4.6 Review

Adipokines in Non-Alcoholic Fatty Liver Disease: Are We on the Road toward New Biomarkers and Therapeutic Targets?

期刊

BIOLOGY-BASEL
卷 11, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/biology11081237

关键词

adipokines; NAFLD; liver; steatosis; inflammation; fibrosis; biomarkers; therapy; clinical trials; preclinical studies

类别

资金

  1. Instituto de Salud Carlos III (ISCIII)
  2. European Social Fund Plus (ESF+) through a Miguel Servet Program [CP21/00025]
  3. Spanish Ministry of Science and Innovation [PID2020-120336RB-I00]
  4. European Regional Development Fund (FEDER)
  5. Generalitat Valenciana [PROMETEO/2019/032]
  6. ISCIII [RD21/0002/0025, PI20/00902]
  7. FEDER
  8. Research Executive Agency of the European Union [734899]
  9. Xunta de Galicia, Conselleria de Educacion, Universidade e Formacion Profesional
  10. Conselleria de Economia, Emprego e Industria (GAIN) [GPC IN607B2019/10]

向作者/读者索取更多资源

Non-alcoholic fatty liver disease (NAFLD) is a significant medical concern due to its high incidence, severe consequences, and lack of effective diagnostic tools and drugs. This review examines the role of adipokines, cytokine-like hormones secreted by adipose tissue, in NAFLD and their potential as diagnostic biomarkers and therapeutic targets. The limitations of current research are discussed and future directions are outlined. NAFLD is a leading cause of chronic liver disease and associated with other non-communicable diseases. The communication between adipose tissue and liver plays a key role in NAFLD pathophysiology. Adipokines have been linked to the development and progression of NAFLD. This review provides an overview of the current knowledge on specific adipokines and their impact on NAFLD, as well as the potential of using adipokines as therapeutic targets and biomarkers for NAFLD management.
Simple Summary Non-alcoholic fatty liver disease (NAFLD) is an unmet medical need due to its increasingly high incidence, severe clinical consequences, and the absence of feasible diagnostic tools and effective drugs. This review summarizes the preclinical and clinical data on adipokines, cytokine-like hormones secreted by adipose tissue, and NAFLD. The aim is to establish the potential of adipokines as diagnostic and prognostic biomarkers, as well as their potential as therapeutic targets for NAFLD. The limitations of current research are also discussed, and future perspectives are outlined. Non-alcoholic fatty liver disease (NAFLD) has become the major cause of chronic hepatic illness and the leading indication for liver transplantation in the future decades. NAFLD is also commonly associated with other high-incident non-communicable diseases, such as cardiovascular complications, type 2 diabetes, and chronic kidney disease. Aggravating the socio-economic impact of this complex pathology, routinely feasible diagnostic methodologies and effective drugs for NAFLD management are unavailable. The pathophysiology of NAFLD, recently defined as metabolic associated fatty liver disease (MAFLD), is correlated with abnormal adipose tissue-liver axis communication because obesity-associated white adipose tissue (WAT) inflammation and metabolic dysfunction prompt hepatic insulin resistance (IR), lipid accumulation (steatosis), non-alcoholic steatohepatitis (NASH), and fibrosis. Accumulating evidence links adipokines, cytokine-like hormones secreted by adipose tissue that have immunometabolic activity, with NAFLD pathogenesis and progression; however, much uncertainty still exists. Here, the current knowledge on the roles of leptin, adiponectin, ghrelin, resistin, retinol-binding protein 4 (RBP4), visfatin, chemerin, and adipocyte fatty-acid-binding protein (AFABP) in NAFLD, taken from preclinical to clinical studies, is overviewed. The effect of therapeutic interventions on adipokines' circulating levels are also covered. Finally, future directions to address the potential of adipokines as therapeutic targets and disease biomarkers for NAFLD are discussed.

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