Literature DB >> 34540943

Excess Body Weight and Metabolic (Dysfunction)-Associated Fatty Liver Disease (MAFLD).

Elke Roeb1.   

Abstract

BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) describes a continuum of liver abnormalities from simple nonalcoholic fatty liver (NAFL) to nonalcoholic fatty liver hepatitis or steatohepatitis (NASH) to NASH fibrosis. It has a variable course, but just like alcoholic fatty liver disease, it can lead to liver cirrhosis and cancer (hepatocellular carcinoma).
SUMMARY: NAFLD is a clinical entity characterized by the presence of liver steatosis, which affects at least 5% of hepatocytes. Affected are people who consume little or no alcohol and who have no secondary cause of liver steatosis such as viral hepatitis, drug intake (e.g., tamoxifen, amiodarone, methotrexate, etc.), or lipodystrophy. NAFLD is, nowadays, the most common liver disease in Europe, with an estimated prevalence of 25%. The currently widely recognized recommendation for the therapy of NAFLD is a lifestyle modification with the goal of weight loss. Although no drugs are currently approved for the treatment of NAFLD, several candidates are in clinical trials. Besides weight loss and physical activity, corresponding single active ingredients or combination therapies are intended to stop the progression of the disease and, in the best case, reverse it. The newly propagated name MAFLD (metabolic-associated fatty liver disease) should indicate that the disease is associated with metabolic disorders. The term MAFLD also implies multiple overlapping causes and drivers of this soaring disease. KEY MESSAGES: The prevalence of NAFLD continues to rise worldwide. NAFLD, NASH, and fibrosis in NAFLD occur predominantly in patients with obesity and type 2 diabetes (T2DM) or else precede these conditions. The progression of NAFLD is highly dependent on changes in glucose, lipid metabolism, and fibrogenesis. A new definition and nomenclature of fatty liver disease, "metabolic associated fatty liver disease" (MAFLD), should be discussed carefully, since around 40% of the global population with NAFLD are classified as non-obese and almost 1/5 as lean. Since the pathogenesis of fatty liver disease, obesity, and glucose and lipid metabolism diseases are very closely related, it is important to continue to look for mechanisms that these diseases have in common and develop new therapeutic approaches.
Copyright © 2021 by S. Karger AG, Basel.

Entities:  

Keywords:  Fatty liver; Fibrosis; Metabolic-associated fatty liver disease (MAFLD); Metabolism; Nonalcoholic fatty liver disease (NAFLD); Nonalcoholic fatty liver hepatitis or steatohepatitis (NASH)

Year:  2021        PMID: 34540943      PMCID: PMC8406344          DOI: 10.1159/000515445

Source DB:  PubMed          Journal:  Visc Med        ISSN: 2297-4725


  41 in total

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Authors:  E Roeb; H M Steffen; H Bantel; U Baumann; A Canbay; M Demir; U Drebber; A Geier; J Hampe; C Hellerbrand; A Pathil-Warth; J M Schattenberg; C Schramm; H K Seitz; N Stefan; F Tacke; A Tannapfel; P Lynen Jansen; J Bojunga
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Review 3.  Nonalcoholic fatty liver disease.

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Journal:  Prog Liver Dis       Date:  1986

Review 4.  Genetics and epigenetics of NAFLD and NASH: Clinical impact.

Authors:  Mohammed Eslam; Luca Valenti; Stefano Romeo
Journal:  J Hepatol       Date:  2017-11-06       Impact factor: 25.083

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Authors:  Zobair M Younossi
Journal:  J Hepatol       Date:  2018-11-09       Impact factor: 25.083

6.  Obeticholic acid for the treatment of non-alcoholic steatohepatitis: interim analysis from a multicentre, randomised, placebo-controlled phase 3 trial.

Authors:  Zobair M Younossi; Vlad Ratziu; Rohit Loomba; Mary Rinella; Quentin M Anstee; Zachary Goodman; Pierre Bedossa; Andreas Geier; Susanne Beckebaum; Philip N Newsome; David Sheridan; Muhammad Y Sheikh; James Trotter; Whitfield Knapple; Eric Lawitz; Manal F Abdelmalek; Kris V Kowdley; Aldo J Montano-Loza; Jerome Boursier; Philippe Mathurin; Elisabetta Bugianesi; Giuseppe Mazzella; Antonio Olveira; Helena Cortez-Pinto; Isabel Graupera; David Orr; Lise Lotte Gluud; Jean-Francois Dufour; David Shapiro; Jason Campagna; Luna Zaru; Leigh MacConell; Reshma Shringarpure; Stephen Harrison; Arun J Sanyal
Journal:  Lancet       Date:  2019-12-05       Impact factor: 79.321

Review 7.  Genetic Factors That Affect Risk of Alcoholic and Nonalcoholic Fatty Liver Disease.

Authors:  Quentin M Anstee; Devanshi Seth; Christopher P Day
Journal:  Gastroenterology       Date:  2016-02-10       Impact factor: 22.682

Review 8.  NAFLD and diabetes mellitus.

Authors:  Herbert Tilg; Alexander R Moschen; Michael Roden
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2016-10-12       Impact factor: 46.802

9.  High-protein diet more effectively reduces hepatic fat than low-protein diet despite lower autophagy and FGF21 levels.

Authors:  Chenchen Xu; Mariya Markova; Nicole Seebeck; Anne Loft; Silke Hornemann; Thomas Gantert; Stefan Kabisch; Kathleen Herz; Jennifer Loske; Mario Ost; Verena Coleman; Frederick Klauschen; Anke Rosenthal; Volker Lange; Jürgen Machann; Susanne Klaus; Tilman Grune; Stephan Herzig; Olga Pivovarova-Ramich; Andreas F H Pfeiffer
Journal:  Liver Int       Date:  2020-07-21       Impact factor: 5.828

10.  Adiposity amplifies the genetic risk of fatty liver disease conferred by multiple loci.

Authors:  Stefan Stender; Julia Kozlitina; Børge G Nordestgaard; Anne Tybjærg-Hansen; Helen H Hobbs; Jonathan C Cohen
Journal:  Nat Genet       Date:  2017-04-24       Impact factor: 38.330

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  1 in total

Review 1.  Diagnostic and Therapy of Nonalcoholic Fatty Liver Disease: A Narrative Review.

Authors:  Elke Roeb
Journal:  Visc Med       Date:  2021-10-26
  1 in total

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