AI Article Synopsis

  • Cholestasis is a condition where bile flow from the liver to the small intestine is disrupted, leading to similar symptoms across different causes.
  • Researchers analyzed the liver protein profiles of cholestatic patients and found 263 proteins that were expressed differently between healthy individuals and those with cholestasis, highlighting the molecular changes involved.
  • A machine learning approach was used to identify 20 key proteins that can effectively differentiate between various types of cholestasis, offering promising insights for tailored treatment strategies in precision medicine.

Article Abstract

Cholestasis is characterized by disrupted bile flow from the liver to the small intestine. Although etiologically different cholestasis displays similar symptoms, diverse factors can contribute to the progression of the disease and determine the appropriate therapeutic option. Therefore, stratifying cholestatic patients is essential for the development of tailor-made treatment strategies. Here, we have analyzed the liver proteome from cholestatic patients of different etiology. In total, 7161 proteins were identified and quantified, of which 263 were differentially expressed between control and cholestasis groups. These differential proteins point to deregulated cellular processes that explain part of the molecular framework of cholestasis progression. However, the clustering of different cholestasis types was limited. Therefore, a machine learning pipeline was designed to identify a panel of 20 differential proteins that segregate different cholestasis groups with high accuracy and sensitivity. In summary, proteomics combined with machine learning algorithms provides valuable insights into the molecular mechanisms of cholestasis progression and a panel of proteins to discriminate across different types of cholestasis. This strategy may prove useful in developing precision medicine approaches for patient care.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11011353PMC
http://dx.doi.org/10.3390/ijms25073684DOI Listing

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