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A novel machine learning-based radiomic model for diagnosing high bleeding risk esophageal varices in cirrhotic patients

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Abstract

Background and aim

To develop and validate a novel machine learning-based radiomic model (RM) for diagnosing high bleeding risk esophageal varices (HREV) in patients with cirrhosis.

Methods

A total of 796 qualified participants were enrolled. In training cohort, 218 cirrhotic patients with mild esophageal varices (EV) and 240 with HREV RM were included to training and internal validation groups. Additionally, 159 and 340 cirrhotic patients with mild EV and HREV RM, respectively, were used for external validation. Interesting regions of liver, spleen, and esophagus were labeled on the portal venous-phase enhanced CT images. RM was assessed by area under the receiver operating characteristic curves (AUROC), sensitivity, specificity, calibration and decision curve analysis (DCA).

Results

The AUROCs for mild EV RM in training and internal validation were 0.943 and 0.732, sensitivity and specificity were 0.863, 0.773 and 0.763, 0.763, respectively. The AUROC, sensitivity, and specificity were 0.654, 0.773 and 0.632, respectively, in external validation. Interestingly, the AUROCs for HREV RM in training and internal validation were 0.983 and 0.834, sensitivity and specificity were 0.948, 0.916 and 0.977, 0.969, respectively. The related AUROC, sensitivity and specificity were 0.736, 0.690 and 0.762 in external validation. Calibration and DCA indicated RM had good performance. Compared with Baveno VI and its expanded criteria, HREV RM had a higher accuracy and net reclassification improvements that were as high as 49.0% and 32.8%.

Conclusion

The present study developed a novel non-invasive RM for diagnosing HREV in cirrhotic patients with high accuracy. However, this RM still needs to be validated by a large multi-center cohort.

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Availability of data and material

The datasets used and analyzed during the current study are available from the corresponding author.

Abbreviations

ALB:

Albumin

ALT:

Alanine aminotransferase

AST:

Aspartate aminotransferase

AUROC:

Under the receiver operating characteristic curves

Cr:

Creatinine

CT:

Computed tomography

DCA:

Decision curve analysis

DCE:

Dynamic contrast enhancement

EV:

Esophageal varices

HOG:

Histogram of oriented gradient

HREV:

High-risk esophageal varices

HVPG:

Hepatic venous pressure gradient

INR:

International normalized ratio

NRI:

Net reclassification improvement

PCA:

Principal components analysis

PLT:

Platelets counts

PT:

Prothrombin time

PTA:

Prothrombin time activity

RM:

Radiomic model

ROI:

Regions of interest

SVM:

Support vector machine

TB:

Total bilirubin

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Funding

This study was supported by the State Key Projects Specialized on Infectious Diseases (No. 2017ZX10203202-004), Digestive Medical Coordinated Development Center of Beijing Hospitals Authority (No. XXT24 and XXZ0801) and Sino-German Cooperation Group (No. GZ1517).

Author information

Authors and Affiliations

Authors

Contributions

YY, YL and CF were contributed equally to collecting the data, development and validation RM. HD designed the project and was in charge of the manuscript. ZD and KH performed the language polishing and scientific editing. LL and HD were contributed equally to writing and editing. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Lei Li or Huiguo Ding.

Ethics declarations

Conflict of interest

Yijie Yan, Yue Li, Chunlei Fan, Yuening Zhang, Shibin Zhang, Zhi Wang, Tehui Huang, Zhenjia Ding, Keqin Hu, Lei Li, and Huiguo Ding declare no conflict of interest.

Ethics statements

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008.

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Yan, Y., Li, Y., Fan, C. et al. A novel machine learning-based radiomic model for diagnosing high bleeding risk esophageal varices in cirrhotic patients. Hepatol Int 16, 423–432 (2022). https://doi.org/10.1007/s12072-021-10292-6

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  • DOI: https://doi.org/10.1007/s12072-021-10292-6

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