| Literature DB >> 26432021 |
Giovanni Musso1, Maurizio Cassader2, Solomon Cohney3, Silvia Pinach2, Francesca Saba2, Roberto Gambino2.
Abstract
Mounting evidence connects non-alcoholic fatty liver disease (NAFLD) to chronic kidney disease (CKD). We review emerging mechanistic links between NAFLD and CKD, including altered activation of angiotensin converting enzyme (ACE)-2, nutrient/energy sensors sirtuin-1 and AMP-activated kinase, as well as impaired antioxidant defense mediated by nuclear factor erythroid 2-related factor-2 (Nrf2). Dietary fructose excess may also contribute to NAFLD and CKD. NAFLD affects renal injury through lipoprotein dysmetabolism and altered secretion of the hepatokines fibroblast growth factor-21, fetuin-A, insulin-like growth factor-1, and syndecan-1. CKD may mutually aggravate NAFLD and associated metabolic disturbances through altered intestinal barrier function and microbiota composition, the accumulation of uremic toxic metabolites, and alterations in pre-receptor glucocorticoid metabolism. We conclude by discussing the implications of these findings for the treatment of NAFLD and CKD.Entities:
Keywords: CKD; NAFLD; NASH; eGFR; renal function
Mesh:
Year: 2015 PMID: 26432021 DOI: 10.1016/j.molmed.2015.08.005
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951