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10.1097/MOG.0000000000000352

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suck abstract from ncbi


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pmid28257308
      Curr+Opin+Gastroenterol 2017 ; 33 (3 ): 149-157
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  • Emerging pharmacologic therapies for primary sclerosing cholangitis #MMPMID28257308
  • Cheung AC ; Lazaridis KN ; LaRusso NF ; Gores GJ
  • Curr Opin Gastroenterol 2017[May]; 33 (3 ): 149-157 PMID28257308 show ga
  • PURPOSE OF REVIEW: The only currently approved treatment for primary sclerosing cholangitis (PSC) is liver transplantation, with a median time to transplant of 12-18 years after diagnosis. There are a number of emerging drugs that have the potential to meet this critically unmet need that will be summarized and discussed herein. RECENT FINDINGS: Although the cause of PSC is unknown, there are a number of novel therapeutics under development. These drugs target presumed pathogenic mechanisms largely extrapolated from ex-vivo and in-vivo preclinical models, as well as translational observations. SUMMARY: Future therapeutic strategies for PSC may include a multitude of complex pathogenic mechanisms encompassing pathways of immunomodulation, the microbiome and inflammation-related fibrosis.
  • |Anti-Bacterial Agents/therapeutic use [MESH]
  • |Chenodeoxycholic Acid/analogs & derivatives/therapeutic use [MESH]
  • |Cholangitis, Sclerosing/*drug therapy/microbiology [MESH]
  • |Clinical Trials as Topic/methods [MESH]
  • |Fecal Microbiota Transplantation [MESH]
  • |Fibric Acids/therapeutic use [MESH]
  • |Gastrointestinal Microbiome/drug effects [MESH]
  • |Humans [MESH]
  • |Immunologic Factors/therapeutic use [MESH]
  • |Molecular Targeted Therapy/*methods/trends [MESH]
  • |Organic Anion Transporters, Sodium-Dependent/antagonists & inhibitors [MESH]
  • |Probiotics/therapeutic use [MESH]
  • |Symporters/antagonists & inhibitors [MESH]


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