Literature DB >> 23815295

Liver diseases and aging: friends or foes?

Fareeba Sheedfar1, Stefano Di Biase, Debby Koonen, Manlio Vinciguerra.   

Abstract

The liver is the only internal human organ capable of natural regeneration of lost tissue, as little as 25% of a liver can regenerate into a whole liver. The process of aging predisposes to hepatic functional and structural impairment and metabolic risk. Therefore, understanding how aging could affect the molecular pathology of liver diseases is particularly important, and few studies to date have tackled this complex process. The most common liver disease, affecting one-third of the overall population, is nonalcoholic fatty liver disease (NAFLD), characterized by an intrahepatic accumulation of lipids. NAFLD can evolve into nonalcoholic steatohepatitis (NASH) in the presence of oxidative stress and inflammation. NASH is a serious risk factor for disabling and deadly liver diseases such as cirrhosis and hepatocellular carcinoma (HCC). Old age seems to favor NAFLD, NASH, and ultimately HCC, in agreement with the inflamm-aging theory, according to which aging accrues inflammation. However, the incidence of HCC drops significantly in the very elderly (individuals aged more than 70) and the relationship between the progression of NAFLD/NASH/HCC and very old age is obscure. In this review, we discuss the literature and we argue that there might be an age window in which the liver becomes resistant to the development of injury; this needs to be studied to understand fully the interaction between age and liver diseases from a therapeutic perspective.
© 2013 the Anatomical Society and John Wiley & Sons Ltd.

Entities:  

Keywords:  NAFLD; NASH; aging; cytokines; demography; injury; insulin/IGF-1 signalling; mouse models; reactive oxygen species

Mesh:

Substances:

Year:  2013        PMID: 23815295     DOI: 10.1111/acel.12128

Source DB:  PubMed          Journal:  Aging Cell        ISSN: 1474-9718            Impact factor:   9.304


  68 in total

1.  Global gene expression profile of normal and regenerating liver in young and old mice.

Authors:  Monica Pibiri; Pia Sulas; Vera Piera Leoni; Andrea Perra; Marta Anna Kowalik; Angela Cordella; Pasquale Saggese; Giovanni Nassa; Maria Ravo
Journal:  Age (Dordr)       Date:  2015-06-03

2.  Genetic ablation of macrohistone H2A1 leads to increased leanness, glucose tolerance and energy expenditure in mice fed a high-fat diet.

Authors:  F Sheedfar; M Vermeer; V Pazienza; J Villarroya; F Rappa; F Cappello; G Mazzoccoli; F Villarroya; H van der Molen; M H Hofker; D P Koonen; M Vinciguerra
Journal:  Int J Obes (Lond)       Date:  2014-05-21       Impact factor: 5.095

Review 3.  Aging and liver disease.

Authors:  In Hee Kim; Tatiana Kisseleva; David A Brenner
Journal:  Curr Opin Gastroenterol       Date:  2015-05       Impact factor: 3.287

4.  The hepatic microenvironment essentially determines tumor cell dormancy and metastatic outgrowth of pancreatic ductal adenocarcinoma.

Authors:  Lennart Lenk; Maren Pein; Olga Will; Beatriz Gomez; Fabrice Viol; Charlotte Hauser; Jan-Hendrik Egberts; Jan-Paul Gundlach; Ole Helm; Sanjay Tiwari; Ralf Weiskirchen; Stefan Rose-John; Christoph Röcken; Wolfgang Mikulits; Patrick Wenzel; Günter Schneider; Dieter Saur; Heiner Schäfer; Susanne Sebens
Journal:  Oncoimmunology       Date:  2017-10-26       Impact factor: 8.110

Review 5.  Nonalcoholic fatty liver disease and aging: epidemiology to management.

Authors:  Marco Bertolotti; Amedeo Lonardo; Chiara Mussi; Enrica Baldelli; Elisa Pellegrini; Stefano Ballestri; Dante Romagnoli; Paola Loria
Journal:  World J Gastroenterol       Date:  2014-10-21       Impact factor: 5.742

6.  Osteocalcin protects against nonalcoholic steatohepatitis in a mouse model of metabolic syndrome.

Authors:  Anisha A Gupte; Omaima M Sabek; Daniel Fraga; Laurie J Minze; Satoru K Nishimoto; Joey Z Liu; Solmaz Afshar; Lillian Gaber; Christopher J Lyon; A Osama Gaber; Willa A Hsueh
Journal:  Endocrinology       Date:  2014-10-03       Impact factor: 4.736

7.  Hepatic NAD(+) deficiency as a therapeutic target for non-alcoholic fatty liver disease in ageing.

Authors:  Can-Can Zhou; Xi Yang; Xia Hua; Jian Liu; Mao-Bing Fan; Guo-Qiang Li; Jie Song; Tian-Ying Xu; Zhi-Yong Li; Yun-Feng Guan; Pei Wang; Chao-Yu Miao
Journal:  Br J Pharmacol       Date:  2016-06-27       Impact factor: 8.739

8.  Aging increases the susceptibility of hepatic inflammation, liver fibrosis and aging in response to high-fat diet in mice.

Authors:  In Hee Kim; Jun Xu; Xiao Liu; Yukinori Koyama; Hsiao-Yen Ma; Karin Diggle; Young-Hyun You; Jan M Schilling; Dilip Jeste; Kumar Sharma; David A Brenner; Tatiana Kisseleva
Journal:  Age (Dordr)       Date:  2016-08-30

9.  DNA Hypomethylation and Histone Variant macroH2A1 Synergistically Attenuate Chemotherapy-Induced Senescence to Promote Hepatocellular Carcinoma Progression.

Authors:  Michela Borghesan; Caterina Fusilli; Francesca Rappa; Concetta Panebianco; Giovanni Rizzo; Jude A Oben; Gianluigi Mazzoccoli; Chris Faulkes; Illar Pata; Antonella Agodi; Farhad Rezaee; Shane Minogue; Alessandra Warren; Abigail Peterson; John M Sedivy; Julien Douet; Marcus Buschbeck; Francesco Cappello; Tommaso Mazza; Valerio Pazienza; Manlio Vinciguerra
Journal:  Cancer Res       Date:  2016-01-15       Impact factor: 12.701

10.  Anthocyanins Delay Ageing-Related Degenerative Changes in the Liver.

Authors:  Jie Wei; Guokun Zhang; Xiao Zhang; Dexin Xu; Jun Gao; Jungang Fan
Journal:  Plant Foods Hum Nutr       Date:  2017-12       Impact factor: 3.921

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