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Evolution of the liver biopsy and its future
Dhanpat Jain 1 , Richard Torres 2 , Romulo Celli 1 , Jeremy Koelmel 3 , Georgia Charkoftaki 3 , Vasilis Vasiliou 3
Affiliations
Affiliations
1
Department of Anatomic Pathology, Yale University School of Medicine, New Haven, CT, USA.
2
Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA.
3
Department of Environmental Health Sciences, Yale School of Public Health, New Haven, CT, USA.
PMID: 33824924 PMCID: PMC7829074 DOI: 10.21037/tgh.2020.04.01
Abstract
Liver biopsies are commonly used to evaluate a wide variety of medical disorders, including neoplasms and post-transplant complications. However, its use is being impacted by improved clinical diagnosis of disorders, and non-invasive methods for evaluating liver tissue and as a result the indications of a liver biopsy have undergone major changes in the last decade. The evolution of highly effective treatments for some of the common indications for liver biopsy in the last decade (e.g., viral hepatitis B and C) has led to a decline in the number of liver biopsies in recent years. At the same time, the emergence of better technologies for histologic evaluation, tissue content analysis and genomics are among the many new and exciting developments in the field that hold great promise for the future and are going to shape the indications for a liver biopsy in the future. Recent advances in slide scanners now allow creation of "digital/virtual" slides that have image of the entire tissue section present in a slide [whole slide imaging (WSI)]. WSI can now be done very rapidly and at very high resolution, allowing its use in routine clinical practice. In addition, a variety of technologies have been developed in recent years that use different light sources and/or microscopes allowing visualization of tissues in a completely different way. One such technique that is applicable to liver specimens combines multiphoton microscopy (MPM) with advanced clearing and fluorescent stains known as Clearing Histology with MultiPhoton Microscopy (CHiMP). Although it has not yet been extensively validated, the technique has the potential to decrease inefficiency, reduce artifacts, and increase data while being readily integrable into clinical workflows. Another technology that can provide rapid and in-depth characterization of thousands of molecules in a tissue sample, including liver tissues, is matrix assisted laser desorption/ionization (MALDI) mass spectrometry. MALDI has already been applied in a clinical research setting with promising diagnostic and prognostic capabilities, as well as being able to elucidate mechanisms of liver diseases that may be targeted for the development of new therapies. The logical next step in huge data sets obtained from such advanced analysis of liver tissues is the application of machine learning (ML) algorithms and application of artificial intelligence (AI), for automated generation of diagnoses and prognoses. This review discusses the evolving role of liver biopsies in clinical practice over the decades, and describes newer technologies that are likely to have a significant impact on how they will be used in the future.
Keywords: Clearing Histology with MultiPhoton Microscopy (CHiMP); Liver biopsy; matrix assisted laser desorption imaging (MALDI); whole slide imaging (WSI).
2021 Translational Gastroenterology and Hepatology. All rights reserved. |
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