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Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease

Background: Gut microbiota are considered to be intrinsic regulators of thyroid autoimmunity. We designed a cross-sectional study to examine the makeup and metabolic function of microbiota in Graves' disease (GD) patients, with the ultimate aim of offering new perspectives on the diagnosis and...

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Autores principales: Jiang, Wen, Yu, Xiaqing, Kosik, Russell Oliver, Song, Yingchun, Qiao, Tingting, Tong, Junyu, Liu, Simin, Fan, Suyun, Luo, Qiong, Chai, Li, Lv, Zhongwei, Li, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110022/
https://www.ncbi.nlm.nih.gov/pubmed/33234057
http://dx.doi.org/10.1089/thy.2020.0193
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author Jiang, Wen
Yu, Xiaqing
Kosik, Russell Oliver
Song, Yingchun
Qiao, Tingting
Tong, Junyu
Liu, Simin
Fan, Suyun
Luo, Qiong
Chai, Li
Lv, Zhongwei
Li, Dan
author_facet Jiang, Wen
Yu, Xiaqing
Kosik, Russell Oliver
Song, Yingchun
Qiao, Tingting
Tong, Junyu
Liu, Simin
Fan, Suyun
Luo, Qiong
Chai, Li
Lv, Zhongwei
Li, Dan
author_sort Jiang, Wen
collection PubMed
description Background: Gut microbiota are considered to be intrinsic regulators of thyroid autoimmunity. We designed a cross-sectional study to examine the makeup and metabolic function of microbiota in Graves' disease (GD) patients, with the ultimate aim of offering new perspectives on the diagnosis and treatment of GD. Methods: The 16S ribosomal RNA (rRNA) V3–V4 DNA regions of microbiota were obtained from fecal samples collected from 45 GD patients and 59 controls. Microbial differences between the two groups were subsequently analyzed based on high-throughput sequencing. Results: Compared with controls, GD patients had reduced alpha diversity (p < 0.05). At the phylum level, GD patients had a significantly lower proportion of Firmicutes (p = 0.008) and a significantly higher proportion of Bacteroidetes (p = 0.002) compared with the controls. At the genus level, GD patients had greater numbers of Bacteroides and Lactobacillus, although fewer Blautia, [Eubacterium]_hallii_group, Anaerostipes, Collinsella, Dorea, unclassified_f_Peptostreptococcaceae, and [Ruminococcus]_torques_group than controls (all p < 0.05). Subgroup analysis of GD patients revealed that Lactobacillus may play a key role in the pathogenesis of autoimmune thyroid diseases. Nine distinct genera showed significant correlations with certain thyroid function tests. Functional prediction revealed that Blautia may be an important microbe in certain metabolic pathways that occur in the hyperthyroid state. In addition, linear discriminant analysis (LDA) and effect size (LEfSe) analysis showed that there were significant differences in the levels of 18 genera between GD patients and controls (LDA >3.0, all p < 0.05). A diagnostic model using the top nine genera had an area under the curve of 0.8109 [confidence interval: 0.7274–0.8945]. Conclusions: Intestinal microbiota are different in GD patients. The microbiota we identified offer an alternative noninvasive diagnostic methodology for GD. Microbiota may also play a role in thyroid autoimmunity, and future research is needed to further elucidate the role.
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spelling pubmed-81100222021-05-11 Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease Jiang, Wen Yu, Xiaqing Kosik, Russell Oliver Song, Yingchun Qiao, Tingting Tong, Junyu Liu, Simin Fan, Suyun Luo, Qiong Chai, Li Lv, Zhongwei Li, Dan Thyroid Immunology, Autoimmunity, and Graves' Ophthalmopathy Background: Gut microbiota are considered to be intrinsic regulators of thyroid autoimmunity. We designed a cross-sectional study to examine the makeup and metabolic function of microbiota in Graves' disease (GD) patients, with the ultimate aim of offering new perspectives on the diagnosis and treatment of GD. Methods: The 16S ribosomal RNA (rRNA) V3–V4 DNA regions of microbiota were obtained from fecal samples collected from 45 GD patients and 59 controls. Microbial differences between the two groups were subsequently analyzed based on high-throughput sequencing. Results: Compared with controls, GD patients had reduced alpha diversity (p < 0.05). At the phylum level, GD patients had a significantly lower proportion of Firmicutes (p = 0.008) and a significantly higher proportion of Bacteroidetes (p = 0.002) compared with the controls. At the genus level, GD patients had greater numbers of Bacteroides and Lactobacillus, although fewer Blautia, [Eubacterium]_hallii_group, Anaerostipes, Collinsella, Dorea, unclassified_f_Peptostreptococcaceae, and [Ruminococcus]_torques_group than controls (all p < 0.05). Subgroup analysis of GD patients revealed that Lactobacillus may play a key role in the pathogenesis of autoimmune thyroid diseases. Nine distinct genera showed significant correlations with certain thyroid function tests. Functional prediction revealed that Blautia may be an important microbe in certain metabolic pathways that occur in the hyperthyroid state. In addition, linear discriminant analysis (LDA) and effect size (LEfSe) analysis showed that there were significant differences in the levels of 18 genera between GD patients and controls (LDA >3.0, all p < 0.05). A diagnostic model using the top nine genera had an area under the curve of 0.8109 [confidence interval: 0.7274–0.8945]. Conclusions: Intestinal microbiota are different in GD patients. The microbiota we identified offer an alternative noninvasive diagnostic methodology for GD. Microbiota may also play a role in thyroid autoimmunity, and future research is needed to further elucidate the role. Mary Ann Liebert, Inc., publishers 2021-05-01 2021-05-03 /pmc/articles/PMC8110022/ /pubmed/33234057 http://dx.doi.org/10.1089/thy.2020.0193 Text en © Wen Jiang et al., 2021; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by-nc/4.0/This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License [CC-BY-NC] (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Immunology, Autoimmunity, and Graves' Ophthalmopathy
Jiang, Wen
Yu, Xiaqing
Kosik, Russell Oliver
Song, Yingchun
Qiao, Tingting
Tong, Junyu
Liu, Simin
Fan, Suyun
Luo, Qiong
Chai, Li
Lv, Zhongwei
Li, Dan
Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title_full Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title_fullStr Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title_full_unstemmed Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title_short Gut Microbiota May Play a Significant Role in the Pathogenesis of Graves' Disease
title_sort gut microbiota may play a significant role in the pathogenesis of graves' disease
topic Immunology, Autoimmunity, and Graves' Ophthalmopathy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110022/
https://www.ncbi.nlm.nih.gov/pubmed/33234057
http://dx.doi.org/10.1089/thy.2020.0193
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