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Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation
Alternations of gut microbiota (GM) in atrial fibrillation (AF) with elevated diversity, perturbed composition and function have been described previously. The current work aimed to assess the association of GM composition with AF recurrence (RAF) after ablation based on metagenomic sequencing and m...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701499/ https://www.ncbi.nlm.nih.gov/pubmed/33058365 http://dx.doi.org/10.1111/jcmm.15959 |
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author | Li, Jing Zuo, Kun Zhang, Jing Hu, Chaowei Wang, Pan Jiao, Jie Liu, Zheng Yin, Xiandong Liu, Xiaoqing Li, Kuibao Yang, Xinchun |
author_facet | Li, Jing Zuo, Kun Zhang, Jing Hu, Chaowei Wang, Pan Jiao, Jie Liu, Zheng Yin, Xiandong Liu, Xiaoqing Li, Kuibao Yang, Xinchun |
author_sort | Li, Jing |
collection | PubMed |
description | Alternations of gut microbiota (GM) in atrial fibrillation (AF) with elevated diversity, perturbed composition and function have been described previously. The current work aimed to assess the association of GM composition with AF recurrence (RAF) after ablation based on metagenomic sequencing and metabolomic analyses and to construct a GM‐based predictive model for RAF. Compared with non‐AF controls (50 individuals), GM composition and metabolomic profile were significantly altered between patients with recurrent AF (17 individuals) and non‐RAF group (23 individuals). Notably, discriminative taxa between the non‐RAF and RAF groups, including the families Nitrosomonadaceae and Lentisphaeraceae, the genera Marinitoga and Rufibacter and the species Faecalibacterium spCAG:82, Bacillus gobiensis and Desulfobacterales bacterium PC51MH44, were selected to construct a taxonomic scoring system based on LASSO analysis. After incorporating the clinical factors of RAF, taxonomic score retained a significant association with RAF incidence (HR = 2.647, P = .041). An elevated AUC (0.954) and positive NRI (1.5601) for predicting RAF compared with traditional clinical scoring (AUC = 0.6918) were obtained. The GM‐based taxonomic scoring system theoretically improves the model performance, and the nomogram and decision curve analysis validated the clinical value of the predicting model. These data provide novel possibility that incorporating the GM factor into future recurrent risk stratification. |
format | Online Article Text |
id | pubmed-7701499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77014992020-12-08 Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation Li, Jing Zuo, Kun Zhang, Jing Hu, Chaowei Wang, Pan Jiao, Jie Liu, Zheng Yin, Xiandong Liu, Xiaoqing Li, Kuibao Yang, Xinchun J Cell Mol Med Original Articles Alternations of gut microbiota (GM) in atrial fibrillation (AF) with elevated diversity, perturbed composition and function have been described previously. The current work aimed to assess the association of GM composition with AF recurrence (RAF) after ablation based on metagenomic sequencing and metabolomic analyses and to construct a GM‐based predictive model for RAF. Compared with non‐AF controls (50 individuals), GM composition and metabolomic profile were significantly altered between patients with recurrent AF (17 individuals) and non‐RAF group (23 individuals). Notably, discriminative taxa between the non‐RAF and RAF groups, including the families Nitrosomonadaceae and Lentisphaeraceae, the genera Marinitoga and Rufibacter and the species Faecalibacterium spCAG:82, Bacillus gobiensis and Desulfobacterales bacterium PC51MH44, were selected to construct a taxonomic scoring system based on LASSO analysis. After incorporating the clinical factors of RAF, taxonomic score retained a significant association with RAF incidence (HR = 2.647, P = .041). An elevated AUC (0.954) and positive NRI (1.5601) for predicting RAF compared with traditional clinical scoring (AUC = 0.6918) were obtained. The GM‐based taxonomic scoring system theoretically improves the model performance, and the nomogram and decision curve analysis validated the clinical value of the predicting model. These data provide novel possibility that incorporating the GM factor into future recurrent risk stratification. John Wiley and Sons Inc. 2020-10-14 2020-11 /pmc/articles/PMC7701499/ /pubmed/33058365 http://dx.doi.org/10.1111/jcmm.15959 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Li, Jing Zuo, Kun Zhang, Jing Hu, Chaowei Wang, Pan Jiao, Jie Liu, Zheng Yin, Xiandong Liu, Xiaoqing Li, Kuibao Yang, Xinchun Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title | Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title_full | Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title_fullStr | Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title_full_unstemmed | Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title_short | Shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
title_sort | shifts in gut microbiome and metabolome are associated with risk of recurrent atrial fibrillation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701499/ https://www.ncbi.nlm.nih.gov/pubmed/33058365 http://dx.doi.org/10.1111/jcmm.15959 |
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