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2017 ; 33
(3
): 149-157
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gab.com Text
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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]