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Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis

Non-alcoholic fatty liver disease (NAFLD) is an important common comorbidity in individuals with type 2 diabetes (T2DM). Although some glucagon-like peptide-1 receptor agonists (GLP-1RAs) have beneficial effects on NAFLD, the efficacy of once-weekly semaglutide has not been established. This was a s...

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Autores principales: Nomoto, Hiroshi, Takahashi, Yuka, Takano, Yoshinari, Yokoyama, Hiroki, Tsuchida, Kazuhisa, Nagai, So, Miya, Aika, Kameda, Hiraku, Cho, Kyu Yong, Nakamura, Akinobu, Atsumi, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459529/
https://www.ncbi.nlm.nih.gov/pubmed/37631377
http://dx.doi.org/10.3390/pharmaceutics15082163
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author Nomoto, Hiroshi
Takahashi, Yuka
Takano, Yoshinari
Yokoyama, Hiroki
Tsuchida, Kazuhisa
Nagai, So
Miya, Aika
Kameda, Hiraku
Cho, Kyu Yong
Nakamura, Akinobu
Atsumi, Tatsuya
author_facet Nomoto, Hiroshi
Takahashi, Yuka
Takano, Yoshinari
Yokoyama, Hiroki
Tsuchida, Kazuhisa
Nagai, So
Miya, Aika
Kameda, Hiraku
Cho, Kyu Yong
Nakamura, Akinobu
Atsumi, Tatsuya
author_sort Nomoto, Hiroshi
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) is an important common comorbidity in individuals with type 2 diabetes (T2DM). Although some glucagon-like peptide-1 receptor agonists (GLP-1RAs) have beneficial effects on NAFLD, the efficacy of once-weekly semaglutide has not been established. This was a subanalysis of the SWITCH-SEMA 1 study, a multicenter, prospective, randomized, parallel-group trial comparing switching from liraglutide or dulaglutide to once-weekly semaglutide in subjects with T2DM (SWITCH) versus continuing current GLP-1RAs (Continue) for 24 weeks. This subanalysis consisted of participants who were suspected to have NAFLD [fatty liver index (FLI) ≥ 30]. In total, 58 participants met the criteria of this subanalysis. There were no statistical differences in baseline characteristics between the SWITCH (n = 31) and Continue groups (n = 27). FLI significantly improved during treatment in the SWITCH group (68.6 to 62.7) but not in the Continue group (71.1 to 72.3) (p < 0.01). The improvement of FLI in the SWITCH group was greater in switching from dulaglutide to semaglutide and significantly correlated with older age (p = 0.016) and lower baseline FLI (p < 0.01). The multiple linear regression analysis revealed that the switch from dulaglutide was associated with an improvement in FLI (p = 0.041). Switching from conventional GLP-1RAs to once-weekly semaglutide might be beneficial for individuals with NAFLD complicated with T2DM.
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spelling pubmed-104595292023-08-27 Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis Nomoto, Hiroshi Takahashi, Yuka Takano, Yoshinari Yokoyama, Hiroki Tsuchida, Kazuhisa Nagai, So Miya, Aika Kameda, Hiraku Cho, Kyu Yong Nakamura, Akinobu Atsumi, Tatsuya Pharmaceutics Article Non-alcoholic fatty liver disease (NAFLD) is an important common comorbidity in individuals with type 2 diabetes (T2DM). Although some glucagon-like peptide-1 receptor agonists (GLP-1RAs) have beneficial effects on NAFLD, the efficacy of once-weekly semaglutide has not been established. This was a subanalysis of the SWITCH-SEMA 1 study, a multicenter, prospective, randomized, parallel-group trial comparing switching from liraglutide or dulaglutide to once-weekly semaglutide in subjects with T2DM (SWITCH) versus continuing current GLP-1RAs (Continue) for 24 weeks. This subanalysis consisted of participants who were suspected to have NAFLD [fatty liver index (FLI) ≥ 30]. In total, 58 participants met the criteria of this subanalysis. There were no statistical differences in baseline characteristics between the SWITCH (n = 31) and Continue groups (n = 27). FLI significantly improved during treatment in the SWITCH group (68.6 to 62.7) but not in the Continue group (71.1 to 72.3) (p < 0.01). The improvement of FLI in the SWITCH group was greater in switching from dulaglutide to semaglutide and significantly correlated with older age (p = 0.016) and lower baseline FLI (p < 0.01). The multiple linear regression analysis revealed that the switch from dulaglutide was associated with an improvement in FLI (p = 0.041). Switching from conventional GLP-1RAs to once-weekly semaglutide might be beneficial for individuals with NAFLD complicated with T2DM. MDPI 2023-08-20 /pmc/articles/PMC10459529/ /pubmed/37631377 http://dx.doi.org/10.3390/pharmaceutics15082163 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nomoto, Hiroshi
Takahashi, Yuka
Takano, Yoshinari
Yokoyama, Hiroki
Tsuchida, Kazuhisa
Nagai, So
Miya, Aika
Kameda, Hiraku
Cho, Kyu Yong
Nakamura, Akinobu
Atsumi, Tatsuya
Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title_full Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title_fullStr Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title_full_unstemmed Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title_short Effect of Switching to Once-Weekly Semaglutide on Non-Alcoholic Fatty Liver Disease: The SWITCH-SEMA 1 Subanalysis
title_sort effect of switching to once-weekly semaglutide on non-alcoholic fatty liver disease: the switch-sema 1 subanalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10459529/
https://www.ncbi.nlm.nih.gov/pubmed/37631377
http://dx.doi.org/10.3390/pharmaceutics15082163
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