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Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients

This study aimed to investigate the association between serum uric acid (SUA) level and nonalcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes (T2DM). T2DM patients hospitalized in the Department of Hepatology, Yantai Qishan Hospital, between April 2012 and December 2018 were clas...

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Autores principales: Yu, Haifeng, Zhao, Ling, Liu, Lijuan, Li, Yanfang, Sun, Jing, Liu, Youde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376353/
https://www.ncbi.nlm.nih.gov/pubmed/34414956
http://dx.doi.org/10.1097/MD.0000000000026946
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author Yu, Haifeng
Zhao, Ling
Liu, Lijuan
Li, Yanfang
Sun, Jing
Liu, Youde
author_facet Yu, Haifeng
Zhao, Ling
Liu, Lijuan
Li, Yanfang
Sun, Jing
Liu, Youde
author_sort Yu, Haifeng
collection PubMed
description This study aimed to investigate the association between serum uric acid (SUA) level and nonalcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes (T2DM). T2DM patients hospitalized in the Department of Hepatology, Yantai Qishan Hospital, between April 2012 and December 2018 were classified into the NAFLD group and the non-NAFLD group. Clinical data, glucose and lipid metabolism biomarkers, and liver and kidney function parameters were retrospectively collected. Five hundred eighty-three T2DM patients met the inclusion and exclusion criteria; 227 patients were included in the non-NAFLD group and 356 patients were included in the NAFLD group. Multiple linear regression analyses showed that SUA was positively correlated with body mass index (P = .003), triglycerides (P = .009), aspartate aminotransferase (P = .036), and alanine aminotransferase (P = .038) and negatively correlated with estimated glomerular filtration rate (P < .001) in T2DM patients. Multivariate regression analyses demonstrated that after adjusting for confounding factors, the SUA tertile was still significantly associated with NAFLD occurrence in T2DM patients (P for trend = .008). With reference to SUA tertile I, the odds ratios for NAFLD in the SUA tertile II and tertile III groups were 1.729 (95% confidence interval [CI]: 1.086–2.753) and 2.315 (95% CI: 1.272–4.213), respectively. The level of SUA in T2DM patients was associated with the occurrence of NAFLD. Elevated SUA was associated with a significantly increased prevalence of NAFLD. The SUA level was an independent risk factor for NAFLD occurrence in patients with T2DM.
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spelling pubmed-83763532021-08-21 Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients Yu, Haifeng Zhao, Ling Liu, Lijuan Li, Yanfang Sun, Jing Liu, Youde Medicine (Baltimore) 4500 This study aimed to investigate the association between serum uric acid (SUA) level and nonalcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes (T2DM). T2DM patients hospitalized in the Department of Hepatology, Yantai Qishan Hospital, between April 2012 and December 2018 were classified into the NAFLD group and the non-NAFLD group. Clinical data, glucose and lipid metabolism biomarkers, and liver and kidney function parameters were retrospectively collected. Five hundred eighty-three T2DM patients met the inclusion and exclusion criteria; 227 patients were included in the non-NAFLD group and 356 patients were included in the NAFLD group. Multiple linear regression analyses showed that SUA was positively correlated with body mass index (P = .003), triglycerides (P = .009), aspartate aminotransferase (P = .036), and alanine aminotransferase (P = .038) and negatively correlated with estimated glomerular filtration rate (P < .001) in T2DM patients. Multivariate regression analyses demonstrated that after adjusting for confounding factors, the SUA tertile was still significantly associated with NAFLD occurrence in T2DM patients (P for trend = .008). With reference to SUA tertile I, the odds ratios for NAFLD in the SUA tertile II and tertile III groups were 1.729 (95% confidence interval [CI]: 1.086–2.753) and 2.315 (95% CI: 1.272–4.213), respectively. The level of SUA in T2DM patients was associated with the occurrence of NAFLD. Elevated SUA was associated with a significantly increased prevalence of NAFLD. The SUA level was an independent risk factor for NAFLD occurrence in patients with T2DM. Lippincott Williams & Wilkins 2021-08-20 /pmc/articles/PMC8376353/ /pubmed/34414956 http://dx.doi.org/10.1097/MD.0000000000026946 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle 4500
Yu, Haifeng
Zhao, Ling
Liu, Lijuan
Li, Yanfang
Sun, Jing
Liu, Youde
Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title_full Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title_fullStr Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title_full_unstemmed Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title_short Relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
title_sort relationship between serum uric acid level and nonalcoholic fatty liver disease in type 2 diabetes patients
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8376353/
https://www.ncbi.nlm.nih.gov/pubmed/34414956
http://dx.doi.org/10.1097/MD.0000000000026946
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