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Metabolic syndrome and transaminases: systematic review and meta-analysis

BACKGROUND: Metabolic syndrome (MetS) is a group of metabolic abnormalities characterised by hypertension, central obesity, dyslipidaemia and dysregulation of blood glucose, associated with the risk of diabetes, cardiovascular disease and overall mortality. The presence of elevated liver enzymes may...

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Autores principales: Raya-Cano, Elena, Molina-Luque, Rafael, Vaquero-Abellán, Manuel, Molina-Recio, Guillermo, Jiménez-Mérida, Rocío, Romero-Saldaña, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614379/
https://www.ncbi.nlm.nih.gov/pubmed/37899468
http://dx.doi.org/10.1186/s13098-023-01200-z
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author Raya-Cano, Elena
Molina-Luque, Rafael
Vaquero-Abellán, Manuel
Molina-Recio, Guillermo
Jiménez-Mérida, Rocío
Romero-Saldaña, Manuel
author_facet Raya-Cano, Elena
Molina-Luque, Rafael
Vaquero-Abellán, Manuel
Molina-Recio, Guillermo
Jiménez-Mérida, Rocío
Romero-Saldaña, Manuel
author_sort Raya-Cano, Elena
collection PubMed
description BACKGROUND: Metabolic syndrome (MetS) is a group of metabolic abnormalities characterised by hypertension, central obesity, dyslipidaemia and dysregulation of blood glucose, associated with the risk of diabetes, cardiovascular disease and overall mortality. The presence of elevated liver enzymes may precede the development of MetS, with alterations of the liver being observed that are directly related to metabolic problems. The study aims to provide the best evidence on the association between liver enzymes (ALT, AST, GGT) and MetS by determining the effect size of these biomarkers. METHODS: A systematic review and meta-analysis of studies indexed in PubMed and Scopus databases were performed. Study quality was assessed using the STROBE tool. The Grade Pro tool was used to evaluate the evidence, and the quantitative synthesis was performed using RevMan (Cochrane Collaboration). RESULTS: Seventeen articles comparing liver enzyme concentrations between 76,686 with MetS (MetS+) and 201,855 without MetS (MetS-) subjects were included. The concentration of ALT, AST and GGT in the MetS + subjects was significantly higher than in the control group 7.13 IU/L (CI95% 5.73–8.54; p < 0.00001; I(2) = 96%), 2.68 IU/L (CI95% 1.82–3.54; p < 0.00001; I(2) = 96%) and 11.20 IU/L (CI95% 7.11–15.29; p < 0.00001; I(2) = 96%), respectively. CONCLUSIONS: The evaluation of the relationship of liver enzymes in the pathophysiological process of MetS could lead to new insights into early diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01200-z.
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spelling pubmed-106143792023-10-31 Metabolic syndrome and transaminases: systematic review and meta-analysis Raya-Cano, Elena Molina-Luque, Rafael Vaquero-Abellán, Manuel Molina-Recio, Guillermo Jiménez-Mérida, Rocío Romero-Saldaña, Manuel Diabetol Metab Syndr Review BACKGROUND: Metabolic syndrome (MetS) is a group of metabolic abnormalities characterised by hypertension, central obesity, dyslipidaemia and dysregulation of blood glucose, associated with the risk of diabetes, cardiovascular disease and overall mortality. The presence of elevated liver enzymes may precede the development of MetS, with alterations of the liver being observed that are directly related to metabolic problems. The study aims to provide the best evidence on the association between liver enzymes (ALT, AST, GGT) and MetS by determining the effect size of these biomarkers. METHODS: A systematic review and meta-analysis of studies indexed in PubMed and Scopus databases were performed. Study quality was assessed using the STROBE tool. The Grade Pro tool was used to evaluate the evidence, and the quantitative synthesis was performed using RevMan (Cochrane Collaboration). RESULTS: Seventeen articles comparing liver enzyme concentrations between 76,686 with MetS (MetS+) and 201,855 without MetS (MetS-) subjects were included. The concentration of ALT, AST and GGT in the MetS + subjects was significantly higher than in the control group 7.13 IU/L (CI95% 5.73–8.54; p < 0.00001; I(2) = 96%), 2.68 IU/L (CI95% 1.82–3.54; p < 0.00001; I(2) = 96%) and 11.20 IU/L (CI95% 7.11–15.29; p < 0.00001; I(2) = 96%), respectively. CONCLUSIONS: The evaluation of the relationship of liver enzymes in the pathophysiological process of MetS could lead to new insights into early diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01200-z. BioMed Central 2023-10-30 /pmc/articles/PMC10614379/ /pubmed/37899468 http://dx.doi.org/10.1186/s13098-023-01200-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Raya-Cano, Elena
Molina-Luque, Rafael
Vaquero-Abellán, Manuel
Molina-Recio, Guillermo
Jiménez-Mérida, Rocío
Romero-Saldaña, Manuel
Metabolic syndrome and transaminases: systematic review and meta-analysis
title Metabolic syndrome and transaminases: systematic review and meta-analysis
title_full Metabolic syndrome and transaminases: systematic review and meta-analysis
title_fullStr Metabolic syndrome and transaminases: systematic review and meta-analysis
title_full_unstemmed Metabolic syndrome and transaminases: systematic review and meta-analysis
title_short Metabolic syndrome and transaminases: systematic review and meta-analysis
title_sort metabolic syndrome and transaminases: systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614379/
https://www.ncbi.nlm.nih.gov/pubmed/37899468
http://dx.doi.org/10.1186/s13098-023-01200-z
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