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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 523A<br />

64% with an average intensity of 1.7 + 0.9 (scale 1-4). Over<br />

90% of participants were willing to donate biospecimens and<br />

be contacted for clinical research. Conclusions: Participants in<br />

the PSC Partners Registry are similar to other cohorts but are<br />

majority female, more symptomatic, and are a resource for<br />

future research.<br />

for PBC, a clear and important unmet need persists, as corroborated<br />

by variable UDCA response. The ongoing unmet need<br />

for PSC is striking, despite widespread UDCA use, and in the<br />

face of rising rates of transplantation for other liver diseases.<br />

Table 1. Comparison of Confirmed versus Unconfirmed PSC<br />

Cases<br />

Disclosures:<br />

Gregory T. Everson - Advisory Committees or Review Panels: Roche/Genentech,<br />

Abbvie, Galectin, Boehringer-Ingelheim, Eisai, Bristol-Myers Squibb, HepC<br />

Connection, BioTest, Gilead, Merck; Board Membership: HepQuant LLC, PSC<br />

Partners, HepQuant LLC; Consulting: Abbvie, BMS, Gilead, Bristol-Myers Squibb;<br />

Grant/Research Support: Roche/Genentech, Pharmassett, Vertex, Abbvie, Bristol-Myers<br />

Squibb, Merck, Eisai, Conatus, PSC Partners, Vertex, Tibotec, GlobeImmune,<br />

Pfizer, Gilead; Management Position: HepQuant LLC, HepQuant LLC;<br />

Patent Held/Filed: Univ of Colorado; Speaking and Teaching: Abbvie, Gilead<br />

Christopher L. Bowlus - Advisory Committees or Review Panels: Gilead Sciences,<br />

Inc; Grant/Research Support: Gilead Sciences, Inc, Intercept Pharmaceuticals,<br />

Bristol Meyers Squibb, Takeda, Lumena, Merck; Speaking and Teaching: Gilead<br />

Sciences, Inc<br />

The following authors have nothing to disclose: Rachel Gomel, Ricky Safer, Jesse<br />

A. King, Estella M. Geraghty, Keith D. Lindor<br />

631<br />

Cholestatic liver disease and liver transplantation in the<br />

UK: a twenty year review<br />

Gwilym Webb 1,2 , James W. Ferguson 2 , David Jones 4 , James Neuberger<br />

2,3 , Gideon Hirschfield 1,2 ; 1 NIHR Centre for Liver Research,<br />

University of Birmingham, Birmingham, United Kingdom; 2 Hepatology,<br />

Queen Elizabeth Hospital, Birmingham, United Kingdom;<br />

3 NHS Blood and Transplant, Bristol, United Kingdom; 4 Newcastle<br />

University, Newcastle, United Kingdom<br />

Background: Primary biliary cirrhosis (PBC) and primary sclerosing<br />

cholangitis (PSC) represent major indications for orthotopic<br />

liver transplantation (OLT). Ursodeoxycholic acid (UDCA) has<br />

been prescribed in the UK for most patients with PBC and PSC,<br />

with consensus for efficacy only in PBC. Aim: To analyse transplant<br />

listing and transplantation for PBC and PSC over the last<br />

20 years of UK-wide practice. Results: We analysed national<br />

transplant registry data for 1995 to 2014 inclusive. Records for<br />

12,935 listings and 10,512 OLTs were reviewed. Listings for<br />

all indications increased from 494 to 976/year (21.2±2.3/<br />

year; r 2 =0.82; p

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