PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of escheartLink to Publisher's site
 
ESC Heart Fail. 2017 August; 4(3): 282–290.
Published online 2017 April 21. doi:  10.1002/ehf2.12155
PMCID: PMC5542738

Heart failure is associated with depletion of core intestinal microbiota

Abstract

Aims

In spite of current medical treatment approaches, mortality of chronic heart failure (HF) remains high and novel treatment modalities are thus urgently needed. A recent theory proposes a possible impact of the intestinal microbiome on the incidence and clinical course of heart failure. This study sought to systematically investigate, if there are specific changes of the intestinal microbiome in heart failure patients.

Methods and results

The intestinal microbiome of 20 patients with heart failure with reduced ejection fraction due to ischemic or dilated cardiomyopathy was investigated by applying high‐throughput sequencing of the bacterial 16S rRNA gene. Microbial profiles were compared to those of matched controls in which heart failure was ruled out by clinical assessment and NT‐proBNP serum levels (n = 20). According to the Shannon diversity index (which measures the intra‐individual alpha‐diversity) based on the distribution of operational taxonomic units (OTUs), HF cases showed a nominally significantly lower diversity index compared to controls (P nom. = 0.01), and testing for genera abundance showed a tendency towards a decreased alpha diversity of HF patients. Beta‐diversity measures (inter‐individual diversity) revealed a highly significant separation of HF cases and controls, (e.g. P weighted UniFracv = 0.004). Assessing the individual abundance of core measurable microbiota (CMM), a significant decrease of Coriobacteriaceae, Erysipelotrichaceae and Ruminococcaceae was observed on the family level. In line with that, Blautia, Collinsella, uncl. Erysipelotrichaceae and uncl. Ruminococcaceae showed a significant decrease in HF cases compared to controls on the genus level.

Conclusions

Heart failure patients showed a significantly decreased diversity of the intestinal microbiome as well as a downregulation of key intestinal bacterial groups. Our data point to an altered intestinal microbiome as a potential player in the pathogenesis and progression of heart failure.

Keywords: Heart failure, Gut microbiome, Microbiota, 16S, Diversity

Introduction

In spite of modern treatment options, chronic heart failure (HF) remains associated with poor prognosis and high mortality, exceeding 50% in 5 years.1 Moreover, its increasing prevalence leads to huge economic burden, making HF a major challenge of the future.2 Therefore, deeper insights into the pathophysiology of the disease are urgently needed, since these efforts might give rise to new disease concepts and ultimately novel therapeutic prospects.

In this context, it has been proposed that heart failure should not be regarded solely as a cardiac disease but rather a systemic multi‐organ failure.3 This view might even be extended by the concept of the holobiont, defining a host and all of its symbiotic microorganisms as a target of analytic and therapeutic interventions. With regard to heart failure, potential interactions between the human host and gut microbiota have been discussed. Dysbiosis of gut bacteria communities has been proposed to be a pathogenic factor in several diseases, e.g. type 2 diabetes.4 Recent publications suggest that intestinal dysbiosis may also play an important role in the pathogenesis of heart failure, putting forward a “gut hypothesis” of heart failure.5

Recently, it has been reported that HF is associated with disrupted intestinal epithelial function, likely as a consequence of reduced intestinal perfusion and ischemia.6, 7 Bowel wall thickness and epithelial permeability increase, whereas absorptive function decreases.8 It has been proposed that intestinal bacteria and/or endotoxins such as lipopolysaccharides (LPS) translocate to the systemic circulation.9 High LPS concentrations in hepatic veins of heart failure patients are consistent with intestinal translocation processes of gut microbes.10 LPS levels in the blood directly correlate with systemic inflammation in decompensated HF patients and decrease after recompensation.6

It is well known that HF is associated with a chronic state of inflammation,11 which might be induced or aggravated by this pathomechanism and thereby indirectly affect cardiomyocyte function.

Of note, an augmented intestinal juxtamucosal bacterial biofilm has been reported in patients with HF, correlating with an enhanced immunoglobulin A‐antilipopolysaccharide response.7, 8 In patients with stable HF, intestinal overgrowth of pathogenic bacteria like Campylobacter, Shigella, Salmonella, and Yersinia, as well as Candida species has been observed.12

The present study aims at a first comprehensive description of the intestinal bacterial profile in patients with acute decompensated or stable HF. Gut microbiome data from a community‐based sample served as comparison group. Intra‐ and inter‐individual analysis of bacterial diversity was performed based on high‐resolution 16S rDNA sequencing.

Materials and methods

Study population

Twenty patients with HF due to frequent etiologies like ischemic cardiomyopathy (ICMP) and dilated cardiomyopathy (DCM) were studied. All participants had a highly reduced left ventricular ejection fraction (LVEF ≤ 35%). Seventy percent were in an acute state of cardiac decompensation and 30% in a stable state of HF. Demographic and clinical patients’ characteristics are shown in Table 1. Patients received drug treatment according to current HF treatment guidelines, including usage of angiotensin converting enzyme (ACE) inhibitors, beta‐blockers, diuretic agents, aldosterone antagonists and antiarrhythmic/heart rate (HR) modulating agents as appropriate. These agents were considered in statistical analysis as they were sorted and examined in groups defined by their mechanism of action. Further medication was classified into groups defined by their indication. Three participants did not receive any drugs at the time of inclusion.

Table 1
Characteristics of HF patients and controls

Exclusion criteria included acute infection, gastrointestinal diseases or malabsorptive disorders, antibiotic or probiotic treatments within the previous three months and cancer. Any other diseases like respiratory disease, apoplexia cerebri and migraine that could possibly influence the intestinal microbiome, were not significantly prevalent in both groups. All patients consumed a mixed European diet. To minimize confounding effects of hospital surrounding, diet and contact to other patients, we collected faecal samples within the first 24 hours after admission to hospital.

The control group consisted of twenty case‐matched individuals (matched in terms of age, gender, body mass index (BMI) and smoking status) from a community‐based sample, free of any heart and/or gastrointestinal disease as well as of cancer. According to the recent ESC guidelines on the diagnosis of heart failure,13 we defined the control group on the basis of prior diagnoses, the absence of HF related clinical signs and symptoms as well as NT‐proBNP measurements. Any medication of subjects from the control group has been considered in statistical analysis. Individuals were obtained from the PopGen biobank.14, 15

The study was performed at the University Medical Centre Schleswig‐Holstein, Campus Kiel, Germany after approval by the local ethics committee. All study participants gave their written, informed consent.

Study protocol and clinical assessment

In HF patients, body height and weight, systolic and diastolic blood pressure and body temperature were measured by clinical staff and obtained from medical records. Blood samples were obtained by nurses or physicians. In the control sample, blood pressure, height and weight were determined by trained study nurses following a standardized protocol.

Body mass index (BMI) was calculated as weight/height.2 A standardised survey on pre‐existing illnesses, dietary habits and several lifestyle factors was completed by all patients and controls and a standardised interview was performed. In HF patients, cardiac function was evaluated by transthoracic Doppler echocardiography according to current guidelines. All imaging studies were judged by an experienced cardiologist unaware of the study protocol and archived digitally.

In HF patients, faecal samples were collected in standard stool collection tubes within the first 24 hours after admission to hospital and stored at −80°C until further processing. Control participants collected faecal samples at home in standard stool collection tubes. The samples were shipped immediately (within 24 hours) at RT and were also stored at −80°C until processing.

DNA extraction, 16S rDNA sequencing and quality control

DNA was extracted using the QIAcube and the QIAamp DNA stool kit (Qiagen) and a prior beat‐beating step. Variable regions v1‐v2 of the 16S rRNA gene were amplified using the primers described in Caporaso et al.16 PCR products were normalized using the SequalPrep Normalization Plate Kit (Life Technologies), pooled based on Qubit dsDNA BR Assay Kit measurements (Thermo Fisher) and sequenced on an Illumina MiSeq (2 × 300 bp). Demultiplexing was based on zero mismatches in the barcode sequences. Forward and reverse reads were merged using FLASh software allowing an overlap of the reads between 250 and 300 bp.17 Sequences with a sequences quality below 30 in less than 95% of the nucleotides as well as chimeras were removed using UCHIME.18

Dataset generation

After quality control unique sequences from all samples were combined and de novo OTU picking was performed with Usearch19 (v7, Edgar). For each sample, 10 000 random sequences were picked to construct the OTU abundance table. The OTU sequences were aligned using Muscle20, 21 and from the alignment a Maximum‐Likelihood Phylogenetic Tree was constructed using a generally time‐reversible model in FastTree.22, 23 Using this tree and the OTU abundance table unweighted and weighted UniFrac24 and phylogenetic diversity25 were calculated using the unifrac.unweighted, unifrac.weighted and phylo.diversity function, respectively, in Mothur.26 Further, these sequences were taxonomically annotated using the RDP classifier27 and most recent Training Set provided on the RDP website (v14; https://rdp.cme.msu.edu/). The taxonomic information was used to construct abundance tables on different taxonomic levels from phylum to genus. Genera with a classification score lower than 0.8 were assigned to the corresponding group named ‘unclassified [family]’.

Statistical analysis

Statistical analysis was carried out in r.28 Alpha‐diversity measures and Bray‐Curtis dissimilarities were calculated using the respective functions of the vegan package29 for r. When testing for differences in alpha‐diversity, Wilcoxon rank sum test was used when value distribution deviated from normality, two samples T‐test was used when not. Unconstrained MDS plots of beta diversity measures were generated using the cmdscale function in r. To test for differences in beta diversity, permutational MANOVA was performed using the adonis function of the vegan package with the option sqrt.dist=T when using abundance tables, but not when using UniFrac distances, and 10 000 permutations. The best fitting ordination model was calculated using db‐RDA (capscale) and the respective distance matrices. AIC was used to select the best fitting model adding single a single explanatory variable to a model correcting for age, gender, BMI and smoking habits. F‐statistics and P‐values were calculated using anova.cca to compare the model with and without the added variable. Enrichments/depletions of taxonomic groups were calculated on a core‐measurable microbiota (CMM). In the CMM we included all taxonomic groups having a mean abundance of at least 1% (0.5% for OTUs) in one of the groups. Additionally for OTUs, the OTU had to be present in at least 40% of the samples. Model fitting and calculations were performed using the manyglm and anova.manyglm functions from the mvabund package,30 using a negative binomial distribution. For the ANOVA, the number of permutations was set to 10 000 and permutation of residuals was used as resampling method, age, gender, BMI and smoking habits were used as covariates. Correction for multiple testing was done by applying Benjamini–Hochberg correction.31

Results

Differences between HF cases and controls with regard to alpha and beta diversity

With regard to alpha diversity, reflecting intra‐individual bacterial variance, the Shannon diversity index based on OTU distribution showed a nominally significantly lower diversity index in HF cases compared to controls (P nom. = 0.01192; Figure 1 A). Indices based on genera abundance showed a tendency of decreased diversity as well, but these differences were not statistically significant upon correction for multiple testing (data not shown).

Figure 1
(A) Alpha diversity: Shannon Index based on OTU abundance for controls and HF patients. (B) Beta diversity: PCoA plot of weighted UniFrac distances.

Assessment of beta diversity (PerMANOVA), a parameter which represents inter‐individual variances, showed a significant separation of HF cases and controls after adjustment for gender, age, BMI and smoking habits on Bray‐Curtis dissimilarity based on genera abundance (explained variance R 2 = 5.5%, P = 0.0124,) as well as OTU abundance (R 2 = 3.9%, P = 0.0099) and in the weighted UniFrac analysis (R 2 = 8.3%, P = 0.0043; Figure 1 B). These results provide evidence for a shift in the community composition of the gut microbiota induced by heart failure. No significant differences were found using the unweighted UniFrac distance metric in this analysis. Of note, none of the additional explanatory variables included in the distance‐based RDA yielded better results than the discrimination between HF cases and controls.

Figure 2 gives an overview of the abundances of the core‐measurable microbiota (CMM) for the control group and the group of HF patients (Fig. 2 A), as well as for each individual in each of the groups (Fig. 2 B).

Figure 2
Genus level abundances of CMM for controls and HF cases. (A) Mean relative abundances of the two groups. (B) Relative abundances for the individual samples.

When looking at families, genera and OTUs contributing to the differences between HF cases and controls in a GLM‐based model, Coriobacteriaceae, Erysipelotrichaceae and Ruminococcaceae showed a significant decrease in HF cases compared to controls (Table 2). Furthermore, Blautia, Collinsella, uncl. Erysipelotrichaceae and uncl. Ruminococcaceae showed a significant decrease in HF cases compared to controls on genus level. Escherichia/Shigella were enriched in HF cases, but this signal did not pass the correction for multiple testing (Table 2, Figure 3). The analysis on OTU basis revealed only nominally significant values in bacterial abundance, however reflecting the findings on genus and family level (Table 2, Figure 3).

Figure 3
Taxonomic groups of CMM (family to OTU level) found with different abundances between HF cases and controls. ns: not significant (P > 0.05), *: P < 0.05, **: P < 0.01, ***: P < 0.001. ...
Table 2
Significant bacteria on family, genus and OTU level based on a GLM model

Differences in the stool microbiome within HF cases

To investigate whether certain variables are associated with inter‐individual variation of the gut microbial community in HF, the PerMANOVA (adonis) approach was applied to the HF cases, testing all available clinical factors (gender, age, BMI, systolic and diastolic blood pressure, aetiology of HF, LVEF ≤ or > 20%, NYHA class, serum levels of NT‐proBNP and CRP, medication and smoking habits) for significant association with genus and OTU composition. None of the variables showed a significant influence on the overall composition.

Discussion

In the present study, we sought to assess the composition and structure of the intestinal luminal microbiota in patients with heart failure due to typical aetiologies like ICMP and DCM, using non‐invasively obtainable faecal samples. Furthermore, we compared the stool microbiome of HF patients to a community‐based control sample from the same geographical area, with each control being matched to a case, based on age, gender, body mass index, and smoking behaviour. The microbiome data of our control group were consistent with available previous research on “normal” gut microbiome constellation.32, 33

To our knowledge, this is the first systematic analysis of the intestinal bacterial microbiota of HF patients using high‐throughput sequencing of bacterial 16S rRNA gene sequences. Our analysis revealed distinct differences in HF patients as compared to controls with respect to the abundance of taxonomic groups on the family to OTU level. These changes were also reflected in differences in beta diversity measures. In addition, a trend of reduced bacterial alpha diversity was observed in HF patients compared to controls.

Analysing intestinal bacterial profile, we could not detect a significantly enhanced abundance of particular (potentially pathogenic) bacteria on OTU level, questioning an infectious disease theory. Instead, observed shifts on family and genus level suggest functional adaptation to altered environmental conditions.

A recent study based on culture dependent methods demonstrated an intestinal enrichment of potential pathogenic bacteria, such as Campylobacter, Shigella, Salmonella, and Yersinia enterocolitica, and Candida species in HF patients.12 In line with these results, we could demonstrate an increase of Enterobacteriaceae in HF patients, especially belonging to the Escherichia/Shigella cluster, using culture‐independent high‐throughput amplicon sequencing data. However, these results did either not meet the significance threshold (Enterobacteriacea) or did not pass the correction for multiple testing (Escherichia/Shigella).

Rather than enrichment, we could show a significant decrease of other families and genera in HF patients. Our study illustrates changes in bacterial diversity mainly driven by significant depletion of the bacterial genera Blautia and Collinsella, as well as two unknown genera belonging to the families Erysipelotrichaceae and Ruminococcaceae. This constellation seems to be a specific attribute of heart failure, as there is no other disease entity reported to be accompanied by this alteration. It is conceivable that depletion of these genera contributes to HF pathogenesis, as recent findings from other inflammatory diseases suggest: For example, Collinsella bacteria have been reported to be associated with systemic atherosclerosis and type 2 diabetes mellitus (T2DM).34, 35 Interestingly, this genus seems to be enriched in patients suffering from atherosclerosis or T2DM, whereas we could demonstrate its depletion in HF patients. Remarkably, Collinsella was also downregulated in HF patients suffering from DM or ischemic heart disease. Thus, the downregulating effects of HF seem to overweigh opposing effects of these comorbidities in our patients. Therefore, we conclude that the depletion of Collinsella may be highly specific to HF. Moreover, recent research demonstrated that Blautia might be associated with anti‐inflammatory mechanisms, as its intestinal abundance is associated with reduced death and improved overall survival in Graft‐versus‐Host‐Disease.36 Furthermore, a reduction in the butyrate‐producing genus Faecalibacterium is observed in HF patients. Faecalibacterium prausnitzii was identified as an anti‐inflammatory commensal and reduced abundance in species belonging to this genus were shown to have an adverse effect on intestinal permeability.37, 38 These interesting findings outline that further in vitro studies need to be performed to further assess the functional role of these genera in heart failure.

Discussing possible confounders, multiple external factors (e.g. food intake, medical drug usage, environmental surrounding) and internal factors yield influence on the gut microbiome balance, possibly contributing to the observed effects. We intended to minimize the impact of dietary habits (e.g. high‐fat diets) by excluding patients consuming unbalanced nutrition, although individual effects of nutrition cannot be excluded, as acute decompensated patients followed no standardized diet. Patients’ medication has been considered in the statistical analyses.

Equally probable, internal changes due to HF may affect intestinal bacterial profile. For example, it is well known that HF is associated with a chronic state of inflammation11, 39 and the intestinal microbiome might not only be addressed as a target of systemic inflammation, but also as a trigger for this pathomechanism. Of note, this linkage has been proposed in several other inflammatory diseases such as rheumatoid arthritis.40 Due to systemic inflammation, intestinal epithelial dysfunction and ultimately increased permeability possibly give rise to new immunogenic epitopes that induce increased autoantibody production and further activate inflammatory pathways, aggravating the primary inflammatory disease.41 It appears possible, that this concept of the intestine acting as a “percolator” of systemic inflammation, might also be functionally relevant in heart failure.

In addition to systemic inflammation, impaired fluid balance in HF patients might be important, worsening bowel perfusion, and causing hypoxemia and epithelial dysfunction. Effectively reduced bowel motility entails the intestinal content (bacteria and food components) to stay longer in the gut and thereby modifies bacterial supply of energy substrates possibly inducing a bacterial shift.42 To a certain degree, diuretic agents might modulate this effect. Since we could not exclude these agents in our study, as they are essential part of current treatment guidelines, we examined their effects on gut bacterial diversity, which did not yield a significant association between use of diuretics and composition of the gut microbiome.

All of these structural and functional changes may jointly affect the bacterial habitat (e.g. by oxygen availability, pH value, immunological competence), constraining dynamic adjustments of bacterial colonisation. Potential consequences might either be induced by the enrichment of pathogen effectors (e.g. bacteria, bacterial toxins, metabolic products, immune modulation) or the relative repression of beneficial bacteria in the compounded balance.

The current general opinion favours the concept that intestinal imbalance arises as a consequence of cardiac dysfunction. However, a functional relevance of an impaired and/or altered bacterial profile as a primary risk factor or early disease marker for the initial onset of heart failure seems to be conceivable as well. Of note, recent studies have shown that intestinal bacterial‐dependent generated trimethylamine‐N‐oxide (TMAO) levels in blood are a prognostic factor for long‐term mortality risk in HF patients independent of traditional risk factors and indices.43, 44 In our study we focused on HF patients mostly in an acute state of decompensation. Future studies may assess if alterations of disease status during the progression of heart failure are mirrored by alterations of intestinal gut microbial composition, similar to e.g. Crohn's disease.45

Overall, significant decreases of bacterial families and genera indicate a complex multifactorially induced remodelling of the intestinal bacterial structure rather than an overgrowth of certain genera. Of note, this mechanism may not be a unique feature of heart failure but has been demonstrated in other widespread diseases as well, like diabetes and chronic kidney disease. However, the pattern of depleted genera Blautia and Collinsella, as well as two unknown genera belonging to the families Erysipelotrichaceae and Ruminococcaceae seems to be HF specific and may even offer the basis for novel specific therapies in the future.

Conclusions

In this study, we could show that significant structural alterations of the intestinal bacterial microbiome can be found in HF patients. It seems possible that altered bacterial gut colonisation, most likely the depletion of distinct core intestinal microbiota, acts as a risk factor and disease marker for HF, enhancing disease progression in a vicious cycle. Future studies should focus on the pathomechanisms involved, e.g. altered inflammatory pathways.

Limitations

Our results are based on relatively small group sizes. Further largescale studies are necessary to prove our findings.

Furthermore, since the recent concept of advanced heart failure proposes a transition to multi‐organ failure when reaching critical disease status,13 we cannot exclude that multiple factors occurring at this stage might superimpose the specific alterations we observed in heart failure patients, e.g. accompanying kidney failure, prolonged treatment on intensive care units, hospital acquired infections and repetitively required antibiotic therapy. Further longitudinal studies, that evaluate alterations of the intestinal microbiome during the course of disease, may help to better separate primary heart failure‐specific alterations from these possible biases.

Conflict of interest

None declared.

Funding

This work was supported by the Deutsche Forschungsgemeinschaft (DFG) Cluster of Excellence “Inflammation at Interfaces”; the German Federal Ministry of Education and Research (BMBF) within the framework of the e:Med research and funding program sysINFLAME [01ZX1306A]; the biobank PopGen (popgen 2.0 network is supported by a grant from the German Ministry for Education and Research [01EY1103]); the Medical faculty of the Christian‐Albrechts‐University of Kiel, Kiel, Germany [F355913] and the “Deutsche Herzstiftung e.V.” [K/11/15 to T.W.].

Acknowledgements

The authors would like to express their gratitude to Vanessa Mangels for her technical support.

Notes

Luedde M., Winkler T., Heinsen F.‐A., Rühlemann M. C., Spehlmann M. E., Bajrovic A., Lieb W., Franke A., Ott S. J., and Frey N. (2017) Heart failure is associated with depletion of core intestinal microbiota. ESC Heart Failure, 4: 282–290. doi: 10.1002/ehf2.12155.

Contributor Information

Mark Luedde, ed.hsku@eddeul.kram.

Femke‐Anouska Heinsen, ed.leik-inu.bmki@nesnieh.f.

Norbert Frey, ed.hsku@yerf.trebron.

References

1. Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE Jr, Drazner MH, Fonarow GC, Geraci SA, Horwich T, Januzzi JL, Johnson MR, Kasper EK, Levy WC, Masoudi FA, McBride PE, McMurray JJ, Mitchell JE, Peterson PN, Riegel B, Sam F, Stevenson LW, Tang WH, Tsai EJ, Wilkoff BL. 2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. Circulation 2013; 128: e240–e327. [PubMed]
2. Go AS, Mozaffarian D, Roger VL, Benjamin EJ, Berry JD, Blaha MJ, Dai S, Ford ES, Fox CS, Franco S, Fullerton HJ, Gillespie C, Hailpern SM, Heit JA, Howard VJ, Huffman MD, Judd SE, Kissela BM, Kittner SJ, Lackland DT, Lichtman JH, Lisabeth LD, Mackey RH, Magid DJ, Marcus GM, Marelli A, Matchar DB, McGuire DK, Mohler ER 3rd, Moy CS, Mussolino ME, Neumar RW, Nichol G, Pandey DK, Paynter NP, Reeves MJ, Sorlie PD, Stein J, Towfighi A, Turan TN, Virani SS, Wong ND, Woo D, Turner MB. Heart disease and stroke statistics‐‐2014 update: a report from the American Heart Association. Circulation 2014; 129: e28–e292. [PubMed]
3. Warriner D, Sheridan P, Lawford P. Heart failure: not a single organ disease but a multisystem syndrome. Br J Hosp Med (London, England : 2005) 2015; 76: 330–336. [PubMed]
4. Zhang YJ, Li S, Gan RY, Zhou T, Xu DP, Li HB. Impacts of Gut Bacteria on Human Health and Diseases. Int J Mol Sci 2015; 16: 7493–7519. [PubMed]
5. Nagatomo Y, Tang WH. Intersections Between Microbiome and Heart Failure: Revisiting the Gut Hypothesis. J Card Fail 2015; 21: 973–980. [PubMed]
6. Sandek A, Bjarnason I, Volk HD, Crane R, Meddings JB, Niebauer J, Kalra PR, Buhner S, Herrmann R, Springer J, Doehner W, von Haehling S, Anker SD, Rauchhaus M. Studies on bacterial endotoxin and intestinal absorption function in patients with chronic heart failure. Int J Cardiol 2012; 157: 80–85. [PubMed]
7. Sandek A, Swidsinski A, Schroedl W, Watson A, Valentova M, Herrmann R, Scherbakov N, Cramer L, Rauchhaus M, Grosse‐Herrenthey A, Krueger M, von Haehling S, Doehner W, Anker SD, Bauditz J. Intestinal blood flow in patients with chronic heart failure: a link with bacterial growth, gastrointestinal symptoms, and cachexia. J Am Coll Cardiol 2014; 64: 1092–1102. [PubMed]
8. Sandek A, Bauditz J, Swidsinski A, Buhner S, Weber‐Eibel J, von Haehling S, Schroedl W, Karhausen T, Doehner W, Rauchhaus M, Poole‐Wilson P, Volk HD, Lochs H, Anker SD. Altered intestinal function in patients with chronic heart failure. J Am Coll Cardiol 2007; 50: 1561–1569. [PubMed]
9. Anker SD, Egerer KR, Volk HD, Kox WJ, Poole‐Wilson PA, Coats AJ. Elevated soluble CD14 receptors and altered cytokines in chronic heart failure. Am J Cardiol 1997; 79: 1426–1430. [PubMed]
10. Peschel T, Schonauer M, Thiele H, Anker SD, Schuler G, Niebauer J. Invasive assessment of bacterial endotoxin and inflammatory cytokines in patients with acute heart failure. Eur J Heart Fail 2003; 5: 609–614. [PubMed]
11. Thierer J, Acosta A, Vainstein N, Sultan M, Francesia A, Marino J, Prado AH, Guglielmone R, Trivi M, Boero L, Brites F, Anker S. Relation of left ventricular ejection fraction and functional capacity with metabolism and inflammation in chronic heart failure with reduced ejection fraction (from the MIMICA Study). Am J Cardiol 2010; 105: 977–983. [PubMed]
12. Pasini E, Aquilani R, Testa C, Baiardi P, Angioletti S, Boschi F, Verri M, Dioguardi F. Pathogenic Gut Flora in Patients With Chronic Heart Failure. JACC Heart Fail 2016; 4: 220–227. [PubMed]
13. Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JG, Coats AJ, Falk V, Gonzalez‐Juanatey JR, Harjola VP, Jankowska EA, Jessup M, Linde C, Nihoyannopoulos P, Parissis JT, Pieske B, Riley JP, Rosano GM, Ruilope LM, Ruschitzka F, Rutten FH, van der Meer P, Authors/Task Force M , Document R . 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail 2016; 18: 891–975. [PubMed]
14. Krawczak M, Nikolaus S, von Eberstein H, Croucher PJ, El Mokhtari NE, Schreiber S. PopGen: population‐based recruitment of patients and controls for the analysis of complex genotype‐phenotype relationships. Community Genet 2006; 9: 55–61. [PubMed]
15. Nothlings U, Krawczak M. PopGen. A population‐based biobank with prospective follow‐up of a control group. Bundesgesundheitsbl 2012; 55: 831–835. [PubMed]
16. Caporaso JG, Lauber CL, Walters WA, Berg‐Lyons D, Lozupone CA, Turnbaugh PJ, Fierer N, Knight R. Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. Proc Natl Acad Sci U S A 2011; 108: 4516–4522. [PubMed]
17. Magoc T, Salzberg SL. FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics (Oxford, England) 2011; 27: 2957–2963. [PMC free article] [PubMed]
18. Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R. UCHIME improves sensitivity and speed of chimera detection. Bioinformatics (Oxford, England) 2011; 27: 2194–2200. [PMC free article] [PubMed]
19. Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics (Oxford, England) 2010; 26: 2460–2461. [PubMed]
20. Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 2004; 32: 1792–1797. [PubMed]
21. Edgar RC. MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics 2004; 5: 113. [PubMed]
22. Price MN, Dehal PS, Arkin AP. FastTree: computing large minimum evolution trees with profiles instead of a distance matrix. Mol Biol Evol 2009; 26: 1641–1650. [PubMed]
23. Price MN, Dehal PS, Arkin AP. FastTree 2‐‐approximately maximum‐likelihood trees for large alignments. PLoS One 2010; 5: e9490. [PMC free article] [PubMed]
24. Lozupone C, Knight R. UniFrac: a new phylogenetic method for comparing microbial communities. Appl Environ Microbiol 2005; 71: 8228–8235. [PubMed]
25. Faith DP. Conservation evaluation and phylogenetic diversity. Biol Conserv 1992. ; 61: 1–10.1992/01/01
26. Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF. Introducing mothur: open‐source, platform‐independent, community‐supported software for describing and comparing microbial communities. Appl Environ Microbiol 2009; 75: 7537–7541. [PubMed]
27. 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]
28. Team RDC . R: A language and environment for statistical computing. Vienna, Austria: Foundation for Statistical Computing; 2008.
29. Oksanen J, Blanchet F, Kindt R, Legendre P, Minchin P, O’Hara R, Simpson G, Solymos P, Stevens H, Wagner H. Vegan: Community Ecology Package. R package version 2.3‐0. 2015.
30. Wang Y, Naumann U, Wright ST, Warton DI. mvabund– an R package for model‐based analysis of multivariate abundance data. Methods Ecol Evol 2012; 3: 471–474.
31. Benjamini Y, Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc B Methodol 1995; 57: 289–300.
32. Human Microbiome Project C . Structure, function and diversity of the healthy human microbiome. Nature 2012; 486: 207–214. [PubMed]
33. Falony G, Joossens M, Vieira‐Silva S, Wang J, Darzi Y, Faust K, Kurilshikov A, Bonder MJ, Valles‐Colomer M, Vandeputte D, Tito RY, Chaffron S, Rymenans L, Verspecht C, De Sutter L, Lima‐Mendez G, D'Hoe K, Jonckheere K, Homola D, Garcia R, Tigchelaar EF, Eeckhaudt L, Fu J, Henckaerts L, Zhernakova A, Wijmenga C, Raes J. Population‐level analysis of gut microbiome variation. Science (New York, NY) 2016; 352: 560–564. [PubMed]
34. Karlsson FH, Fak F, Nookaew I, Tremaroli V, Fagerberg B, Petranovic D, Backhed F, Nielsen J. Symptomatic atherosclerosis is associated with an altered gut metagenome. Nat Commun 2012; 3: 1245. [PubMed]
35. Lambeth SM, Carson T, Lowe J, Ramaraj T, Leff JW, Luo L, Bell CJ, Shah VO. Composition, Diversity and Abundance of Gut Microbiome in Prediabetes and Type 2 Diabetes. J Diabetes Obes 2015; 2: 1–7. [PMC free article] [PubMed]
36. Jenq RR, Taur Y, Devlin SM, Ponce DM, Goldberg JD, Ahr KF, Littmann ER, Ling L, Gobourne AC, Miller LC, Docampo MD, Peled JU, Arpaia N, Cross JR, Peets TK, Lumish MA, Shono Y, Dudakov JA, Poeck H, Hanash AM, Barker JN, Perales M‐A, Giralt SA, Pamer EG, van den Brink MRM. Intestinal Blautia Is Associated with Reduced Death from Graft‐versus‐Host Disease. Biol Blood Marrow Transplant 2015; 21: 1373–1383. [PubMed]
37. Sokol H, Pigneur B, Watterlot L, Lakhdari O, Bermudez‐Humaran LG, Gratadoux JJ, Blugeon S, Bridonneau C, Furet JP, Corthier G, Grangette C, Vasquez N, Pochart P, Trugnan G, Thomas G, Blottiere HM, Dore J, Marteau P, Seksik P, Langella P. Faecalibacterium prausnitzii is an anti‐inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients. Proc Natl Acad Sci U S A 2008; 105: 16731–16736. [PubMed]
38. Martin R, Miquel S, Chain F, Natividad JM, Jury J, Lu J, Sokol H, Theodorou V, Bercik P, Verdu EF, Langella P, Bermudez‐Humaran LG. Faecalibacterium prausnitzii prevents physiological damages in a chronic low‐grade inflammation murine model. BMC Microbiol 2015; 15: 67. [PubMed]
39. Dick SA, Epelman S. Chronic Heart Failure and Inflammation: What Do We Really Know? Circ Res 2016; 119: 159–176. [PubMed]
40. Scher JU, Littman DR, Abramson SB. Microbiome in Inflammatory Arthritis and Human Rheumatic Diseases. Arthritis Rheumatol (Hoboken, NJ) 2016; 68: 35–45. [PMC free article] [PubMed]
41. Lerner A, Matthias T. Rheumatoid arthritis‐celiac disease relationship: joints get that gut feeling. Autoimmun Rev 2015; 14: 1038–1047. [PubMed]
42. Btaiche IF, Chan LN, Pleva M, Kraft MD. Critical illness, gastrointestinal complications, and medication therapy during enteral feeding in critically ill adult patients. Nutr Clin Pract: official publication of the American Society for Parenteral and Enteral Nutrition 2010; 25: 32–49. [PubMed]
43. Tang WH, Wang Z, Fan Y, Levison B, Hazen JE, Donahue LM, Wu Y, Hazen SL. Prognostic value of elevated levels of intestinal microbe‐generated metabolite trimethylamine‐N‐oxide in patients with heart failure: refining the gut hypothesis. J Am Coll Cardiol 2014; 64: 1908–1914. [PubMed]
44. Suzuki T, Heaney LM, Bhandari SS, Jones DJ, Ng LL. Trimethylamine N‐oxide and prognosis in acute heart failure. Heart (British Cardiac Society) 2016; 102: 841–848. [PubMed]
45. Wills ES, Jonkers D, Savelkoul PH, Masclee AA, Pierik MJ, Penders J. Fecal Microbial Composition of Ulcerative Colitis and Crohn's Disease Patients in Remission and Subsequent Exacerbation. PLoS One 2014; 9: e90981. [PMC free article] [PubMed]

Articles from ESC Heart Failure are provided here courtesy of Wiley-Blackwell