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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 793A<br />

could potentially select F0–2 treatment-naïve G4 patients suitable<br />

to shorten SMV+PR therapy to 12 weeks.<br />

Disclosures:<br />

Tarik Asselah - Consulting: Jannsen, AbbVie, Achillion, BMS, Gilead, Merck,<br />

Roche; Speaking and Teaching: Jannsen, AbbVie, Achillion, BMS, Gilead,<br />

Merck, Roche<br />

Christophe Moreno - Consulting: Abbvie, Janssen, Gilead, BMS; Grant/Research<br />

Support: Janssen, Gilead, Roche, Astellas<br />

Christoph Sarrazin - Advisory Committees or Review Panels: Bristol-Myers<br />

Squibb, Janssen, Merck/MSD, Gilead, Roche, Abbvie, Janssen, Merck/MSD;<br />

Consulting: Merck/MSD, Merck/MSD; Grant/Research Support: Abbott, Roche,<br />

Merck/MSD, Gilead, Janssen, Abbott, Roche, Merck/MSD, Qiagen; Speaking<br />

and Teaching: Gilead, Novartis, Abbott, Roche, Merck/MSD, Janssen, Siemens,<br />

Falk, Abbvie, Bristol-Myers Squibb, Achillion, Abbott, Roche, Merck/MSD, Janssen<br />

Michael Gschwantler - Advisory Committees or Review Panels: Janssen, BMS,<br />

Gilead, AbbVie; Speaking and Teaching: Janssen, BMS, Gilead, AbbVie<br />

Graham R. Foster - Advisory Committees or Review Panels: GlaxoSmithKline,<br />

Novartis, Boehringer Ingelheim, Tibotec, Chughai, Gilead, Janssen, Idenix,<br />

GlaxoSmithKline, Novartis, Roche, Tibotec, Chughai, Gilead, Merck, Janssen,<br />

Idenix, BMS; Board Membership: Boehringer Ingelheim; Grant/Research Support:<br />

Chughai, Roche, Chughai; Speaking and Teaching: Roche, Gilead, Tibotec,<br />

Merck, BMS, Boehringer Ingelheim, Gilead, Janssen<br />

Peter Buggisch - Advisory Committees or Review Panels: Janssen, AbbVie, BMS;<br />

Speaking and Teaching: Roche, MSD, Gilead, Merz Pharma<br />

Faisal M. Sanai - Advisory Committees or Review Panels: Merck Sharpe Dohme,<br />

Bristol Myers Squibb, Janssen Pharmaceuticals, Gilead Sciences; Grant/<br />

Research Support: Roche Pharmaceuticals, Bristol Myers Squibb; Speaking and<br />

Teaching: Roche Pharmaceuticals, Janssen Pharmaceuticals, Gilead Sciences,<br />

Bayer Schering<br />

Robert Ryan - Employment: Janssen Pharmaceuticals; Stock Shareholder: Janssen<br />

Pharmaceutical<br />

Oliver Lenz - Employment: Janssen; Stock Shareholder: Janssen (J&J)<br />

Gino Van Dooren - Stock Shareholder: Johnson and Johnson<br />

Isabelle Londjon-Domanec - Employment: Janssen<br />

Catherine Nalpas - Employment: Janssen pharmaceuticals<br />

Michael Schlag - Employment: Janssen Cilag Pharma; Stock Shareholder: Johnson<br />

& Johnson<br />

Maria Buti - Advisory Committees or Review Panels: Gilead, Janssen, MSD;<br />

Grant/Research Support: Gilead, Janssen; Speaking and Teaching: Gilead,<br />

Janssen, BMS<br />

The following authors have nothing to disclose: Antonio Craxi<br />

1180<br />

Rapid drop in serum glucose and hypoglycemia in<br />

chronic hepatitis C patients with diabetes during oral<br />

HCV therapy<br />

Laura M. Benítez-Gutiérrez 1 , Vincent Soriano 2 , Isabella Esposito 1 ,<br />

Pablo Barreiro 2 , Ana Maria Duca 1 , Silvia Requena 1 , Isolina<br />

Baños 1 , Ana Treviño 1 , Valentin Cuervas-Mons 1 , Carmen de Mendoza<br />

1 ; 1 Internal Medicine, Hospital Universitario Puerta de Hierro<br />

Majadahonda, Madrid, Spain; 2 Infectious Disease Unit,, La Paz<br />

University Hospital & IdiPAZ, Madrid, Spain<br />

Introduction: Chronic HCV infection is associated with metabolism<br />

abnormalities, including insulin resistance. Up to 15-25%<br />

of chronic hepatitis C patients will develop diabetes lifelong.<br />

New DAA allow HCV suppression within a very short-time<br />

frame. Little is known on the metabolic effects seen in chronic<br />

hepatitis C patients on DAA. Methods: All chronic hepatitis C<br />

patients that received sofosbuvir (SOF)-based regimens during<br />

at least 4 weeks at two reference hepatitis clinics in Madrid<br />

were retrospectively examined. Results: A total of 61 chronic<br />

hepatitis C patients begun SOF-based regimens and had<br />

weeks 0 and 4 controls. Regimens were as follows: SOF+simeprevir<br />

(16), SOF+daclatasvir (13), SOF+ledipasvir (27) and<br />

SOF+ribavirin (5). At 4 weeks 63% had undetectable viremia<br />

and the rest had

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