Next Article in Journal
Reply to Comment: Evaluation of the Association of Omentin 1 rs2274907 A > T and rs2274908 G > A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case–Control Study
Next Article in Special Issue
Altered Gut Microbiota in Irritable Bowel Syndrome and Its Association with Food Components
Previous Article in Journal
Comment: “Evaluation of the Association of Omentin 1 rs2274907 A>T and rs2274908 G>A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case Control Study”
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
JPM
Volume 10
Issue 4
10.3390/jpm10040192
jpm-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Differential Microbial Pattern Description in Subjects with Autoimmune-Based Thyroid Diseases: A Pilot Study

by
Isabel Cornejo-Pareja
1,2,†,
Patricia Ruiz-Limón
1,2,†,
Ana M. Gómez-Pérez
1,
María Molina-Vega
1,
Isabel Moreno-Indias
1,2,* and
Francisco J. Tinahones
1,2,3
1
Unidad de Gestión Clínica de Endocrinología y Nutrición, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Clínico Virgen de la Victoria, 29010 Málaga, Spain
2
CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, 28029 Madrid, Spain
3
Department of Medicine and Dermatology, University of Málaga, 29010 Málaga, Spain
*
Author to whom correspondence should be addressed.
†
These authors share first authorship.
J. Pers. Med. 2020, 10(4), 192; https://doi.org/10.3390/jpm10040192
Submission received: 15 September 2020 / Revised: 14 October 2020 / Accepted: 20 October 2020 / Published: 26 October 2020
(This article belongs to the Special Issue Targeting the Microbiome for Disease Diagnosis and Therapy: New Frontiers for Personalized Medicine)
Browse Figures
Versions Notes

Abstract

:
The interaction between genetic susceptibility, epigenetic, endogenous, and environmental factors play a key role in the initiation and progression of autoimmune thyroid diseases (AITDs). Studies have shown that gut microbiota alterations take part in the development of autoimmune diseases. We have investigated the possible relationship between gut microbiota composition and the most frequent AITDs. A total of nine Hashimoto’s thyroiditis (HT), nine Graves–Basedow’s disease (GD), and 11 otherwise healthy donors (HDs) were evaluated. 16S rRNA pyrosequencing and bioinformatics analysis by Quantitative Insights into Microbial Ecology and Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) were used to analyze the gut microbiota. Beta diversity analysis showed that gut microbiota from our groups was different. We observed an increase in bacterial richness in HT and a lower evenness in GD in comparison to the HDs. GD showed a significant increase of Fusobacteriaceae, Fusobacterium and Sutterella compared to HDs and the core microbiome features showed that Prevotellaceae and Prevotella characterized this group. Victivallaceae was increased in HT and was part of their core microbiome. Streptococcaceae, Streptococcus and Rikenellaceae were greater in HT compared to GD. Core microbiome features of HT were represented by Streptococcus, Alistipes, Anaerostipes, Dorea and Haemophilus. Faecalibacterium decreased in both AITDs compared to HDs. PICRUSt analysis demonstrated enrichment in the xenobiotics degradation, metabolism, and the metabolism of cofactors and vitamins in GD patients compared to HDs. Moreover, correlation studies showed that some bacteria were widely correlated with autoimmunity parameters. A prediction model evaluated a possible relationship between predominant concrete bacteria such as an unclassified genus of Ruminococcaceae, Sutterella and Faecalibacterium in AITDs. AITD patients present altered gut microbiota compared to HDs. These alterations could be related to the immune system development in AITD patients and the loss of tolerance to self-antigens.

1. Introduction

Autoimmune thyroid diseases (AITDs) are the most common organ-specific autoimmune disorders. Within AITDs, Hashimoto’s thyroiditis and Graves–Basedow’s disease are the most frequent conditions.
Hashimoto’s thyroiditis (HT) is identified by lymphocytes infiltration in the thyroid gland which leads to the destruction of thyroid follicles, and the production of autoantibodies against thyroid peroxidase (TPO, 90–95%) and thyroglobulin (TG, 20–50%) [1,2].
On the other hand, Graves’ disease (GD) is identified by the production of autoantibodies of the immunoglobulin G1 subclass that are directed against the thyrotropin receptor which induces thyroid hormone overproduction and also causing hypertrophy and hyperplasia of thyroid cells [3].
The etiology of AITDs is thought to be multifactorial, arising from an interaction between genetic susceptibility, epigenetic, and various endogenous and environmental factors [4].
Several studies have provided evidence for genetic factors, however, the concordance rate for AITDs among monozygotic twins is in the range of 35–55% compared with 3% in dizygotic twins, emphasizing that other important factors, such as the environment, are implicated in the pathogenesis of AITD [5,6,7].
Gut microbiota takes part in the homeostasis of the host, and especially in the regulation of the immune system. Gut microbiota is a promising agent for the development of personalized medicine as it collects information about its host, like diet or environmental factors [8]. Recent evidence suggest that the alteration of gut microbiota may have connection with autoimmune diseases [9,10,11,12].
Notwithstanding, the pathogenic link between gut microbiota and AITDs has not been fully elucidated, with only a few studies in humans [13,14,15]. Zhao et al., demonstrated that HT patients had an altered gut microbiota profile compared with the healthy population and this profile correlated with clinical parameters [16].
In the present study, we aimed to investigate the gut microbiota profile in patients affected by AITD, both HT and GD; and its relationship with autoimmunity markers.

2. Materials and Methods

2.1. Participants

A total of 18 AITD patients (nine GD patients and nine HT patients) were recruited at the Department of Endocrinology and Nutrition of Virgen de la Victoria University Hospital (Málaga, Spain). Moreover, we included 11 otherwise healthy donors (HDs) with similar anthropometric features as study groups, without thyroid disease and without family history of thyroid disease. These HDs were euthyroid and goiter was not evident on physical examination. Individuals were included from those who were attended at the hospital during the first half of 2018.
All participants with GD were receiving synthetic antithyroid (Neo-tomizol, 5–20 mg of dose) and HT patients were receiving levothyroxine treatment (Eutirox, 50–175 µg of dose) and presented an acceptable control of the disease which allowed us to focus on the pathophysiology of autoimmunity and not on thyroid dysfunction. The exclusion criteria were: pregnancy; type 1 or type 2 diabetes mellitus; other autoimmune disease; and chronic and/or severe gastrointestinal disorders. We also excluded patients and HDs with extreme diets, those exposed to antibiotic therapy (current or previous 3 months), chronic drugs different to AITDs medication that alter microbiota profile, those taking probiotic agents, and the non-acceptance of informed consent.
The study protocol was approved by the Medical Ethics Committee of Virgen de la Victoria University Hospital and conducted according to principals of the Declaration of Helsinki. All participants enrolled provided their written informed consent and were also verbally informed of the characteristics of the study.

2.2. Anthropometric and Laboratory Measurements

Anthropometric measurements, including body weight, height, and waist and hip circumferences, were collected. Peripheral venous blood samples were obtained after 8 hours of fasting. The serum was centrifuged at 4000 rpm for 15 min at 4 °C and frozen at −80 °C until analysis. Levels of cholesterol, triglycerides, HDL-cholesterol, and glucose were analyzed by enzymatic methods (Randox Laboratories Ltd., Crumlin, UK) and glycosylated hemoglobin (HbA1c) was determined by Dimension Vista autoanalyzer (Siemens Healthcare Diagnostics, Munich, Germany).
Laboratory markers of autoimmunity [thyroid stimulating immunoglobulin (TSI), anti- thyroperoxidase (Anti-TPO)] and thyroid profile [thyroid-stimulating hormone (TSH), free thyroxine (FT4), free triiodothyronine (FT3)] were quantified as part of the routine patient management in the case of AITD patients, with exception of HDs. Reference ranges were for TSH 0.4–5 μIU/mL; FT4 11–22 pmol/L; and FT3 2–5 pmol/L. TSI was measured by Elecsys Anti-TSHR test following the manufacturer’s protocols (Roche, Basel, Switzerland) in a Roche electrochemiluminometric analyzer (Cobas e 801, Roche, Basel, Switzerland). Anti-TPO was detected by Atellica IM Anti-Thyroid Peroxidase assay (SIEMENS Healthineers, Erlangen, Germany) using the Atellica IM Analyzer (SIEMENS Healthineers, Erlangen, Germany). Reference ranges were for TPO-Ab > 60 IU/mL and TSI-Ab > 2 IU/mL.

2.3. DNA Extraction from Faecal Samples

Faecal samples were obtained by the volunteers, immediately refrigerated, and carried to the laboratory, where they were stored at −80 °C for subsequent analysis.
DNA was extracted from 200 mg of stool using the QIAamp DNA stool Mini kit (Qiagen, Hilden, Germany) according to the manufacturer’s protocols. DNA concentration was measured by absorbance at 260 nm, and the purity was verified by determining the A260/A280 ratio with a Nanodrop spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA).

2.4. Sequencing of 16S rRNA and Bioinformatic Analysis

The Ion 16S Metagenomics Kit (Thermo-Fisher Scientific Inc., Waltham, MA, USA) was used to amplified the ribosomal 16S rRNA gene region from stool DNA, with two primer sets (V2–4–8 and V3–6, 7–9) covering the most of the hypervariable regions of the 16S rRNA region in bacteria. The libraries were created using the Ion Plus Fragment Library Kit (Thermo Fisher Scientific, Waltham, MA, USA). Barcodes were added to each sample using the Ion Xpress Barcode Adapters kit (Thermo Fisher Scientific, Waltham, MA, USA). Emulsion PCR and sequencing of the amplicon libraries were carried out on an Ion 520 chip (Ion 520TM Chip Kit) using the Ion Chef System and Torrent S5TM system, respectively, using the Ion 520TM/530TM Kit-Chef (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instructions. Torrent Suite™ Server software (Thermo Fisher Scientific, Waltham, MA, USA), version 5.4.0, with default parameters for the 16S Target Sequencing (bead loading ≤30, key signal ≤30, and usable sequences ≤30) was used to base calling and run demultiplexing. Raw data is stored at the public repository SRA database (NCBI) with the BioProject PRJNA666641.
The open-source Quantitative Insights into Microbial Ecology (QIIME2, version 2019.7) software was used to analyze the quality sequences [17,18] and also was used for diversity analysis and subsequent taxonomic analysis through clustering with search [19] and the reference base Greengenes version 13_8 at 97% of identity.
Metagenome function was predicted by Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) analysis through picking operational taxonomic units (OTUs) from the Greengenes database, as described elsewhere [20]. The resulting OTU table was employed to predict the metagenome at three different Kyoto Encyclopedia of Genes and Genomes (KEGG) Orthology (KO) levels (level (L) 1 to L3).

2.5. Statistical Analysis

The open-source Statistical Analysis of Metagenomic Profiles [STAMP (v 2.1.3)] [21] was used to compare the differential abundances of taxa, KEGG categories, and subcategories, with the White’s non-parametric test. α- and β-diversities were analyzed within QIIME2, through the diversity plugin: β-diversity metrics employed a permutational multivariate analysis of variance (PERMANOVA) with 999 permutations, while α-diversity metrics involved a Kruskal–Wallis test.
Anthropometric and clinical characteristics were analyzed with the IBM SPSS Statistics 25 (IBM, Armonk, NY, USA). The relationship between gut microbiota and thyroid variables was analyzed using Spearman´s correlations models. Binary logistic regression models were fitted to assess the relationship between thyroid profile and autoimmunity markers with particular features as independent predictors. To control for potential confounding factors, their results were adjusted by age (years), sex (male or female) and body mass index (BMI, kg/m2). The results were described as mean and dispersion (standard deviation, SD) for quantitative variables and as a proportion for qualitative variables. Statistical significance was established at p < 0.05. p values were corrected for multiple comparisons using the Benjamini–Hochberg method at 0.1, and reported as q-value, when appropriate.

3. Results

3.1. Clinical Data Study

All subjects (n = 29) were of Spanish nationality and born and grown in the Andalusian community. The study groups showed similar clinical characteristics about age, sex, anthropometric parameters, or metabolic profile, without finding statistically significant differences (p > 0.05). Our AITD patients had normalized thyroid function by medical treatment, substitution with levothyroxine in HT patients, or antithyroid drugs in patients with GD. However, we found significant differences in autoimmunity between the three study groups. TPO-Ab was significantly increased in HT and TSI-Ab was significantly increased in GD. HDs values of TPO-Ab resulted in slightly increased levels than expected for healthy individuals. In addition, according to serum TSH range our HDs were euthyroid. These demographic and clinical data of the subjects are summarized in Table 1.

3.2. Gut Microbiota Diversity in AITD Patients

After the quality assessment, a total of 2,785,614 quality 16S rRNA gene sequences with an average of 26,056 ± 29,024 sequences per sample passed the filters. In order to compare the populations of the different groups, dimensional Principal Coordinates Analysis plots of UniFrac distances were used. Qualitative (Unweighted UniFrac distance) and quantitative (Weighted Unifrac distance) relationships showed differences among the groups (p = 0.003 and p = 0.002, respectively) (Figure 1A,B). Further analysis showed that our AITD patients did not show significant differences (p > 0.05), but they showed statistically significant differences with respect to HDs (p < 0.05 in groups, AITD patients related to HDs) (Figure S1).
Alpha diversity was assessed using rarefaction curves. Richness, estimated by the observed features index, demonstrated a significant increase in HT patients versus HDs (p = 0.022), while no differences were found between the other groups. Evenness, calculated by the Pielou index, showed a significant decreased in GD patients compared with HDs (p = 0.03) and no significant differences among the other groups. Finally, biodiversity, estimated by the Shannon index, suggested no significant differences among the study groups (Figure 1C).

3.3. Gut Microbiota Profile in AITD Patients

Dominant bacterial phyla were Bacteroidetes and Firmicutes, while Proteobacteria, Actinobacteria, and Tenericutes shared smaller proportions, between 1–10%, in the different study groups. No differences were observed between our study groups at this taxa level (Figure 2A).
At the family level, Fusobacteriaceae was significantly increased in GD patients when compared with HT patients and HDs (q = 0.01). Furthermore, a significantly higher abundance was found in HT patients when compared with HDs for Victivallaceae (q = 0.03). In addition, Rikenellaceae was significantly decreased in GD patients compared with HT patients (q = 0.04) (Figure 2B).
Finally, at the genus level, Fusobacterium was significantly higher in GD patients compared with HDs and also compared with HT patients (q = 0.02 and q = 0.009, respectively). Faecalibacterium was significantly lower in GD patients compared to HDs and also compared with HT patients (q = 0.02 and q = 0.07, respectively). An unclassified genus of the family Rikenellaceae was significantly lower in GD patients compared to HT patients (q = 0.03). The genus Sutterella was significantly higher in GD patients compared to HDs (q = 0.10) (Figure 2C).

3.4. Core Microbiome in AITD Patients and HDs

After studying the differences between groups, we wondered if each group was characterized by a concrete core gut microbiome. We investigated the core microbiome of each group, meaning those features that were shared among the 85% of the samples of each study group. At the family level, we observed that a total of 15 identified families were shared by all the volunteers of the study (See the complete list in Table S1). Interestingly, Pasteurellaceae was only shared between AITD patients. Victivallaceae and Streptococcaceae were characteristic of the HT group and Prevotellaceae of GD group; while Christensenellaceae seemed to be characteristic of the HDs group (Figure 3A). On the other hand, 12 identified genera were shared between the three groups (See the complete list in Table S1). Collinsella and Roseburia belonged to the core microbiome of both AITDs, while Butyricimonas was shared by GD patients and HDs. HT patients were the group with a greater number of characteristic features: Streptococcus, Alistipes, Anaerostipes, Dorea and Haemophilus; while Prevotella was characteristic of the GD group. No characteristic genus was found in the HDs group (Figure 3B).

3.5. Differences in the Metabolic Profiles of Gut Microbiota between AITD Patients and HDs

PICRUSt metagenome predictions were used to identify those microbial functions that were enriched or degraded in AITD patients and HDs. In tier 2 of the KO categories, we observed no significant differences between HT patients and HDs or between both pathologies. However, we found pathways significantly different between GD patients and HDs at this level (Figure 3C).
Moreover, in tier 3 of the KO categories, we have not observed changes between HT patients and HDs. Nevertheless, we have detected a high number of pathways significantly different between GD patients and HDs at this level. The 27 pathways can be observed in detail in Figure S2.

3.6. AITDs Could Be Related to Bacterial Profile

Correlation studies were performed to establish a relationship between the thyroid autoimmunity of the study groups and their gut microbiota. Significant univariate correlations were found between the number of specific bacteria with thyroid autoimmunity markers like thyroperoxidase antibody (TPO-ab) (positive correlation with Alistipes; Ruminococcaceae unclassified and Enterobacteriaceae, so negative correlation with Faecalibacterium) and thyroid stimulating immunoglobulin antibody (TSI-ab) (positive correlation with Lactobacillus and Pasteurellaceae and negative correlation with Faecalibacterium) (Table 2).
When we evaluated the possible implication of the gut microbial community in global AITDs, we found that an unclassified genus of Ruminococcaceae was associated with a 49.4% rise in the odds of the TPO-ab presence in the crude model. This trend was also maintained in the adjusted model by BMI, age, and sex (Table 3). Likewise, we found that Sutterella could influence in TSI-ab presence, with a 35.1% increase in either the crude model or the adjusted model. However, Faecalibacterium was associated with a decrease of 94.1% in the odds of presenting positive TSI autoimmunity in the crude model, so this relationship is maintained in the adjusted model (Table 4).

4. Discussion

Our study has pointed out that the AITDs share common as well as particular gut microbiome profile features that differ from the stool profile of HDs and those dysbiotic amounts of particular taxa could be related with the development of the disease.
Autoimmune disease initiation has been linked to gut microbiota dysbiosis by different mechanisms such as molecular mimicry, the by-stander activation, and the epitope spreading. In recent years, patients bearing with an already established AITDs have also been reported to show alterations of the gut microbial composition [22,23,24].
Gut microbiome profiles from our study groups are different according to beta diversity analysis. However, further comparisons showed that the main differences belonged to the microbiota populations of HDs and each one of the AITDs studied. Thus, AITDs could share some patterns of their microbiota profiles. AITDs microbial changes have been classically attributed to morphological changes. Interestingly, patients with HT presented ultrastructural morphological changes of distal duodenum enterocytes, a variation in microvillus thickness, and a leaky gut condition [22]. On the other hand, GD frequently impacts the hollow organs with lower levels of gastric acid production, increased the intestinal motility which along with autoimmune gastritis contributing to diarrhea. Thus, GD might reshape the intestinal microbial composition through intestinal physiological modifications [7].
The increased bacterial richness that we have observed in our HT patients might be related to the bacterial overgrowth in the intestinal tract of these hypothyroid patients [25,26]. On the other hand, our GD patients showed a lower evenness in their microbiota populations in comparison to the HDs, which could indicate that in this population, could be dominant features. However, biodiversity did not show any significant differences among our study groups, which was aligned with reported works [15,27,28].
Our core microbiome results have demonstrated that the identified features at family and genus levels were mainly shared by our three study groups. However, despite this apparent normality, we have found some specific bacteria characteristic of each particular condition.
Taking together the differences in the feature abundances of each group and their respective core microbiomes, we have found important trends associated with each study group. About GD patients, we found a significant increase in the Fusobacteriaceae family and its Fusobacterium genus in GD. Fusobacterium is a well-recognized pro-inflammatory bacterium [29] and Fusobacterium nucleatum has been already reported in GD patients [30]. Sutterella was found higher in abundance in GD patients than in HDs. Sutterella has been positively related to prediabetes and inflammatory bowel disease [31,32] and it has an immunomodulatory role and pro-inflammatory capacity in the human gastrointestinal tract [33]. Moreover, we have also found a remarkable relationship between Prevotellaceae family and Prevotella genus with GD group through the core microbiome analysis. Prevotella has been linked with GD patients [27] and other autoimmune diseases like rheumatoid arthritis [34]. Thus, Fusobacterium, Sutterella and Prevotella, features relative to GD disease, have been linked to processes related to inflammation and autoimmunity.
In the case of HT patients, the family Victivallaceae is increased and is part of their core microbiome. Nevertheless, the role of these bacteria is little known, only some reports linking Victivallaceae with diet and obesity [35]. Another member of the core microbiome is the family Streptococcaceae and its genus Streptococcus that in combination with Rikenellaceae, which has been found increased in the HT patients concerning GD, have been reported to take part in the decrease in alpha-diversity in type 1 diabetes, with the capacity to behave as pathogens [36]. This is also the case of Haemophilus, which most of its species are considered pathobionts. H. influenzae has been reported to induce autoimmune disease by molecular mimicry of an epitope [37]. Furthermore, other core microbiome features of HT like Alistipes, Anaerostipes or Dorea could also be treated as pathobionts that within the disease environment could develop the capacity to damage the host. Together these results suggest that it could be possible that with a larger study these pathobionts from the core microbiome of the tested groups could reach a statistical significance between them.
About HDs related to AITDs, the core microbiome launched that Christensenellaceae was characteristic of this group. This result is compatible with studies that identify Christensenellaceae family as an important player in human health, associated with human longevity [38] and with lower levels of BMI [39]. As in the other groups, maybe a longer study could trigger differences in the abundance of Christensenellaceae with respect to the AITDs. Moreover, our study showed that Faecalibacterium genus decreases in autoimmune thyroid conditions compared to HDs, which is aligned with previous works [16,27]. It is important to remark that, although HDs were appropriate for the comparison with the other groups attending to their anthropometric and biochemical variables (no differences were observed with respect to the tested groups), the election of volunteers with a lower BMI could be beneficial for greater differences with respect to the tested groups. This fact could be also considered about the election of volunteers without TPO-Ab, although it is known that low levels are not relevant for the clinical practice if they are not accompanied by other variables [40]. These issues will be considered in future studies.
According to the PICRUSt analysis, GD disease is characterized by enrichment in xenobiotics degradation and metabolism as well as the metabolism of cofactors and vitamins in comparison to HDs. This could be related to the fact that GD patients are characterized by hypermetabolism [41] and could be translated into their microbiota profiles. Moreover, the enrichment in xenobiotics degradation could be related to the fact of these patients are medicated. This result could be indicative of some kind of intervention of the gut microbiota in the medication action, as it has been reported with other drugs [42].
Further analysis was performed to establish a possible relationship between autoimmunity parameters and specific features. Our analyses showed a positive correlation of TSI-ab with Pasteurellaceae family shared by AITDs patients. Pasteurellaceae family has been previously correlated with GD patients [27]. Thus, our correlation studies showed that some members of the gut microbiota were widely correlated with autoimmunity parameters, indicating that the gut microbiota might be closely related to the AITDs. Our findings may support future research on the interaction of the gut microbiota to the development of the AITDs. Likewise, a prediction model evaluated a possible relationship between predominant concrete bacteria in the AITDs. An unclassified genus of the Ruminococcaeae family and Sutterella were related to HT patients and GD patients, increasing the risk of presenting positive TPO-ab and TSI-ab, respectively. On one hand, Ruminococcaceae has been found as a part of the shared core microbiome of our volunteers [43]. On the other hand, we have already shown the implication of Sutterella in inflammatory conditions.
The most promising feature seems to be Faecalibacterium. Faecalibacterium has been related to a decrease of 94.1% in TSI immunity. In addition, inflammatory processes like inflammatory bowel diseases and colorectal cancer are favored when Faecalibacterium is decreased [44,45]. Moreover, in our study, Faecalibacterium has been shown as a protective factor, reducing the probability of presenting TSI-ab related to GD patients. The decrease of Faecalibacterium could indicate a real dysbiosis in these patients.
Although this study has several strengths, as the complete characterization of the microbiota, several limitations to this research must be acknowledged, like the low number of subjects because of the pilot study nature of our investigation. In this manner, this fact has been advertized throughout the document. Although further longitudinal investigations are necessary to evaluate the progression of the AITDs, these results contribute to the increase in scarce knowledge about the relationship between the gut microbiota and AITDs.

5. Conclusions

In this pilot study, our observations demonstrated a gut dysbiosis in AITD patients, may be able to contribute to thyroid disease development. Thus, gut dysbiosis might be related to the immune system development in AITD patients and the loss of tolerance to self-antigens including thyroglobulin and the autoimmunity that triggers AITD. Even though the studies of microbiome and their association to predict disease states are useful for personalized medicine, a deeper understanding of the microbiome might be necessary for the development of evidence-based microbial therapeutics in AITDs. Furthermore, studies with a greater number of subjects and longitudinal studies investigations might be required to evaluate the progression of the AITDs. Nevertheless, our results contribute to the increase in scarce knowledge about the relationship between the gut microbiota and AITDs.

Supplementary Materials

The following are available online at https://www.mdpi.com/2075-4426/10/4/192/s1, Table S1: Shared families and genera from each core microbiomes of the study group. Figure S1: Clustering of fecal bacterial communities according to the different study groups by PCoA using unweighted and weighted UniFrac distances. Figure S2: Significant differences in predicted functional composition at the level 3 of KEGG Pathways of the gut microbiota among HDs and GD patients.

Author Contributions

Conceptualization, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; methodology, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; validation, I.C.-P., P.R.-L., A.M.G.-P., M.M.-V., I.M.-I. and F.J.T.; formal analysis, I.C.-P., P.R.-L., A.M.G.-P., M.M.-V., I.M.-I. and F.J.T.; investigation, I.C.-P., P.R.-L., A.M.G.-P., M.M.-V., I.M.-I. and F.J.T.; resources, I.C.-P., P.R.-L., A.M.G.-P., M.M.-V., I.M.-I. and F.J.T.; data curation, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; writing—original draft preparation, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; writing—review and editing, I.C.-P., P.R.-L., A.M.G.-P., M.M.-V., I.M.-I. and F.J.T.; visualization, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; supervision, I.M.-I. and F.J.T.; project administration, I.C.-P., P.R.-L., I.M.-I. and F.J.T.; funding acquisition, I.M.-I. and F.J.T. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by Instituto de Salud Carlos III co-founded by Fondo Europeo de Desarrollo Regional—FEDER (CP16/00163, PI18/01160), Madrid, Spain. ICP was supported by Rio Hortega and now for Juan Rodes from the Spanish Ministry of Economy and Competitiveness (ISCIII) and cofounded by Fondo Europeo de Desarrollo Regional-FEDER (CM 17/00169, JR 19/00054). PRL was supported by the “Sara Borrell” program from ISCIII; Madrid, Spain and cofounded by Fondo Europeo de Desarrollo Regional–FEDER (CD19/00216). AMGP was supported by a research contract from Servicio Andaluz de Salud (B-0033-2014). MMV was supported by Rio Hortega from the Spanish Ministry of Economy and Competitiveness (ISCIII) and cofounded by Fondo Europeo de Desarrollo Regional-FEDER (CM18/00120). IMI was supported by the “MS type I” program from ISCIII; Madrid, Spain, cofounded by Fondo Europeo de Desarrollo Regional—FEDER (CP16/00163).

Acknowledgments

The authors thank the Metagenomic Platform of the CIBER Physiopathology of Obesity and Nutrition (CIBERobn), ISCIII, Madrid, Spain, especially to Pablo Rodríguez.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Pearce, E.N.; Farwell, A.P.; Braverman, L.E. Thyroiditis. N. Engl. J. Med. 2003, 348, 2646–2655. [Google Scholar] [CrossRef] [PubMed]
  2. Devdhar, M.; Ousman, Y.H.; Burman, K.D. Hypothyroidism. Endocrinol. Metab. Clin. North Am. 2007, 36, 595–615. [Google Scholar] [CrossRef] [PubMed]
  3. De Leo, S.; Lee, S.Y.; Braverman, L.E. Hyperthyroidism. Lancet 2016, 388, 906–918. [Google Scholar] [CrossRef] [Green Version]
  4. Hasham, A.; Tomer, Y. Genetic and epigenetic mechanisms in thyroid autoimmunity. Immunol. Res. 2012, 54, 204–213. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Tozzoli, R.; Barzilai, O.; Ram, M.; Villalta, D.; Bizzaro, N.; Sherer, Y.; Shoenfeld, Y. Infections and autoimmune thyroid diseases: Parallel detection of antibodies against pathogens with proteomic technology. Autoimmun. Rev. 2008, 8, 112–115. [Google Scholar] [CrossRef] [PubMed]
  6. Prummel, M.F.; Strieder, T.; Wiersinga, W.M. The environment and autoimmune thyroid diseases. Eur. J. Endocrinol. 2004, 150, 605–618. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Ebert, E.C. The Thyroid and the Gut. J. Clin. Gastroenterol. 2010, 44, 402–406. [Google Scholar] [CrossRef] [PubMed]
  8. Behrouzi, A.; Nafari, A.H.; Siadat, S.D. The significance of microbiome in personalized medicine. Clin. Transl. Med. 2019, 8, 16. [Google Scholar] [CrossRef]
  9. Leiva-Gea, I.; Sánchez-Alcoholado, L.; Martín-Tejedor, B.; Castellano-Castillo, D.; Moreno-Indias, I.; Urda-Cardona, A.; Tinahones, F.J.; Fernández-García, J.C.; Queipo-Ortuño, M.I. Gut Microbiota Differs in Composition and Functionality Between Children With Type 1 Diabetes and MODY2 and Healthy Control Subjects: A Case-Control Study. Diabetes Care 2018, 41, 2385–2395. [Google Scholar] [CrossRef] [Green Version]
  10. Vázquez, N.M.; Ruiz-Limón, P.; Moreno-Indias, I.; Manrique-Arija, S.; Tinahones, F.J.; Fernandez-Nebro, A. Expansion of Rare and Harmful Lineages is Associated with Established Rheumatoid Arthritis. J. Clin. Med. 2020, 9, 1044. [Google Scholar] [CrossRef] [Green Version]
  11. Edwards, C.J.; Costenbader, K. Epigenetics and the microbiome: Developing areas in the understanding of the aetiology of lupus. Lupus 2014, 23, 505–506. [Google Scholar] [CrossRef] [PubMed]
  12. Sellitto, M.; Bai, G.; Serena, G.; Fricke, W.F.; Sturgeon, C.; Gajer, P.; White, J.R.; Koenig, S.S.K.; Sakamoto, J.; Boothe, D.; et al. Proof of Concept of Microbiome-Metabolome Analysis and Delayed Gluten Exposure on Celiac Disease Autoimmunity in Genetically At-Risk Infants. PLoS ONE 2012, 7, e33387. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Zhou, J.S.; Gill, H.S. Immunostimulatory probiotic Lactobacillus rhamnosus HN001 and Bifidobacterium lactis HN019 do not induce pathological inflammation in mouse model of experimental autoimmune thyroiditis. Int. J. Food Microbiol. 2005, 103, 97–104. [Google Scholar] [CrossRef] [PubMed]
  14. Penhale, W.J.; Young, P.R. The influence of the normal microbial flora on the susceptibility of rats to experimental autoimmune thyroiditis. Clin. Exp. Immunol. 1988, 72, 288–292. [Google Scholar]
  15. Ishaq, H.M.; Mohammad, I.S.; Guo, H.; Shahzad, M.; Hou, Y.J.; Ma, C.; Naseem, Z.; Wu, X.; Shi, P.; Xu, J. Molecular estimation of alteration in intestinal microbial composition in Hashimoto’s thyroiditis patients. Biomed. Pharmacother. 2017, 95, 865–874. [Google Scholar] [CrossRef]
  16. Zhao, F.; Feng, J.; Li, J.; Zhao, L.; Liu, Y.; Chen, H.; Jin, Y.; Zhu, B.; Wei, Y. Alterations of the Gut Microbiota in Hashimoto’s Thyroiditis Patients. Thyroid. 2018, 28, 175–186. [Google Scholar] [CrossRef]
  17. Bolyen, E.; Rideout, J.R.; Dillon, M.R.; Bokulich, N.A.; Abnet, C.; Al-Ghalith, G.A.; Alexander, H.; Alm, E.J.; Arumugam, M.; Asnicar, F.; et al. QIIME 2: Reproducible, interactive, scalable, and extensible microbiome data science. Nat. Biotechnol. 2019, 37, 852–857. [Google Scholar] [CrossRef]
  18. Callahan, B.J.; McMurdie, P.J.; Rosen, M.J.; Han, A.W.; Johnson, A.J.A.; Holmes, S.P. DADA2: High-resolution sample inference from Illumina amplicon data. Nat. Methods 2016, 13, 581–583. [Google Scholar] [CrossRef] [Green Version]
  19. Rognes, T.; Flouri, T.; Nichols, B.; Quince, C.; Mahé, F. VSEARCH: A versatile open source tool for metagenomics. PeerJ 2016, 4, e2584. [Google Scholar] [CrossRef]
  20. Benjamini, Y.; Hochberg, Y. Benjamini-1995.pdf. J. R. Stat. Soc. B 1995, 57, 289–300. [Google Scholar]
  21. Parks, D.H.; Tyson, G.W.; Hugenholtz, P.; Beiko, R.G. STAMP: Statistical analysis of taxonomic and functional profiles. Bioinformatics 2014, 30, 3123–3124. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Sasso, F.C.; Carbonara, O.; Torella, R.; Mezzogiorno, A.; Esposito, V.; DeMagistris, L.; Secondulfo, M.; Carratu’, R.; Iafusco, D.; Cartenì, M. Ultrastructural changes in enterocytes in subjects with Hashimoto’s thyroiditis. Gut 2004, 53, 1878–1880. [Google Scholar] [CrossRef] [Green Version]
  23. Virili, C.; Fallahi, P.; Antonelli, A.; Benvenga, S.; Centanni, M. Gut microbiota and Hashimoto’s thyroiditis. Rev. Endocr. Metab. Disord. 2018, 19, 293–300. [Google Scholar] [CrossRef] [PubMed]
  24. Mu, Q.; Kirby, J.; Reilly, C.M.; Luo, X.M. Leaky Gut As a Danger Signal for Autoimmune Diseases. Front. Immunol. 2017, 8, 598. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Lauritano, E.C.; Bilotta, A.L.; Gabrielli, M.; Scarpellini, E.; Lupascu, A.; Laginestra, A.; Novi, M.; Sottili, S.; Serricchio, M.; Cammarota, G.; et al. Association between Hypothyroidism and Small Intestinal Bacterial Overgrowth. J. Clin. Endocrinol. Metab. 2007, 92, 4180–4184. [Google Scholar] [CrossRef] [Green Version]
  26. Ghoshal, U.C.; Shukla, R.; Ghoshal, U.; Gwee, K.-A.; Ng, S.C.; Quigley, E.M.M. The Gut Microbiota and Irritable Bowel Syndrome: Friend or Foe? Int. J. Inflamm. 2012, 2012, 1–13. [Google Scholar] [CrossRef]
  27. Ishaq, H.M.; Mohammad, I.S.; Shahzad, M.; Ma, C.; Raza, M.A.; Wu, X.; Guo, H.; Shi, P.; Xu, J. Molecular Alteration Analysis of Human Gut Microbial Composition in Graves’ disease Patients. Int. J. Biol. Sci. 2018, 14, 1558–1570. [Google Scholar] [CrossRef] [Green Version]
  28. Chen, J.; Chia, N.; Kalari, K.R.; Yao, J.Z.; Novotna, M.; Soldan, M.M.P.; Luckey, D.H.; Marietta, E.V.; Jeraldo, P.R.; Chen, X.; et al. Multiple sclerosis patients have a distinct gut microbiota compared to healthy controls. Sci. Rep. 2016, 6, 28484. [Google Scholar] [CrossRef] [Green Version]
  29. Liu, H.; Redline, R.W.; Han, Y.W. Fusobacterium nucleatum Induces Fetal Death in Mice via Stimulation of TLR4-Mediated Placental Inflammatory Response. J. Immunol. 2007, 179, 2501–2508. [Google Scholar] [CrossRef] [Green Version]
  30. Zhou, L.; Li, X.; Ahmed, A.; Wu, D.; Liu, L.; Qiu, J.; Yan, Y.; Jin, M.; Xin, Y. Gut Microbe Analysis Between Hyperthyroid and Healthy Individuals. Curr. Microbiol. 2014, 69, 675–680. [Google Scholar] [CrossRef]
  31. Allin, K.H.; Tremaroli, V.; Caesar, R.; Jensen, B.A.H.; Damgaard, M.T.F.; Bahl, M.I.; Licht, T.R.; Hansen, T.H.; Nielsen, T.; Dantoft, T.M.; et al. Aberrant intestinal microbiota in individuals with prediabetes. Diabetologia 2018, 61, 810–820. [Google Scholar] [CrossRef] [Green Version]
  32. Lavelle, A.; Lennon, G.; O’Sullivan, O.; Docherty, N.; Balfe, A.; Maguire, A.; Mulcahy, H.E.; Doherty, G.; O’Donoghue, D.; Hyland, J.; et al. Spatial variation of the colonic microbiota in patients with ulcerative colitis and control volunteers. Gut 2015, 64, 1553–1561. [Google Scholar] [CrossRef] [Green Version]
  33. Hiippala, K.; Kainulainen, V.; Kalliomäki, M.; Arkkila, P.; Satokari, R. Mucosal Prevalence and Interactions with the Epithelium Indicate Commensalism of Sutterella spp. Front. Microbiol. 2016, 7, 1706. [Google Scholar] [CrossRef] [Green Version]
  34. Scher, J.U.; Sczesnak, A.; Longman, R.S.; Segata, N.; Ubeda, C.; Bielski, C.; Rostron, T.; Cerundolo, V.; Pamer, E.G.; Abramson, S.B.; et al. Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis. eLife 2013, 2, e01202. [Google Scholar] [CrossRef] [PubMed]
  35. Kaplan, R.C.; Wang, Z.; Usyk, M.; Sotres-Alvarez, D.; Daviglus, M.L.; Schneiderman, N.; Talavera, G.A.; Gellman, M.D.; Thyagarajan, B.; Moon, J.-Y.; et al. Gut microbiome composition in the Hispanic Community Health Study/Study of Latinos is shaped by geographic relocation, environmental factors, and obesity. Genome Biol. 2019, 20, 219–221. [Google Scholar] [CrossRef] [PubMed]
  36. Kostic, A.D.; Gevers, D.; Siljander, H.; Vatanen, T.; Hyötyläinen, T.; Hämäläinen, A.-M.; Peet, A.; Tillmann, V.; Pöhö, P.; Mattila, I.; et al. The Dynamics of the Human Infant Gut Microbiome in Development and in Progression toward Type 1 Diabetes. Cell Host Microbe 2015, 17, 260–273. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Croxford, J.L.; Anger, H.A.; Miller, S.D. Viral Delivery of an Epitope fromHaemophilus influenzaeInduces Central Nervous System Autoimmune Disease by Molecular Mimicry. J. Immunol. 2005, 174, 907–917. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Waters, J.L.; Ley, R.E. The human gut bacteria Christensenellaceae are widespread, heritable, and associated with health. BMC Biol. 2019, 17, 1–11. [Google Scholar] [CrossRef]
  39. Goodrich, J.K.; Waters, J.L.; Poole, A.C.; Sutter, J.L.; Koren, O.; Blekhman, R.; Beaumont, M.; Van Treuren, W.; Knight, R.; Bell, J.T.; et al. Human Genetics Shape the Gut Microbiome. Cell 2014, 159, 789–799. [Google Scholar] [CrossRef] [Green Version]
  40. Prummel, M.F.; Wiersinga, W.M. Thyroid peroxidase autoantibodies in euthyroid subjects. Best Pr. Res. Clin. Endocrinol. Metab. 2005, 19, 1–15. [Google Scholar] [CrossRef]
  41. Gelfand, R.A.; Hutchinson-Williams, K.A.; Bonde, A.A.; Castellino, P.; Sherwin, R.S. Catabolic effects of thyroid hormone excess: The contribution of adrenergic activity to hypermetabolism and protein breakdown. Metabolism 1987, 36, 562–569. [Google Scholar] [CrossRef]
  42. Koppel, N.; Rekdal, V.M.; Balskus, E.P. Chemical transformation of xenobiotics by the human gut microbiota. Science 2017, 356, eaag2770. [Google Scholar] [CrossRef] [PubMed]
  43. Punzalan, C.; Qamar, A. Probiotics for the Treatment of Liver Disease. In The Microbiota in Gastrointestinal Pathophysiology: Implications for Human Health, Prebiotics, Probiotics, and Dysbiosis, 1st ed.; Elsevier Inc.: London, UK, 2017; pp. 373–381. ISBN 9780128040621. [Google Scholar]
  44. Louis, P.; Flint, H.J. Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine. FEMS Microbiol. Lett. 2009, 294, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Ferreira-Halder, C.V.; Faria, A.V.D.S.; Andrade, S.S. Action and function of Faecalibacterium prausnitzii in health and disease. Best Pract. Res. Clin. Gastroenterol. 2017, 31, 643–648. [Google Scholar] [CrossRef]
Jpm 10 00192 g001 550
Figure 1. Estimation of diversity in healthy donors (HDs), Graves–Basedow’s disease (GD) patients, and Hashimoto’s thyroiditis (HT) patients. Clustering of fecal bacterial communities according to the different study groups by PCoA using unweighted and weighted UniFrac distances. Statistical differences were observed between groups. (A) Unweighted UniFrac distances, p = 0.003; and (B) Weighted UniFrac distances, p = 0.002. Dots belong to the HDs group; square to GD patients and cone to HT patients. (C) Shannon Diversity and Evenness indexes and estimated richness among different groups were compared. All values are mean ± SD. * p < 0.05 GD patients vs. HDs; $ p < 0.05 HT patients vs. HDs. Circles belong to the HDs; squares to GD patients and triangles to HT patients.
Figure 1. Estimation of diversity in healthy donors (HDs), Graves–Basedow’s disease (GD) patients, and Hashimoto’s thyroiditis (HT) patients. Clustering of fecal bacterial communities according to the different study groups by PCoA using unweighted and weighted UniFrac distances. Statistical differences were observed between groups. (A) Unweighted UniFrac distances, p = 0.003; and (B) Weighted UniFrac distances, p = 0.002. Dots belong to the HDs group; square to GD patients and cone to HT patients. (C) Shannon Diversity and Evenness indexes and estimated richness among different groups were compared. All values are mean ± SD. * p < 0.05 GD patients vs. HDs; $ p < 0.05 HT patients vs. HDs. Circles belong to the HDs; squares to GD patients and triangles to HT patients.
Jpm 10 00192 g001
Jpm 10 00192 g002 550
Figure 2. (A) Microbiota profile of faecal samples from the study groups at the phylum level. (B) Families statistically significant between the study groups. (C) Genera statistically significant between the study groups. * Indicates significant differences between groups, q < 0.1 (q = p-FDR-corrected).
Figure 2. (A) Microbiota profile of faecal samples from the study groups at the phylum level. (B) Families statistically significant between the study groups. (C) Genera statistically significant between the study groups. * Indicates significant differences between groups, q < 0.1 (q = p-FDR-corrected).
Jpm 10 00192 g002
Jpm 10 00192 g003 550
Figure 3. (A) Venn diagram of the core microbiome from the study groups at the family level. (B) Venn diagram of the core microbiome from the study groups at the genus level. (C) Significant differences in predicted functional composition at level 2 of Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathways of the gut microbiota among HDs (white) and GD patients (dark grey). Only functional capacities with p < 0.1 are shown; q = p-value FDR-corrected.
Figure 3. (A) Venn diagram of the core microbiome from the study groups at the family level. (B) Venn diagram of the core microbiome from the study groups at the genus level. (C) Significant differences in predicted functional composition at level 2 of Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathways of the gut microbiota among HDs (white) and GD patients (dark grey). Only functional capacities with p < 0.1 are shown; q = p-value FDR-corrected.
Jpm 10 00192 g003
Table
Table 1. Clinical and demographic characteristics of patients and healthy donors.
Table 1. Clinical and demographic characteristics of patients and healthy donors.
ParametersHT Patients
(n = 9)		GD Patients
(n = 9)		HDs
(n = 11)		p-Value
Sex (M/F, % F)(0/10, 100)(2/7, 77.8)(4/7, 63.5)0.113
Age (years, mean ± SD)40.3 ± 9.646.2 ± 8.648.8 ± 6.20.062
Smokers (%)3044.4-----0.515
Family history of Thyroid disease (%)5033.3-----0.484
Time of evolution of thyroid disease (months, mean ± SD)134.4 ± 101.316.4 ± 22.6-----0.001 *
Anthropometry
Weight (kg, mean ± SD)63.4 ± 11.766.6 ± 13.069.5 ± 8.10.354
BMI (kg/m2, mean ± SD)24.9 ± 5.825.2 ± 4.725.0 ± 2.00.831
Waist c. (cm, mean ± SD)81.4 ± 13.886.1 ± 10.987.9 ± 8.40.321
Hip c. (cm, mean ± SD)98.3 ± 10.7101.6 ± 11.397.0 ± 4.10.391
Blood pressure
Systolic (mmHg, mean ± SD)121.6 ± 11.3119.6 ± 16.2128.8 ± 17.30.636
Diastolic (mmHg, mean ± SD)75.3 ± 5.175.0 ± 15.478.6 ± 8.70.449
Analytical metabolic
Glucose (mg/dL, mean ± SD)86.6 ± 6.593.4 ± 4.191.0 ± 8.30.078
HbA1c (%, mean ± SD)5.1 ± 0.35.3 ± 0.45.3 ± 0.30.29
Total-C (mg/dL, mean ± SD)178.5 ± 44.7192.2 ± 29.6192.4 ± 47.80.568
LDL-c (mg/dL, mean ± SD)107.7 ± 39.1109.4 ± 10.2110.1 ± 38.10.758
HDL-c (mg/dL, mean ± SD)56.8 ± 11.765.6 ± 22.260.5 ± 12.90.666
TGs (mg/dL, mean ± SD)70.1 ± 16.685.2 ± 31.9108.8 ± 59.00.132
CRP (mg/dL, mean ± SD)3.1 ± 0.03.2 ± 0.44.1 ± 1.40.116
Thyroid profile
TSH (µIU/mL, mean ± SD)2.6 ± 2.83.3 ± 8.52.2 ± 1.00.030 *
FT4 (pmol/L, mean ± SD)15.4 ± 2.215.2 ± 3.115.2 ± 1.30.76
FT3 (pmol/L, mean ± SD)3.8 ± 0.25.5 ± 2.34.8 ± 0.40.002 *
TPO-Ab (IU/mL, mean ± SD)1186.7 ± 358.4792.0 ± 621.7160.3 ± 381.30.001 *
TPO-Ab > 60 IU/mL (P/N, % P)(10/0, 100)(6/3, 66.7)(2/9, 18.2)0.000 *
TSI-Ab (IU/mL, mean ± SD)3.5 ± 7.216.8 ± 34.10.8 ± 0.10.000 *
TSI-Ab > 2 IU/mL (P/N, % P)(1/9, 10)(9/0, 100)(0/11, 0)0.000 *
BMI, body mass index; CRP, C-reactive protein; FT3, free triiodothyronine; FT4, free thyroxine; GD, Graves–Basedow’s disease; HDs, healthy donors; HDL-c, high-density lipoprotein; Hip c. hip circumference; HT, Hashimoto’s thyroiditis; LDL-c, low-density lipoprotein cholesterol; M/F, male/female; P/N, positive/negative ratio; TGs, triglycerides; Total-C, total cholesterol; TPO-Ab, thyroperoxidase antibody; TSI-Ab thyroid stimulating immunoglobulin antibody; Waist c. waist circumference. * Significant differences p < 0.05.
Table
Table 2. Simple linear correlation relationship of autoimmunity and thyroid profile with gut microbiota (taxa abundances: samples at phylum, family, and genus levels).
Table 2. Simple linear correlation relationship of autoimmunity and thyroid profile with gut microbiota (taxa abundances: samples at phylum, family, and genus levels).
Plylum LevelFamily or Genus LevelTPO-AbTSI-Ab
Bacteroidetes ----------
Alistipesr = 0.432; p = 0.019-----
Firmicutes ----------
Lactobacillaceae-----r = 0.517; p = 0.006
Lactobacillus-----r = 0.517; p = 0.006
Faecalibacteriumr = −0.453; p = 0.014r = −0.406; p = 0.036
Ruminococcaceae unclasificatedr = 0.408; p = 0.028-----
Proteobacteria ----------
Enterobacteriaceaer = 0.416; p = 0.025-----
Pasteurellaceae-----r = 0.441; p = 0.021
TPO-Ab, thyroperoxidase antibody; TSI-Ab, thyroid stimulating immunoglobulin antibody.
Table
Table 3. Adjusted model for autoimmunity thyroid profile (Positive TPO-Ab >60 IU/mL)—Gut microbiota community.
Table 3. Adjusted model for autoimmunity thyroid profile (Positive TPO-Ab >60 IU/mL)—Gut microbiota community.
Positive TPO Autoimmunity (TPO-Ab >60 IU/mL)
Ruminococcaeae unclassified
OR (CI)p
Crude model1.494 (1.041–2.145)0.029
Model 11.474 (1.026–2.413)0.038
Binary logistic regression analysis: Odds ratio (OR) and 95% confidence interval (CI) for the association between positive thyroid autoimmunity and gut microbiota. Positive levels of TPO antibody were defined as a level >60 IU/mL. Dependent variable: positive TPO autoimmunity—TPO-Ab levels <60 IU/mL (0) vs. TPO-Ab levels >60 IU/mL (1). Model 1: adjusted for sex, age, and BMI.
Table
Table 4. Adjusted model for autoimmunity thyroid profile (Positive TSI-Ab >2 IU/mL)—Gut microbiota community.
Table 4. Adjusted model for autoimmunity thyroid profile (Positive TSI-Ab >2 IU/mL)—Gut microbiota community.
Positive TSI Autoimmunity (TSI-Ab >2 IU/mL)
SutterellaFaecalibacterium
OR (CI)pOR (CI)p
Crude model1.351 (1.053–1.734)0.0180.059 (0.004–0.958)0.047
Model 11.499 (1.041–2.158)0.0300.025 (0.001–0.900)0.044
Binary logistic regression analysis: ddds ratio (OR) and 95% confidence interval (CI) for the association between positive thyroid autoimmunity and gut microbiota. Positive levels of TSI antibody were defined as a level >2 IU/mL. Dependent variable: positive TSI autoimmunity—TSI-Ab levels <2 IU/mL (0) vs. TSI-Ab levels >2 IU/mL (1). Model 1: adjusted for sex, age, and BMI.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Cornejo-Pareja, I.; Ruiz-Limón, P.; Gómez-Pérez, A.M.; Molina-Vega, M.; Moreno-Indias, I.; Tinahones, F.J. Differential Microbial Pattern Description in Subjects with Autoimmune-Based Thyroid Diseases: A Pilot Study. J. Pers. Med. 2020, 10, 192. https://doi.org/10.3390/jpm10040192

AMA Style

Cornejo-Pareja I, Ruiz-Limón P, Gómez-Pérez AM, Molina-Vega M, Moreno-Indias I, Tinahones FJ. Differential Microbial Pattern Description in Subjects with Autoimmune-Based Thyroid Diseases: A Pilot Study. Journal of Personalized Medicine. 2020; 10(4):192. https://doi.org/10.3390/jpm10040192

Chicago/Turabian Style

Cornejo-Pareja, Isabel, Patricia Ruiz-Limón, Ana M. Gómez-Pérez, María Molina-Vega, Isabel Moreno-Indias, and Francisco J. Tinahones. 2020. "Differential Microbial Pattern Description in Subjects with Autoimmune-Based Thyroid Diseases: A Pilot Study" Journal of Personalized Medicine 10, no. 4: 192. https://doi.org/10.3390/jpm10040192

APA Style

Cornejo-Pareja, I., Ruiz-Limón, P., Gómez-Pérez, A. M., Molina-Vega, M., Moreno-Indias, I., & Tinahones, F. J. (2020). Differential Microbial Pattern Description in Subjects with Autoimmune-Based Thyroid Diseases: A Pilot Study. Journal of Personalized Medicine, 10(4), 192. https://doi.org/10.3390/jpm10040192

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop