Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis

被引:130
|
作者
Younossi, Zobair M. [1 ,2 ]
Loomba, Rohit [3 ]
Rinella, Mary E. [4 ]
Bugianesi, Elisabetta [5 ]
Marchesini, Giulio [6 ]
Neuschwander-Tetri, Brent A. [7 ]
Serfaty, Lawrence [8 ]
Negro, Francesco [9 ]
Caldwell, Stephen H. [10 ]
Ratziu, Vlad [11 ,12 ]
Corey, Kathleen E. [13 ]
Friedman, Scott L. [14 ]
Abdelmalek, Manal F. [15 ]
Harrison, Stephen A. [16 ]
Sanyal, Arun J. [17 ]
Lavine, Joel E. [18 ]
Mathurin, Philippe [19 ]
Charlton, Michael R. [20 ]
Chalasani, Naga P. [21 ]
Anstee, Quentin M. [22 ]
Kowdley, Kris V. [23 ]
George, Jacob [24 ,25 ]
Goodman, Zachary D. [1 ,2 ]
Lindor, Keith [26 ]
机构
[1] Inova Hlth Syst, Dept Med, Falls Church, VA USA
[2] Inova Hlth Syst, Betty & Guy Beatty Ctr Integrated Res, Falls Church, VA USA
[3] Univ Calif San Diego, Dept Gastroenterol, La Jolla, CA 92093 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Gastroenterol, Chicago, IL 60611 USA
[5] Univ Torino, Dept Med Sci, Turin, Italy
[6] Univ Bologna, Dept Med, Bologna, Italy
[7] St Louis Univ, Div Gastroenterol & Hepatol, St Louis, MO 63103 USA
[8] St Antoine Hosp, Paris, France
[9] Univ Hosp Geneva, Dept Gastroenterol, Geneva, Switzerland
[10] Univ Virginia, Div Gastroenterol & Hepatol, Charlottesville, VA USA
[11] Inst Cardiometab & Nutr, Paris, France
[12] Hosp Pitie Salpetriere, Paris, France
[13] Massachusetts Gen Hosp, Div Gastroenterol, Cambridge, MA USA
[14] Icahn Sch Med Mt Sinai, Div Liver Dis, New York, NY 10029 USA
[15] Duke Univ, Div Gastroenterol & Hepatol, Durham, NC USA
[16] Pinnacle Clin Res, San Antonio, TX USA
[17] Virginia Commonwealth Univ, Div Gastroenterol, Richmond, VA USA
[18] Columbia Coll Phys & Surg, Dept Pediat, New York, NY USA
[19] Hop Claude Huriez Rue Michel Polonowski, Lille, France
[20] Univ Chicago, Dept Med, 5841 S Maryland Ave, Chicago, IL 60637 USA
[21] Indiana Univ Sch Med, Div Gastroenterol & Hepatol, Indianapolis, IN 46202 USA
[22] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[23] Swedish Med Ctr, Liver Care Network & Organ Care Res, Seattle, WA USA
[24] Westmead Hosp, Dept Gastroenterol & Hepatol, Sydney, NSW, Australia
[25] Sydney West Local Hlth Dist, Sydney, NSW, Australia
[26] Arizona State Univ, Coll Hlth Solut, Phoenix, AZ USA
关键词
MAGNETIC-RESONANCE ELASTOGRAPHY; BARIATRIC SURGERY; FIBROSIS STAGE; LIFE-STYLE; CARDIOVASCULAR-DISEASE; AMERICAN ASSOCIATION; RESISTANCE EXERCISE; PHYSICAL-ACTIVITY; REDUCES FEATURES; MEDICAL THERAPY;
D O I
10.1002/hep.29724
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) and its progressive form non-alcoholic steatohepatitis (NASH), are rapidly becoming among the top causes of cirrhosis, hepatocellular carcinoma, and indications for liver transplantation. Other than lifestyle modification through diet and exercise, there are currently no other approved treatments for NASH/NAFLD. Although weight loss can be effective, it is difficult to achieve and sustain. In contrast, bariatric surgery can improve metabolic conditions associated with NAFLD, and has been shown to improve liver histology. To have approved regimens for the treatment of NASH/NAFLD, several issues must be addressed. First, all stakeholders must agree on the most appropriate clinical trial endpoints for NASH. Currently, resolution of NASH (without worsening fibrosis) or reduction of fibrosis stage (without worsening NASH) are the accepted endpoints by the regulatory authorities. It is important to recognize the prognostic implication of histologic features of NASH. In this context, although histologic NASH has been associated with advanced fibrosis, it is not an independent predictor of long-term mortality. In contrast, there are significant data to suggest that fibrosis stage is the only robust and independent predictor of liver-related mortality. In addition to the primary endpoints, several important secondary endpoints, including noninvasive biomarkers, long-term outcomes, and patient-reported outcomes must be considered. In 2018, a few phase 3 clinical trials for the treatment of NASH have been initiated. Additionally, a number of phase 2a and 2b clinical trials targeting different pathogenic pathways in NASH are in the pipeline of emerging therapies. Conclusion: Over the next 5 years, some of these regimens are expected to provide potential new treatment options for patients with NASH/NAFLD. (Hepatology 2018;68:361-371)
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页码:361 / 371
页数:11
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