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

瘤胃球菌 生物 厚壁菌 真细菌 肠道菌群 发病机制 拟杆菌 乳酸菌 拟杆菌 链球菌 疾病 医学 内科学 失调 微生物群 免疫学 免疫系统 微生物学 甲状腺 16S核糖体RNA 遗传学 细菌
作者
Wen Jiang,Xiaqing Yu,Russell O Kosik,Yingchun Song,Tingting Qiao,Junyu Tong,Simin Liu,Suyun Fan,Qiong Luo,Li Chai,Zhongwei Lv,Dan Li
出处
期刊:Thyroid [Mary Ann Liebert, Inc.]
卷期号:31 (5): 810-820 被引量:22
标识
DOI:10.1089/thy.2020.0193
摘要

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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