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Review article

Association of Gut Microbial Dysbiosis and Hypertension: A Systematic Review


Hypertension (HTN) is one of the most prevalent and dangerous cardiovascular diseases worldwide. Recently, its direct or indirect association with gut dysbiosis has been an interest of study for many. It also includes the metabolomic and functional gene changes in hypertensives compared with healthy individuals. This systematic review aims to study quantitative and qualitative interactions between the two and re-defining the heart-gut axis. We have strictly followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), 2020, guidelines. We conducted an in-depth search of databases such as PubMed, PubMed Central (PMC), Medline, and ScienceDirect to find relevant studies for our topic of interest. After the final quality check, we included eight articles in the systematic review. A significant difference in richness and diversity in gut microbiota was observed in hypertensive patients compared with healthy controls. There was an increased abundance of many bacteria such as Catabacter, Robinsoleilla, Serratia, Enterobacteriaceae, Ruminococcus torques, Parasutterella, Escherichia, Shigella, and Klebsiella, while a decreased abundance of Sporobacter, Roseburia hominis, Romboutsia spp., and Roseburia. Alteration of the composition also varied based on diet, age, ethnicity, and severity of HTN. Short-chain fatty acids (SCFAs)-producing bacteria are found to be on the lower side in hypertensives owing to the protective property of SCFAs against inflammation, especially butyric acid. From the perspective of metabolomic changes, harmful metabolites for cardiovascular health such as intestinal fatty acid binding protein (I-FABP), lipopolysaccharides (LPSs), zonulin, sphingomyelins, acylcarnitines, and trimethylamine N-oxide (TMAO) were found to be increased in hypertensives. Changes in these biomarkers further establish the relation between gut epithelial health and high blood pressure (BP). Participants affected by diseases have an overall lower rate of acquiring new genes, which results in a low richness of genes in them compared with healthy individuals. There is increased expression of the choline utilization (cutC) gene and reduced expression of genes associated with biosynthesis and transport of amino acids in high-BP participants. The unique changes in the composition of the microbiota, functional changes in genes, and metabolome collectively help for a better understanding of the pathogenesis of HTN and also suggest the gut as a promising new therapeutic target for HTN. To establish a further causal relationship between the two, more research is required.

Introduction & Background

Hypertension (HTN), a major health concern worldwide, is one of the major risk factors for cardiovascular diseases. The American Heart Association statistics for 2009-2012 show approximately 80 million adults aged over 20 years have HTN. In 10 years (2003 and 2013), high blood pressure (BP) accounts for 34% of deaths [1]. Even with aggressive management by antihypertensive drugs and lifestyle modifications, only one out of five hypertensive patients manage to control BP adequately. For many researchers, it has become a center of attention mainly because its prevention can aid in reducing the number of kidney diseases and stroke in addition to cardiovascular complications [2]. As we know, lifestyle and environmental factors also contribute to the pathogenesis of HTN, such as daily salt consumption in the diet, alcohol intake, and exercise routine [3]. Recently, the gut microbiome has been newly identified as a risk factor for HTN [4,5].

Gut microbiome and gut dysbiosis are two important concepts. The human body is a host to a variety of microbial species, known as the gut microbiome, which outnumbers the cells of our body [6-8]. They are present in the oral, vaginal, gastrointestinal, and skin communities [6,7,9-11]. Their contribution ranges from playing a major role in nutrition to susceptibility to disease [11]. The imbalance in bacterial composition, alterations in their metabolic activities, or changes in bacterial diversity within the gut is called gut dysbiosis. Dysbiosis has a huge influence on the cause of many diseases such as inflammatory bowel disease, type 1 diabetes, type 2 diabetes, allergies, cancer, obesity, dyslipidemia, and metabolic syndrome [12-18].

Many animal and human studies are showing interest in evaluating a relationship between gut microbial dysbiosis and the development of cardiovascular diseases, mainly atherosclerosis and HTN. Furthermore, the gut microbiome has been recognized as having a key role in obstructive sleep apnea-induced HTN [19]. Proposed mechanisms include the effects of gut microbiota on systemic inflammation, production of pro-atherosclerotic metabolite (trimethylamine N-oxide, or TMAO), and short-chain fatty acids (SCFAs) [20,21]. Decreased microbial diversity has been observed in both animal models and human samples of HTN. Population-based human studies have revealed significant associations between microbial metabolites and BP [22].

The exact association between the gut microbiome and HTN is not well studied even if there is a growing interest in the topic. There has been a lack of adequate evidence on the unique alterations in the composition of gut microbiota and metabolic profiles in hypertensives, and whether these changes are a causative factor or a consequence of high BP is still unknown. If the relationship will become more established, the outcome will be greater in the terms of newer therapeutic targets for the prevention of HTN.

This systematic literature review highlights the influence of gut dysbiosis on the pathogenesis of HTN. Further research is required to demonstrate the temporal relationship between dysbiosis and HTN if any.



We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), 2020, guidelines while conducting the systematic review [23]. Our main aim is to identify an association between hypertension (HTN) and gut dysbiosis if any.

Literature Search Strategy

For articles that studied an association between intestinal microbial dysbiosis and HTN between 2012 and 2022, we searched the following four databases in detail: PubMed, PubMed Central (PMC), Medline, and ScienceDirect. A systematic search strategy using Medical Subject Headings (MeSH) terms and keywords were developed and used to find the relevant articles for this study. We included the following keywords: “hypertension,” “gut microbiome,” “dysbiosis,” “intestinal dysbiosis,” and “intestinal microbiome.” We also combined the aforementioned keywords and MeSH strategy using the Boolean method to extract all the relevant articles from the databases. The summary of the search strategy for the different databases has been described in Table 1.

Database Strategy Number of results before inclusion/exclusion criteria Results after inclusion/exclusion criteria (studies from past 10 years, adult population)
PubMed, PMC, and Medline (((gutdysbiosis) OR (gut microbiome) OR (intestinal symbiosis) OR (microbiome)) AND ((hypertension)))      1,291 137
  (("Hypertension/adverse effects"[Majr] OR "Hypertension/complications"[Majr] OR "Hypertension/epidemiology"[Majr] OR "Hypertension/microbiology"[Majr] OR "Hypertension/physiopathology"[Majr] )) AND (( "Dysbiosis/diagnosis"[Majr] OR "Dysbiosis/etiology"[Majr] OR "Dysbiosis/pathology"[Majr] OR "Dysbiosis/physiology"[Majr] OR "Dysbiosis/physiopathology"[Majr] )) 13 3
  ("Dysbiosis"[Mesh]) AND (( "Hypertension/adverse effects"[Majr] OR "Hypertension/complications"[Majr] OR "Hypertension/epidemiology"[Majr] OR "Hypertension/microbiology"[Majr] OR "Hypertension/physiopathology"[Majr] )) 31 3
  (("Dysbiosis/diagnosis"[Majr] OR "Dysbiosis/etiology"[Majr] OR "Dysbiosis/pathology"[Majr] OR "Dysbiosis/physiology"[Majr] OR "Dysbiosis/physiopathology"[Majr] )) AND ("Hypertension"[Mesh]) 26 6
ScienceDirect  (((gut dysbiosis) OR (gut microbiome) OR (intestinal dysbiosis) OR (microbiome)) AND ((hypertension) OR (high blood pressure)) AND ("adults")) 6,506 330

Inclusion Criteria and Exclusion Criteria

Inclusion and exclusion criteria are mentioned in Table 2.

Inclusion criteria Exclusion criteria
Papers from last 10 years Unpublished literature
Papers published in English Gray literature
Papers focusing on adult population (19+ years) Papers discussing pediatric population (less than 19 years)  
Papers with free full-text articles  
Papers included humans as cases and controls  

Data Extraction and Quality Appraisal of Included Studies

For data extraction, we screened all the included articles first by their title, abstract, and full text to understand their degree of relevance. Consequently, we extracted data including the year of publication, sample size, age of patients, inclusion criteria, results, and conclusions.

For quality appraisal, the Joanna Briggs Institute (JBI, Adelaide, Australia) tool was used. The articles that satisfied >70% of the criteria were finally studied in detail to conduct this study.


Study Selection

First, a total of 7,867 articles, from the four databases - PubMed, PubMed Central (PMC), Medline and ScienceDirect, were identified. Consequently, we excluded duplicates, articles older than 10 years, articles focusing on the pediatric population, and animal studies. Then, 3,457 articles remained for further screening based on title, abstracts, and inclusion and exclusion criteria. Among the remaining 23 articles, we excluded the articles that did not fulfill the criteria during quality appraisal using the JBI tool. At last, eight articles were selected to include in this study. All the articles were cross-sectional observational studies. The PRISMA flowchart is shown in Figure 1.

Study Population

The patients (cases) who participated in the study were having systolic BP (SBP) ≥ 140 mmHg and diastolic BP (DBP) ≥ 90 mmHg. Patients were also included from different grades of HTN, including prehypertension (pHTN), grade 1 HTN, and grade 3 HTN.

Gut Composition

Gut microbiota is widely diverse, containing trillions of microorganisms [24]. Most of the studies used the method of 16S ribosomal RNA (rRNA) gene amplification and sequencing for evaluating the changes in richness and diversity of gut microbiota in hypertensives. One study also used newly introduced metagenomic sequencing. All these studies concluded that there was a significant difference in the beta diversity (interindividual diversity) in both groups.

The pertinent characteristics of the studies have been discussed in Table 3.

Authors Year of publication Total number of patients (n) Conclusion/results
Palmu et al. [25] 2020 6,953 (829 for urinary sodium analysis) Most of the observed changes belonged to the Firmicutes phylum. Analysis was conducted to establish a correlation between sodium intake, gut Lactobacillus abundance, and BP.
Sun et al. [22] 2019 529 Associations between within-person and between-person gut microbial community diversity, taxonomic composition, and blood pressure in a diverse population-based cohort of middle-aged adults were seen.
Wang et al. [26] 2021 1,082 (with 1,003 and 434 adults included in the microbiota and metabolomics analysis samples, respectively) Positive associations of metabolites such as sphingomyelins, acylcarnitines, and cholesterol and potential roles of microbiota and metabolites in BP regulation were seen.
Kim et al. [27] 2018 22 A strong correlation of SBP with gut bacteria and barrier dysfunction existed. Butyrate production is inversely proportional to SBP.
Verhaar et al. [28] 2020 4,672  Substantial differences between gut microbiota composition and high BP in-between ethnic groups were found. A positive correlation was found between BP and fecal SCFA levels.
Mushtaq et al.  [29] 2019 80 (50 cases of grade 3 hypertension and 30 controls) Differences were observed in the bacterial populations, with a critically increased F/B ratio in the patients with grade 3 hypertension.
Li et al. [19] 2017 196 (inclusion of 41 healthy controls, 56 with pHTN, and 99 with primary hypertension) Significant and minimal differences were found in the structure of gut microbiota between healthy and hypertension and pHTN and hypertension, respectively.
Yan et al. [30] 2017 120 (60 patients with primary hypertension and 60 healthy controls of Chinese origin) Alterations were found in microbial diversity, genes, and functions of the gut microbiome in hypertensive patients.


It is still challenging to identify and understand the exact mechanism of HTN owing to its complex nature. However, many recent advances are establishing an interplay between gut dysbiosis and HTN. Four phyla dominate the adult human gut: Firmicutes, Bacteroidetes, Actinobacteria, and Proteobacteria. The general idea of how gut dysbiosis and high BP are associated has been shown in Figure 2.

In this study, we have mainly discussed the compositional gut microbiota changes along with the functional changes in genes and metabolome in hypertensive patients to get a detailed picture of the association between the two.

Gut Microbial Richness and Diversity in HTN

A bidirectional communication of gut microbiota exists with the human host and the environment. The human gut is a habitat of trillions of microbiomes, which do have a crucial role in maintaining homeostasis and immunity of the host. Alpha diversity is a diversity observed within a sample (number of species), whereas beta diversity is defined as between-sample diversity (type and abundance of the species). In the following sections, we have discussed altered gut microbiota diversity and richness observed in hypertensive patients. HTN is defined as SBP ≥ 140 mmHg and/or DBP ≥ 90 mmHg [26]. Some basic characteristics of patients, samples, and alterations in the composition have been summarized in Table 4.

Author Age (years) Method used to evaluate bacterial DNA from fecal samples Changes in gut microbial diversity and richness in HTN patients Elevated relative abundance in HTN patients Reduced relative abundance in HTN patients
Palmu et al. [25] 25-74 Shallow shotgun metagenome sequencing In models adjusted for age and sex, alpha diversity was inversely associated with systolic BP. For age- and sex-adjusted models, all BP indices were significantly associated with beta diversity. Lactobacillus paracasei Lactobacillus salivarius
Sun et al. [22] 18-30 MoBio PowerSoil kit (Qiagen, Hilden, Germany) Sequencing (of hypervariable V3 and V4 region of 16S rRNA) on the Illumina MiSeq (San Diego, CA, USA) platform (2×300) Alpha diversity was inversely associated Significant differences in beta diversity Catabacter and Robinsoleilla Sporobacter and Anaerovorax
Wang et al. [26] 30-69 TIANGEN (Beijing, China) DNA extraction kits Sequencing for 16S rRNA targeting the V4 hypervariable region performed on the Illumina MiSeq PE250 platform Differences in beta diversity Rothia, Serratia, Enterobacteriaceae, Leuconostocaceae, and Fusobacterium Coprococcus, Adlercreutzia, Eggerthella, and Raistonia
Kim et al. [27] >18 With PowerFecal DNA extraction kit (Qiagen) - Ruminococcus torques, Eubacterium siraeum, and Alistipes finegoldii Bacteroides thetaiotaomicron
Verhaar et al. [28] 18-70 Sequencing the V4 region of the 16S rRNA gene on Illumina MiSeq Alpha diversity difference stronger with young female (Dutch) Streptococcus spp. and Klebsiella spp. Roseburia spp., Clostridium sensu stricto spp., Roseburia hominis, Romboutsia spp., and Ruminococcaceae
Mushtaq et al. [29] 40-75 16S rRNA gene amplification using the QIAamp MiniStool kit (Qiagen) Alpha diversity significantly higher in the hypertension group Veillonellaceae family, Prevotella, Megasphaera, Parasutterella, Escherichia, and Shigella Faecalibacterium prausnitzii and Bacteroides uniformis
Li et al. [19] - TIANGEN kit Inversely related alpha diversity in both pHTN and HTN groups Prevotella and Klebsiella Faecalibacterium, Oscillibacter, Roseburia, Bifidobacterium, Coprococcus, and Butyrivibrio
Yan et al. [30] - QIAamp DNA mini kit (Qiagen) Alpha diversity inversely associated in hypertensives Klebsiella, Streptococcus, and Parabacteroides (P. merdae) F. prausnitzii, Roseburia spp., and Synergistetes

Palmu et al. studied the alpha and beta diversities, and they found a significant change in beta diversity with SBP and DBP, but an inverse association of alpha diversity with SBP in age- and sex-adjusted studies [25]. In multi-variable-adjusted models, beta diversity with DBP was only identified. Among the observed changes in taxonomic composition, most of them belonged to the Firmicutes phylum. To offer novel insights, a more focused analysis was conducted to establish a correlation between sodium intake, gut Lactobacillus abundance, and BP. They highlighted the potential mechanism of a diet contributing to change the gut microbiome, resulting in high BP by observing the abundance of Lactobacillus paracasei with decreased urinary sodium excretion and Lactobacillus salivarius with increased urinary sodium excretion. It cannot be ignored that the method used for sequencing and labeling DNA (shallow shotgun metagenome) is a new field with reported limitations.

Sun et al. found that the richness in various taxonomic groups was inversely related to high BP. Inverse cross-sectional relation of alpha diversity with systolic BP was observed in Coronary Artery Risk Development in Young Adults (CARDIA) participants [22]. They observed elevated representation of Catabacter and Robinsoleilla and decreased representation of Sporobacter and Anaerovorax. However, findings were found to be sensitive after adjustment of covariants such as body mass index (BMI). The major limitation of the study was that one-third of the patients included were taking antihypertensives.

To minimize the effect of antihypertensives on the results, Wang et al. conducted a study. They took participants from China Health and Nutrition Survey (CHNS) due to the presence of the highest number of undiagnosed and untreated hypertensive patients in addition to the presence of high prevalence of HTN in China. Hence, according to them, China might be the ideal place to study HTN [26]. Additionally, a few patients who were using medication to control BP were excluded from the study. The essential characteristics were a positive correlation of HTN with Rothia, Serratia, Enterobacteriaceae, Leuconostocaceae, and Fusobacterium, while a negative correlation with Coprococcus, Adlercreutzia, Eggerthella, and Raistonia.

The focus of the study by Verhaar et al. was to recognize an association and to find substantial differences between gut microbiota composition with high BP between ethnic groups within the population-based HEalthy Life In an Urban Setting (HELIUS) cohort [28]. The study showed the most significant alpha diversity in young female Dutch hypertensives among other ethnic groups. They noted the elevated abundance of Streptococcus spp. and Klebsiella spp. and a reduced abundance of Roseburia spp., Clostridium sensu stricto spp., Roseburia hominis, Romboutsia spp., and Ruminococcaceae. SCFAs are end products of intestinal fermentation done by gut microbiota, which are otherwise indigestible dietary products. Some examples of SCFA are propionate, acetate, and butyrate. Butyrate is majorly used by colonocytes, while acetate and propionate are consumed by the liver. SCFAs regulate gut inflammation and metabolism by functioning as an important colonocytes energy source and signaling molecules, indicating a low level of SCFA production in gut microbiota may act as a risk factor for multiple metabolic syndromes, including HTN. G-protein coupled free fatty acid receptors (FFARs) are present in the renal arteries, resulting in arterial vasodilation when attached with SCFAs. The positive correlation found between BP and fecal SCFA levels in the study was conflicting, with the negative correlation found between BP and SCFA-producing bacteria. With further research, researchers understood that they were measuring fecal SCFA levels as a proxy for intestinal SCFA production, which could be not reflecting the exact level of intestinal SCFA production. The measured fecal SCFA might reflect the amount after subtracting SCFA absorption. Consequently, they hypothesized that higher microbial SCFA production increases intestinal SCFA absorption, resulting in lower levels of SCFAs excretion in feces.

Kim et al. observed that bacterial taxa such as Ruminococcus torques, Eubacterium siraeum, and Alistipes finegoldii were increased in patients [27]. R. torques have been studied to participate in mucus degradation and eventually in gut barrier dysfunction. E. siraeum and A. finegoldii are known to trigger intestinal inflammation. In contrast, a decreased number of Bacteroides thetaiotaomicron was observed, which boosts the immunity of the host by strengthening the mucosal barrier. Depletion of Eubacterium rectale, one of the most significant butyrate-producing bacteria of the human gut, was observed. The study elucidated that butyrate production is inversely proportional to SBP. The finding was additionally validated by plasma butyrate measurements that were on the lower side. Furthermore, Rosebria and Eubacterium were on the higher side in the healthy people, which are the major butyrate-producing genera. Apart from being a small sample-size study, participants were divided without considering possible confounding factors such as diet, culture, demographics, and race.

Another study by Mushtaq et al. was unique as they took patients with grade 3 HTN and compared with the healthy controls. Firmicutes and Bacteroidetes are two of the four phyla that dominate the human gut flora. The Firmicutes/Bacteroidetes ratio (F/B ratio) was used to characterize gut dysbiosis. An increased ratio in the HTN group compared with the control group was identified. An increased F/B ratio could be due to an increase in Firmicutes or a decrease in Bacteroidetes [29]. An increase in abundance was noted of the Veillonellaceae at the family level and Prevotella, Megasphaera, Parasutterella, and Escherichia‑Shigella at the genus level compared with the control group. Veillonellaceae produces acetate and propionate in high amounts. Prevotella copri promotes inflammation by expressing a superoxide reductase. They did not find any major differences among Klebsiella spp., Streptococcus spp., and Parabacteroides merdae.

Yan et al. reported frequent distribution of them in hypertensives. Using the Metagenome-wide Association Studies (MGWAS) method, 31 Metagenome Linkage Groups (MLGs) were found to be higher in patients while 37 in controls [30]. In controls, MLGs of Roseburia and Faecalibacterium prausnitzii were on a higher side. They hypothesized a gross dose-response relationship between the abundance of HTN/control-enriched MLGs and the severity of HTN. At the phylum level, patients had higher levels of Proteobacteria but fewer Actinobacteria. At the genus level, Klebsiella, Clostridium, Streptococcus, Parabacteroides, Eggerthella, and Salmonella were frequently distributed in the hypertensives, while Faecalibacterium, Roseburia, and Synergistetes were found to be higher in the control group. F. prausnitzii and Roseburia are the major SCFA producers in the human colon, which might lead to the depletion of SCFA-producing enzymes in hypertensives. The major limitation was that 35% of patients had taken antihypertensive drugs or specific nutritious supplements.

A most unique part of the study conducted by Li et al. is that they included three groups to study the association: hypertensives, prehypertensives (pHTN), and healthy controls. On top of that, all the subjects included in the HTN group were newly diagnosed hypertensives. Thus, patients were not exposed to antihypertensive medication. According to them, the rate of acquiring new genes in controls surpassed the rate for the same in disease samples, which directly indicated a low richness of genes in hypertensives [19]. Prevotella and Klebsiella were found to be increased in HTN. Inflammation due to an immune response triggered by lipopolysaccharide (LPS) is the fundamental feature of gram-negative bacteria’s pathogenesis, such as Prevotella and Klebsiella. In addition to that, Prevotella is also associated with stearic acid, an important metabolite in HTN. Faecalibacterium, Oscillibacter, Roseburia, Bifidobacterium, Coprococcus, and Butyrivibrio were enriched in controls. Faecalibacterium and Roseburia in the intestines are very important for butyric acid production. Moreover, Bifidobacterium is necessary probiotics for gut microbial homeostasis, LPS reduction, and gut barrier. In pHTN also, they observed somewhat similar alterations in the bacterial diversity, enterotype, composition, and metabolic functions. After observing a minute difference in the characteristic of gut microbiota between pHTN and HTN, they recognized that pHTN is, in fact, a state in which gut dysbiosis has already occurred and not only a transitional period between normotensive and hypertensive status. As a result, they emphasized intervening early in pHTN patients instead of neglecting pHTN populations. However, it was a small sample size study.

Functional and Metabolomic Alterations in HTN

A study of changes in the functional expressions of the genes and the metabolome may fill the gap and allow us to understand the communication between gut microbiota and elevated BP in more detail. The metabolome is like a snapshot of different metabolic pathways by which we can identify new biomarkers responsible for elevation of the blood pressure. So along with studying compositional changes, it is beneficial to study these changes as well.

Wang et al. found positive associations of metabolites such as sphingomyelins, acylcarnitines, and cholesterol with both SBP and DBP [26]. Ceramide, a precursor of sphingolipids, has been shown to be detrimental to the heart in many ways. One of them is to impair vasodilation. When fatty acids surpass the energy requirement or storage room of a cell, an overabundance of sphingolipids takes place. They inferred sphingolipids as a potential biomarker for cardiovascular diseases in humans. Acylcarnitines, byproducts of incomplete β-oxidation, can accumulate in the blood when fatty acids are in excess for the oxidation process. They stimulate proinflammatory pathways involving nuclear factor-kappa B, which eventually results in high BP.

Another study that reflected on metabolomic changes was done by Kim et al. They evaluated impaired gut barrier function in the high BP cohort by measuring intestinal fatty acid binding protein (I-FABP), LPS, and soluble form of zonulin in plasma, which are biomarkers for gut epithelial health [27]. Zonulin is a protein present in the gut epithelial tight junction, which helps in the regulation of the junction. Moreover, they observed a significant increase in Th17 cells expressing CD161 and CCR6/integrin β7 in the HTN cohort, which are markers for gut inflammation. A constellation of these changes could be suggesting the interrelation between decreased gut barrier function and increased inflammation in patients with HTN.

From a metabolomic perspective, Yan et al. revealed that HTN-enriched taxonomic groups were involved more in membrane transport, LPS biosynthesis, and steroid degradation. Healthy controls demonstrated microbiota involved in the metabolism of other amino acids, cofactors, and vitamins (including folate biosynthesis and metabolism, riboflavin metabolism, and ubiquinone biosynthesis) [30]. Furthermore, the gut microbial enzymes, which are involved in trimethylamine N-oxide (TMAO) production, were enriched and the SCFA-producing enzymes were depleted in hypertensives. The choline utilization (cutC) gene, a gene that degrades the choline into trimethylamine, was identified in a variety of human gut commensals. Functional analysis also demonstrated the abundance of cutC genes in the gut microbiota of the hypertensives. Notably, several genera such as Klebsiella and Streptococcus, which were found to be in higher numbers, are choline degraders. These findings suggested that choline intake and TMAO production by gut microbiota could contribute to the pathogenesis of HTN.

Li et al. observed depletion in genes associated with biosynthesis and transport of amino acids, such as lysine, histidine, leucine, and serine, which are essential for human health in HTN patients [19]. An analysis of bacterial gene functions suggested that overproduction of LPS by gut bacteria could contribute to HTN pathogenesis; on the other hand, biosynthesis of amino acids, fatty acid utilization, and purine metabolism by gut bacteria might prevent the development of HTN.

Palmu et al. suggested the possibility of an association between microbiome-driven processes related to lipid metabolism, gluconeogenesis, and xenobiotic metabolism with blood pressure [25]. However, they proposed further validation of the hypothesis of functional changes by experimental studies with detailed sequencing.


The sampling method determines results. Ideally, mucosal biopsy should be used for studying microbiota composition and diversity instead of fecal sampling because it is only a proxy. Mucosal microbiota can be different from stool microbiota. Mucosal sampling has its own limitations too, such as disruption of the biofilm while taking the biopsy and also the impact of bowel preparation before a colonoscopy. The gut microbiota is affected by many factors, including age, diet, medications, exercise, and other coexisting diseases such as gut malignancy. Many studies did not take them into consideration or only took one factor into consideration. Many articles are present in the Chinese language on a similar subject, but due to the language barrier, we could not include them in this study. No clinical trial studies have been included in this study. Thus, large-scale, multicenter longitudinal studies are required for a better understanding of the association between gut dysbiosis and HTN, if any.


This study demonstrates a consistent relationship between high BP and gut microbiota ecology. Continuous cross-talk between the two signifies the potential mechanism of HTN pathogenesis. The richness and composition also depend on the diet, age, ethnicity, and severity of HTN. Metabolomic changes seen in hypertensives alter the previously well-maintained homeostasis and promote a proinflammatory state. Metabolites present in plasma and feces such as I-FABP, LPS, zonulin, sphingomyelins, acylcarnitines, and TMAO require validation by further studies to explore their potential as biomarkers. To establish a further causal relationship, more studies are warranted.


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Review article

Association of Gut Microbial Dysbiosis and Hypertension: A Systematic Review

Author Information

Shaili S. Naik Corresponding Author

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Internal Medicine, Surat Municipal Institute of Medical Education and Research (SMIMER) Hospital and Medical College, Surat, IND

Shivana Ramphall

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Research, American University of Antigua, Osbourn, ATG

Swarnima Rijal

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Vishakh Prakash

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Internal Medicine, Government Medical College Kozhikode, Kozhikode, IND

Heba Ekladios

Department of Psychiatry, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Jiya Mulayamkuzhiyil Saju

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Internal Medicine, Sree Narayana Institute of Medical Sciences, Ernakulam, IND

General Surgery, Government Medical College, Thiruvananthapuram, Trivandrum, IND

Naishal Mandal

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Internal Medicine, Surat Municipal Institute of Medical Education and Research (SMIMER) Hospital and Medical College, Surat, IND

Nang I. Kham

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Rabia Shahid

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Sathish Venugopal

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA

Ethics Statement and Conflict of Interest Disclosures

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.


The author (S.S. Naik) would like to thank Dr. Hassaan Tohid, the mentor from the California Institute of Behavioral Neurosciences & Psychology (CIBNP), and coauthors for their assistance in this study. In addition, the author would like to thank Dr. Aditya Desai, Dr. Darshi Desai, and Dr. Naishal Mandal for guiding and encouraging the author through the whole process.

Review article

Association of Gut Microbial Dysbiosis and Hypertension: A Systematic Review

Figures etc.


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