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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Editorial Department of Journal of Clinical Hepatology
2016-03-01
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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 |
work_keys_str_mv |
AT xubeibei nonalcoholicfattyliverdiseaseandserumuricacid AT wangbingyuan nonalcoholicfattyliverdiseaseandserumuricacid |
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