Abstract
Helicobacter pylori is a Gram-negative microorganism that causes chronic dyspepsia, gastritis, mucosa-associated lymphoid tissue (MALT) lymphoma, and gastric adenocarcinoma. Various antibiotic regimens are employed to eradicate it; however, antibiotic resistance has skyrocketed in recent years, resulting in a reduction in eradication rates. As a result, numerous novel therapeutic approaches are being adopted in clinical practice, and probiotics are being extensively investigated. Probiotics are living bacteria that, when consumed, offer many medicinal advantages that may be accomplished by altering the amount or activity of gut flora. Their beneficial influence on gut health, immune system modulation, and cancer therapy is the subject of extensive investigation. This is owing to their perceived safety and simplicity of use. The primary objective of this review is to learn about and investigate the function of probiotics in the eradication of H. pylori, either alone or in conjunction with traditional treatments.
Data have been collected from PubMed, PubMed Central, Medline, Cochrane, and Google Scholar, and relevant articles have been chosen following the PRISMA guidelines. Our search resulted in 2489 records, of which 123 full-text articles were screened for eligibility. Two reviewers independently performed the quality appraisal of 16 relevant articles, and ultimately 11 high-quality studies are included in this review. In conclusion, probiotic monotherapy does not have a significant effect on the eradication rates of H. pylori, but in conjunction with standard treatment regimens, there was mild improvement in the eradication rates but a significant reduction of side effects due to antibiotics.
Keywords: hpylori, probiotics and microbiome, gastritis, eradication, dietary supplements, yogurt
Introduction and background
Infection with Helicobacter pylori is one of the most prevalent chronic bacterial illnesses in humans, affecting roughly 4.4 billion people globally [1]. H. pylori is a Gram-negative, flagellated bacterium that inhabits the human stomach and causes prolonged gastric inflammation leading to gastritis, predisposing to gastric cancer and MALT lymphoma [1,2]. Gastric cancer constitutes nine percent of all cancer-related deaths, and hence H. pylori eradication has been demonstrated to lower the incidence of stomach cancer [1]. Until recently, triple therapy consisting of omeprazole, amoxicillin, and clarithromycin was considered the conventional first-line regimen. However, antibiotic resistance caused by the emergence of point mutations leads to increased failure rates [2]. In developed nations like Europe and the United States of America, quadruple therapy, which includes bismuth sub-citrate potassium, metronidazole, tetracycline, and omeprazole, is suggested as the primary treatment [3]. The quadruple regimen continues to have significant adverse effects like abdominal pain, nausea, vomiting, and bloating, leading to poor patient adherence to the medication, which further encouraged the emergence of antibiotic-resistant strains, and therefore, new treatment options are being explored [4].
Probiotics are live microorganisms, which when ingested, have numerous medical benefits that can be achieved by modifying the quantity or activity of the gut flora [5]. The two main species utilized as probiotics are Lactobacillus and Bifidobacterium, which are non-spore-forming, Gram-positive rods [6]. The resilience to low pH and endurance to a broad variety of temperatures define these bacteria, and their native habitat is the digestive system, oral mucous membranes, and genital tracts. These are being widely researched for their positive impact on gut health, immune system modification, and cancer therapies [6]. These dietary supplements are gaining popularity due to their perceived safety and ease of usage [5].
The selected suitable antimicrobials, their optimal combination, dosage, frequency, duration of treatment, and the necessity to use adjuvants are the parts of successful management of an infectious process [7]. Any disturbance in the equilibrium of the beneficial and harmful microorganisms in the body can trigger an inflammatory response, which causes epithelial malfunction [8]. H. pylori alter the host microbiome, most likely through changes in the gut microenvironment and acid-base balance. Hence probiotic supplementation may be beneficial in the treatment of inflammatory and infectious diseases [8,9]. Some studies have shown that adding probiotics to the traditional antibiotic regimen in H. pylori treatment can minimize the adverse effects of the antibiotics, most likely by re-establishing the balance of intestinal microbes [3]. Also, some of the probiotics are known to improve the success rates of H. pylori eradication, by both immunological and non-immunological mechanisms, like inhibiting H. pylori adhesion to the mucous membrane or by altering the pH [9]. However, other investigations have revealed that the use of probiotics has not improved the outcomes [4]. Furthermore, depending on the mechanism of action of various strains, pairing several strains of probiotics may be useful for boosting the eradication rate of infection [10]. These conflicting results have led to clinical confusion as to how this condition is best treated.
The primary goal of this systematic review is to determine the therapeutic value of probiotics, either alone or in conjunction with conventional treatment regimens, in the management of H. pylori eradication in adults.
Review
Methods
Relevant studies were found by searching PubMed, PubMed Central, Medline, Cochrane Library, and Google Scholar. This review was carried out using the preferred reporting items for systematic review and meta-analysis (PRISMA) guidelines. The following keywords were used for the search: Helicobacter pylori, Campylobacter pylori, proteobacteria, Helicobacteraceae, Gram-negative bacteria, Spiral Bacterium, eradication, gastritis, Lactobacillus, Bifidobacteria, Saccharomyces, probiotics, yogurt, microbiome, and dietary supplements. Additionally, a combination of the above regular keywords and MeSH strategy was used to identify relevant records from the PubMed databases.
Only studies that satisfied the following criteria were considered: (1) research conducted in the previous 10 years, which is 2011 through 2021, (2) free full-text articles, (3) studies conducted only on human subjects, (4) patient population 18 years or older. All animal studies, articles in languages other than English, books, and documents were excluded. Furthermore, research and review articles published before 2011 were omitted to provide a greater emphasis on the most recent advancements in therapies while keeping antibiotic resistance in mind. The literature selection process is outlined in the following PRISMA flow diagram [11] (Figure 1).
Figure 1. PRISMA Flow Diagram .
PRISMA: preferred reporting items for systematic reviews and meta-analysis [11]
Results
Our search yielded 354,238 records from PubMed, PubMed Central, and Medline; 43 records from Cochrane, and five records from Google scholar. After eliminating duplicates and irrelevant articles, 123 full-text articles were screened for eligibility. For our data analysis, we used EndNote basic (Clarivate, London, United Kingdom) as a reference manager. Sixteen studies were pre-qualified for quality evaluation out of 123. Two authors independently analyzed the results of these 16 papers using the standardized tools listed under; the Cochrane quality assessment tool for randomized clinical trials and the AMSTAR Checklist (Ottawa, Canada) for systematic reviews. This review eventually incorporated 10 studies. Table 1 summarizes the findings of the studies included in this review, as well as the conclusions drawn from each.
Table 1. Study analysis and review .
H. pylori: Helicobacter pylori, ITT: intention to treat, RCT: randomized control trial, BQT: bismuth containing quadruple therapy, GI: gastrointestinal
No | Authors | Year Published | Study design | Study Population | H.pylori Diagnostic test | Eradication Regimen | Probiotics used | Outcomes |
1 | Giuseppe Losurdo [2] | Jan-18 | Systematic review | 11 studies were selected. Probiotics eradicated H. pylori in 50 out of 403 patients. | N/A | Probiotic monotherapy | N/A | Probiotics alone show a minimal effect on H. pylori clearance, suggesting a likely direct role. |
2 | Lynne V McFarland [4] | Oct-15 | Systematic review and meta-analysis | 19 RCTs with 2730 participants using six different types of multi-strain probiotics | N/A | N/A | N/A | Adjunctive use of some multi-strain probiotics may improve H. pylori eradication rates and prevent the development of adverse effects and, but not all mixtures were effective |
3 | Maria Pina Dore [7] | Apr-19 | Randomized control trial | 56 H. pylori positive subjects assigned in 1:1 ratio into active or placebo group | Upper endoscopy with biopsy and 13C urea breath test | Probiotics and Pantoprazole or Placebo and Pantoprazole | Limosilactobacillus reuteri | The cure rate in the active group is 10.7% for ITT analysis versus 3.5% for the placebo group |
4 | Jin Young Yoon [8] | Jul-19 | Randomized control trial | 142 patients allocated to treatment or placebo group | 13C Urea Breath test, campylobacter-like organism test or histological examination | Subjects were randomized in 1:1 ratio into fermented milk with Lactobacillus paracasei HP7 and Glycyrrhiza glabra group or fermented milk only group for eight weeks | Lactobacillus paracasei and Glycyrrhiza glabra | The combination of Lactobacillus paracasei and Glycyrrhiza glabra improved GI symptoms, reduced H. pylori density and inflammation |
5 | Luyi Chen [9] | Aug-18 | Randomized control trial | 70 H. pylori positive patients were randomized into two groups | Esophagogastroduodenoscopy and histology | Bismuth containing quadruple therapy versus probiotics, and Bismuth containing quadruple therapy for 14 days | Clostridium butyricum | Eradication rates were 88.6% for the BQT group and 85.7% for probiotic and BQT group. No significant differences in eradication but there was a significant improvement in GI symptoms |
6 | Rahmatollah Rafiei [10] | Dec-20 | Randomized control trial | 106 H. pylori positive patients were assigned into two groups | Endoscopy | Triple therapy or probiotics and triple therapy | Lactobacillus rhamnosus, Lactobacillus casei, Streptococcus thermophiles, Lactobacillus bulgaricus, Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium longum, | The eradication rate is 88.5% in the probiotic and triple therapy group and 63.3% in triple therapy group |
7 | Wen Ji [11] | Sep-18 | Randomized control trial | 526 H. pylori positive patients were randomized into two groups in equal ratio | 14C-Urea breath test and electronic gastroscopy | Quadruple therapy or quadruple therapy with probiotics for 14 days | Compound Lactobacillus acidophilus | N/A |
8 | Ryuzo Deguchi [12] | Nov-11 | Randomized control trial | 229 patients with H. pylori were randomized into two groups | A bacterial culture or rapid urea breath test | Triple therapy or probiotics and triple therapy for one week along with pretreatment with probiotics alone for three weeks | Lactobacillus gasseri containing yogurt | The eradication rate for the probiotic group was 38.5% versus 28% for the triple therapy alone group. |
9 | Jian Zhang [13] | Sep-20 | Randomized, single-arm pilot trial | 150 positive patients were randomly allocated to different probiotic regimens | C13/14-Urea Breath Test, rapid urease test, stool antigen test or histology exam and culture | Clostridium butyricum in group A, Bacillus coagulans in group B and C. butyricum plus B coagulans in group C for eight weeks | Clostridium butyricum and Bacillus coagulans | The eradication rates were 18%, 20% and 26% in three groups, respectively. Hence C butyricum and B coagulans may effectively inhibit H. pylori to some extent. |
10 | Muhan Lu [14] | Oct-16 | Meta-analysis of randomized control trials | 13 randomized controlled trials, including 2306 patients | N/A | N/A | N/A | Probiotic supplementation may be effective in improving eradication rates and alleviating the disease related adverse effects |
Discussion
Helicobacter pylori have been known to infect humans for about 58,000 years, yet it wasn't found until 1982 [15]. H. pylori have been extensively studied by scientists all over the world since its isolation and culture by J. Robin Warren and Barry J. Marshall in 1982 [16]. Potentially treatable conditions caused by H. pylori include dyspepsia, peptic ulcer disease, Mucosa-associated lymphoid tissue lymphoma, and gastric adenocarcinoma [15]. It is surprising to learn that H. pylori are related to several diseases that are just not gastroenterological but also include several cardiovascular, hematological, and neurological conditions [15]. Probiotics generate bacteriostatic chemicals that limit H. pylori colonization and minimize treatment-related adverse effects such as antibiotic-associated diarrhea [16]. They also play an increasingly important role in health and disease, and there is an expanding body of data on the therapeutic potential of probiotics in many gastrointestinal diseases, including irritable bowel syndrome and other conditions [17]. However, several studies have contradictory findings on the efficacy and safety of probiotics in aiding with eradication [16]. Despite earlier research focusing on probiotic addition, the time and duration of probiotic treatment remain unknown.
This systematic review was conducted to investigate in depth and gain a better understanding of what is known, what is unknown, and what needs to be focused on in the future for the management of H. pylori and the significance of probiotics in the same. As a result, we have included a brief overview of H. pylori’s pathophysiology, its associations, typical treatment regimens, and antibiotic resistance to assist us in going through our review.
H. Pylori Pathogenesis and Its Associations
H. pylori infection is extremely common, possibly affecting more than half of the world’s population [18]. Africa has the highest prevalence (79.1%), followed by Latin America and the Caribbean (63.4%) and Asia (54.7%). North America (37.1%) and Oceania (24.4%), on the other hand, have the lowest H. pylori prevalence rates [19]. Pathogenic variables linked with chronic Helicobacter infection include its motility, bacterial chemotaxis, adherence, and CagA positive strains [20]. Chronic gastritis induced by H. pylori infection progresses to gastric adenocarcinoma, which develops as a result of a chain of events that includes gastritis, atrophy, intestinal metaplasia, dysplasia, and cancer [18]. The risk of gastric carcinogenesis in individuals infected with Cag PAI (Cag pathogenicity island) positive strains is double that of Cag PAI-negative strains [20]. Gastric epithelial proliferation and carcinoma development are induced by CagA transgenic expression in mice, and CagA suppresses apoptosis both in vitro and in vivo, indicating that CagA is a bacterial oncoprotein [21].
H. pylori colonization is known to be related to a variety of diseases. Some of its disease associations include Alzheimer’s disease, multiple sclerosis, rosacea, psoriasis, pernicious anemia, iron deficiency anemia, chorioretinitis, insulin resistance syndrome, Type 1 DM, metabolic syndrome, stroke, asthma, and many more [22]. This bacterium has been linked to an increased incidence of both diffuse and intestinal gastric cancer [18]. As a result of all these clinical interconnections and the most frequent gastric and duodenal ulcers, we must eliminate its colonization [18,22]. Figure 2 demonstrates some of the associations of H. pylori.
Figure 2. Helicobacter pylori associations.
Management and Antibiotic Resistance
Multiple regimens are available to treat H. pylori infection. The most popular regimens are triple therapy which consists of standard proton pump inhibitor, clarithromycin, and amoxicillin, and quadruple therapy with standard proton pump inhibitor, bismuth, tetracycline, and metronidazole [23]. Other less common but emerging regimens are sequential therapy, concomitant therapy, hybrid therapy (sequential-concomitant therapy), quinolone-based therapy, and salvage therapy [23]. The Maastricht V consensus recommended quadruple therapy containing PPI, bismuth, and two antibiotics as the first-line therapy for H. pylori eradication [12].
In the early 1990s, triple therapy consisting of a proton pump inhibitor, clarithromycin, and amoxicillin (CAM) was widely used, and the cure rate was about 80% [24]. Eventually, various factors led to the development of antibiotic resistance, which reduced the cure rates and brought the need for new treatment regimens. The most important factors are poor patient compliance, greater bacterial loads, biofilm formation, improper and insufficient regimens, and gene polymorphisms [24]. Prolonged treatment with such high dose antibiotics also caused increased adverse effects like imbalance in the gut microbial environment, antibiotic-related diarrhea, and Clostridium difficile infections, which further lead to poor compliance and antibiotic resistance [12]. Another vital factor for the failure of eradication is CAM (clarithromycin and amoxicillin) resistance due to 23S rRNA gene mutation [13].
Role of Probiotics
Researchers believe that probiotics may help treat diarrhea, constipation, irritable bowel syndrome, and other gastrointestinal disorders [14]. Several experimental investigations have suggested that different probiotics may have an antagonistic impact on H. pylori; however, the specific mechanisms are yet to be discovered [25]. Lactobacillus predominates in the non-acidic areas of the stomach, and Saccharomyces predominates in the acidic areas [26]. Chronic H. pylori infection reduces the Lactobacillus density in the stomach as well as alters the quality and quantity of the gut microbial flora [26]. The capacity of probiotics to inhibit H. pylori from attaching epithelial cells is typically caused by several processes such as competing for adhesion sites or nutrients, creating steric hindrance, and secreting antimicrobial compounds [25]. Additionally, probiotics also can partially stabilize or restore normal endogenous microbiota and suppress H. pylori growth [26]. Few studies also mentioned that probiotics increase IgA production, which supports the mucosal barrier against pathogens [25]. Hence they have recently been proposed as a novel therapeutic option against H. pylori [26]. However, this increase in the H. pylorieradication rates and reduction in adverse responses may be strain-specific [27].
In this study, we looked at the impact of several kinds of probiotics on H. pylori eradication, either alone or in conjunction with other conventional regimens. In a randomized controlled study with Limosilactobacillus Reuteri, Maria Pina Dore et al. reported that probiotics combined with pantoprazole had an eradication rate of 10.7% compared to 3.5% in the pantoprazole alone group [7]. In another study, Luyi Chen et al. found that bismuth quadruple therapy plus Clostridium had no significant difference in eradication rates when compared to bismuth quadruple therapy alone [9]. In contrast, Jian Zhang et al. found in their study that C. butyricum and B. coagulans can eliminate H. pylori to some level and can be utilized as an alternate therapy in antibiotic-resistant individuals [14]. When clarithromycin-based triple therapy was combined with probiotics, tolerance rose to more than 85%, and GI symptoms decreased from 76% in the usual triple therapy to 15% [28]. Furthermore, as indicated by Guiseppe Losurdo, Muhan Lu, and Lynne V McFarland's systematic reviews and meta-analysis, probiotics may have a little influence in the eradication of H. pylori and aid in the reduction of antibiotic-related adverse effects. These three reviews together looked at a total of 43 randomized control studies [2,4,26].
Concurrent probiotic and eradication therapy administration is usually believed to be more effective than other treatment regimens; nevertheless, clinical investigations have found varying outcomes about the optimal periods for providing probiotics [14]. However, most studies concluded that probiotics alone had no meaningful influence on eradication, although they did minimize the adverse effects of extended antibiotic therapy. This might be attributed to the probiotics repairing the disrupted microbial ecology in the stomach, which helped minimize nausea, GI distress, or diarrhea-like side effects and led to improved patient compliance. Thus, probiotics, when used in conjunction with conventional treatment regimens, showed a substantial improvement in eradication rates, particularly when used in conjunction with quadruple or triple therapy, while probiotic monotherapy had unsatisfactory results.
Limitations
Our study has numerous limitations, including a small number of publications included, evaluation of only free full-text papers, small sample sizes, and no consideration of recurrence rates; hence, any conclusions reached here are based on restricted data. Our findings should be interpreted with caution due to the high level of heterogeneity across the studies included in our analysis. Antibiotic resistance varies by area, and so eradication rates vary accordingly.
Conclusions
In conclusion, probiotics alone do not play a role in the eradication of Helicobacter pylori, but when combined with traditional treatment regimens, there is a slight increase in the eradication rates, which could be due to a reduction in the antibiotic-associated side effects, which leads to better patient adherence to the regimen. Furthermore, their effect might be strain-specific, dose-specific, or duration-specific. Additionally, pretreatment with probiotics, as well as supplementation throughout the therapy, resulted in higher eradication rates. The current comprehensive analysis showed significant evidence for the therapeutic benefit of probiotics in decreasing antibiotic-associated adverse effects. Though H. pylori eradication is studied worldwide, it has mostly been investigated in certain geographical locations such as China, Korea, Europe, and the Middle East. Hence, more well-designed, randomized, and thorough studies with high sample sizes in diverse locations should be undertaken, taking into account antibiotic resistance dependent on geography. It is also necessary to investigate the precise mechanism by which probiotics affect helicobacter elimination. As previously stated, only a few probiotics have a favorable impact; hence future researchers must investigate the precise strain and dose, as well as the specific duration, to improve the outcome of this chronic illness.
Acknowledgments
Dr. Hassan Tohid, who made this study feasible, deserves my sincere appreciation and thanks. His advice and support were extremely valuable throughout the course of completing my paper. I'd also want to thank Dr. Lubna, my mentor, and my co-authors for their steadfast support throughout the process.
The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.
Footnotes
The authors have declared that no competing interests exist.
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