a proof-of-concept. |
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Uchikov, P.; Khalid, U.; Vankov, N.; Kraeva, M.; Kraev, K.; Hristov, B.; Sandeva, M.; Dragusheva, S.; Chakarov, D.; Petrov, P.; et al. The Role of Artificial Intelligence in the Diagnosis and Treatment of Ulcerative Colitis. Diagnostics 2024, 14, 1004. https://doi.org/10.3390/diagnostics14101004
Uchikov P, Khalid U, Vankov N, Kraeva M, Kraev K, Hristov B, Sandeva M, Dragusheva S, Chakarov D, Petrov P, et al. The Role of Artificial Intelligence in the Diagnosis and Treatment of Ulcerative Colitis. Diagnostics. 2024; 14(10):1004. https://doi.org/10.3390/diagnostics14101004
Chicago/Turabian StyleUchikov, Petar, Usman Khalid, Nikola Vankov, Maria Kraeva, Krasimir Kraev, Bozhidar Hristov, Milena Sandeva, Snezhanka Dragusheva, Dzhevdet Chakarov, Petko Petrov, and et al. 2024. "The Role of Artificial Intelligence in the Diagnosis and Treatment of Ulcerative Colitis" Diagnostics 14, no. 10: 1004. https://doi.org/10.3390/diagnostics14101004
APA StyleUchikov, P., Khalid, U., Vankov, N., Kraeva, M., Kraev, K., Hristov, B., Sandeva, M., Dragusheva, S., Chakarov, D., Petrov, P., Dobreva-Yatseva, B., & Novakov, I. (2024). The Role of Artificial Intelligence in the Diagnosis and Treatment of Ulcerative Colitis. Diagnostics, 14(10), 1004. https://doi.org/10.3390/diagnostics14101004