Hepatology highlights
Jean‐François Dufour – 10 September 2014
Jean‐François Dufour – 10 September 2014
Chien‐Hsieh Chiang, Kuo‐Chin Huang – 10 September 2014
Jean‐François Dufour – 10 September 2014
Natalie E. Nierenberg, Debra D. Poutsiaka, Jennifer K. Chow, Jeffrey Cooper, Lori Lyn Price, Richard B. Freeman, Richard Rohrer, David R. Snydman – 10 September 2014 – Infection after liver transplantation (LT) remains a leading cause of morbidity and mortality. The risk of infection after LT is highest in those who are most immunosuppressed, but to date, no standard blood marker of one's degree of immunosuppression or risk index has been established.
Priya Grewal – 9 September 2014
Eric G. Meissner, Yu‐Jin Lee, Anu Osinusi, Zayani Sims, Jing Qin, Dan Sturdevant, John McHutchison, Mani Subramanian, Maureen Sampson, Susanna Naggie, Keyur Patel, Alan T. Remaley, Henry Masur, Shyam Kottilil – 9 September 2014 – Hepatitis C virus (HCV) modulates intrahepatic cholesterol biosynthetic pathways to promote viral replication. Chronic HCV infection is associated with altered metabolism, including dyslipidemia and insulin resistance (IR), which contributes to disease progression and influences response to therapy.
Joseph A. Boscarino, Mei Lu, Anne C. Moorman, Stuart C. Gordon, Loralee B. Rupp, Philip R. Spradling, Eyasu H. Teshale, Mark A. Schmidt, Vinutha Vijayadeva, Scott D. Holmberg, for the Chronic Hepatitis Cohort Study (CHeCS) Investigators – 9 September 2014 – Our objective was to assess the extent and risk factors for depression and poor physical health among patients with chronic hepatitis C virus (HCV) infection. We surveyed HCV‐infected patients seen at four large healthcare systems participating in the Chronic Hepatitis Cohort Study (CHeCS).
Mariko Esumi, Mariko Ishibashi, Hiromi Yamaguchi, Satomi Nakajima, Yuhi Tai, Sachiko Kikuta, Masahiko Sugitani, Tadatoshi Takayama, Maino Tahara, Makoto Takeda, Takaji Wakita – 9 September 2014 – The human liver reacts to hepatitis C virus (HCV) with a balanced response consisting of host anti‐ and proviral activities. To explore these subtle host responses, we used oligonucleotide microarrays to investigate the differential gene expression between two groups of liver samples with high and low HCV loads (>100‐fold difference).
Linjie Lv, Qingwang Han, Yinghao Chu, Muzi Zhang, Lin Sun, Wanguo Wei, Caixia Jin, Wenlin Li – 9 September 2014
Timothy J.S. Cross – 9 September 2014