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The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin

The pandemic of COVID-19 has highlighted the intricate relationship between gut microbiome and overall health. Recent studies have shown that the Firmicutes/Bacteroidetes ratio in the gut microbiome may be linked to various diseases including COVID-19 and type 2 diabetes (T2D). Understanding the lin...

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Autores principales: Petakh, Pavlo, Oksenych, Valentyn, Kamyshnyi, Aleksandr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Masson SAS. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183625/
https://www.ncbi.nlm.nih.gov/pubmed/37196542
http://dx.doi.org/10.1016/j.biopha.2023.114892
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author Petakh, Pavlo
Oksenych, Valentyn
Kamyshnyi, Aleksandr
author_facet Petakh, Pavlo
Oksenych, Valentyn
Kamyshnyi, Aleksandr
author_sort Petakh, Pavlo
collection PubMed
description The pandemic of COVID-19 has highlighted the intricate relationship between gut microbiome and overall health. Recent studies have shown that the Firmicutes/Bacteroidetes ratio in the gut microbiome may be linked to various diseases including COVID-19 and type 2 diabetes (T2D). Understanding the link between gut microbiome and these diseases is essential for developing strategies for prevention and treatment. In this study, 115 participants were recruited and divided into three groups: 1st group: T2D patients and healthy controls, 2nd group: COVID-19 patients with and without T2D, 3rd group: T2D patients with COVID-19 treated with or without metformin. Gut microbial composition at the phylum level was assessed using qRT-PCR with universal primers targeting the bacterial 16 S rRNA gene and specific primers for Firmicutes and Bacteroidetes. Data was analyzed using one-way ANOVA, logistic regression, and Spearman's rank correlation coefficient. The study found that the ratio of Firmicutes to Bacteroidetes (F/B) was higher in patients with both T2D and COVID-19 compared to those with only T2D or COVID-19. Additionally, the F/B ratio was positively correlated with C-reactive protein (CRP) in T2D and COVID-19 patients. The study also suggests that metformin treatment may affect this correlation. Logistic regression analysis showed that the F/B ratio was significantly associated with CRP. These findings suggest that the F/B ratio may be a potential biomarker for inflammation in T2D and COVID-19 patients and metformin treatment may have an effect on the correlation between F/B and CRP levels.
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spelling pubmed-101836252023-05-15 The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin Petakh, Pavlo Oksenych, Valentyn Kamyshnyi, Aleksandr Biomed Pharmacother Article The pandemic of COVID-19 has highlighted the intricate relationship between gut microbiome and overall health. Recent studies have shown that the Firmicutes/Bacteroidetes ratio in the gut microbiome may be linked to various diseases including COVID-19 and type 2 diabetes (T2D). Understanding the link between gut microbiome and these diseases is essential for developing strategies for prevention and treatment. In this study, 115 participants were recruited and divided into three groups: 1st group: T2D patients and healthy controls, 2nd group: COVID-19 patients with and without T2D, 3rd group: T2D patients with COVID-19 treated with or without metformin. Gut microbial composition at the phylum level was assessed using qRT-PCR with universal primers targeting the bacterial 16 S rRNA gene and specific primers for Firmicutes and Bacteroidetes. Data was analyzed using one-way ANOVA, logistic regression, and Spearman's rank correlation coefficient. The study found that the ratio of Firmicutes to Bacteroidetes (F/B) was higher in patients with both T2D and COVID-19 compared to those with only T2D or COVID-19. Additionally, the F/B ratio was positively correlated with C-reactive protein (CRP) in T2D and COVID-19 patients. The study also suggests that metformin treatment may affect this correlation. Logistic regression analysis showed that the F/B ratio was significantly associated with CRP. These findings suggest that the F/B ratio may be a potential biomarker for inflammation in T2D and COVID-19 patients and metformin treatment may have an effect on the correlation between F/B and CRP levels. The Author(s). Published by Elsevier Masson SAS. 2023-07 2023-05-15 /pmc/articles/PMC10183625/ /pubmed/37196542 http://dx.doi.org/10.1016/j.biopha.2023.114892 Text en © 2023 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Petakh, Pavlo
Oksenych, Valentyn
Kamyshnyi, Aleksandr
The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title_full The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title_fullStr The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title_full_unstemmed The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title_short The F/B ratio as a biomarker for inflammation in COVID-19 and T2D: Impact of metformin
title_sort f/b ratio as a biomarker for inflammation in covid-19 and t2d: impact of metformin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183625/
https://www.ncbi.nlm.nih.gov/pubmed/37196542
http://dx.doi.org/10.1016/j.biopha.2023.114892
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