Literature DB >> 27973461

Bone metabolism in non-alcoholic fatty liver disease: vitamin D status and bone mineral density.

Ahad Eshraghian1.   

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and abnormal liver enzyme worldwide. NAFLD is reported to be associated with other extra-hepatic diseases including cardiovascular disease, diabetes mellites and thyroid gland abnormalities. Liver is also the source of many proteins involved in bone metabolism and is the regulator of several bone metabolism pathways. Although underlying pathogenesis is not clear, the association between NAFLD and low bone mineral density (BMD) in the forms of osteoporosis and osteopenia has been recently reported. This study aimed to review current evidences supporting the association between bone metabolism including low BMD and serum vitamin D level in patients with NAFLD. Epidemiolocal studies indicating lower BMD and vitamin D in patients with NAFLD have been reviewed. The main pathophysiological mechanisms including association of insulin resistance, serum adiponectin, ghrelin, osteopontin, osteoprotegerin, and osteocalcin with NAFLD and low BMD have been briefly reviewed and summarized. Results of current clinical trials investigating the role of vitamin D supplementation for treatment of hepatic steatosis and non-alcoholic steatohepoatitis (NASH) have been also summarized. As a conclusion, increasing evidences are now available suggesting low BMD in patients with NAFLD. Some of these studies showed association of NAFLD severity with low vitamin D and BMD. Screening and surveillance of skeletal system regarding osteoporosis/osteomalacia in patients with NAFLD may be considered in future strategies and guidelines for NAFLD management.

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Year:  2016        PMID: 27973461     DOI: 10.23736/S0391-1977.16.02587-6

Source DB:  PubMed          Journal:  Minerva Endocrinol        ISSN: 0391-1977            Impact factor:   2.184


  5 in total

1.  Relationship between Serum 25-hydroxy-vitamin D Concentration and Risk of Metabolic Syndrome in Patients with Fatty Liver.

Authors:  Hee-Sook Lim; Tae-Hee Kim; Hae-Hyeog Lee; Soon-Kyung Kim; Bora Lee; Yoon-Hyung Park
Journal:  J Bone Metab       Date:  2017-11-30

2.  Current and emerging pharmacological therapy for non-alcoholic fatty liver disease.

Authors:  Ahad Eshraghian
Journal:  World J Gastroenterol       Date:  2017-11-14       Impact factor: 5.742

3.  Hepatomusculoskeletal disorders: Coining a new term might improve the management of the musculoskeletal manifestations of chronic liver disease.

Authors:  Christos Tsagkaris; Stavros P Papadakos; Dimitrios V Moysidis; Andreas S Papazoglou; Alexandra Koutsogianni; Marios Papadakis
Journal:  World J Gastrointest Pathophysiol       Date:  2022-07-22

4.  Association of Nonalcoholic Fatty Liver Disease With Osteoporotic Fractures: A Cross-Sectional Retrospective Study of Chinese Individuals.

Authors:  Yanmao Wang; Gen Wen; Runhua Zhou; Wanrun Zhong; Shengdi Lu; Chengfang Hu; Yimin Chai
Journal:  Front Endocrinol (Lausanne)       Date:  2018-07-23       Impact factor: 5.555

5.  Increased risk of osteoporosis in patients with nonalcoholic fatty liver disease: A population-based retrospective cohort study.

Authors:  Hon-Jhe Chen; Hao-Yu Yang; Kuang-Chieh Hsueh; Cheng-Che Shen; Ru-Yi Chen; Hsien-Chung Yu; Tzu-Lin Wang
Journal:  Medicine (Baltimore)       Date:  2018-10       Impact factor: 1.889

  5 in total

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