AI Article Synopsis

  • Celiac Disease (CD) is an autoimmune disorder triggered by gluten, leading to malnutrition and developmental issues in children, while Environmental Enteropathy (EE) also causes malnutrition due to barrier dysfunction, but is linked to infections, especially in low-income regions.
  • Both conditions require tissue biopsy for diagnosis, but they share similar histopathological features, making differentiation challenging.
  • The study introduces a convolutional neural network (CNN) to classify duodenal biopsy images, achieving high accuracy rates for identifying CD, EE, and healthy controls, demonstrating its effectiveness in medical diagnostics.

Article Abstract

Celiac Disease (CD) and Environmental Enteropathy (EE) are common causes of malnutrition and adversely impact normal childhood development. CD is an autoimmune disorder that is prevalent worldwide and is caused by an increased sensitivity to gluten. Gluten exposure destructs the small intestinal epithelial barrier, resulting in nutrient mal-absorption and childhood under-nutrition. EE also results in barrier dysfunction but is thought to be caused by an increased vulnerability to infections. EE has been implicated as the predominant cause of under-nutrition, oral vaccine failure, and impaired cognitive development in low-and-middle-income countries. Both conditions require a tissue biopsy for diagnosis, and a major challenge of interpreting clinical biopsy images to differentiate between these gastrointestinal diseases is striking histopathologic overlap between them. In the current study, we propose a convolutional neural network (CNN) to classify duodenal biopsy images from subjects with CD, EE, and healthy controls. We evaluated the performance of our proposed model using a large cohort containing 1000 biopsy images. Our evaluations show that the proposed model achieves an area under ROC of 0.99, 1.00, and 0.97 for CD, EE, and healthy controls, respectively. These results demonstrate the discriminative power of the proposed model in duodenal biopsies classification.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536862PMC
http://dx.doi.org/10.1007/978-3-030-32520-6_55DOI Listing

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