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Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes

OBJECTIVE: Patients with type 2 diabetes have a high risk of non-alcoholic fatty liver disease (NAFLD) and related liver fibrosis. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated efficacy in improving NAFLD, while their effectiveness on liver fibrosis is limited in type 2 diab...

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Autores principales: Tan, Yijiong, Zhen, Qin, Ding, Xiaoying, Shen, Tingting, Liu, Fang, Wang, Yufan, Zhang, Qidi, Lin, Renkun, Chen, Lili, Peng, Yongde, Fan, Nengguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399467/
https://www.ncbi.nlm.nih.gov/pubmed/36034438
http://dx.doi.org/10.3389/fendo.2022.935180
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author Tan, Yijiong
Zhen, Qin
Ding, Xiaoying
Shen, Tingting
Liu, Fang
Wang, Yufan
Zhang, Qidi
Lin, Renkun
Chen, Lili
Peng, Yongde
Fan, Nengguang
author_facet Tan, Yijiong
Zhen, Qin
Ding, Xiaoying
Shen, Tingting
Liu, Fang
Wang, Yufan
Zhang, Qidi
Lin, Renkun
Chen, Lili
Peng, Yongde
Fan, Nengguang
author_sort Tan, Yijiong
collection PubMed
description OBJECTIVE: Patients with type 2 diabetes have a high risk of non-alcoholic fatty liver disease (NAFLD) and related liver fibrosis. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated efficacy in improving NAFLD, while their effectiveness on liver fibrosis is limited in type 2 diabetic patients. MATERIALS/METHODS: A prospective cohort study was performed in type 2 diabetic patients. The study subjects were divided into two groups based on the use of liraglutide or not, and propensity score matching (PSM) was also conducted. After 12 months follow-up, liver fibrosis was assessed by NAFLD fibrosis score (NFS) fibrosis-4 (FIB-4), and liver stiffness measurement (LSM). The association between liraglutide use and liver fibrosis was analyzed by multivariable linear regression. RESULTS: In the current study, a total of 1,765 type 2 diabetic patients were enrolled. 262 patients were liraglutide user and 1,503 were nouser. After 12 months follow-up, liraglutide use tended to be associated with reduced prevalence of advanced fibrosis (3.1% vs. 6.1%, P = 0.218). After adjustment for confounding factors, multivariable linear regression revealed that liraglutide use was negatively associated with decreased NFS (β= -0.34, P = 0.043), FIB4 (β= -0.26, P = 0.044) and LSM (β= -4.95, P = 0.007) in type 2 diabetics. The results after PSM were similar to those before PSM. CONCLUSIONS: Liraglutide treatment is associated with decreased liver fibrosis in type 2 diabetic subjects.
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spelling pubmed-93994672022-08-25 Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes Tan, Yijiong Zhen, Qin Ding, Xiaoying Shen, Tingting Liu, Fang Wang, Yufan Zhang, Qidi Lin, Renkun Chen, Lili Peng, Yongde Fan, Nengguang Front Endocrinol (Lausanne) Endocrinology OBJECTIVE: Patients with type 2 diabetes have a high risk of non-alcoholic fatty liver disease (NAFLD) and related liver fibrosis. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated efficacy in improving NAFLD, while their effectiveness on liver fibrosis is limited in type 2 diabetic patients. MATERIALS/METHODS: A prospective cohort study was performed in type 2 diabetic patients. The study subjects were divided into two groups based on the use of liraglutide or not, and propensity score matching (PSM) was also conducted. After 12 months follow-up, liver fibrosis was assessed by NAFLD fibrosis score (NFS) fibrosis-4 (FIB-4), and liver stiffness measurement (LSM). The association between liraglutide use and liver fibrosis was analyzed by multivariable linear regression. RESULTS: In the current study, a total of 1,765 type 2 diabetic patients were enrolled. 262 patients were liraglutide user and 1,503 were nouser. After 12 months follow-up, liraglutide use tended to be associated with reduced prevalence of advanced fibrosis (3.1% vs. 6.1%, P = 0.218). After adjustment for confounding factors, multivariable linear regression revealed that liraglutide use was negatively associated with decreased NFS (β= -0.34, P = 0.043), FIB4 (β= -0.26, P = 0.044) and LSM (β= -4.95, P = 0.007) in type 2 diabetics. The results after PSM were similar to those before PSM. CONCLUSIONS: Liraglutide treatment is associated with decreased liver fibrosis in type 2 diabetic subjects. Frontiers Media S.A. 2022-08-10 /pmc/articles/PMC9399467/ /pubmed/36034438 http://dx.doi.org/10.3389/fendo.2022.935180 Text en Copyright © 2022 Tan, Zhen, Ding, Shen, Liu, Wang, Zhang, Lin, Chen, Peng and Fan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Tan, Yijiong
Zhen, Qin
Ding, Xiaoying
Shen, Tingting
Liu, Fang
Wang, Yufan
Zhang, Qidi
Lin, Renkun
Chen, Lili
Peng, Yongde
Fan, Nengguang
Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title_full Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title_fullStr Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title_full_unstemmed Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title_short Association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
title_sort association between use of liraglutide and liver fibrosis in patients with type 2 diabetes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399467/
https://www.ncbi.nlm.nih.gov/pubmed/36034438
http://dx.doi.org/10.3389/fendo.2022.935180
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