Basic Study Open Access
Copyright ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Diabetes. Jun 15, 2023; 14(6): 862-882
Published online Jun 15, 2023. doi: 10.4239/wjd.v14.i6.862
Alteration of intestinal microbiota is associated with diabetic retinopathy and its severity: Samples collected from southeast coast Chinese
Xue-Mei Gu, Qi-Han Zhu, Department of Endocrinology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China
Xue-Mei Gu, Qi-Han Zhu, Wenzhou Key Laboratory of Diabetes Research, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China
Chao-Yin Lu, Department of Endocrinology, Taizhou Central Hospital (Taizhou University Hospital), Taizhou 318000, Zhejiang Province, China
Jian Pan, Department of Ophthalmology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China
Jian-Zhong Ye, Department of Clinical Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang Province, China
ORCID number: Xue-Mei Gu (0000-0002-2851-368X); Jian-Zhong Ye (0000-0001-8174-2580); Qi-Han Zhu (0000-0003-0319-7665).
Author contributions: Gu XM and Lu CY have contributed equally to this work and share first authorship; Gu XM performed data analysis and co-wrote the first draft of the manuscript; Lu CY performed data analysis, specimen collection, and co-wrote the first draft of the manuscript; Pan J performed specimen collection and data collection; Ye JZ performed data analysis, experimental design, co-chief investigator of the study, and co-guarantor of this work; Zhu QH performed data analysis, experimental design, essay modification, co-chief investigator of the study, and co-guarantor of this work; all authors have provided substantial intellectual input and approved the final version for publication.
Supported by Wenzhou Science and Technology Bureau, No. Y20190129 and No. Y2020263.
Institutional review board statement: The studies involving human participants were reviewed and approved by Research Ethics Committee of the First Affiliated Hospital of Wenzhou Medical University.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Data sharing statement: The datasets presented in this study can be found in online repositories: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA786292. The names of the repository/repositories and accession number(s) can be found below: NCBI SRA (accession: SRP349289).
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Qi-Han Zhu, MM, Attending Doctor, Department of Endocrinology, The First Affiliated Hospital of Wenzhou Medical University, The South of Shangcai Village, Nanbaixiang Town, Ouhai District, Wenzhou 325000, Zhejiang Province, China. dr_zhuqihan@163.com
Received: March 9, 2023
Peer-review started: March 9, 2023
First decision: March 23, 2023
Revised: April 9, 2023
Accepted: April 27, 2023
Article in press: April 27, 2023
Published online: June 15, 2023
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Abstract
BACKGROUND

Current approaches for the therapy of diabetic retinopathy (DR), which was one of leading causes of visual impairment, have their limitations. Animal experiments revealed that restructuring of intestinal microbiota can prevent retinopathy.

AIM

To explore the relationship between intestinal microbiota and DR among patients in the southeast coast of China, and provide clues for novel ways to prevention and treatment methods of DR.

METHODS

The fecal samples of non-diabetics (Group C, n = 15) and diabetics (Group DM, n = 30), including 15 samples with DR (Group DR) and 15 samples without DR (Group D), were analyzed by 16S rRNA sequencing. Intestinal microbiota compositions were compared between Group C and Group DM, Group DR and Group D, as well as patients with proliferative diabetic retinopathy (PDR) (Group PDR, n = 8) and patients without PDR (Group NPDR, n = 7). Spearman correlation analyses were performed to explore the associations between intestinal microbiota and clinical indicators.

RESULTS

The alpha and beta diversity did not differ significantly between Group DR and Group D as well as Group PDR and Group NPDR. At the family level, Fusobacteriaceae, Desulfovibrionaceae and Pseudomonadaceae were significantly increased in Group DR than in Group D (P < 0.05, respectively). At the genera level, Fusobacterium, Pseudomonas, and Adlercreutzia were increased in Group DR than Group D while Senegalimassilia was decreased (P < 0.05, respectively). Pseudomonas was negatively correlated with NK cell count (r = -0.39, P = 0.03). Further, the abundance of genera Eubacterium (P < 0.01), Peptococcus, Desulfovibrio, Acetanaerobacterium and Negativibacillus (P < 0.05, respectively) were higher in Group PDR compared to Group NPDR, while Pseudomonas, Alloprevotella and Tyzzerella (P < 0.05, respectively) were lower. Acetanaerobacterium and Desulfovibrio were positively correlated with fasting insulin (r = 0.53 and 0.61, respectively, P < 0.05), when Negativibacillus was negatively correlated with B cell count (r = -0.67, P < 0.01).

CONCLUSION

Our findings indicated that the alteration of gut microbiota was associated with DR and its severity among patients in the southeast coast of China, probably by multiple mechanisms such as producing short-chain fatty acids, influencing permeability of blood vessels, affecting levels of vascular cell adhesion molecule-1, hypoxia-inducible factor-1, B cell and insulin. Modulating gut microbiota composition might be a novel strategy for prevention of DR, particularly PDR in population above.

Key Words: Intestinal microbiota; Diabetic retinopathy; Occurrence; Progression; Southeast coast of China

Core Tip: Current approaches for the therapy of diabetic retinopathy (DR) have their limitations. Our study revealed that alteration of gut microbiota was associated with DR and its progression, and further, this association was mediated by multiple mechanisms including producing short-chain fatty acids, influencing permeability of blood vessels, affecting levels of vascular cell adhesion molecule-1, hypoxia-inducible factor-1, B cell and insulin. Hence, reconstruction of gut microbiota might be a promising strategy for prevention of DR.



INTRODUCTION

For the moment, diabetes is one of the fastest developing and worldwide metabolic diseases, with multiple complications such as diabetic retinopathy (DR). Global pool analysis of DR in 2010 revealed the proportion of DR, and vision-threatening DR in diabetics was 34.6%, 10.2% respectively[1]. DR will cause visual impairment and even blindness in adults aged 20 to 74 years old, and is considered as one of the primary causes[2]. DR is subdivided into non-proliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR). PDR is less common in patients but more threatening to vision compared with NPDR[3]. The treatment of PDR and visually threatening diabetic macular edema (DME) is a main research topic on DR. Laser therapy, anti-angiogenic therapy, anti-inflammatory therapy and surgery are major treatments for PDR. Laser therapy is a classic tool for severe NPDR and PDR, aiming to preserve visual acuity[4]. However, laser would impair the central vision and night vision[5]. As a main anti-angiogenic therapy, anti-vascular endothelial growth factor (VEGF) is a recommended therapy of DR refractory to laser treatment and DME. Contrast to laser monotherapy, anti-VEGF therapy can improve visual acuity in inpatients with DME or PDR[6,7]. However, considering limited half-life time of anti-VEGF agents, the repetitive injections of anti-VEGF are required at one or two months intervals, causing increased financial burden, increased occurrence of endophthalmitis and elevated intraocular pressure[8]. Besides, the long-term therapy of anti-VEGF would reduce patient compliance, increase the incidence of treatment interruption, and result in deterioration finally[9]. Almost nearly 50% patients are insensitive or even non-responsive to anti-VEGF therapy, but new approved anti-angiogenic therapies as well as effective and evidence-based replacement treatments are absent[10,11]. Although glucocorticoids can be used in patients who failed to respond to anti-VEGF, the role in treating PDR still need further confirmation and the side effect of elevating blood glucose constrains its application in diabetics[9]. Other treatments including anti-protein kinase C, angiotensin receptor blockers, fenofibrate have their own flaws[12-16].

Chronic low-grade inflammations are already recognized as pivotal players in the development of diabetes and its complications including DR. Besides the anti-inflammatory effect via generating short chain fatty acid such as butyrate[17], intestinal microbiota also plays a pro-inflammatory role by increasing intestinal permeability, releasing lipopolysaccharide (LPS) which was relevant with distant inflammatory response and impacted cytokines such as TNF-α and IL-6[18,19]. The roles of microbiota on inflammation may explain its possible contribution on occurrence and development of DR. An animal experiments showed that intermittent fasting can prevent the occurrence of DR[10]. Only four studies aiming at the relationship between human intestinal microbiota and DR have been found[20-23]. Jayasudha et al[21] performed Illumina sequencing of the internal transcribed spacer 2 region which mainly detects fungus. Three other studies performed 16S rRNA sequencing to distinguish the microbiota between diabetics with DR and without DR[20,22,23]. Moubayed et al[20] only analyzed fecal genus Bacteroides among healthy volunteers, diabetic patients with DR and without DR, lack of analysis of the other microbial community types. As for the other two studiers, one of their limits was that diabetics enrolled are always treated with metformin[22,23]. Metformin can reduce the severity of DR and incidence of NPDR independently and the mechanisms might be anti-angiogenesis and anti-inflammation[24-27]. Notwithstanding no studies have demonstrated that intestinal microbiota involves in the effect of metformin on DR, metformin should also be considered as a confounding factor which may affect the accuracy of the conclusion about relationship between intestinal microbiota and DR stated by Huang et al[22]. Moreover, the effect of metformin on different microbiota were inconsistent in type 2 diabetes mellitus (T2DM) patients, which possibly be impacted by duration of diabetes, gender and race[28]. Thus, metformin taken by whole T2DM subjects still probably complicate the analysis of gut microbiota[24]. The abundance of intestinal microbiota was obviously affected by diet and geographic proximity[29,30]. Different intestinal microbiota may be relevant to same diseases among different persons from different areas and with different dietary habits. Our study is focus on exploring the differential bacteria between diabetic patients with DR and without DR, as well as diabetic patients with PDR and NPDR in south Zhejiang and north Fujian in China, aiming to unravel the link between intestinal microflora and DR, and find a new therapeutic target for DR, especially PDR.

MATERIALS AND METHODS
Study population and sample collection

For this study, 45 samples were obtained from patients who are hospitalized in the department of endocrinology in the 1st Affiliated Hospital of Wenzhou medical university from August, 2018 to September, 2020. Patients were divided into non-diabetics (Group C, n = 15) and T2DM patients (Group DM, n = 30), which was further divided into patients with DR (Group DR, n = 15) and patients without DR (Group D, n = 15). Further, Group DR was divided into patients with PDR (Group PDR, n = 8) and patients without PDR (Group NPDR, n = 7). The enrolled patients are aged between 30-80 years old without conditions as pregnant, lactation, current smoker, current drinker, BMI ≥ 27, prescribed for metformin, alpha glycosidase inhibitor, antibiotics, probiotics, glucocorticoids, cathartics or PPI within 3 mo, rheumatoid arthritis, inflammatory bowel disease, or gastrointestinal tract operation. After admitted into our department, demographic, medical history, physical examination data were collected and several biochemical tests were performed. Participants self-collected a fecal sample, which were collected by patients, and stored at -80 ℃ later in less than 24 h. This study was approved by the Ethics Committee of the 1st Affiliated Hospital of Wenzhou medical university. All participants gave their informed consent. The trial register number is 2018-129.

DNA extraction and amplification

Fecal samples were snap frozen and stored at -80 ℃ after collection. Bacterial DNA was isolated from the fecal samples using MagPure Soil DNA LQ Kit (Magen, United States) following the manufacturer’s instructions. DNA concentration and integrity were measured by Nano Drop 2000 spectrophotometer (Thermo Fisher Scientific, Waltham, MA, United States) and agarose gel electrophoresis, respectively. Polymerase chain reaction (PCR) amplification of the V3-V4 hypervariable regions of the bacterial 16S rRNA gene was carried out in a 25 μL reaction using universal primer pairs (343F: 5′-TACGGRAGGCAGCAG-3′; 798R: 5′-AGGGTATCTAATCCT-3′). The reverse primer contained a sample barcode and both primers were connected with an Illumina sequencing adapter.

Library construction and sequencing

The amplicon quality was visualized using gel electrophoresis. The PCR products were purified with Agencourt AMPure XP beads (Beckman Coulter Co., United States) and quantified using Qubit dsDNA assay kit. The concentrations were then adjusted for sequencing. 16S rDNA sequencing were performed using Illumina MiSeq platform at Shanghai OE Biotech Co., Ltd.

Bioinformatic analysis

Paired-end reads were preprocessed using Trimmomatic software to detect and cut off ambiguous bases(N)[31]. It also cut off low quality sequences with average quality score below 20 using sliding window trimming approach. After trimming, paired-end reads were assembled using FLASH software[32]. Parameters of assembly were: 10 bp of minimal overlapping, 200 bp of maximum overlapping and 20% of maximum mismatch rate. Sequences were performed further denoising as follows: Reads with ambiguous, homologous sequences or below 200 bp were abandoned. Reads with 75% of bases above Q20 were retained using QIIME software (version 1.8.0)[33]. Then, reads with chimera were detected and removed using VSEARCH[34]. Clean reads were subjected to primer sequences removal and clustering to generate operational taxonomic units (OTUs) using VSEARCH software with 97% similarity cutoff[34]. The representative read of each OTU was selected using QIIME package. All representative reads were annotated and blasted against Silva database (Version 123) using Ribosomal Database Project classifier (confidence threshold was 70%)[35]. The microbial diversity in fecal samples was estimated using the alpha diversity that include Chao1 index, Shannon index and Simpson index. The Unifrac distance matrix performed by QIIME software was used for weighted Unifrac principal coordinates analysis (PCoA) construction. The 16S rRNA gene amplicon sequencing and analysis were conducted by OE Biotech Co., Ltd. (Shanghai, China).

Statistical analysis

Data with normal distribution and homogeneity of variance were compared using independant samples t test, otherwise, were compared using Wilcoxon test. Comparisons between groups were performed with the clinical characteristics. For associations between clinical characteristics and gut microbial, Spearman correlation analysis were performed using R version 3.6.1. Correction for multiple testing was performed using false discovery rate with the Benjamini–Hochberg. False discovery rate values < 0.05 were considered statistically significant.

RESULTS
Clinical and biochemical characteristics

The clinical and biochemical characteristics were compared between Group DM and C as well as Group D and DR, Group PDR and NPDR (Tables 1 and 2). The age, sex proportion and BMI did not differ between the three pairs mentioned above. Further, the other indexes were comparable between Group DM and C except for fasting blood glucose, glycated hemoglobin A1c (Tables 1 and 2). Compared to Group D, neutrophil to lymphocyte ratio, CD4+ T cell count were significantly increased in Group DR (P < 0.05, P < 0.05), whereas, B cell count, CD8+ T cell count, NK cell count, percentage of NK cell were decreased (P < 0.01, P < 0.05, P < 0.01, P < 0.05, Table 2). Patients in Group PDR had a significantly lower level of estimated glomerular filtration rate (eGFR) and B cell count (P < 0.05, P < 0.01), and a higher level of fasting insulin compared with NPDR (P < 0.05, Table 2).

Table 1 Basic characteristics compared between Group DM and Group C.
Characteristic
Group DM vs Group C
Group DM (n = 30)
Group C (n = 15)
P value
Age55.93 ± 9.5859.73 ± 16.46NS
Gender, male/female19/119/6NS
Height165.70 ± 8.07162.20 ± 7.78NS
Weight64.75 ± 7.6762.53 ± 8.29NS
Body mass index23.47 ± 2.2123.73 ± 2.27NS
Waist circumference84.75 ± 7.7884.67 ± 8.36NS
Hip circumference91.42 ± 7.3292.07 ± 7.29NS
Waist hip ratio0.93 ± 0.050.92 ± 0.08NS
Waist height ratio0.51 ± 0.050.52 ± 0.05NS
Systolic blood pressure128.43 ± 11.98127.80 ± 14.03NS
Fasting glucose8.29 ± 2.795.34 ± 0.95< 0.01
HbA1c9.94 ± 1.965.63 ± 0.31< 0.01
Triglycerides1.81 ± 1.821.72 ± 0.77NS
LDL-C3.00 ± 0.972.94 ± 0.88NS
eGFR92.29 ± 27.6587.21 ± 30.00NS
Table 2 Basic characteristics compared between samples with diabetic retinopathy and samples without diabetic retinopathy, as well as patients with proliferative diabetic retinopathy vs patients without proliferative diabetic retinopathy.
Characteristic
Group DR vs Group D
Group PDR vs Group NPDR
Group DR (n = 15)
Group D (n = 15)
P value
Group PDR (n = 8)
Group NPDR (n = 7)
P value
Age55.87 ± 10.5456.00 ± 8.90NS58.75 ± 11.8552.57 ± 8.44NS
Gender, male/female9/610/5NS3/53/4NS
Diabetes duration14.27 ± 7.274.045 ± 4.67NS15.50 ± 4.9912.87 ± 9.49< 0.01
height165.13 ± 9.26166.27 ± 6.97NS165.75 ± 10.12164.43 ± 8.90NS
Weight64.83 ± 9.1164.67 ± 6.24NS65.19 ± 9.6464.43 ± 9.22NS
Body mass index23.49 ± 1.9923.45 ± 2.48NS23.07 ± 1.2423.97 ± 2.62NS
Waist circumference83.47 ± 8.4086.03 ± 7.17NS85.75 ± 9.7780.86 ± 6.20NS
Hip circumference89.53 ± 8.8393.30 ± 5.03NS92.88 ± 8.1785.71 ± 8.50NS
Waist hip ratio0.93 ± 0.060.92 ± 0.05NS0.92 ± 0.070.95 ± 0.03NS
Waist height ratio0.51 ± 0.050.52 ± 0.05NS0.52 ± 0.070.49 ± 0.02NS
Systolic blood pressure131.93 ± 13.27124.93 ± 9.74NS135.75 ± 13.79127.57 ± 12.15NS
Fasting glucose9.24 ± 2.957.34 ± 2.35NS9.61 ± 1.838.81 ± 4.00NS
HbA1c10.01 ± 1.639.87 ± 2.31NS9.26 ± 1.6210.87 ± 1.24NS
Triglycerides2.18 ± 2.501.44 ± 0.57NS2.42 ± 2.901.90 ± 2.14NS
LDL-C2.78 ± 0.903.22 ± 1.02NS2.51 ± 1.163.09 ± 0.34NS
eGFR88.08 ± 32.0996.51 ± 22.72NS69.33 ± 33.84109.51 ± 7.88< 0.05
Urine albumin creatine ratio527.22 ± 1055.3030.90 ± 52.89NS508.40 ± 731.68548.74 ± 1404.61NS
Serum creatinine clearance value97.59 ± 52.53114.66 ± 41.75NS94.24 ± 60.68101.41 ± 45.96NS
Urea nitrogen7.65 ± 5.665.87 ± 2.24NS9.60 ± 7.245.41 ± 1.58NS
Fasting insulin61.34 ± 24.0670.91 ± 57.40NS73.31 ± 19.8447.66 ± 21.96< 0.05
HOMA-IR3.82 ± 2.133.10 ± 2.00NS4.53 ± 1.6223.00 ± 2.46NS
HOMA-B0.40 ± 0.250.80 ± 1.02NS0.36 ± 0.130.45 ± 0.36NS
Platelet217.60 ± 55.49203.67 ± 63.63NS196.63 ± 43.45241.57 ± 61.04NS
Mean platelet volume11.13 ± 0.8510.99 ± 0.79NS11.40 ± 0.8810.83 ± 0.76NS
Platelet distribution width13.79 ± 1.5813.95 ± 1.55NS14.05 ± 1.5513.49 ± 1.67NS
Neutrophil to lymphocyte ratio2.85 ± 0.992.10 ± 0.86< 0.052.75 ± 0.902.97 ± 1.15NS
T cell count1165.87 ± 373.691518.00 ± 335.85NS1092.75 ± 504.021249.43 ± 119.08NS
B cell count249.67 ± 82.72378.87 ± 124.49< 0.01198.00 ± 57.65308.71 ± 66.81< 0.01
CD4+ T cell count733.87 ± 299.45953.2 ± 226.40< 0.05684.13 ± 413.77790.72 ± 49.25NS
CD8+ T cell count389.40 ± 116.23490.47 ± 137.90< 0.05371.88 ± 145.83409.43 ± 76.37NS
CD4+ to CD8+ T cell ratio1.91 ± 0.602.01 ± 0.42NS1.85 ± 0.791.98 ± 0.31NS
NK cell count220.20 ± 85.18462.27 ± 250.54< 0.01240.00 ± 114.91197.57 ± 20.12NS
NK cell percent12.66 ± 3.6519.41 ± 9.48< 0.0514.05 ± 4.5211.07 ± 1.33NS
Sequencing summary

Total 890469 sequences read with an average of 19788.2 reads per sample were obtained among the 45 samples. 46551 OTUs were observed totally, with a mean of 1034.467 OTUs. The phyla Bacteroidete was the dominant intestinal microbiota with approximately 40% (Figure 1). The other three phyla dominated in microbiota were Firmicutes, Proteobacteria and Actinobacteria, with average relative abundances of 29.1%, 19.6% and 5.2% respectively (Figure 1).

Figure 1
Figure 1 The pie shows average relative abundances of the most four dominated phyla. Relative abundances are presented as percentage.
Fecal microbiota diversity

The Chao1, Shannon, simpson indexes were significantly higher in Group C compared with Group DM (P < 0.001, P < 0.001, P < 0.001, Figure 2A-C). However, they did not differ significantly between Group D and Group DR as well as between Group PDR and Group NPDR (P > 0.05, Figure 2D-I).

Figure 2
Figure 2 Alpha diversity analysis of microbiota in the six groups. A: The Chao1 index between Group DM and Group C; B: The Shannon index between Group DM and Group C; C: The simpson index between Group DM and Group C; D: The Chao1 index between Group DR and Group D; E: The Shannon index between Group DR and Group D; F: The simpson index between Group DR and Group D; G: The Chao1 index between Group PDR and Group NPDR; H: The Shannon index between Group PDR and Group NPDR; I: The simpson index between Group PDR and Group NPDR. aP < 0.05. NS: Not significant. Group C: Samples with non-diabetics; Group DM: Samples with diabetics; Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.

Weighted and unweighted PCoA showed a distinct distance between Group C and Group DM (Adonis, P < 0.01, P < 0.01, Figure 3A and B), whereas Group D and Group DR had no distinction (P > 0.05, P > 0.05, P > 0.05, P > 0.05, Figure 3C and D). However, the microbiota community in Group PDR was not differed from Group NPDR (P > 0.05, P > 0.05, Figure 3E and F).

Figure 3
Figure 3 Beta diversity analysis of microbiota in the six groups. A and B: Weighted and unweighted PCoA between between Group DM and Group C; C and D: Weighted and unweighted PCoA between between Group DR and Group D; E and F: Weighted and unweighted PCoA between between Group PDR and Group NPDR. Differences were assessed by Adonis. Group C: Samples with non-diabetics; Group DM: Samples with diabetics; Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.
The composition of fecal microbiota

At the phylum level, Proteobacteria was the most abundant in Group C followed by Bacteroidetes (Figure 4A). The abundance of Firmicutes, Bacteroidetes, Proteobacteria and Actinobacteria varied between Group DM and Group C (Figure 4A). The Firmicutes to Bacteroidetes ratio was slightly higher in Group DM compared with Group C, however, there was no significant difference (r = 0.86 vs r = 0.81, P = 0.53).

Figure 4
Figure 4 The composition at phylum level in the six groups. A: The composition at phylum level in Group DM and Group C. The abundance of Firmicutes, Bacteroidetes, Proteobacteria and Actinobacteria varied between the two groups; B: The composition at phylum level in Group DR and Group D. The relative mean abundance of phylum Bacteroidetes and Firmicutes between Group D and Group DR were similar (P = 0.33, P = 0.37); C: The composition at phylum level in Group PDR and Group NPDR. The relative mean abundance of phylum Bacteroidetes, Firmicutes and showed a similarity between Group PDR and NPDR (P = 0.71, P = 0.33). Group C: Samples with non-diabetics; Group DM: Samples with diabetics; Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.

At the phylum level, the majority composition of microbiome in Group D and DR were Bacteroidetes and Firmicutes (Figure 4B). The relative mean abundance of phylum Bacteroidetes and Firmicutes as well as Firmicutes to Bacteroidetes ratio between Group D and Group DR were similar (P = 0.33, P = 0.37, P = 0.52, Figure 4B). The relative mean abundance of phylum Bacteroidetes, Firmicutes and Firmicutes to Bacteroidetes ratio showed a similarity between Group PDR and NPDR (P = 0.71, P = 0.33, P = 0.54, Figure 4C).

The linear discriminant analysis effect size revealed that Fusob Cteriaceae, Fusobacteriales, Fusobacteriia, Fusobacteriaceae, Desulfovibrionales, Delta Proteobacteria, Burkholderiaceae and Beta Proteobacteriales were dominant in Group DR (Figure 5A). Meanwhile, Eubacteriaceae and Pseudomonadaceae were dominant in PDR and Group NPDR respectively (Figure 5B).

Figure 5
Figure 5 Results of linear discriminant analysis effect size in the six groups. Wilcoxon signed rank test was used for statistical analyzing. The threshold of linear discriminant analysis score was set to 2.0. A and B: Red nodes designated microorganism that only been detected in Group DR. The regions marked with yellow indicated no significant difference between Group DR and Group D as well as Group PDR and NPDR. Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.

At the phylum level, Fusobacteria was significant higher in Group DR than in Group D (P < 0.05, Figure 6A). In addition, at the family level, Fusobacteriaceae, Burkholderiaceae, Desulfovibrionaceae and Pseudomonadaceae were significantly increased in Group DR than in Group D (P < 0.05, P < 0.05, P < 0.05, P < 0.05, Figure 6B). At the genus level, the abundance of Senegalimassilia, S5-A14a and Lachnospiraceae_UCG-008 were significantly decreased in Group DR than in Group D (P < 0.05, P < 0.05, P < 0.05), whereas, Fusobacterium, Pseudomonas, Lachnospiraceae_UCG-010 and Adlercreutzia were significantly increased (P < 0.05, P < 0.05, P < 0.05, P < 0.05, Figure 6C). Further, Eubacterium, Peptococcus, Desulfovibrio, Acetanaerobacterium, Negativibacillus and Family_XIII_UCG-001 were significantly increased in Group PDR compared with Group NPDR (P < 0.01, P < 0.05, P < 0.05, P < 0.05, P < 0.05, P < 0.05), wherereas, Pseudomonas, Alloprevotella, Tyzzerella and Tyzzerella-3 had a reduction (P < 0.05, P < 0.05, P < 0.05, P < 0.05, Figure 6D).

Figure 6
Figure 6 Relative abundance of microbiota displayed by Box and whiskers plots. A-C: Box and whiskers plots display relative abundance of microbiota in different level between Group DR and Group D; D: Box and whiskers plots display relative abundance of genera between Group PDR and NPDR. Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.

Spearman’s correlations between the relative abundance of bacterial families, clinical indices and biochemical characteristics were performed between Group DR and Group D as well as Group PDR and NPDR. In Group D and Group DR, Pseudomonas had a negative correlation with NK cell count (r = -0.39, P < 0.05, Figure 7A). However, Senegalimassilia had a positive correlation with NK cell% (r = 0.42, P < 0.05, Figure 7A). Meanwhile, in Group PDR and Group NPDR, Acetanaerobacterium (r = 0.53, P < 0.05) and Desulfovibrio were positively correlated with fasting insulin (r = 0.61, P < 0.05, Figure 7B), when Negativibacillus was negatively correlated with B cell count (r = -0.67, P < 0.01) and eGFR (r = -0.66, P < 0.01, Figure 7C).

Figure 7
Figure 7 Correlation heatmap between gut microbiota and clinical indices. A: Correlation heatmap between gut microbiota and clinical indices in Group DM (Group DR vs Group D); B and C: Correlation heatmap between gut microbiota and clinical indices in Group DR (Group PDR vs Group NPDR). Different colors represent correlation level. Different colors represent correlation level (blue represents for negative correlation, red represents for positive correlation). aP < 0.05; bP < 0.01. Group C: Samples with non-diabetics; Group DM: Samples with diabetics; Group DR: Samples with diabetic retinopathy; Group D: Samples without diabetic retinopathy; Group PDR: Patients with proliferative diabetic retinopathy; Group NPDR: Patients without proliferative diabetic retinopathy.
DISCUSSION

Disorder in intestinal microbiota composition has been implicated in occurrence and development of diabetes mellitus (DM)[36,37]. Intestinal microbiota dysbiosis induces oxidative stress, inflammation, insulin resistance and vascular permeability, which probably involves in progression of diabetic complication including DR[37,38]. However, the association between intestinal microbiota and DR remains unclear. Moubayed et al[20] found diabetic patients have higher relative abundance of Bacteroides than non-diabetic patients, however microbiota differences between patients with DR and without DR were not detected. A study presented microbiota biomarkers to help diagnosing DR, but not analyze the relation between them and clinical markers[22]. Considering existing mature examination to make a definite diagnosis of DR, microbiota biomarkers did not contribute much to the diagnosis. Besides, there was no evidence to prove that the relationship between biomarkers and DR was not accidental. The primary aim of the current study was to assess the gut flora differences of persons with DM and healthy controls, of diabetic patients with DR and without DR separately, applying 16S rRNA gene sequencing. In addition, the analysis of the correlation between the gut flora differences and clinical indexes was taken.

PCOA analysis revealed that the α diversity was decreased significantly in Group DM compared those in Group C, which was in line with previous study[22]. Lower bacterial richness was associated with several common metabolic markers including overall adiposity, insulin resistance and dyslipidaemia coexisted in T2DM[39]. Maintenance of gut nomobiosis played a protective role in glycolipid metabolism[40], on the contrary, gut dysbiosis characteristed with reduced microbiota diversity induced expansion of pathogenic bacteria, gut inflammation and deterioration of diabetes[41,42]. Signifificant variations of gut microbiota between T2DM patients and nondiabetic controls revealed in PCoA was showed by a previous report[43], which was accordant with ours. In addition, in accordance with previous study, α diversity indexes did not differ significantly between Group DR and Group D[22,23]. The α and β diversity did not significantly change between Group DR and Group D as well as between Group NPDR and PDR in our study.

At phylum level, Bacteroidota, Firmicutes, Proteobacteria and Actinobacteriota occupied more than 80% of community abundance were regarded as the most dominant phyla in each group. A study found that the abundance of Firmicutes and Bacteroidetes increased in Group DM compared with Group C, with slightly higher Firmicutes/Bacteroidetes ratio in Group DM, consistent to our study[43]. Further, the investigation performed by Li et al[44] got the similar results in Han population. Of interests, we found that Firmicutes were more abundant in Group DR than Group D, while Bacteroidetes were less abundant in Group DR via Wilcoxon test. However, Huang et al[22] got an opposite result. Although the result in our study was lack of statistical difference, this distinction also got our attention. Metformin may influence Firmicutes abundance[45]. We guessed that metformin received by most diabetic patients without DR stated by Huang et al[22] might led to lower abundance of Firmicutes in Group DM without DR. Compared with Group D, there was a significant increase abundance of Fusobacteria in Group DR. However, the study performed by Sisinthy Shivaji was discordant with ours[23], which possibly due to the inconsistent effect of metformin on Fusobacteria[28].

Our results indicated that Fusobacteriacee, Desulfovibrionaceae, Burkholderiaceae and Pseudomonadaceae at the family level increased in Group DR compared with Group D. Further, Eubacteriaceae and Pseudomonadaceae were predominant in Group PDR and Group NPDR respectively. Fusobacteria and Fusobacteriaceae produced short-chain fatty acids including acetate and propionate and their abundance increased in non-alcoholic steatohepatitis (NASH) subjects compared to nonalcoholic fatty liver and healthy controls[46]. Elevated and propionate in faeces of human NASH subjects were relevant to the increase of Th17 in peripheral blood[46]. An study in animal model showed that blocking the IL-23-Th17-IL-17A pathway would help alleviating DR in mice[47]. Therefore, our results suggested that increased Fusobacteria and Fusobacteriaceae may contribute to producing acetate and propionate, increasing Th17 and causing DR. Fusobacteriaceae is a gram-negative bacterium producing endotoxin, LPS[48]. A study found that Fusobacteriaceae increased and induced LPS in pigs with NASH[48]. And, in hyperglycaemic mice, elevation of systemic LPS contributed to the occurrence of DR[49]. Thus, higher abundance of Fusobacteriaceae possibly produce LPS and cause DR in our study. Eubacteriaceae is one of the bacteria that can metabolize aromatic amino acids to produce p-Cresy lsulfate (a prototype protein-bound uremic toxin)[50]. P-Cresy lsulfate induced renal cell carcinoma to overexpress hypoxia-inducible factor (HIF)-1α[51]. In our study, eGFR was lower in Group PDR than NPDR. P-Cresy lsulfate which was one of metabolites of great uremic solutes produced by Eubacteriaceae may deteriorate DR by elevate the level of HIF-1α in retina in our study.

Compared to Group D, the genera Fusobacterium, Pseudomonas, Adlercreutzia and Lachnospiraceae_UCG-010 were increased, but Senegalimassilia, Lachnospiraceae_UCG-008 and S5-A14a were decreased in Group DR. Huang et al[22] found that compared with patients with diabetic patients without DR , Group DR had decreased Blautia and Lactobacillus and less of them took metformin. Besides preventing the occurrence of DR, metformin also increase Blautia and Lactobacillus[27,52]. Accordingly, despite lack of statistical differences in the numbers of patients using metformin between the two groups stated by Huang et al[22], we speculated that increased Blautia and Lactobacillus and lower incidence of DR were relevant to metformin, and the causal relationship between Blautia, Lactobacillus and DR remained uncertain. Patients in Group DR had a larger proportion of Fusobacterium, suggesting a possible larger proportion of Fusobacterium Nucleatum (Fn) than in Group D. As a most frequent Fusobacterium Specie, FN secreted adhesins recognized vascular endothelial cell receptors and increased the vascular permeability contributing to the development of retinopathy possibly[53,54]. This may explain why diabetic patients with higher Fusobacterium are more likely to develop DR. Pseudomonas aeruginosa was one of Pseudomonas species which was a common pathogen in human body[55]. Pseudomonas aeruginosa could help secreting exotoxin to induce hyperpermeability and thrombosis of pulmonary vessels[56]. Besides, our study found that Pseudomonas was negatively correlated with absolute value of NK cells, consistent to other studies[57,58]. We presumed that Pseudomonas increased the permeability of retinal blood vessels and decreased NK cells, resulting in the occurrence of DR. Further experiments were needed to confirm the supposition. Adlercreutzia was positively correlated with leptin level which was positively correlated with the severity of DR[59,60]. Therefore, Adlercreutzia may promote the occurrence of DR by influencing leptin. Senegalimassilia had the genome that produced enterolactone, which was one of the two kinds of lignans in mammals and negatively correlated with white blood cells and C-reactive protein[50,61,62]. Increased Senegalimassilia would inhibit inflammatory response by producing enterolactone, and prevent DR consequently. The relationship between Lachnospiraceae_UCG-010, Lachnospiraceae_UCG-008, S5-A14a and diabetic complications had not been reported.

Eubacterium, Peptococcus, Desulfovibrio, Acetanaerobacterium, Negativibacillus and Family_XIII_UCG-001 were higher in Group PDR compared to Group NPDR, while Pseudomonas, Alloprevotella and Tyzzerella were lower. Eubacterium is known as a butyrate producer[63]. Sodium butyrate in low concentration can promote angiogenesis whereas high concentration sodium butyrate has anti-angiogenic effect[64,65]. However, whether Eubacterium in our study promotes DR by generating low concentration sodium butyrate needs to be further clarified. Diabetes had a close relationship with cognitive impairment[66-68]. Diabetics with DR were more likely to suffer cognitive impairment (CI) and patients with higher severity of DR were more likely to have higher incidence of CI[69]. In addition, retinal vessel and cerebral small vessel had similar embryological origin, size and structure, suggesting that DR and CI may have similar pathophysiological basis[69]. A study showed patients with T2DM who had CI had higher level of Peptococcus and our study showed patients in Group PDR had a higher level of Peptococcus than Group NPDR[70]. Peptococcus may inspire both CI and DR progression in diabetic patients. Desulfovibrio desulfuricans was one of three species isolated from human faeces and could induce endothelial cell to produce vascular cell adhesion molecule-1 (VCAM-1) relating to the severity of DR[71,72]. Elevated level of Desulfovibrio desulfuricans may involve in the progression of PDR. The conclusion needs to be further explored due to the lack of analyzing species levels in genera Desulfovibrio.Desulfovibrio and Acetanaerobacterium were positively correlated with fasting insulin level and their abundance were higher in Group PDR than Group NPDR in our study. Insulin could induce HIF and neovascularization by PI3K and MAPK pathway[73]. Hyperinsulinemia may be the mechanism of Desulfovibrio and Acetanaerobacterium promoting PDR. Our study showed that Negativibacillus was negatively correlated with B lymphocyte. Considering immune cells including B lymphocyte inhibited the formation of pulmonary neovascularization by ischemi, Negativibacillus may promote retinal neovascularization by decreasing B lymphocyte[74]. As stated earlier, Pseudomonas aeruginosa increased the incidence of DR by promoting increased vascular permeability. However, Pseudomonas aeruginosa decreased in Group PDR than Group NPDR. Pseudomonas aeruginosa inhibited HIF, a key molecule of developing PDR[75]. Reason for the phenomenon that Pseudomonas aeruginosa was related higher incidence of DR but lower incidence of PDR needed further exploration. Butyric acid exhibited anti-angiogenic effect by inhibit expression of VEGF/KDR gene, and the higher abundance of Alloprevotella in the Group NPDR may suppress angiogenesis via butyric acids, thus delay the onset of PDR[76]. Tyzzerella produced much propionate which was capable of reducing the expression of VCAM-1 and intercellular adhesion molecule-1 (ICAM-1) induced by cytokine[77,78]. The levels of VCAM-1 and ICAM-1 in serum and eyes of patients in Group PDR were elevated compared with Group NPDR[79]. Hence, Tyzzerella may have slowed the progression of DR by reducing VCAM-1 and ICAM-1. The effect of Family XIII UCG-001 on DR was still unknown.

CONCLUSION

Our study explored the differences of intestinal microbiota between group DR and group D, as well as group PDR and group NPDR in the Chinese population of the southeast coastal region, rid of the interference of metformin. At the family level and genus level, much different microbiota was found between group DR and group D, and they may promote the occurrence of DR by affecting immune cells mediated by short-chain fatty acids, pro-inflammation response or anti-inflammation, inducing HIF and influencing permeability of blood vessels in the fundus. On the genus level, we found that besides Pseudomonas, the variation of microbiota composition between group PDR and group NPDR was completely different from that between group DR and group D. Some differential bacteria between group PDR and group NPDR may affect the level of butyrate or butyric acid, participate in the production of VCAM-1, decrease the level of HIF, affect the brain-eye barrier, promote insulin secretion and reduce B lymphocytes to promote or postpone the progress of DR. Accordingly, we speculated that the disorder of intestinal microbiota may be involved in the occurrence and development of DR, providing a possible novel therapeutic target for DR. However, our study lacked the detection at species level, as well as the measurement of microbial metabolites and related clinical indicators. The causal relationship between intestinal microbiota and the occurrence and development of DR remained unclear. Consider the limitation mentioned above, further investigation was required.

ARTICLE HIGHLIGHTS
Research background

For the therapy of diabetic retinopathy (DR), current approaches showed their own limitations. Modulation of gut flora was capable of preventing DR, which was revealed by animal experiment.

Research motivation

To provide clues for novel ways to prevention and treatment methods of DR.

Research objectives

This study aims to explore the relationship between intestinal microbiota and DR among patients in the southeast coast of China.

Research methods

By 16S rRNA sequencing, fecal samples of non-diabetics (Group C, n = 15) and diabetics (Group DM, n = 30) were analyzed. Spearman correlation analyses were performed to explore the associations between intestinal microbiota and clinical indicators.

Research results

The alpha and beta diversity did not differ significantly between Group DR and Group D as well as Group PDR and Group NPDR. At the genera level, Pseudomonas, Fusobacterium and Adlercreutzia were increased in Group DR than Group D while Senegalimassilia was decreased (P < 0.05, respectively). At the family level, Pseudomonadaceae, Desulfovibrionaceae and Fusobacteriaceae were significantly increased in Group DR than in Group D (P < 0.05, respectively). Pseudomonas was negatively correlated with NK cell count (r = -0.39, P = 0.03). In addition, the abundance of Pseudomonas, Alloprevotella and Tyzzerella (P < 0.05, respectively) were lower in Group PDR compared to Group NPDR, while genera Eubacterium (P < 0.01), Peptococcus, Desulfovibrio, Acetanaerobacterium and Negativibacillus (P < 0.05, respectively) were higher. Desulfovibrio and Acetanaerobacterium were positively associated with fasting insulin (r = 0.53 and 0.61, respectively, P < 0.05), when Negativibacillus was negatively associated with B cell count (r = −0.67, P < 0.01).

Research conclusions

Our research revealed that dysbiosis of gut flora was correlated with DR and its progression among diabetics in the southeast coast of China, probably via several mechanisms including producing influencing permeability of blood vessels, short-chain fatty acids, affecting levels of vascular cell adhesion molecule-1, hypoxia-inducible factor-1, B cell and insulin. Manipulating gut microbiota might be a novel way for prevention of DR, particularly PDR in population above.

Research perspectives

This research perspectives are as fellow: (1) Current treatments for DR did not acquire satisfied effect; (2) Animal experiment revealed that reconstruction of gut microbiota could prevent DR; and (3) Does alteration of gut microbiota has connection with DR in human?

ACKNOWLEDGEMENTS

We would like to appreciate all the participating patients.

Footnotes

Provenance and peer review: Unsolicited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Endocrinology and metabolism

Country/Territory of origin: China

Peer-review report’s scientific quality classification

Grade A (Excellent): 0

Grade B (Very good): B

Grade C (Good): C

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Baraka B, United States; Millman JR, United States S-Editor: Gong ZM L-Editor: A P-Editor: Fan JR

References
1.  Yau JW, Rogers SL, Kawasaki R, Lamoureux EL, Kowalski JW, Bek T, Chen SJ, Dekker JM, Fletcher A, Grauslund J, Haffner S, Hamman RF, Ikram MK, Kayama T, Klein BE, Klein R, Krishnaiah S, Mayurasakorn K, O'Hare JP, Orchard TJ, Porta M, Rema M, Roy MS, Sharma T, Shaw J, Taylor H, Tielsch JM, Varma R, Wang JJ, Wang N, West S, Xu L, Yasuda M, Zhang X, Mitchell P, Wong TY; Meta-Analysis for Eye Disease (META-EYE) Study Group. Global prevalence and major risk factors of diabetic retinopathy. Diabetes Care. 2012;35:556-564.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2576]  [Cited by in F6Publishing: 2882]  [Article Influence: 240.2]  [Reference Citation Analysis (3)]
2.  Cheung N, Mitchell P, Wong TY. Diabetic retinopathy. Lancet. 2010;376:124-136.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1781]  [Cited by in F6Publishing: 2081]  [Article Influence: 148.6]  [Reference Citation Analysis (0)]
3.  Sivaprasad S, Gupta B, Crosby-Nwaobi R, Evans J. Prevalence of diabetic retinopathy in various ethnic groups: a worldwide perspective. Surv Ophthalmol. 2012;57:347-370.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 204]  [Cited by in F6Publishing: 228]  [Article Influence: 19.0]  [Reference Citation Analysis (0)]
4.  Wang W, Lo ACY. Diabetic Retinopathy: Pathophysiology and Treatments. Int J Mol Sci. 2018;19.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 327]  [Cited by in F6Publishing: 623]  [Article Influence: 103.8]  [Reference Citation Analysis (0)]
5.  Fong DS, Girach A, Boney A. Visual side effects of successful scatter laser photocoagulation surgery for proliferative diabetic retinopathy: a literature review. Retina. 2007;27:816-824.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 94]  [Cited by in F6Publishing: 113]  [Article Influence: 6.6]  [Reference Citation Analysis (0)]
6.  Writing Committee for the Diabetic Retinopathy Clinical Research Network; Gross JG, Glassman AR, Jampol LM, Inusah S, Aiello LP, Antoszyk AN, Baker CW, Berger BB, Bressler NM, Browning D, Elman MJ, Ferris FL 3rd, Friedman SM, Marcus DM, Melia M, Stockdale CR, Sun JK, Beck RW. Panretinal Photocoagulation vs Intravitreous Ranibizumab for Proliferative Diabetic Retinopathy: A Randomized Clinical Trial. JAMA. 2015;314:2137-2146.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 487]  [Cited by in F6Publishing: 492]  [Article Influence: 54.7]  [Reference Citation Analysis (0)]
7.  Mitchell P, Bandello F, Schmidt-Erfurth U, Lang GE, Massin P, Schlingemann RO, Sutter F, Simader C, Burian G, Gerstner O, Weichselberger A; RESTORE study group. The RESTORE study: ranibizumab monotherapy or combined with laser versus laser monotherapy for diabetic macular edema. Ophthalmology. 2011;118:615-625.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 845]  [Cited by in F6Publishing: 969]  [Article Influence: 74.5]  [Reference Citation Analysis (0)]
8.  Jorge R, Costa RA, Calucci D, Cintra LP, Scott IU. Intravitreal bevacizumab (Avastin) for persistent new vessels in diabetic retinopathy (IBEPE study). Retina. 2006;26:1006-1013.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 172]  [Cited by in F6Publishing: 184]  [Article Influence: 10.8]  [Reference Citation Analysis (0)]
9.  Villegas VM, Schwartz SG. Current and Future Pharmacologic Therapies for Diabetic Retinopathy. Curr Pharm Des. 2018;24:4903-4910.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 11]  [Article Influence: 2.2]  [Reference Citation Analysis (0)]
10.  Beli E, Yan Y, Moldovan L, Vieira CP, Gao R, Duan Y, Prasad R, Bhatwadekar A, White FA, Townsend SD, Chan L, Ryan CN, Morton D, Moldovan EG, Chu FI, Oudit GY, Derendorf H, Adorini L, Wang XX, Evans-Molina C, Mirmira RG, Boulton ME, Yoder MC, Li Q, Levi M, Busik JV, Grant MB. Restructuring of the Gut Microbiome by Intermittent Fasting Prevents Retinopathy and Prolongs Survival in db/db Mice. Diabetes. 2018;67:1867-1879.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 247]  [Cited by in F6Publishing: 224]  [Article Influence: 37.3]  [Reference Citation Analysis (0)]
11.  Ferris FL 3rd, Maguire MG, Glassman AR, Ying GS, Martin DF. Evaluating Effects of Switching Anti-Vascular Endothelial Growth Factor Drugs for Age-Related Macular Degeneration and Diabetic Macular Edema. JAMA Ophthalmol. 2017;135:145-149.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 43]  [Cited by in F6Publishing: 49]  [Article Influence: 7.0]  [Reference Citation Analysis (0)]
12.  He Y, Qin MZ, Chen YW. Liver injury caused by fenofibrate within 48 h after first administration: a case report. BMC Gastroenterol. 2021;21:298.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 4]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
13.  Dohmen K, Wen CY, Nagaoka S, Yano K, Abiru S, Ueki T, Komori A, Daikoku M, Yatsuhashi H, Ishibashi H. Fenofibrate-induced liver injury. World J Gastroenterol. 2005;11:7702-7703.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 15]  [Cited by in F6Publishing: 15]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
14.  Sjølie AK, Klein R, Porta M, Orchard T, Fuller J, Parving HH, Bilous R, Chaturvedi N; DIRECT Programme Study Group. Effect of candesartan on progression and regression of retinopathy in type 2 diabetes (DIRECT-Protect 2): a randomised placebo-controlled trial. Lancet. 2008;372:1385-1393.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 320]  [Cited by in F6Publishing: 307]  [Article Influence: 19.2]  [Reference Citation Analysis (0)]
15.  Antonetti DA, Klein R, Gardner TW. Diabetic retinopathy. N Engl J Med. 2012;366:1227-1239.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1061]  [Cited by in F6Publishing: 1168]  [Article Influence: 97.3]  [Reference Citation Analysis (0)]
16.  Kawata R, Yokoi T. Analysis of a Skeletal Muscle Injury and Drug Interactions in Lovastatin- and Fenofibrate-Coadministered Dogs. Int J Toxicol. 2019;38:192-201.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
17.  Segain JP, Raingeard de la Blétière D, Bourreille A, Leray V, Gervois N, Rosales C, Ferrier L, Bonnet C, Blottière HM, Galmiche JP. Butyrate inhibits inflammatory responses through NFkappaB inhibition: implications for Crohn's disease. Gut. 2000;47:397-403.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 886]  [Cited by in F6Publishing: 919]  [Article Influence: 38.3]  [Reference Citation Analysis (0)]
18.  Janssen AW, Kersten S. Potential mediators linking gut bacteria to metabolic health: a critical view. J Physiol. 2017;595:477-487.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 44]  [Cited by in F6Publishing: 56]  [Article Influence: 7.0]  [Reference Citation Analysis (0)]
19.  Allam-Ndoul B, Castonguay-Paradis S, Veilleux A. Gut Microbiota and Intestinal Trans-Epithelial Permeability. Int J Mol Sci. 2020;21.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 56]  [Cited by in F6Publishing: 171]  [Article Influence: 42.8]  [Reference Citation Analysis (0)]
20.  Moubayed NM, Bhat RS, Al Farraj D, Dihani NA, El Ansary A, Fahmy RM. Screening and identification of gut anaerobes (Bacteroidetes) from human diabetic stool samples with and without retinopathy in comparison to control subjects. Microb Pathog. 2019;129:88-92.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 23]  [Article Influence: 4.6]  [Reference Citation Analysis (0)]
21.  Jayasudha R, Das T, Kalyana Chakravarthy S, Sai Prashanthi G, Bhargava A, Tyagi M, Rani PK, Pappuru RR, Shivaji S. Gut mycobiomes are altered in people with type 2 Diabetes Mellitus and Diabetic Retinopathy. PLoS One. 2020;15:e0243077.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 51]  [Article Influence: 12.8]  [Reference Citation Analysis (0)]
22.  Huang Y, Wang Z, Ma H, Ji S, Chen Z, Cui Z, Chen J, Tang S. Dysbiosis and Implication of the Gut Microbiota in Diabetic Retinopathy. Front Cell Infect Microbiol. 2021;11:646348.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 77]  [Article Influence: 25.7]  [Reference Citation Analysis (0)]
23.  Das T, Jayasudha R, Chakravarthy S, Prashanthi GS, Bhargava A, Tyagi M, Rani PK, Pappuru RR, Sharma S, Shivaji S. Alterations in the gut bacterial microbiome in people with type 2 diabetes mellitus and diabetic retinopathy. Sci Rep. 2021;11:2738.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 41]  [Cited by in F6Publishing: 86]  [Article Influence: 28.7]  [Reference Citation Analysis (0)]
24.  Li Y, Ryu C, Munie M, Noorulla S, Rana S, Edwards P, Gao H, Qiao X. Association of Metformin Treatment with Reduced Severity of Diabetic Retinopathy in Type 2 Diabetic Patients. J Diabetes Res. 2018;2018:2801450.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 34]  [Article Influence: 5.7]  [Reference Citation Analysis (0)]
25.  Esfahanian N, Shakiba Y, Nikbin B, Soraya H, Maleki-Dizaji N, Ghazi-Khansari M, Garjani A. Effect of metformin on the proliferation, migration, and MMP-2 and -9 expression of human umbilical vein endothelial cells. Mol Med Rep. 2012;5:1068-1074.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 86]  [Cited by in F6Publishing: 94]  [Article Influence: 7.8]  [Reference Citation Analysis (0)]
26.  Xavier DO, Amaral LS, Gomes MA, Rocha MA, Campos PR, Cota BD, Tafuri LS, Paiva AM, Silva JH, Andrade SP, Belo AV. Metformin inhibits inflammatory angiogenesis in a murine sponge model. Biomed Pharmacother. 2010;64:220-225.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 52]  [Article Influence: 3.5]  [Reference Citation Analysis (0)]
27.  Fan YP, Wu CT, Lin JL, Hsiung CA, Liu HY, Lai JN, Yang CC. Metformin Treatment Is Associated with a Decreased Risk of Nonproliferative Diabetic Retinopathy in Patients with Type 2 Diabetes Mellitus: A Population-Based Cohort Study. J Diabetes Res. 2020;2020:9161039.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 16]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
28.  Zhang Q, Hu N. Effects of Metformin on the Gut Microbiota in Obesity and Type 2 Diabetes Mellitus. Diabetes Metab Syndr Obes. 2020;13:5003-5014.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 55]  [Cited by in F6Publishing: 95]  [Article Influence: 23.8]  [Reference Citation Analysis (0)]
29.  García-Vega ÁS, Corrales-Agudelo V, Reyes A, Escobar JS. Diet Quality, Food Groups and Nutrients Associated with the Gut Microbiota in a Nonwestern Population. Nutrients. 2020;12.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 21]  [Article Influence: 5.3]  [Reference Citation Analysis (0)]
30.  Hansen MEB, Rubel MA, Bailey AG, Ranciaro A, Thompson SR, Campbell MC, Beggs W, Dave JR, Mokone GG, Mpoloka SW, Nyambo T, Abnet C, Chanock SJ, Bushman FD, Tishkoff SA. Population structure of human gut bacteria in a diverse cohort from rural Tanzania and Botswana. Genome Biol. 2019;20:16.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 59]  [Article Influence: 11.8]  [Reference Citation Analysis (0)]
31.  Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014;30:2114-2120.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30322]  [Cited by in F6Publishing: 36776]  [Article Influence: 3677.6]  [Reference Citation Analysis (1)]
32.  Reyon D, Tsai SQ, Khayter C, Foden JA, Sander JD, Joung JK. FLASH assembly of TALENs for high-throughput genome editing. Nat Biotechnol. 2012;30:460-465.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 835]  [Cited by in F6Publishing: 887]  [Article Influence: 73.9]  [Reference Citation Analysis (0)]
33.  Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, Fierer N, Peña AG, Goodrich JK, Gordon JI, Huttley GA, Kelley ST, Knights D, Koenig JE, Ley RE, Lozupone CA, McDonald D, Muegge BD, Pirrung M, Reeder J, Sevinsky JR, Turnbaugh PJ, Walters WA, Widmann J, Yatsunenko T, Zaneveld J, Knight R. QIIME allows analysis of high-throughput community sequencing data. Nat Methods. 2010;7:335-336.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23810]  [Cited by in F6Publishing: 23006]  [Article Influence: 1643.3]  [Reference Citation Analysis (0)]
34.  Rognes T, Flouri T, Nichols B, Quince C, Mahé F. VSEARCH: a versatile open source tool for metagenomics. PeerJ. 2016;4:e2584.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4320]  [Cited by in F6Publishing: 4973]  [Article Influence: 621.6]  [Reference Citation Analysis (0)]
35.  Wang Q, Garrity GM, Tiedje JM, Cole JR. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol. 2007;73:5261-5267.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12842]  [Cited by in F6Publishing: 12614]  [Article Influence: 742.0]  [Reference Citation Analysis (0)]
36.  Qin J, Li Y, Cai Z, Li S, Zhu J, Zhang F, Liang S, Zhang W, Guan Y, Shen D, Peng Y, Zhang D, Jie Z, Wu W, Qin Y, Xue W, Li J, Han L, Lu D, Wu P, Dai Y, Sun X, Li Z, Tang A, Zhong S, Li X, Chen W, Xu R, Wang M, Feng Q, Gong M, Yu J, Zhang Y, Zhang M, Hansen T, Sanchez G, Raes J, Falony G, Okuda S, Almeida M, LeChatelier E, Renault P, Pons N, Batto JM, Zhang Z, Chen H, Yang R, Zheng W, Yang H, Wang J, Ehrlich SD, Nielsen R, Pedersen O, Kristiansen K. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature. 2012;490:55-60.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3971]  [Cited by in F6Publishing: 4523]  [Article Influence: 376.9]  [Reference Citation Analysis (0)]
37.  Karlsson FH, Tremaroli V, Nookaew I, Bergström G, Behre CJ, Fagerberg B, Nielsen J, Bäckhed F. Gut metagenome in European women with normal, impaired and diabetic glucose control. Nature. 2013;498:99-103.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1766]  [Cited by in F6Publishing: 1823]  [Article Influence: 165.7]  [Reference Citation Analysis (0)]
38.  Allin KH, Nielsen T, Pedersen O. Mechanisms in endocrinology: Gut microbiota in patients with type 2 diabetes mellitus. Eur J Endocrinol. 2015;172:R167-R177.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 144]  [Cited by in F6Publishing: 138]  [Article Influence: 15.3]  [Reference Citation Analysis (0)]
39.  Le Chatelier E, Nielsen T, Qin J, Prifti E, Hildebrand F, Falony G, Almeida M, Arumugam M, Batto JM, Kennedy S, Leonard P, Li J, Burgdorf K, Grarup N, Jørgensen T, Brandslund I, Nielsen HB, Juncker AS, Bertalan M, Levenez F, Pons N, Rasmussen S, Sunagawa S, Tap J, Tims S, Zoetendal EG, Brunak S, Clément K, Doré J, Kleerebezem M, Kristiansen K, Renault P, Sicheritz-Ponten T, de Vos WM, Zucker JD, Raes J, Hansen T; MetaHIT consortium, Bork P, Wang J, Ehrlich SD, Pedersen O. Richness of human gut microbiome correlates with metabolic markers. Nature. 2013;500:541-546.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2727]  [Cited by in F6Publishing: 2791]  [Article Influence: 253.7]  [Reference Citation Analysis (1)]
40.  Prakash S, Rodes L, Coussa-Charley M, Tomaro-Duchesneau C. Gut microbiota: next frontier in understanding human health and development of biotherapeutics. Biologics. 2011;5:71-86.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 70]  [Cited by in F6Publishing: 108]  [Article Influence: 8.3]  [Reference Citation Analysis (0)]
41.  Weiss GA, Hennet T. Mechanisms and consequences of intestinal dysbiosis. Cell Mol Life Sci. 2017;74:2959-2977.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 393]  [Cited by in F6Publishing: 346]  [Article Influence: 49.4]  [Reference Citation Analysis (0)]
42.  Sharma S, Tripathi P. Gut microbiome and type 2 diabetes: where we are and where to go? J Nutr Biochem. 2019;63:101-108.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 148]  [Cited by in F6Publishing: 230]  [Article Influence: 38.3]  [Reference Citation Analysis (0)]
43.  Wang J, Li W, Wang C, Wang L, He T, Hu H, Song J, Cui C, Qiao J, Qing L, Li L, Zang N, Wang K, Wu C, Qi L, Ma A, Zheng H, Hou X, Liu F, Chen L. Enterotype Bacteroides Is Associated with a High Risk in Patients with Diabetes: A Pilot Study. J Diabetes Res. 2020;2020:6047145.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 54]  [Article Influence: 13.5]  [Reference Citation Analysis (0)]
44.  Li SC, Xiao Y, Wu RT, Xie D, Zhao HH, Shen GY, Wu EQ. Comparative analysis of type 2 diabetes-associated gut microbiota between Han and Mongolian people. J Microbiol. 2021;59:693-701.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3]  [Cited by in F6Publishing: 3]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
45.  Wu H, Esteve E, Tremaroli V, Khan MT, Caesar R, Mannerås-Holm L, Ståhlman M, Olsson LM, Serino M, Planas-Fèlix M, Xifra G, Mercader JM, Torrents D, Burcelin R, Ricart W, Perkins R, Fernàndez-Real JM, Bäckhed F. Metformin alters the gut microbiome of individuals with treatment-naive type 2 diabetes, contributing to the therapeutic effects of the drug. Nat Med. 2017;23:850-858.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 824]  [Cited by in F6Publishing: 846]  [Article Influence: 120.9]  [Reference Citation Analysis (0)]
46.  Rau M, Rehman A, Dittrich M, Groen AK, Hermanns HM, Seyfried F, Beyersdorf N, Dandekar T, Rosenstiel P, Geier A. Fecal SCFAs and SCFA-producing bacteria in gut microbiome of human NAFLD as a putative link to systemic T-cell activation and advanced disease. United European Gastroenterol J. 2018;6:1496-1507.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 110]  [Cited by in F6Publishing: 196]  [Article Influence: 32.7]  [Reference Citation Analysis (0)]
47.  Xu H, Cai M, Zhang X. Effect of the blockade of the IL-23-Th17-IL-17A pathway on streptozotocin-induced diabetic retinopathy in rats. Graefes Arch Clin Exp Ophthalmol. 2015;253:1485-1492.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 25]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
48.  Panasevich MR, Meers GM, Linden MA, Booth FW, Perfield JW 2nd, Fritsche KL, Wankhade UD, Chintapalli SV, Shankar K, Ibdah JA, Rector RS. High-fat, high-fructose, high-cholesterol feeding causes severe NASH and cecal microbiota dysbiosis in juvenile Ossabaw swine. Am J Physiol Endocrinol Metab. 2018;314:E78-E92.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 66]  [Cited by in F6Publishing: 66]  [Article Influence: 11.0]  [Reference Citation Analysis (0)]
49.  Vagaja NN, Binz N, McLenachan S, Rakoczy EP, McMenamin PG. Influence of endotoxin-mediated retinal inflammation on phenotype of diabetic retinopathy in Ins2 Akita mice. Br J Ophthalmol. 2013;97:1343-1350.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 25]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
50.  McCann SE, Hullar MAJ, Tritchler DL, Cortes-Gomez E, Yao S, Davis W, O'Connor T, Erwin D, Thompson LU, Yan L, Lampe JW. Enterolignan Production in a Flaxseed Intervention Study in Postmenopausal US Women of African Ancestry and European Ancestry. Nutrients. 2021;13.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 4]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
51.  Wu TK, Wei CW, Pan YR, Hsu RJ, Wu CY, Yu YL. The uremic toxin p-cresyl sulfate induces proliferation and migration of clear cell renal cell carcinoma via microRNA-21/ HIF-1α axis signals. Sci Rep. 2019;9:3207.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 8]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
52.  Zhang X, Zhao Y, Xu J, Xue Z, Zhang M, Pang X, Zhang X, Zhao L. Modulation of gut microbiota by berberine and metformin during the treatment of high-fat diet-induced obesity in rats. Sci Rep. 2015;5:14405.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 370]  [Cited by in F6Publishing: 445]  [Article Influence: 49.4]  [Reference Citation Analysis (0)]
53.  Afra K, Laupland K, Leal J, Lloyd T, Gregson D. Incidence, risk factors, and outcomes of Fusobacterium species bacteremia. BMC Infect Dis. 2013;13:264.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 62]  [Cited by in F6Publishing: 82]  [Article Influence: 7.5]  [Reference Citation Analysis (0)]
54.  Fardini Y, Wang X, Témoin S, Nithianantham S, Lee D, Shoham M, Han YW. Fusobacterium nucleatum adhesin FadA binds vascular endothelial cadherin and alters endothelial integrity. Mol Microbiol. 2011;82:1468-1480.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 153]  [Cited by in F6Publishing: 182]  [Article Influence: 14.0]  [Reference Citation Analysis (0)]
55.  Silby MW, Winstanley C, Godfrey SA, Levy SB, Jackson RW. Pseudomonas genomes: diverse and adaptable. FEMS Microbiol Rev. 2011;35:652-680.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 553]  [Cited by in F6Publishing: 578]  [Article Influence: 44.5]  [Reference Citation Analysis (0)]
56.  Machado GB, de Assis MC, Leão R, Saliba AM, Silva MC, Suassuna JH, de Oliveira AV, Plotkowski MC. ExoU-induced vascular hyperpermeability and platelet activation in the course of experimental Pseudomonas aeruginosa pneumosepsis. Shock. 2010;33:315-321.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 24]  [Cited by in F6Publishing: 24]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
57.  Chung JW, Piao ZH, Yoon SR, Kim MS, Jeong M, Lee SH, Min JK, Kim JW, Cho YH, Kim JC, Ahn JK, Kim KE, Choi I. Pseudomonas aeruginosa eliminates natural killer cells via phagocytosis-induced apoptosis. PLoS Pathog. 2009;5:e1000561.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 21]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
58.  Broquet A, Roquilly A, Jacqueline C, Potel G, Caillon J, Asehnoune K. Depletion of natural killer cells increases mice susceptibility in a Pseudomonas aeruginosa pneumonia model. Crit Care Med. 2014;42:e441-e450.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 38]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
59.  Afarid M, Attarzadeh A, Farvardin M, Ashraf H. The Association of Serum Leptin Level and Anthropometric Measures With the Severity of Diabetic Retinopathy in Type 2 Diabetes Mellitus. Med Hypothesis Discov Innov Ophthalmol. 2018;7:156-162.  [PubMed]  [DOI]  [Cited in This Article: ]
60.  Dekker Nitert M, Mousa A, Barrett HL, Naderpoor N, de Courten B. Altered Gut Microbiota Composition Is Associated With Back Pain in Overweight and Obese Individuals. Front Endocrinol (Lausanne). 2020;11:605.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 22]  [Cited by in F6Publishing: 43]  [Article Influence: 10.8]  [Reference Citation Analysis (0)]
61.  Adlercreutz H. Lignans and human health. Crit Rev Clin Lab Sci. 2007;44:483-525.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 363]  [Cited by in F6Publishing: 315]  [Article Influence: 19.7]  [Reference Citation Analysis (0)]
62.  Eichholzer M, Richard A, Nicastro HL, Platz EA, Linseisen J, Rohrmann S. Urinary lignans and inflammatory markers in the US National Health and Nutrition Examination Survey (NHANES) 1999-2004 and 2005-2008. Cancer Causes Control. 2014;25:395-403.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 17]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
63.  Takada T, Watanabe K, Makino H, Kushiro A. Reclassification of Eubacterium desmolans as Butyricicoccus desmolans comb. nov., and description of Butyricicoccus faecihominis sp. nov., a butyrate-producing bacterium from human faeces. Int J Syst Evol Microbiol. 2016;66:4125-4131.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 20]  [Article Influence: 2.5]  [Reference Citation Analysis (0)]
64.  Tracy SC, Tasto JP, Oshima Y, Murata R, Garcia J, Amiel D. The effect of butyric acid on normal tendons: a potential stimulus for extracellular matrix expression. Am J Orthop (Belle Mead NJ). 2011;40:142-147.  [PubMed]  [DOI]  [Cited in This Article: ]
65.  Jahani S, Moslemi HR, Dehghan MM, Sedaghat R, Mazaheri Nezhad R, Rezaee Moghaddam D. The effect of butyric acid with autogenous omental graft on healing of experimental Achilles tendon injury in rabbits. Iran J Vet Res. 2015;16:100-104.  [PubMed]  [DOI]  [Cited in This Article: ]
66.  Wong RH, Scholey A, Howe PR. Assessing premorbid cognitive ability in adults with type 2 diabetes mellitus--a review with implications for future intervention studies. Curr Diab Rep. 2014;14:547.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 42]  [Cited by in F6Publishing: 37]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
67.  Grünblatt E, Bartl J, Riederer P. The link between iron, metabolic syndrome, and Alzheimer's disease. J Neural Transm (Vienna). 2011;118:371-379.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 42]  [Cited by in F6Publishing: 40]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
68.  Biessels GJ, Staekenborg S, Brunner E, Brayne C, Scheltens P. Risk of dementia in diabetes mellitus: a systematic review. Lancet Neurol. 2006;5:64-74.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1346]  [Cited by in F6Publishing: 1445]  [Article Influence: 80.3]  [Reference Citation Analysis (0)]
69.  Gupta P, Gan ATL, Man REK, Fenwick EK, Sabanayagam C, Mitchell P, Cheung CY, Cheung N, Wong TY, Cheng CY, Lamoureux EL. Association between diabetic retinopathy and incident cognitive impairment. Br J Ophthalmol. 2019;103:1605-1609.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 20]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
70.  Zhang Y, Lu S, Yang Y, Wang Z, Wang B, Zhang B, Yu J, Lu W, Pan M, Zhao J, Guo S, Cheng J, Chen X, Hong K, Li G, Yu Z. The diversity of gut microbiota in type 2 diabetes with or without cognitive impairment. Aging Clin Exp Res. 2021;33:589-601.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 30]  [Article Influence: 10.0]  [Reference Citation Analysis (0)]
71.  Weglarz L, Dzierzewicz Z, Skop B, Orchel A, Parfiniewicz B, Wiśniowska B, Swiatkowska L, Wilczok T. Desulfovibrio desulfuricans lipopolysaccharides induce endothelial cell IL-6 and IL-8 secretion and E-selectin and VCAM-1 expression. Cell Mol Biol Lett. 2003;8:991-1003.  [PubMed]  [DOI]  [Cited in This Article: ]
72.  Chen YR, Zhou LZ, Fang ST, Long HY, Chen JY, Zhang GX. Isolation of Desulfovibrio spp. from human gut microbiota using a next-generation sequencing directed culture method. Lett Appl Microbiol. 2019;68:553-561.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 20]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
73.  Zeng Y, Zhang L, Hu Z. Cerebral insulin, insulin signaling pathway, and brain angiogenesis. Neurol Sci. 2016;37:9-16.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 29]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
74.  Wagner EM, Sánchez J, McClintock JY, Jenkins J, Moldobaeva A. Inflammation and ischemia-induced lung angiogenesis. Am J Physiol Lung Cell Mol Physiol. 2008;294:L351-L357.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 31]  [Article Influence: 1.8]  [Reference Citation Analysis (0)]
75.  Legendre C, Reen FJ, Mooij MJ, McGlacken GP, Adams C, O'Gara F. Pseudomonas aeruginosa Alkyl quinolones repress hypoxia-inducible factor 1 (HIF-1) signaling through HIF-1α degradation. Infect Immun. 2012;80:3985-3992.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 33]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
76.  Gururaj AE, Belakavadi M, Salimath BP. Antiangiogenic effects of butyric acid involve inhibition of VEGF/KDR gene expression and endothelial cell proliferation. Mol Cell Biochem. 2003;243:107-112.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 28]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
77.  Isipato M, Dessì P, Sánchez C, Mills S, Ijaz UZ, Asunis F, Spiga D, De Gioannis G, Mascia M, Collins G, Muntoni A, Lens PNL. Propionate Production by Bioelectrochemically-Assisted Lactate Fermentation and Simultaneous CO(2) Recycling. Front Microbiol. 2020;11:599438.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 11]  [Article Influence: 3.7]  [Reference Citation Analysis (0)]
78.  Zapolska-Downar D, Naruszewicz M. Propionate reduces the cytokine-induced VCAM-1 and ICAM-1 expression by inhibiting nuclear factor-kappa B (NF-kappaB) activation. J Physiol Pharmacol. 2009;60:123-131.  [PubMed]  [DOI]  [Cited in This Article: ]
79.  Adamiec-Mroczek J, Oficjalska-Młyńczak J, Misiuk-Hojło M. Proliferative diabetic retinopathy-The influence of diabetes control on the activation of the intraocular molecule system. Diabetes Res Clin Pract. 2009;84:46-50.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 29]  [Article Influence: 1.9]  [Reference Citation Analysis (0)]