Pathophysiological background in different phenotypes of nonalcoholic fatty liver disease (NAFLD) remains to be elucidated. The aim was to investigate the association between fecal and blood microbiota profiles and the presence of NAFLD in obese versus lean subjects. Demographic and clinical data were reviewed in 268 health checkup examinees, whose fecal and blood samples were available for microbiota analysis. NAFLD was diagnosed with ultrasonography, and subjects with NAFLD were further categorized as obese (body mass index (BMI) ≥25) or lean (BMI <25). Fecal and blood microbiota communities were analyzed by sequencing of the V3-V4 domains of the 16S rRNA genes. Correlation between microbiota taxa and NAFLD was assessed using zero-inflated Gaussian mixture models, with adjustment of age, sex, and BMI, and Bonferroni correction. The NAFLD group (n = 76) showed a distinct bacterial community with a lower biodiversity and a far distant phylotype compared with the control group (n = 192). In the gut microbiota, the decrease in Desulfovibrionaceae was associated with NAFLD in the lean NAFLD group (log2 coefficient (coeff.) = -2.107, P = 1.60E-18), but not in the obese NAFLD group (log2 coeff. = 1.440, P = 1.36E-04). In the blood microbiota, Succinivibrionaceae showed opposite correlations in the lean (log2 coeff. = -1.349, P = 5.34E-06) and obese NAFLD groups (log2 coeff. = 2.215, P = 0.003). Notably, Leuconostocaceae was associated with the obese NAFLD in the gut (log2 coeff. = -1.168, P = 0.041) and blood (log2 coeff. = -2.250, P = 1.28E-10). In conclusion, fecal and blood microbiota profiles showed different patterns between subjects with obese and lean NAFLD, which might be potential biomarkers to discriminate diverse phenotypes of NAFLD.
Citation: Yun Y, Kim H-N, Lee E-j, Ryu S, Chang Y, Shin H, et al. (2019) Fecal and blood microbiota profiles and presence of nonalcoholic fatty liver disease in obese versus lean subjects. PLoS ONE 14(3): e0213692. https://doi.org/10.1371/journal.pone.0213692
Editor: Ming-Lung Yu, Kaohsiung Medical University Chung Ho Memorial Hospital, TAIWAN
Received: December 3, 2018; Accepted: February 26, 2019; Published: March 14, 2019
Copyright: © 2019 Yun et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Ministry of Science and ICT (grant no. 2018R1A5A2025286 [HYK]), and the Ministry of Education (NRF-2018R1D1A1B07050067 [H-LK]). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Nonalcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver diseases. Patients with NAFLD have increased risk of developing cirrhosis or hepatocellular carcinoma, as well as cardiovascular events, malignancies other than hepatocellular carcinoma, and increased mortality.[2, 3] Obesity is a well-documented risk factor for the development of NAFLD. However, the relationship between obesity and NAFLD appears more complicated, considering the absence of NAFLD in obese subjects without any metabolic abnormalities and the presence of NAFLD in lean (body mass index (BMI) <25 kg/m2) individuals with metabolic abnormalities such as insulin resistance. Although the prevalence of lean NAFLD shows ethnic preponderance, particularly Asians, it was also found in approximately 10% of Western population.[6–8] However, the pathogenetic differences between phenotypes of NAFLD remain to be elucidated.
The microbiota found in the human body comprise trillions of microorganisms, with the majority colonizing the gut. Gut microbiota appear to be one of the key regulators in the pathogenesis of obesity, diabetes, and metabolic syndrome.[10–12] Recent studies have suggested that gut microbiota are involved in the pathogenesis of NAFLD. For example, gut-derived endogenous alcohol was suggested to play a role in the pathogenesis of nonalcoholic steatohepatitis. In addition, shifts in the composition of gut microbiota seemed relevant in NAFLD, such as decrease in some members of Firmicutes, or abundance of Bacteroidetes in nonalcoholic steatohepatitis and Ruminococcus in significant fibrosis. However, these studies mostly focused on obese subjects. Because BMI may be one of the major determinants of compositional changes in gut microbiome, microbial characteristics could be different among NAFLD patients with different body habitus. A recent study has reported Firmicutes-poor microbiota along with marked lower overall microbial richness in nonobese NAFLD compared with nonobese control. However, studies linking gut dysbiosis and phenotypic variations of NAFLD in terms of body habitus are scarce.
A recent pilot study demonstrated that changes in blood microbiota are associated with liver fibrosis in obese patients. The liver has a unique vasculature; it receives the majority of its blood supply from the intestine through the portal vein. Thus, disturbances in the intestinal immune system could increase intestinal permeability and bacterial translocation, triggering various pathological sequences including obesity, metabolic and liver diseases. Recently, the predictive role of blood microbiota has been reported in metabolic diseases.[21, 22] Although studies on blood microbiota attract attention with anticipation of their use as potential noninvasive biomarkers, data on the relationship between gut and blood microbiota and the presence of NAFLD in subjects with different body habitus are insufficient. Thus, we aimed to investigate fecal and blood microbiota profiles in obese versus lean subjects with or without NAFLD.
Materials and methods
Health checkup examinees were screened for the eligibility for this study between June and September 2014 at Kangbuk Samsung Hospital Total Healthcare Screening Centers in Seoul, South Korea. The affordable number of participants for analysis within the study budget was less than 300. During the screening period, a total of 296 subjects were found to be eligible showing no evidence of other liver diseases (i.e., positive serology for viral hepatitis B or C, significant alcohol intake (daily alcohol consumption ≥ 30 g [male] or 20 g [female]), other metabolic or hereditary liver diseases, or use of medications such as amiodarone, tamoxifen, methotrexate, or corticosteroids). They gave written informed consents and agreed to provide samples for blood and fecal microbiota analysis. Among these, 268 subjects were finally enrolled in the present study by excluding 28 because of their previous use of antibiotics, probiotics, or cholesterol-lowering medications (n = 22), and the presence of diabetes mellitus (n = 6). Of these 268 participants, NAFLD was diagnosed in 76 subjects based on the presence of ultrasonographic findings suggestive of fatty liver as described below. Because all study participants had no evidence of liver diseases of other etiologies such as alcoholic or viral as described earlier, incident cases with fatty liver were regarded as NAFLD. The control group comprised 192 subjects without any evidence of NAFLD or other liver diseases.
This study was approved by the Institutional Review Board of Kangbuk Samsung Hospital (KBSMC 2013-01-245-008, registered December 23, 2013). All study participants gave their written informed consent to participate in the study. The present study was conducted according to the ethical guidelines of the World Medical Association Declaration of Helsinki.
Clinical, laboratory, and radiologic assessments
Height and weight were measured by trained nurses with the participants wearing a lightweight hospital gown without shoes. Briefly, height was measured to the nearest 0.1 cm using a stadiometer with the participants standing barefoot. Weight was measured to the nearest 0.1 kg on a bioimpedance analyzer (InBody 3.0 and InBody 720, Biospace Co., Seoul, Korea). BMI was calculated as weight in kilograms divided by height in meters squared. Study subjects were categorized according to their BMI based on the criteria established for Asian populations: underweight, BMI <18.5 kg/m2; normal weight, BMI 18.5–23 kg/m2; overweight, BMI 23–25 kg/m2; and obese, BMI ≥25 kg/m2. Insulin resistance was assessed with the homeostasis model assessment of insulin resistance equation, as follows: fasting blood insulin (μU/ml)×fasting blood glucose (mmol/l)/22.5. An ultrasonographic diagnosis of fatty liver was defined as the presence of a diffuse increase in the echogenicity of the liver parenchyma compared with the kidney or spleen.[26, 27] The intra- and inter-observer reliability for the diagnosis of fatty liver was adequately high (kappa statistics of 0.94 and 0.74, respectively).
DNA extraction and sequence data generation
Fecal samples were immediately frozen after collection. Buffy coat consisting mainly of leukocytes was used for blood samples. 16S rRNA genes were extracted and amplified from specimens using the MO-BIO PowerSoil DNA Isolation Kit (MO-BIO Laboratories, Carlsbad, CA) according to the manufacturer’s instructions. Amplification and sequencing were performed in the same batch as previously described for analysis of bacterial communities. The genomic DNA was amplified using fusion primers targeting 16S V3-V4 rRNA gene with indexing barcodes. All samples were pooled for sequencing on the Illumina Miseq platform according to the manufacturer’s specifications.
Quality filtering, chimera removal, and de novo operational taxonomic unit (OTU) clustering were carried out using the UPARSE pipeline, which identifies highly accurate OTU from amplicon sequencing data. The reads were dereplicated, sorted, and clustered into candidate OTU with removing chimeric OTU. Taxonomic assignment for OTU was annotated by RDP reference (version 16) with an identity threshold of 97% using UTAX command in the UPARSE pipeline. OTU table with taxonomic assignments was transformed to “biom” format for the compatibility of QIIME software (version 1.9; http://qiime.org). Finally, 5,668,793 reads/227 OTUs with a mean of 21,152 (SD = 12,674) sequences per fecal sample and 9,786,870 reads/4,066 OTUs with a mean of 36,518 (SD = 24,966) sequences per blood sample were included for the QIIME analysis. Alpha diversity was calculated using chao1 and phylogenetic diversity (PD) by QIIME, which significant difference between case/control was calculated with 999 Monte Carlo permutation and Bonferroni multiple correction. Beta diversity on Cumulative Sum Scaling (CSS) normalized OTU tables by QIIME was performed using the weighted UniFrac distance metrics based on the phylogenetic distance comparison between communities showing principal coordinate analysis plots. Permutational ANOVA for distance matrix was calculated with 999 Monte Carlo permutation and Bonferroni multiple correction.
The zero-inflated Gaussian mixture (fitZIG) model of metagenomeSeq package version 1.14.2  was used for correlation analysis between CSS normalized count data (as dependent variables) and control versus NAFLD (as independent categorical variables). Age, sex, and BMI covariates were adjusted for regression analysis. Each taxa level that was abundant (>50 normalized counts per sample) and prevalent (present in 10% of samples) in each analysis set was applied to the zero-inflated Gaussian mixture model with Bonferroni multiple correction (an adjusted P value <0.05 is significant). This analysis was performed using R software package version 3.2.3 (R Foundation for Statistical Computing, Vienna, Austria).
Table 1 summarizes the baseline characteristics of the entire study subjects (n = 268). Subjects with NAFLD (n = 76, 28.4%) showed significantly higher BMI, blood pressure, and metabolic and liver-related laboratory values than those without NAFLD (i.e., control, n = 192).(all P-values <0.05) Among lean subjects (BMI <25 kg/m2, n = 195), subjects with NAFLD (i.e., “lean NAFLD”; n = 27, 13.8%) also demonstrated significantly higher biometric and laboratory values, except for hemoglobin A1c and aspartate aminotransferase, than lean controls (Table 2). On the contrary, obese subjects (n = 73) showed less distinctive baseline characteristics between those with (i.e., “obese NAFLD”; n = 49, 67.1%) and without NAFLD, particularly without significant difference in age, sex, blood pressure, lipid profiles, and renal function.
Microbial diversity of fecal and blood microbiota in the NAFLD group
Alpha diversity measures diversity within a community. Different metrics have been devised to measure alpha diversity with emphasis on the different aspects of the community structure. In Table 3, overall blood microbiota had higher richness (Chao1) but less PD than fecal microbiota. In fecal data, the NAFLD group showed slightly lower biodiversity than the control group, but it was statistically significant only in fecal microbial PD of total NAFLD (Bonferroni corrected P = 0.011). The biodiversity of the NAFLD group also showed lower tendencies than that of the control group in blood microbiota as well.
Beta diversity measuring the variations in community membership across the different groups was performed to prove the differentiation between groups using OTU abundance with weighted Unifrac metrics, weighting species abundances with phylogenetic relationships among taxa. In principal coordinate analysis plots of both fecal and blood microbiota, only lean NAFLD showed a clustering of the NAFLD group (Fig 1). When it was examined for statistical significance of the distance metrics, permutational ANOVA of blood microbiota exhibited no significant results. However, permutational ANOVA of fecal microbiota showed highly significant difference between the NAFLD and control groups, except obese NAFLD (Table 4). Therefore, the highly significant difference between the NAFLD and control groups is predominantly due to the difference in lean NAFLD (pseudo-F = 3.021, P = 0.001).
NOTE. Nonalcoholic fatty liver disease (black squares) and control (gray circles) groups from total (A [fecal], D [blood]), lean (B [fecal], E [blood]), and obese (C [fecal], F [blood]) samples.
Taxonomic comparison in fecal microbiota
To obtain a featured change of microbial components, we used zero-inflated Gaussian mixture based on the normalized count data of an OTU table. Table 5 shows a summary of significant differential bacterial taxa (Bonferroni corrected P<0.05) with at least 2 times of coefficient effect, adjusted by age, sex, and BMI. The results of total NAFLD (obese and lean NAFLD) resembled those of lean NAFLD. The decrease in five Clostridia, which belong to Firmicutes, was correlated with lean NAFLD. Two Ruminococcaceae (i.e., Fastidiosipila and Faecalibacterium) showed same negative patterns in the lean and obese NAFLD as well as in total NAFLD. In particular, Fastidiosipila was the only bacterium that showed the same pattern across the three groups. This result indicates the unique bacterial feature for NAFLD regardless of the presence or absence of obesity. However, Desulfovibrionaceae under Deltaproteobacteria showed an opposite trend between lean (negative) and obese NAFLD (positive), which resulted in negative correlation with total NAFLD. The decrease in Weissella and its family Leuconostocaceae was associated with only the obese NAFLD group.
Taxonomic comparison in blood microbiota
In contrast to fecal data, blood microbiota of total NAFLD were more shared with obese NAFLD pattern, but the obese NAFLD group showed more unique results (Table 6). Notably, the family Leuconostocaceae was negatively associated with obese NAFLD in blood and fecal microbiota. However, the genus under Leuconostocaceae was Leuconostoc, not Weissella. Associated bacteria including Deinococcus-Thermus and Deferribacteres phyla were much more varied in the blood than in the feces. The decrease in Deferribacteriales incertae sedis was highly associated with obese NAFLD, which was in contrast to lean NAFLD. Anaerobiospirillum and its family Succinivibrionaceae were negatively associated with lean NAFLD, but very positively associated with obese NAFLD. The decrease in rhizobial Beijerinckiaceae and archeal Methanosarcinaceae was highly correlated with obese NAFLD.
The results of the present study demonstrated that lean subjects had different characteristics in blood microbiota in terms of the presence of NAFLD. Furthermore, lean subjects with NAFLD showed different features in blood and gut microbiota compared with obese subjects with NAFLD. These data suggest that the distinctive features of blood microbiota might be diagnostic for the presence of NAFLD in lean population, which may be used as a point-of-care test for early detection of lean NAFLD.
The results suggested unique pattern of reduced PD in fecal and blood microbiota in lean subjects with NAFLD. The beta diversity did not distinguish between subjects with NAFLD and controls. By contrast, when the subjects were stratified based on their BMI, fecal microbiota discriminated subjects with NAFLD in the lean subgroup and in the overall subjects. Interestingly, blood microbiota showed reduced richness in bacterial diversity in lean individuals with NAFLD in contrast to lean controls or obese group. However, such diversity was not distinct in fecal microbiota between subjects with or without NAFLD, or between subgroups with or without obesity (Table 3). Lower PD in fecal microbiota in overall subjects with NAFLD was in consistent with recent studies.[18, 33] We observed a markedly distinct microbial community in fecal microbiota of subjects with lean NAFLD but not in blood. This discrepancy in ecological diversity between blood and fecal microbiota might have resulted from their genuine compositional difference due to the presence of intestinal barrier, filtering function of the liver, and the role of immune cells. In addition, blood microbiota may have oral source other than gut-derived bacteria. Excluding the possibilities of confounding effects of oral disease in the study participants might help clarify phylogenetic characteristics more evidently.
The vast majority of human gut microbiota consist of three bacterial phyla, namely, Bacteroidetes, Actinobacteria, and Firmicutes. Dysbiosis between beneficial and pathogenic bacteria may lead to obesity, insulin resistance, and NAFLD. In particular, both Bacteroidetes and Firmicutes (phylum) encode carbohydrate-digesting enzymes metabolizing complex carbohydrates to the short-chain fatty acids. A greater number of these enzymes are encoded by Bacteroidetes than by Firmicutes. Obese subjects have an increased Bacteroidetes/Firmicutes ratio and higher short-chain fatty acids than lean subjects. Previous studies on fecal microbiota reported a higher Bacteroidetes/Firmicutes ratio in NAFLD patients than in control.[14, 15] This finding is in line with our results on fecal microbiota showing many bacteria which belong to Firmicutes were decreased in subjects with NAFLD regardless of body habitus (Table 5). However, the level of lactobacilli (family Leuconostocaceae and Weisella) was lower only in obese subjects with NAFLD. In addition, the quantities of Desulfovibrionaceae were significantly different between obese NAFLD and lean NAFLD. These differences in the composition of gut microbiota suggest different characteristics in terms of gut dysbiosis, body habitus, and phenotypes of NAFLD. Previous studies on the association between gut microbiota and obesity and metabolic diseases reported controversial results on BMI and lactobacilli; a negative and a positive correlation[41, 42] were found between lactobacilli and BMI.
Based on the potential linkage among disturbances in the intestinal immune system, bacterial translocation, and pathological consequences including obesity, metabolic and liver diseases, we aimed to investigate the potential role of blood microbiota in discriminating the phenotypes of NAFLD. In our results, the negative correlation of the presence of NAFLD, particularly obese NAFLD, and lactobacilli Leuconostocaceae was also observed in blood microbiota, as well as in fecal microbiota. However, other bacteria showed mixed features, especially in obese NAFLD; for example, reduced Actinomycetales and Deferribacteriales versus increased Aeromonadales (Table 6). Among these organisms, distinctly different correlations were observed in Deferribacteriales incertae sedis and Aeromonadales between lean NAFLD and obese NAFLD. Previous studies demonstrated that some microbial metabolites, such as lipopolysaccharide, are found in the plasma of obese subjects and correlated with the degree of liver inflammation. This finding suggests the role of a mediator in the development and progression of NAFLD.[43, 44] Lean subjects with NAFLD might have different degrees of liver injury from obese patients, as was shown in a recent study from Hong Kong. In addition, lean NAFLD is associated with decreased likelihood of having insulin resistance and hypercholesterolemia compared with overweight or obese NAFLD in a Western study. Taken together, patients with lean NAFLD may have different pathogenetic mechanisms and clinical characteristics other than BMI from obese NAFLD, which might be linked with different gut and blood microbiota profiles in a complex manner. Direct evidences to the pathogenetic link between blood microbiota and NAFLD phenotypes are scarce. However, increase in Proteobacteria in the blood of the obese NAFLD group was observed, which shares similar gut microbiome characteristics of alcoholic liver diseases and cirrhosis.[46, 47] The opposite results of the correlation between the abovementioned bacteria and phenotypes of NAFLD (i.e., lean versus obese) might reflect the different degrees of bacterial translocation and resultant low-grade inflammatory state as well as the degrees of insulin resistance and NAFLD between lean and obese subjects.[22, 48, 49]
The results of the present study might serve as a microbiota signature to predict NAFLD particularly in lean subjects, before progression of NAFLD to significant fibrosis or cirrhosis. In addition, a point-of-care test based on our blood microbiota characteristics might be anticipated if these results are properly validated in the near future. On the contrary, this study has several limitations when interpreting our results. First, clinical characteristics including risk factors for NAFLD or disease severity of NAFLD of the study subjects who volunteered for health checkup were deemed similar to those of the general population, compared to patients with established NAFLD or nonalcoholic steatohepatitis. In addition, although the characteristics of the study participants harbors concerns of selection bias, the prevalence of overall participants or lean subgroup was similar to those in the literature.[1, 50–53] Second, lack of histological data prevented further analysis on the relationship between gut and blood microbiota features and the severity of liver disease. Third, the small number of NAFLD subjects (n = 49 [obese] and n = 27 [lean], respectively) could have contributed the absence of difference in alpha and phylogenetic diversity of the blood and fecal microbiota. Diagnosis of NAFLD based on ultrasonographic findings might also have influenced on the number of cases due to the limited sensitivity of ultrasound to detect hepatic steatosis. Other diagnostic technologies with higher sensitivity for hepatic steatosis such as magnetic resonance imaging proton density fat fraction and controlled attenuation parameter using transient elastography were not available as baseline health checkup data. Finally, the results need to be validated in other populations with different characteristics such as body habitus or dietary habits. In addition, causative relationship between the distinctive features of microbiota and NAFLD, instead of merely innocent bystander, warrants further investigation.
In conclusion, our study revealed distinctive features of gut and blood microbiota in terms of the presence of lean and obese NAFLD. The predictive role of the microbiota profiles requires further validation in a larger cohort with histological data.
S1 Table. Significant taxa in fecal microbiota related with NAFLD groups. Both unadjusted and adjusted P-values are provided.
We acknowledge the computing resources by Global Science experimental Data hub Center (GSDC) Project and Korea Research Environment Open NETwork (KREONET) in Korea Institute of Science and Technology Information (KISTI). The datasets used and/or analyzed during the current study are available from CODA (Clinical and Omics data archives) in KNIH (Korea National Institute of Health, Korea).
- 1. Vernon G, Baranova A, Younossi ZM. Systematic review: the epidemiology and natural history of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in adults. Aliment Pharmacol Ther. 2011;34(3):274–85. pmid:21623852.
- 2. European Association for the Study of the Liver, European Association for the Study of Diabetes, European Association for the Study of Obesity. EASL-EASD-EASO Clinical Practice Guidelines for the management of non-alcoholic fatty liver disease. J Hepatol. 2016;64(6):1388–402. pmid:27062661.
- 3. Wong VW, Wong GL, Yip GW, Lo AO, Limquiaco J, Chu WC, et al. Coronary artery disease and cardiovascular outcomes in patients with non-alcoholic fatty liver disease. Gut. 2011;60(12):1721–7. pmid:21602530.
- 4. Subichin M, Clanton J, Makuszewski M, Bohon A, Zografakis JG, Dan A. Liver disease in the morbidly obese: a review of 1000 consecutive patients undergoing weight loss surgery. Surg Obes Relat Dis. 2015;11(1):137–41. pmid:25701959.
- 5. Stefan N, Kantartzis K, Machann J, Schick F, Thamer C, Rittig K, et al. Identification and characterization of metabolically benign obesity in humans. Arch Intern Med. 2008;168(15):1609–16. pmid:18695074.
- 6. Younossi ZM, Stepanova M, Negro F, Hallaji S, Younossi Y, Lam B, et al. Nonalcoholic fatty liver disease in lean individuals in the United States. Medicine (Baltimore). 2012;91(6):319–27. pmid:23117851.
- 7. Nishioji K, Sumida Y, Kamaguchi M, Mochizuki N, Kobayashi M, Nishimura T, et al. Prevalence of and risk factors for non-alcoholic fatty liver disease in a non-obese Japanese population, 2011–2012. J Gastroenterol. 2015;50(1):95–108. pmid:24619537.
- 8. Kim LJ, Nalls MA, Eiriksdottir G, Sigurdsson S, Launer LJ, Koster A, et al. Associations of visceral and liver fat with the metabolic syndrome across the spectrum of obesity: the AGES-Reykjavik study. Obesity (Silver Spring). 2011;19(6):1265–71. pmid:21183935; PubMed Central PMCID: PMCPMC3081537.
- 9. Savage DC. Microbial ecology of the gastrointestinal tract. Annu Rev Microbiol. 1977;31:107–33. pmid:334036.
- 10. Turnbaugh PJ, Hamady M, Yatsunenko T, Cantarel BL, Duncan A, Ley RE, et al. A core gut microbiome in obese and lean twins. Nature. 2009;457(7228):480–4. pmid:19043404; PubMed Central PMCID: PMCPMC2677729.
- 11. Vrieze A, Van Nood E, Holleman F, Salojarvi J, Kootte RS, Bartelsman JF, et al. Transfer of intestinal microbiota from lean donors increases insulin sensitivity in individuals with metabolic syndrome. Gastroenterology. 2012;143(4):913–6 e7. pmid:22728514.
- 12. Qin J, Li Y, Cai Z, Li S, Zhu J, Zhang F, et al. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature. 2012;490(7418):55–60. pmid:23023125.
- 13. Schnabl B, Brenner DA. Interactions between the intestinal microbiome and liver diseases. Gastroenterology. 2014;146(6):1513–24. pmid:24440671; PubMed Central PMCID: PMCPMC3996054.
- 14. Zhu L, Baker SS, Gill C, Liu W, Alkhouri R, Baker RD, et al. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: a connection between endogenous alcohol and NASH. Hepatology. 2013;57(2):601–9. pmid:23055155.
- 15. Raman M, Ahmed I, Gillevet PM, Probert CS, Ratcliffe NM, Smith S, et al. Fecal microbiome and volatile organic compound metabolome in obese humans with nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol. 2013;11(7):868–75 e1-3. pmid:23454028.
- 16. Boursier J, Mueller O, Barret M, Machado M, Fizanne L, Araujo-Perez F, et al. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology. 2016;63(3):764–75. pmid:26600078; PubMed Central PMCID: PMCPMC4975935.
- 17. Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Microbial ecology: human gut microbes associated with obesity. Nature. 2006;444(7122):1022–3. pmid:17183309.
- 18. Wang B, Jiang X, Cao M, Ge J, Bao Q, Tang L, et al. Altered Fecal Microbiota Correlates with Liver Biochemistry in Nonobese Patients with Non-alcoholic Fatty Liver Disease. Sci Rep. 2016;6:32002. pmid:27550547; PubMed Central PMCID: PMCPMC4994089.
- 19. Lelouvier B, Servant F, Paisse S, Brunet AC, Benyahya S, Serino M, et al. Changes in blood microbiota profiles associated with liver fibrosis in obese patients: A pilot analysis. Hepatology. 2016;64(6):2015–27. pmid:27639192.
- 20. Serino M, Luche E, Gres S, Baylac A, Berge M, Cenac C, et al. Metabolic adaptation to a high-fat diet is associated with a change in the gut microbiota. Gut. 2012;61(4):543–53. pmid:22110050; PubMed Central PMCID: PMCPMC3292714.
- 21. Amar J, Lange C, Payros G, Garret C, Chabo C, Lantieri O, et al. Blood microbiota dysbiosis is associated with the onset of cardiovascular events in a large general population: the D.E.S.I.R. study. PLoS One. 2013;8(1):e54461. pmid:23372728; PubMed Central PMCID: PMCPMC3555817.
- 22. Amar J, Serino M, Lange C, Chabo C, Iacovoni J, Mondot S, et al. Involvement of tissue bacteria in the onset of diabetes in humans: evidence for a concept. Diabetologia. 2011;54(12):3055–61. pmid:21976140.
- 23. Chang Y, Jung H-S, Cho J, Zhang Y, Yun KE, Lazo M, et al. Metabolically Healthy Obesity and the Development of Nonalcoholic Fatty Liver Disease. Am J Gastroenterol. 2016. pmid:27185080
- 24. Wen CP, David Cheng TY, Tsai SP, Chan HT, Hsu HL, Hsu CC, et al. Are Asians at greater mortality risks for being overweight than Caucasians? Redefining obesity for Asians. Public Health Nutr. 2009;12(4):497–506. pmid:18547457.
- 25. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28(7):412–9. pmid:3899825.
- 26. Saadeh S, Younossi ZM, Remer EM, Gramlich T, Ong JP, Hurley M, et al. The utility of radiological imaging in nonalcoholic fatty liver disease. Gastroenterology. 2002;123(3):745–50. pmid:12198701.
- 27. Lee DH. Imaging evaluation of non-alcoholic fatty liver disease: focused on quantification. Clin Mol Hepatol. 2017;23(4):290–301. pmid:28994271; PubMed Central PMCID: PMCPMC5760010.
- 28. Kim CW, Yun KE, Jung HS, Chang Y, Choi ES, Kwon MJ, et al. Sleep duration and quality in relation to non-alcoholic fatty liver disease in middle-aged workers and their spouses. J Hepatol. 2013;59(2):351–7. pmid:23578884.
- 29. Fadrosh DW, Ma B, Gajer P, Sengamalay N, Ott S, Brotman RM, et al. An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform. Microbiome. 2014;2:6–. PMC3940169. pmid:24558975
- 30. Edgar RC. UPARSE: highly accurate OTU sequences from microbial amplicon reads. Nature methods. 2013;10(10):996–8. http://www.nature.com/nmeth/journal/v10/n10/abs/nmeth.2604.html#supplementary-information. pmid:23955772
- 31. Navas-Molina JA, Peralta-Sánchez JM, González A, McMurdie PJ, Vázquez-Baeza Y, Xu Z, et al. Advancing our understanding of the human microbiome using QIIME. Methods in enzymology. 2013;531:371–444. PMC4517945. pmid:24060131
- 32. Paulson JN, Stine OC, Bravo HC, Pop M. Differential abundance analysis for microbial marker-gene surveys. Nature methods. 2013;10(12):1200–2. http://www.nature.com/nmeth/journal/v10/n12/abs/nmeth.2658.html#supplementary-information. pmid:24076764
- 33. Del Chierico F, Nobili V, Vernocchi P, Russo A, Stefanis C, Gnani D, et al. Gut microbiota profiling of pediatric nonalcoholic fatty liver disease and obese patients unveiled by an integrated meta-omics-based approach. Hepatology. 2017;65(2):451–64. pmid:27028797.
- 34. Bellot P, Garcia-Pagan JC, Frances R, Abraldes JG, Navasa M, Perez-Mateo M, et al. Bacterial DNA translocation is associated with systemic circulatory abnormalities and intrahepatic endothelial dysfunction in patients with cirrhosis. Hepatology. 2010;52(6):2044–52. pmid:20979050.
- 35. Koren O, Spor A, Felin J, Fak F, Stombaugh J, Tremaroli V, et al. Human oral, gut, and plaque microbiota in patients with atherosclerosis. Proc Natl Acad Sci U S A. 2011;108 Suppl 1:4592–8. pmid:20937873; PubMed Central PMCID: PMCPMC3063583.
- 36. He X, Ji G, Jia W, Li H. Gut Microbiota and Nonalcoholic Fatty Liver Disease: Insights on Mechanism and Application of Metabolomics. Int J Mol Sci. 2016;17(3):300. pmid:26999104; PubMed Central PMCID: PMCPMC4813164.
- 37. Machado MV, Cortez-Pinto H. Diet, Microbiota, Obesity, and NAFLD: A Dangerous Quartet. Int J Mol Sci. 2016;17(4):481. pmid:27043550; PubMed Central PMCID: PMCPMC4848937.
- 38. El Kaoutari A, Armougom F, Gordon JI, Raoult D, Henrissat B. The abundance and variety of carbohydrate-active enzymes in the human gut microbiota. Nat Rev Microbiol. 2013;11(7):497–504. pmid:23748339.
- 39. Schwiertz A, Taras D, Schafer K, Beijer S, Bos NA, Donus C, et al. Microbiota and SCFA in lean and overweight healthy subjects. Obesity (Silver Spring). 2010;18(1):190–5. pmid:19498350.
- 40. Saber SM, Othman HB, ElMasry S, Magdy A, Zidan HF. Correlation between Body Mass Index and Gut Microbiota in Adults. Int J Curr Microbiol App Sci. 2017;6(2):778–87.
- 41. Million M, Angelakis E, Maraninchi M, Henry M, Giorgi R, Valero R, et al. Correlation between body mass index and gut concentrations of Lactobacillus reuteri, Bifidobacterium animalis, Methanobrevibacter smithii and Escherichia coli. Int J Obes (Lond). 2013;37(11):1460–6. pmid:23459324; PubMed Central PMCID: PMCPMC3826031.
- 42. Ignacio A, Fernandes MR, Rodrigues VA, Groppo FC, Cardoso AL, Avila-Campos MJ, et al. Correlation between body mass index and faecal microbiota from children. Clin Microbiol Infect. 2016;22(3):258 e1–8. pmid:26551842.
- 43. Gangarapu V, Ince AT, Baysal B, Kayar Y, Kilic U, Gok O, et al. Efficacy of rifaximin on circulating endotoxins and cytokines in patients with nonalcoholic fatty liver disease. Eur J Gastroenterol Hepatol. 2015;27(7):840–5. pmid:26043290.
- 44. Imajo K, Fujita K, Yoneda M, Nozaki Y, Ogawa Y, Shinohara Y, et al. Hyperresponsivity to low-dose endotoxin during progression to nonalcoholic steatohepatitis is regulated by leptin-mediated signaling. Cell Metab. 2012;16(1):44–54. pmid:22768838.
- 45. Leung JC, Loong TC, Wei JL, Wong GL, Chan AW, Choi PC, et al. Histological severity and clinical outcomes of nonalcoholic fatty liver disease in nonobese patients. Hepatology. 2017;65(1):54–64. pmid:27339817.
- 46. Kirpich IA, Petrosino J, Ajami N, Feng W, Wang Y, Liu Y, et al. Saturated and Unsaturated Dietary Fats Differentially Modulate Ethanol-Induced Changes in Gut Microbiome and Metabolome in a Mouse Model of Alcoholic Liver Disease. Am J Pathol. 2016;186(4):765–76. pmid:27012191.
- 47. Chen Y, Yang F, Lu H, Wang B, Chen Y, Lei D, et al. Characterization of fecal microbial communities in patients with liver cirrhosis. Hepatology. 2011;54(2):562–72. pmid:21574172.
- 48. Cani PD, Amar J, Iglesias MA, Poggi M, Knauf C, Bastelica D, et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes. 2007;56(7):1761–72. pmid:17456850.
- 49. Garidou L, Pomie C, Klopp P, Waget A, Charpentier J, Aloulou M, et al. The Gut Microbiota Regulates Intestinal CD4 T Cells Expressing RORgammat and Controls Metabolic Disease. Cell Metab. 2015;22(1):100–12. pmid:26154056.
- 50. Younossi ZM, Blissett D, Blissett R, Henry L, Stepanova M, Younossi Y, et al. The economic and clinical burden of nonalcoholic fatty liver disease in the United States and Europe. Hepatology. 2016;64(5):1577–86. Epub 2016/10/22. pmid:27543837.
- 51. Jeong EH, Jun DW, Cho YK, Choe YG, Ryu S, Lee SM, et al. Regional prevalence of non-alcoholic fatty liver disease in Seoul and Gyeonggi-do, Korea. Clin Mol Hepatol. 2013;19(3):266–72. Epub 2013/10/18. pmid:24133664; PubMed Central PMCID: PMCPMC3796676.
- 52. Xu C, Yu C, Ma H, Xu L, Miao M, Li Y. Prevalence and risk factors for the development of nonalcoholic fatty liver disease in a nonobese Chinese population: the Zhejiang Zhenhai Study. Am J Gastroenterol. 2013;108(8):1299–304. Epub 2013/04/10. pmid:23567356.
- 53. Sinn DH, Gwak GY, Park HN, Kim JE, Min YW, Kim KM, et al. Ultrasonographically detected non-alcoholic fatty liver disease is an independent predictor for identifying patients with insulin resistance in non-obese, non-diabetic middle-aged Asian adults. Am J Gastroenterol. 2012;107(4):561–7. Epub 2011/11/24. pmid:22108448.
- 54. Lee SS, Park SH, Kim HJ, Kim SY, Kim MY, Kim DY, et al. Non-invasive assessment of hepatic steatosis: prospective comparison of the accuracy of imaging examinations. J Hepatol. 2010;52(4):579–85. pmid:20185194.
- 55. Hannah WN Jr., Harrison SA. Noninvasive imaging methods to determine severity of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Hepatology. 2016;64(6):2234–43. Epub 2016/06/25. pmid:27338123.