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Published January 1, 2025 | Version v1
Journal article Open

Investigating hepatic fibrosis heterogeneity by three-dimensional imaging in metabolic dysfunction-associated steatotic liver disease

Creators

  • 1. Koc Univ, Sch Med, Dept Gastroenterol & Hepatol, TR-34010 Istanbul, Turkiye
  • 2. Koc Univ, Dept Phys, TR-34450 Istanbul, Turkiye
  • 3. Koc Univ, Sch Med, Dept Neurol, TR-34010 Istanbul, Turkiye
  • 4. Fatih Sultan Mehmet Vakif Univ, Dept Comp Engn, TR-34083 Istanbul, Turkiye
  • 5. Koc Univ, Grad Sch Hlth Sci, TR-34010 Istanbul, Turkiye
  • 6. Acibadem Univ, Fac Med, Dept Gen Surg, TR-34752 Istanbul, Turkiye
  • 7. Koc Univ, Sch Med, Dept Gen Surg, TR-34010 Istanbul, Turkiye
  • 8. Koc Univ, Sch Med, Dept Histol & Embryol, TR-34010 Istanbul, Turkiye
  • 9. Acibadem Univ, Fac Med, Dept Pathol, TR-34752 Istanbul, Turkiye

Description

Although liver biopsy is a well-established technique to assess fibrosis it has several limitations, including invasive nature, semi-quantitative assessment methods, significant sampling and observer variability, making precise assessment of hepatic fibrosis challenging. Accurate and reliable modalities are crucial for clinical trials to characterize hepatic fibrosis monitorization effectively. We aimed to perform 3-dimensional imaging of optically transparent liver samples by light-sheet microscopy (LSM) to quantify extracellular matrix (ECM) proteins. Fifty-seven MASLD, thirty-eight chronic hepatitis patients and twelve healthy individuals were included. Liver tissues were cleared with a CLARITY method. 3D imaging of ECM was performed via the newly developed LSM. Collagen Proportionate Volume (CPV) and Elastin Proportionate Volume (EPV) values were calculated by analysis of over 200 sections per sample through morphometry. We have optimized a method which achieves transparency of liver tissues in advanced fibrotic stages of MASLD and optimized non-destructive slide-free fibrosis pathology of whole fresh and FFPE liver biopsy samples. Cut-off values for CPV and EPV were established for fibrotic stages. CPV and EPV analysis showed a considerable optical section heterogeneity resulting in a fibrosis stage of variance within the sample. Volumetric image analysis for fibrosis staging revealed that only 44% and 47% of optical sections would be staged the same for F3 and F4, respectively. For the first time, our findings demonstrate a novel method of analyzing 3D digital pathology of liver fibrosis using in-house LSM. Volumetric imaging of whole liver biopsy samples showed that fibrosis heterogeneity occurs even in different sections.

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