Nonalcoholic fatty liver disease and serum uric acid

Nonalcoholic fatty liver disease (NAFLD) is considered the manifestation of metabolic syndrome (MS) in the liver. Besides glucose and lipid metabolic disorders, the level of serum uric acid (SUA) is also associated with the progression of NAFLD. This article reviews the research achievements in the...

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Main Authors: XU Beibei, WANG Bingyuan
Format: Article
Language:zho
Published: Editorial Department of Journal of Clinical Hepatology 2016-03-01
Series:Linchuang Gandanbing Zazhi
Online Access:http://www.lcgdbzz.org/qk_content.asp?id=7235
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spelling doaj-58fd6f1eac5b44b0a375e0e32ff674962020-11-25T02:45:11ZzhoEditorial Department of Journal of Clinical HepatologyLinchuang Gandanbing Zazhi1001-52561001-52562016-03-0132343744110.3969/j.issn.1001-5256.2016.03.007Nonalcoholic fatty liver disease and serum uric acidXU Beibei0WANG Bingyuan1Department of Geriatric Gastroenterology, The First Affiliated Hospital of China Medical University, Shenyang 110001, ChinaDepartment of Geriatric Gastroenterology, The First Affiliated Hospital of China Medical University, Shenyang 110001, ChinaNonalcoholic fatty liver disease (NAFLD) is considered the manifestation of metabolic syndrome (MS) in the liver. Besides glucose and lipid metabolic disorders, the level of serum uric acid (SUA) is also associated with the progression of NAFLD. This article reviews the research achievements in the association between SUA and NAFLD and points out that SUA can independently predict the risks of MS, type 2 diabetes, and cardiovascular disease in both healthy people and patients. Its mechanism may be that SUA increases the expression of reactive oxygen species (ROS)/thioredoxin-interacting protein (TXNIP) through inducing ROS, and then it activates the NLR pyrin domain containing 3 inflammasome and induces the secretion of interleukin. Both basic and clinical research show that the drugs reducing SUA can inhibit the TXNIP pathway, reduce the blood glucose level, and alleviate liver ROS, inflammation, steatosis, and fibrosis. This article suggests that SUA may be a promising therapeutic method for NAFLD and needs further basic and clinical research. http://www.lcgdbzz.org/qk_content.asp?id=7235
collection DOAJ
language zho
format Article
sources DOAJ
author XU Beibei
WANG Bingyuan
spellingShingle XU Beibei
WANG Bingyuan
Nonalcoholic fatty liver disease and serum uric acid
Linchuang Gandanbing Zazhi
author_facet XU Beibei
WANG Bingyuan
author_sort XU Beibei
title Nonalcoholic fatty liver disease and serum uric acid
title_short Nonalcoholic fatty liver disease and serum uric acid
title_full Nonalcoholic fatty liver disease and serum uric acid
title_fullStr Nonalcoholic fatty liver disease and serum uric acid
title_full_unstemmed Nonalcoholic fatty liver disease and serum uric acid
title_sort nonalcoholic fatty liver disease and serum uric acid
publisher Editorial Department of Journal of Clinical Hepatology
series Linchuang Gandanbing Zazhi
issn 1001-5256
1001-5256
publishDate 2016-03-01
description Nonalcoholic fatty liver disease (NAFLD) is considered the manifestation of metabolic syndrome (MS) in the liver. Besides glucose and lipid metabolic disorders, the level of serum uric acid (SUA) is also associated with the progression of NAFLD. This article reviews the research achievements in the association between SUA and NAFLD and points out that SUA can independently predict the risks of MS, type 2 diabetes, and cardiovascular disease in both healthy people and patients. Its mechanism may be that SUA increases the expression of reactive oxygen species (ROS)/thioredoxin-interacting protein (TXNIP) through inducing ROS, and then it activates the NLR pyrin domain containing 3 inflammasome and induces the secretion of interleukin. Both basic and clinical research show that the drugs reducing SUA can inhibit the TXNIP pathway, reduce the blood glucose level, and alleviate liver ROS, inflammation, steatosis, and fibrosis. This article suggests that SUA may be a promising therapeutic method for NAFLD and needs further basic and clinical research.
url http://www.lcgdbzz.org/qk_content.asp?id=7235
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AT wangbingyuan nonalcoholicfattyliverdiseaseandserumuricacid
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