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The development of artificial intelligence in the histological diagnosis of Inflammatory Bowel Disease (IBD-AI).
Furlanello, Cesare; Bussola, Nicole; Merzi, Nicolò; Pievani Trapletti, Giovanni; Cadei, Moris; Del Sordo, Rachele; Sidoni, Angelo; Ricci, Chiara; Lanzarotto, Francesco; Parigi, Tommaso Lorenzo; Villanacci, Vincenzo.
Afiliación
  • Furlanello C; Orobix Life, Bergamo, Italy; LIGHT Center, Brescia, Italy.
  • Bussola N; Orobix Life, Bergamo, Italy.
  • Merzi N; Orobix Life, Bergamo, Italy.
  • Pievani Trapletti G; Orobix Life, Bergamo, Italy.
  • Cadei M; Institute of Pathology, ASST Spedali Civili and University of Brescia, Brescia, Italy.
  • Del Sordo R; Department of Medicine and Surgery, Section of Anatomic Pathology and Histology, Medical School, University of Perugia, Perugia, Italy.
  • Sidoni A; Department of Medicine and Surgery, Section of Anatomic Pathology and Histology, Medical School, University of Perugia, Perugia, Italy.
  • Ricci C; Gastroenterology Unit, Clinical and Experimental Sciences Department, Spedali Civili Hospital, University of Brescia, Brescia, Italy.
  • Lanzarotto F; Gastroenterology Unit, Clinical and Experimental Sciences Department, Spedali Civili Hospital, University of Brescia, Brescia, Italy.
  • Parigi TL; Division of Immunology, Transplantation and Infectious Disease, University Vita-Salute San Raffaele, Milan, Italy.
  • Villanacci V; Institute of Pathology, ASST Spedali Civili and University of Brescia, Brescia, Italy. Electronic address: villanac@alice.it.
Dig Liver Dis ; 2024 Jun 08.
Article en En | MEDLINE | ID: mdl-38853093
ABSTRACT

BACKGROUND:

Inflammatory bowel disease (IBD) includes Crohn's Disease (CD) and Ulcerative Colitis (UC). Correct diagnosis requires the identification of precise morphological features such basal plasmacytosis. However, histopathological interpretation can be challenging, and it is subject to high variability.

AIM:

The IBD-Artificial Intelligence (AI) project aims at the development of an AI-based evaluation system to support the diagnosis of IBD, semi-automatically quantifying basal plasmacytosis.

METHODS:

A deep learning model was trained to detect and quantify plasma cells on a public dataset of 4981 annotated images. The model was then tested on an external validation cohort of 356 intestinal biopsies of CD, UC and healthy controls. AI diagnostic performance was calculated compared to human gold standard.

RESULTS:

The system correctly found that CD and UC samples had a greater prevalence of basal plasma cells with mean number of PCs within ROIs of 38.22 (95 % CI 31.73, 49.04) for CD, 55.16 (46.57, 65.93) for UC, and 17.25 (CI 12.17, 27.05) for controls. Overall, OR=4.968 (CI 1.835, 14.638) was found for IBD compared to normal mucosa (CD +59 %; UC +129 %). Additionally, as expected, UC samples were found to have more plasma cells in colon than CD cases.

CONCLUSION:

Our model accurately replicated human assessment of basal plasmacytosis, underscoring the value of AI models as a potential aid IBD diagnosis.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Dig Liver Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Dig Liver Dis Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Italia