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The association between BMI and serum uric acid is partially mediated by gut microbiota

Obesity is a risk factor for the development of hyperuricemia, both of which were related to gut microbiota. However, whether alterations in the gut microbiota lie in the pathways mediating obesity’s effects on hyperuricemia is less clear. Body mass index (BMI) and serum uric acid (SUA) were separat...

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Autores principales: Duan, Zhuo, Fu, Jingxiang, Zhang, Feng, Cai, Yijia, Wu, Guangyan, Ma, Wenjun, Zhou, Hongwei, He, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581133/
https://www.ncbi.nlm.nih.gov/pubmed/37747198
http://dx.doi.org/10.1128/spectrum.01140-23
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author Duan, Zhuo
Fu, Jingxiang
Zhang, Feng
Cai, Yijia
Wu, Guangyan
Ma, Wenjun
Zhou, Hongwei
He, Yan
author_facet Duan, Zhuo
Fu, Jingxiang
Zhang, Feng
Cai, Yijia
Wu, Guangyan
Ma, Wenjun
Zhou, Hongwei
He, Yan
author_sort Duan, Zhuo
collection PubMed
description Obesity is a risk factor for the development of hyperuricemia, both of which were related to gut microbiota. However, whether alterations in the gut microbiota lie in the pathways mediating obesity’s effects on hyperuricemia is less clear. Body mass index (BMI) and serum uric acid (SUA) were separately important indicators of obesity and hyperuricemia. Our study aims to investigate whether BMI-related gut microbiota characteristics would mediate the association between BMI and SUA levels. A total of 6,280 participants from Guangdong Gut Microbiome Project were included in this study. Stool samples were collected for 16S rRNA gene sequencing. The results revealed that BMI was significantly and positively associated with SUA. Meanwhile, BMI was significantly associated with the abundance of 102 gut microbial genera, 16 of which were also significantly associated with SUA. The mediation analysis revealed that the association between BMI and SUA was partially mediated by the abundance of Proteobacteria (proportion mediated: 0.94%, P < 0.05). At the genus level, 25 bacterial genera, including Ralstonia, Oscillospira, Faecalibacterium, etc., could also partially mediate the association of BMI with SUA (the highest proportion is mediated by Ralstonia, proportion mediated: 2.76%, P < 0.05). This study provided evidence for the associations among BMI, gut microbiota, and SUA, and the mediation analysis suggested that the association of BMI with SUA was partially mediated by the gut microbiota. IMPORTANCE: Using 16S rRNA sequencing analysis, local interpretable machine learning technique analysis and mediation analysis were used to explore the association between BMI with SUA, and the mediating effects of gut microbial dysbiosis in the association were investigated.
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spelling pubmed-105811332023-10-18 The association between BMI and serum uric acid is partially mediated by gut microbiota Duan, Zhuo Fu, Jingxiang Zhang, Feng Cai, Yijia Wu, Guangyan Ma, Wenjun Zhou, Hongwei He, Yan Microbiol Spectr Research Article Obesity is a risk factor for the development of hyperuricemia, both of which were related to gut microbiota. However, whether alterations in the gut microbiota lie in the pathways mediating obesity’s effects on hyperuricemia is less clear. Body mass index (BMI) and serum uric acid (SUA) were separately important indicators of obesity and hyperuricemia. Our study aims to investigate whether BMI-related gut microbiota characteristics would mediate the association between BMI and SUA levels. A total of 6,280 participants from Guangdong Gut Microbiome Project were included in this study. Stool samples were collected for 16S rRNA gene sequencing. The results revealed that BMI was significantly and positively associated with SUA. Meanwhile, BMI was significantly associated with the abundance of 102 gut microbial genera, 16 of which were also significantly associated with SUA. The mediation analysis revealed that the association between BMI and SUA was partially mediated by the abundance of Proteobacteria (proportion mediated: 0.94%, P < 0.05). At the genus level, 25 bacterial genera, including Ralstonia, Oscillospira, Faecalibacterium, etc., could also partially mediate the association of BMI with SUA (the highest proportion is mediated by Ralstonia, proportion mediated: 2.76%, P < 0.05). This study provided evidence for the associations among BMI, gut microbiota, and SUA, and the mediation analysis suggested that the association of BMI with SUA was partially mediated by the gut microbiota. IMPORTANCE: Using 16S rRNA sequencing analysis, local interpretable machine learning technique analysis and mediation analysis were used to explore the association between BMI with SUA, and the mediating effects of gut microbial dysbiosis in the association were investigated. American Society for Microbiology 2023-09-25 /pmc/articles/PMC10581133/ /pubmed/37747198 http://dx.doi.org/10.1128/spectrum.01140-23 Text en Copyright © 2023 Duan et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Duan, Zhuo
Fu, Jingxiang
Zhang, Feng
Cai, Yijia
Wu, Guangyan
Ma, Wenjun
Zhou, Hongwei
He, Yan
The association between BMI and serum uric acid is partially mediated by gut microbiota
title The association between BMI and serum uric acid is partially mediated by gut microbiota
title_full The association between BMI and serum uric acid is partially mediated by gut microbiota
title_fullStr The association between BMI and serum uric acid is partially mediated by gut microbiota
title_full_unstemmed The association between BMI and serum uric acid is partially mediated by gut microbiota
title_short The association between BMI and serum uric acid is partially mediated by gut microbiota
title_sort association between bmi and serum uric acid is partially mediated by gut microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581133/
https://www.ncbi.nlm.nih.gov/pubmed/37747198
http://dx.doi.org/10.1128/spectrum.01140-23
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