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The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials

Coenzyme Q10 is a potent antioxidant and is necessary for energy production in mitochondria. Clinical data have suggested that coenzyme Q10 (CoQ10) has some beneficial effects on liver function. However, these results are equivocal. This systematic review and meta‐analysis aimed to clarify the effec...

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Autores principales: Soleimani Damaneh, Mohadeseh, Fatahi, Somaye, Aryaeian, Naheed, Bavi Behbahani, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494615/
https://www.ncbi.nlm.nih.gov/pubmed/37701221
http://dx.doi.org/10.1002/fsn3.3478
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author Soleimani Damaneh, Mohadeseh
Fatahi, Somaye
Aryaeian, Naheed
Bavi Behbahani, Hossein
author_facet Soleimani Damaneh, Mohadeseh
Fatahi, Somaye
Aryaeian, Naheed
Bavi Behbahani, Hossein
author_sort Soleimani Damaneh, Mohadeseh
collection PubMed
description Coenzyme Q10 is a potent antioxidant and is necessary for energy production in mitochondria. Clinical data have suggested that coenzyme Q10 (CoQ10) has some beneficial effects on liver function. However, these results are equivocal. This systematic review and meta‐analysis aimed to clarify the effect of coenzyme Q10 supplementation on the serum concentration of liver function enzymes. We searched the online databases using relevant keywords up to April 2022. Randomized clinical trials (RCTs) investigating the effect of CoQ10, compared with a control group, on serum concentrations of liver enzymes were included. We found a significant reduction following supplementation with CoQ10 on serum concentrations of alanine aminotransferase (ALT) based on 15 effect sizes from 13 RCTs (weighted mean difference [WMD] = −5.33 IU/L; 95% CI: −10.63, −0.03; p = .04), aspartate aminotransferase (AST) based on 15 effect sizes from 13 RCTs (WMD = −4.91 IU/L; 95% CI: −9.35, −0.47; p = .03) and gamma‐glutamyl transferase (GGT) based on eight effect sizes from six RCTs (WMD = −8.07 IU/L; 95% CI: −12.82, −3.32; p = .001; I (2) = 91.6%). However, we found no significant effects of CoQ10 supplementation on alkaline phosphatase concentration (WMD = 1.10 IU/L; 95% CI: −5.98, 8.18; p = .76). CoQ10 supplementation significantly improves circulating ALT, AST, and GGT levels; therefore, it might positively affect liver function. Further high‐quality RCTs with more extended intervention periods and larger sample sizes are recommended to confirm our results.
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spelling pubmed-104946152023-09-12 The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials Soleimani Damaneh, Mohadeseh Fatahi, Somaye Aryaeian, Naheed Bavi Behbahani, Hossein Food Sci Nutr Reviews Coenzyme Q10 is a potent antioxidant and is necessary for energy production in mitochondria. Clinical data have suggested that coenzyme Q10 (CoQ10) has some beneficial effects on liver function. However, these results are equivocal. This systematic review and meta‐analysis aimed to clarify the effect of coenzyme Q10 supplementation on the serum concentration of liver function enzymes. We searched the online databases using relevant keywords up to April 2022. Randomized clinical trials (RCTs) investigating the effect of CoQ10, compared with a control group, on serum concentrations of liver enzymes were included. We found a significant reduction following supplementation with CoQ10 on serum concentrations of alanine aminotransferase (ALT) based on 15 effect sizes from 13 RCTs (weighted mean difference [WMD] = −5.33 IU/L; 95% CI: −10.63, −0.03; p = .04), aspartate aminotransferase (AST) based on 15 effect sizes from 13 RCTs (WMD = −4.91 IU/L; 95% CI: −9.35, −0.47; p = .03) and gamma‐glutamyl transferase (GGT) based on eight effect sizes from six RCTs (WMD = −8.07 IU/L; 95% CI: −12.82, −3.32; p = .001; I (2) = 91.6%). However, we found no significant effects of CoQ10 supplementation on alkaline phosphatase concentration (WMD = 1.10 IU/L; 95% CI: −5.98, 8.18; p = .76). CoQ10 supplementation significantly improves circulating ALT, AST, and GGT levels; therefore, it might positively affect liver function. Further high‐quality RCTs with more extended intervention periods and larger sample sizes are recommended to confirm our results. John Wiley and Sons Inc. 2023-06-07 /pmc/articles/PMC10494615/ /pubmed/37701221 http://dx.doi.org/10.1002/fsn3.3478 Text en © 2023 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Soleimani Damaneh, Mohadeseh
Fatahi, Somaye
Aryaeian, Naheed
Bavi Behbahani, Hossein
The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title_full The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title_fullStr The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title_full_unstemmed The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title_short The effect of coenzyme Q10 supplementation on liver enzymes: A systematic review and meta‐analysis of randomized clinical trials
title_sort effect of coenzyme q10 supplementation on liver enzymes: a systematic review and meta‐analysis of randomized clinical trials
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494615/
https://www.ncbi.nlm.nih.gov/pubmed/37701221
http://dx.doi.org/10.1002/fsn3.3478
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