Cargando…
Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials
BACKGROUND: Pioglitazone is considered a potential therapy for non-alcoholic fatty liver disease (NAFLD). However, different effects of pioglitazone on NAFLD have been demonstrated in diabetic and non-diabetic patients. Herein, a meta-analysis of randomized, placebo-controlled trials was carried out...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091905/ https://www.ncbi.nlm.nih.gov/pubmed/37065735 http://dx.doi.org/10.3389/fendo.2023.1111430 |
_version_ | 1785023225030246400 |
---|---|
author | Wang, Zeyu Du, Huiqing Zhao, Ying Ren, Yadi Ma, Cuihua Chen, Hongyu Li, Man Tian, Jiageng Xue, Caihong Long, Guangfeng Xu, Meidong Jiang, Yong |
author_facet | Wang, Zeyu Du, Huiqing Zhao, Ying Ren, Yadi Ma, Cuihua Chen, Hongyu Li, Man Tian, Jiageng Xue, Caihong Long, Guangfeng Xu, Meidong Jiang, Yong |
author_sort | Wang, Zeyu |
collection | PubMed |
description | BACKGROUND: Pioglitazone is considered a potential therapy for non-alcoholic fatty liver disease (NAFLD). However, different effects of pioglitazone on NAFLD have been demonstrated in diabetic and non-diabetic patients. Herein, a meta-analysis of randomized, placebo-controlled trials was carried out to indirectly compare pioglitazone in NAFLD patients with vs. without type 2 diabetes. METHODS: Randomized controlled trials (RCTs) of pioglitazone vs. placebo involving NAFLD patients with or without type 2 diabetes/prediabetes collected from databases were enrolled into this analysis. Methodological quality was employed to evaluate the domains recommended by the Cochrane Collaboration. The analysis covered the changes in histology (fibrosis, hepatocellular ballooning, inflammation, steatosis), liver enzymes, blood lipids, fasting blood glucose (FBS), homeostasis model assessment-IR (HOMA-IR), weight and body mass index (BMI) before and after treatment, and adverse events. RESULTS: The review covered seven articles, with 614 patients in total, of which three were non-diabetic RCTs. No difference was found in patients with vs. without type 2 diabetes in histology, liver enzymes, blood lipids, HOMA-IR, weight, BMI, and FBS. Moreover, no significant difference was revealed in adverse effects between NAFLD patients with diabetes and without DM, except the incidence of edema that was found to be higher in the pioglitazone group than in the placebo group in NAFLD patients with diabetes. CONCLUSIONS: Pioglitazone could exert a certain effect on alleviating NAFLD, which was consistent between non-diabetic NAFLD patients and diabetic NAFLD patients in improving histopathology, liver enzymes, and HOMA-IR and reducing blood lipids. Furthermore, there were no adverse effects, except the incidence of edema which is higher in the pioglitazone group in NAFLD patients with diabetes. However, large sample sizes and well-designed RCTs are required to further confirm these conclusions. |
format | Online Article Text |
id | pubmed-10091905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100919052023-04-13 Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials Wang, Zeyu Du, Huiqing Zhao, Ying Ren, Yadi Ma, Cuihua Chen, Hongyu Li, Man Tian, Jiageng Xue, Caihong Long, Guangfeng Xu, Meidong Jiang, Yong Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Pioglitazone is considered a potential therapy for non-alcoholic fatty liver disease (NAFLD). However, different effects of pioglitazone on NAFLD have been demonstrated in diabetic and non-diabetic patients. Herein, a meta-analysis of randomized, placebo-controlled trials was carried out to indirectly compare pioglitazone in NAFLD patients with vs. without type 2 diabetes. METHODS: Randomized controlled trials (RCTs) of pioglitazone vs. placebo involving NAFLD patients with or without type 2 diabetes/prediabetes collected from databases were enrolled into this analysis. Methodological quality was employed to evaluate the domains recommended by the Cochrane Collaboration. The analysis covered the changes in histology (fibrosis, hepatocellular ballooning, inflammation, steatosis), liver enzymes, blood lipids, fasting blood glucose (FBS), homeostasis model assessment-IR (HOMA-IR), weight and body mass index (BMI) before and after treatment, and adverse events. RESULTS: The review covered seven articles, with 614 patients in total, of which three were non-diabetic RCTs. No difference was found in patients with vs. without type 2 diabetes in histology, liver enzymes, blood lipids, HOMA-IR, weight, BMI, and FBS. Moreover, no significant difference was revealed in adverse effects between NAFLD patients with diabetes and without DM, except the incidence of edema that was found to be higher in the pioglitazone group than in the placebo group in NAFLD patients with diabetes. CONCLUSIONS: Pioglitazone could exert a certain effect on alleviating NAFLD, which was consistent between non-diabetic NAFLD patients and diabetic NAFLD patients in improving histopathology, liver enzymes, and HOMA-IR and reducing blood lipids. Furthermore, there were no adverse effects, except the incidence of edema which is higher in the pioglitazone group in NAFLD patients with diabetes. However, large sample sizes and well-designed RCTs are required to further confirm these conclusions. Frontiers Media S.A. 2023-03-29 /pmc/articles/PMC10091905/ /pubmed/37065735 http://dx.doi.org/10.3389/fendo.2023.1111430 Text en Copyright © 2023 Wang, Du, Zhao, Ren, Ma, Chen, Li, Tian, Xue, Long, Xu and Jiang 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 Wang, Zeyu Du, Huiqing Zhao, Ying Ren, Yadi Ma, Cuihua Chen, Hongyu Li, Man Tian, Jiageng Xue, Caihong Long, Guangfeng Xu, Meidong Jiang, Yong Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title | Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title_full | Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title_fullStr | Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title_full_unstemmed | Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title_short | Response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: A meta-analysis of randomized controlled trials |
title_sort | response to pioglitazone in non-alcoholic fatty liver disease patients with vs. without type 2 diabetes: a meta-analysis of randomized controlled trials |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091905/ https://www.ncbi.nlm.nih.gov/pubmed/37065735 http://dx.doi.org/10.3389/fendo.2023.1111430 |
work_keys_str_mv | AT wangzeyu responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT duhuiqing responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT zhaoying responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT renyadi responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT macuihua responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT chenhongyu responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT liman responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT tianjiageng responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT xuecaihong responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT longguangfeng responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT xumeidong responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials AT jiangyong responsetopioglitazoneinnonalcoholicfattyliverdiseasepatientswithvswithouttype2diabetesametaanalysisofrandomizedcontrolledtrials |