Next Article in Journal
The Significance of Bayesian Pharmacokinetics in Dosing for Critically Ill Patients: A Primer for Clinicians Using Vancomycin as an Example
Next Article in Special Issue
Antibiotic Resistance in Helicobacter pylori Isolates from Northwestern and Central Romania Detected by Culture-Based and PCR-Based Methods
Previous Article in Journal
Polyclonal Multidrug ESBL-Producing Klebsiella pneumoniae and Emergence of Susceptible Hypervirulent Klebsiella pneumoniae ST23 Isolates in Mozambique
Previous Article in Special Issue
Epidemiology of Helicobacter pylori Resistance to Antibiotics (A Narrative Review)
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Antibiotics
Volume 12
Issue 9
10.3390/antibiotics12091440
antibiotics-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Helicobacter pylori Infections in Children

by
Julie Nguyen
1,*,
Kallirroi Kotilea
1,2,
Patrick Bontems
1,2 and
Veronique Yvette Miendje Deyi
2,3
1
Department of Pediatric Gastroenterology, Hopital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, 1000 Brussels, Belgium
2
Belgian Helicobacter and Microbiota Study Group (BHMSG), 1000 Brussels, Belgium
3
Department of Microbiology, Laboratoire Hospitalier Universitaire de Bruxelles-Brussel Universitair Laboratorium (LHUB-ULB), Université Libre de Bruxelles, 1000 Brussels, Belgium
*
Author to whom correspondence should be addressed.
Antibiotics 2023, 12(9), 1440; https://doi.org/10.3390/antibiotics12091440
Submission received: 5 June 2023 / Revised: 6 September 2023 / Accepted: 7 September 2023 / Published: 12 September 2023
(This article belongs to the Special Issue Helicobacter pylori Infection - New Data and Approaches on Diagnosis, Pathogenesis, Antibiotic Resistance and Advances in Therapy)
Versions Notes

Abstract

:
In the context of epidemiology, host response, disease presentation, diagnosis, and treatment management, the manifestation of Helicobacter pylori (H. pylori) infection diverges between children and adults. H. pylori infection stands out as one of the most prevalent bacterial infections globally, and its prevalence in both children and adults is decreasing in many developing countries but some still struggle with a high prevalence of pediatric H. pylori infection and its consequences. The majority of infected children are asymptomatic and pediatric studies do not support the involvement of H. pylori in functional disorders such as recurrent abdominal pain. The pathophysiology of H. pylori infection relies on complex bacterial virulence mechanisms and their interaction with the host immune system and environmental factors. This interaction gives rise to diverse gastritis phenotypes, which subsequently influence the potential development of various gastroduodenal pathologies. In clinical settings, the diagnosis of this infection in childhood requires an upper gastrointestinal endoscopic exam with mucosal biopsy samples for histology and culture, or Polymerase Chain Reaction (PCR) at the very least. When warranted, eradication treatment should be given when good compliance is expected, and there should be systematic use of a treatment adapted to the antimicrobial susceptibility profile. To combat the burgeoning threat of multidrug resistance, vigilant surveillance of resistance patterns and strategic antibiotic management are paramount.

1. Introduction

Helicobacter pylori (H. pylori) is a spiral-shaped and flagellated Gram-negative bacterium that specifically colonizes the human stomach. Its initial description can be traced back to 1983, credited to the work of Barry Marshall and Robin Warren [1].
In the last years, the annual count of registered publications has exceeded 1800, with over 100 of those focused on H. pylori in pediatrics.
This bacterium is generally acquired during childhood and continues throughout the life unless specific treatment is prescribed. It can lead to severe gastroduodenal pathologies, including chronic gastritis, peptic ulcer, gastric cancer, and gastric mucosa-associated lymphoid tissue (MALT) lymphoma.
The prevalence of H. pylori is largely associated with socioeconomic status and living conditions, particularly those marked by overcrowding and poor hygiene [2].
Children differ from adults and have a low rate of severe disease associated with H. pylori and almost an absence of gastric malignancies. Infection is generally asymptomatic in children. Several studies have shown a lack of evidence regarding the relation between abdominal pain or other abdominal symptoms in children and H. pylori infection [3]. Considering these distinctions, guidelines for pediatric care provided by numerous esteemed societies, including the European Society of Pediatric Gastroenterology Hepatology and Nutrition and the North American Society of Pediatric Gastroenterology, Hepatology, and Nutrition, advise against employing a ‘test and treat strategy’ for the management of H. pylori in children [4].
This review, drawing from recent and pertinent publications, seeks to provide a concise overview of H. pylori in pediatric populations, encompassing shifts in its prevalence, risk factors, pathogenesis, clinical manifestations, and discussing the appropriate utilization of relevant diagnostic methods and clinical strategies employed in patient care. Moreover, recent data on resistance rates of H. pylori to currently employed antibiotics are discussed, with a focus on primary resistance and its trend across diverse regions worldwide.

2. Epidemiology

The discovery of H. pylori DNA in Peruvian mummies and other well-preserved human corpses from prehistoric times suggests that the infection has existed in human communities for thousands of years [5]. H. pylori infection is spread worldwide, as there seems to be no population, even in the most remote corners of the world, whose members are exempt from H. pylori. Seven distinct populations and subpopulations of H. pylori are currently identified in the modern context. These modern populations trace their genetic origins back to ancestral groups that emerged in Africa, Central Asia, and East Asia. It is of great interest to note that modern worldwide distributions follow human migratory fluxes [6].
In 2017, a systematic review and meta-analysis with 184 reports from 62 countries showed that the prevalence of H. pylori infection in adults ranges from 24% to 73% across continents, with a pooled global prevalence estimated at more than 50%, depending on geographic location and economic development. According to regional estimates of prevalence, the global population of individuals infected with H. pylori was approximated at 4.4 billion in 2015. Africa exhibited the highest pooled prevalence of H. pylori infection (70.1%; 95% CI, 62.6–77.7%), followed by South America (69.4%; 95% CI, 63.9–74.9%) and Western Asia (66.6%; 95% CI, 56.1–77.0%). In contrast, Oceania (24.4%; 95% CI, 18.5–30.4%), Western Europe (34.3%; 95% CI, 31.3–37.2%), and Northern America (37.1%; 95% CI, 32.3–41.9%) have the lowest prevalence rates [7].
In children, a 2022 systematic review and meta-analysis encompassing 60 countries and involving 152,650 patients across 198 epidemiological studies in the past 30 years, yielded insights into the global prevalence of H. pylori infection. Employing a multilevel mixed-effects meta-regression methodology, this study established that the overall prevalence of H. pylori infection in children worldwide stands at 32.3% (95% CI, 27.3–37.8%), which varied by diagnostic test (28.6% [23.0–35.0] for serology vs. 35.9% [29.2–43.2] for urea breath tests or stool antigen tests) [8]. This prevalence displayed geographical disparities, which were noteworthy even within the confines of the same country. For example, the prevalence ranged from 3.8% to 9.5% depending on the prefecture in Japan. The prevalence of H. pylori is low (6.0%) in children from North–Central Nigeria, whereas it is relatively high (28%) in the Southwest part of the country [9]. Notably, the prevalence of H. pylori infection in children in low-income and middle-income countries (43.2%) is almost twice that in high-income countries (21.7%) [8].
Studies have consistently shown over the past three decades that there has been a significant decrease in the prevalence of H. pylori infection among children on a global scale, particularly in industrialized countries of the Western world. In contrast, prevalence has plateaued at a high level in developing and newly industrialized countries [10]. This declining prevalence is explained by the steady improvements in sanitation and living conditions from the 1950s. In addition, it was speculated that the decreasing birth rate might have led to fewer children per family, thus decreasing the risk of intra-familial infection [11].
In Portugal, we note a significant decreasing trend in the prevalence of H. pylori infection in children [12]. In China, the infection rate has decreased over the past decades from 58.3% (95% CI, 50.7–65.5%) in 1983–1994 to 40.0% (95% CI, 38.2–41.8%) in the period 2015–2019 [13]. In Japan, the prevalence was near 90% among individuals born before 1950, but with a subsequent decreasing trend, reaching less than 2% among the children born between 2000 and 2003 [14]. In a meta-analysis from Taiwan, of the 29 eligible studies including 38,597 subjects, the pooled prevalence of H. pylori infection decreased from 63.8% (95% CI, 55.9–71%) in 1990–2000 to 28.2% (95% CI, 21.8–35.6%) in 2016–2020 [15].

3. Risk Factors Associated with Helicobacter pylori Infection in Children

It is now well known that H. pylori infection is acquired mostly during childhood, mainly during the first decade of life [16]. Intrafamilial transmission is the main route, with potential transmission pathways including oral–oral, fecal–oral, and gastro–oral routes [8]. The global distribution of H. pylori exhibits significant variations, largely influenced by socio-economic status and overcrowding. Regions with lower and middle incomes exhibit a high prevalence ranging from 60% to 80%, attributed to factors such as crowded living conditions, inadequate sanitation facilities, and suboptimal hygiene practices. In sharp contrast, higher income countries present a considerably lower prevalence of H. pylori, ranging from 1.2% to 12.2%.
Results derived from a comprehensive review of seven cohort studies reveal the impact of birth country on the prevalence of H. pylori infection among asymptomatic children under the age of five. Infection rates within this group are documented at 20% to 40% in high-income countries and 30% to 50% in upper-middle-income countries.
Age and ethnicity are additional factors impacting H. pylori prevalence. Torres et al.’s study revealed higher infection rates among older children, ranging from 20% to 50% in those aged 0–5 years and 38% to 79% in older children [17].
Lower maternal education, lower education of both parents, larger family size, having parents, siblings infected with H. pylori, consuming meals in unsanitary conditions, and diarrhea are significantly associated with a higher prevalence of H. pylori infection detected by mixed tests in children [8].

4. Pathogenesis, Natural History, and Clinical Outcome of the Infection

4.1. Natural History

H. pylori is usually acquired in childhood, but infection persists lifelong without treatment. However, spontaneous eradication is described in infants or young children [18]. After successfully colonizing the gastric epithelium cells, chronic gastritis will develop in virtually all persistently colonized persons, but most of them will remain asymptomatic. The clinical course will depend on bacterial and host factors. Patients with a higher acid output are more likely to have gastritis predominantly in the antrum, which predisposes to duodenal ulcers [19]. Patients with a lower acid output are more likely to have gastritis in the body of the stomach, which predisposes them to gastric ulcers, and can initiate a sequence of events that, in rare cases, might lead to gastric carcinoma (0.5–2%) [16,20]. In addition, H. pylori infection induces the formation of mucosa-associated lymphoid tissue (MALT) in the gastric mucosa. Malignant lymphoma arising from MALT is another rare complication of H. pylori infection [21,22,23]. Who will develop the disease depends upon three factors: (a) the virulence of the infecting H. pylori strain, (b) the type and extent of the host immune response to infection, and (c) modulating cofactors such as geography, climate, gastrointestinal (GI) microbiota, medications, and diet [24].

4.2. Pathogenesis and Differences in Immune Response in Children and Adults

Key aspects of bacterial colonization involve flagellar motility, urease activity, mechanisms of adhesion, and damage to the gastric epithelium via vacuolization (vacuolating cytotoxin A-VacA). The Helicobacter pylori pathogenicity island exerts a key role in inflammation, composes a type IV secretory system (T4SS), and promotes the intracellular injection of cytotoxin-associated gene A (CagA) antigen. The host immune response is characterized by initial mucosal invasion with polymorphonuclear cells followed by activation of the innate and adaptive immune system with complex T helper 1 (TH1), TH17, and regulatory T (Treg) cell interactions [16].
Compared to adults, children with H. pylori colonization of the stomach have lower rates of gastroduodenal ulceration that have been attributed to a reduced polymorphonuclear and mononuclear cell infiltration [25]. Several studies have shown that infected children have reduced gastric inflammation compared to adults [25,26,27]. In addition, there is evidence that the immune response to infection in children is lower than in adults with lower mucosal recruitment of neutrophil, CD3+, and CD8+ cells as well as a lower activation status of NF-jB transcription [28]. Sequence analyses suggested that the cagA and vacA genes profiles of the bacteria isolated from infected adults and children might be comparable. Therefore, the lower level of inflammation in infected children contrasted with adults is not due to differences in bacterial strains or common virulence factors [29]. Children with H. pylori infection have a high Treg response but a low Th1 and Th17 response compared to adults [27,30]. Detecting H. pylori-specific Th17/Th1 in chronically infected adults may indicate that the initial regulatory response is gradually lost [31]. Consequently, Th1, Th17, and Treg results may imply gastric mucosal response to H. pylori [32]. Michalkiewicz et al. concluded that H. pylori infection in children was characterized by (a) Th1 expression profile, (b) lack of mRNA over-expression of natural immunity receptors, and (c) solid anti-inflammatory activities in the gastric mucosa, possibly due to increased activity of anti-inflammatory M2 macrophages [33]. A recent study involving 40 H. pylori-infected children and adults analyzed Th17A, Treg response, and gastric inflammation. FOXP3 cells expressed Tregs on antral mucosa and Th1 by Th17A expression. Both pathways were overexpressed in the mucosa of H. pylori-positive patients. Children presented an important regulatory response that inhibits inflammation (with higher FOXP3 cells) and significantly lower Th17A levels during H. pylori infection than adults [34].

4.3. Clinical Outcome

It is estimated that of the H. pylori-infected individuals developing chronic gastritis, approximately 90% will likely remain asymptomatic [35]. However, peptic ulcers and gastric cancer are associated with colonizing H. pylori in the stomach. These complications represent a weak percentage of H. pylori-infected individuals (15–20% for gastritis that might lead to ulcers and less than 2% for gastric cancer). Still, the burden is considerable as those two gastric diseases represent over a million global deaths annually [36,37]. H. pylori has been classified by the International Agency for Research on Cancer (IARC) as a group 1 (‘definite’) carcinogen since 1994 [38]. In 2015, at the Kyoto Consensus aiming in an aetiologic classification of chronic gastritis and duodenitis in adults and its appropriate diagnostic assessment, H. pylori gastritis was designated an infectious disease, meaning it should be treated whether or not associated with symptoms [39]. As of 2019, H. pylori gastritis as an infectious disease is included as a nosological entity in the 11th International Classification of Disease (ICD 11) [40].
The risk of ulceration increases when taking non-steroidal anti-inflammatory drugs (NSAIDs). In a meta-analysis, Huang et al. concluded that, compared to subjects not infected with H. pylori and not taking NSAIDs, the group positive for these two covariates had a relative risk of peptic ulcer disease 6.1 times higher [41]. The risk of duodenal ulcers is also increased by smoking [42]. These environmental factors are more critical in old age than in children or young adults.
H. pylori is additionally correlated with milder GI diseases such as non-ulcer dyspepsia and gastritis. Moreover, several non-GI diseases have been purportedly connected to H. pylori infection, such as iron deficiency anemia, diabetes mellitus, coronary artery diseases, and idiopathic thrombocytopenic purpura. However, it is important to note that the causal role of the bacterium in these associations is not well established. On the other hand, H. pylori infection is negatively associated with several upper GI diseases such as gastroesophageal reflux disease, Barret’s esophagus, eosinophilic esophagitis, and esophageal cancer, as well as non-GI diseases such as asthma, although evidence is still weak for these negative associations [43,44,45,46,47].

5. Clinical Manifestations in Children

The clinical manifestations of H. pylori infection in children are non-specific, and in some cases, they may be justified by the presence of complications. Although less frequent than in adults, H. pylori-associated gastroduodenal ulcers are responsible for abdominal pain and upper gastrointestinal bleeding [28]. Regarding H. pylori infection and gastritis, a meta-analysis of 75 studies with 5990 H. pylori-infected and 17,782 uninfected children evaluated histologic changes in the gastric mucosa according to the Updated Sydney System. H. pylori-positive children presented more cases with nodular gastritis and duodenal ulcer than H. pylori-negative children. The H. pylori infection was also associated with a higher relative risk for gastric antral and corpus chronic inflammation, the presence of neutrophils and lymphoid follicles, but rarely gastric mucosa atrophy. Intestinal metaplasia was only significantly higher in the antral area of patients with chronic active inflammation [48]. Kako et al. from Japan, in a study with mixed pediatric and adult patients, showed different histopathological patterns of gastritis across age categories. In pediatric patients, 84% had a pattern of nodular gastritis, present in 68% of the young adult group and only 8% of the older group. In the latter, inflammatory changes seem more pronounced in the gastric body than in the antrum with strong mucosal inflammation. Persistent nodular gastritis and mononuclear infiltrate may evolve into cancer or atrophy after years of a concurrent balance between Th1 and Th2 immune response [49].
On the other hand, trials in children investigating the role of H. pylori in non-ulcer dyspepsia are inconclusive because they are uncontrolled and of poor quality or do not include sufficient patients [50,51,52,53,54,55]. No clinical manifestations, especially non-recurrent abdominal pain (RAP), are specific to H. pylori infection in children [56]. In a meta-analysis published in 2010, a statistically significant association was documented only for epigastric pain and H. pylori, while vomiting, diarrhea, flatulence, chronic functional abdominal pain, halitosis, regurgitation, constipation, or nausea were not related to H. pylori infection. A more recent prospective observational study of 240 Brazilian children with chronic non-ulcer dyspepsia showed no association between GI symptoms and H. pylori infection except nausea [57]. Among 1558 children aged 6–13 years in Iran, 145 children with RAP, according to the Apley and Naish criteria, were compared with 145 age-matched healthy controls recruited from the same area. The symptoms of H. pylori-positive children were not significantly different from those of H. pylori-negative children [58].
A meta-analysis suggests that H. pylori may have immunoregulatory properties in Inflammatory Bowel Disease (IBD), and the inverse association seems stronger in pediatric patients and those with Crohn’s disease. Further studies are necessary to explore this subject [59,60]. Another meta-analysis supports the inverse relationship of infection with the risk of asthma, especially in CagA+ patients [61].
H. pylori infection is a causal factor in developing Iron Deficiency Anemia (IDA) [62]. Different pathways have been implicated, including decreased absorption of dietary iron due to hypochlorhydria, gastrointestinal blood loss, and enhanced uptake and sequestration of iron by the bacteria [63]. In children and adolescents with H. pylori-associated IDA, increased iron requirements play a significant role as a pathogen. On the other hand, bacterial virulence and host genetic factors remain to be investigated [62]. In some intervention studies, H. pylori eradication has been shown to reduce iron deficiency anemia [64,65,66,67].
Reports in children and adults suggest that when investigating causes of chronic immune thrombocytopenic purpura (ITP), H. pylori infection should be considered. Indeed, partial, or complete remission of thrombocytopenia has been reported in some patients after H. pylori eradication. H. pylori eradication has a significant therapeutic effect in patients with ITP, according to a meta-analysis of four pediatric and two adult randomized trials [68].
There is insufficient data to support the relationship between H. pylori infection and Henoch Schonlein purpura, coeliac disease, obstructive sleep apnea syndrome, and type I diabetes mellitus in children. On the other hand, a recent meta-analysis of 29 studies backs up the hypothesis that H. pylori infection is linked to growth defects in children, particularly height for age scores [69]. Emerging evidence suggests more and more extraintestinal pathologies to be related to H. pylori infection. However, most of them do not occur during childhood. Moreover, it seems that the development of extraintestinal manifestations because of H. pylori infection might also depend on other factors such as age, race, gender, and geographical areas. Therefore, elucidating the role of these demographic and host-related factors in the pathogenesis of H. pylori-associated extraintestinal manifestations should also be the focus of future research [70].

6. Diagnosis

Available diagnostic tools for H. pylori infection include both invasive and non-invasive methods. Using a gastric biopsy specimen obtained from upper gastrointestinal endoscopy, invasive tests include rapid urea testing (RUT), histology, culture, and molecular biology. The non-invasive methods include the 13C urease breath test (UBT), stool antigen test (SAT), serology, and molecular tests on non-invasive specimens (stool samples, saliva, and gastric juice).
Both invasive and non-invasive methods could be used in pediatrics. However, the primary objective of clinical investigation remains rooted in identifying the underlying cause of a child’s symptoms. Presently, existing evidence strongly suggests that an infection of H. pylori does not exhibit a direct link to symptoms in cases where peptic ulcer disease is absent. Consequently, pursuing a non-invasive test to identify the infection and subsequently initiate treatment upon a positive result is not deemed appropriate. As a result, the strategy known as ‘test and treat’, which hinges on employing non-invasive diagnostic methods to diagnose H. pylori infection in children, stands unrecommended and has never been endorsed.
In instances where children display symptoms that raise the suspicion of pathological conditions affecting the upper digestive tract, such as dyspepsia, a thorough evaluation involving upper-gastrointestinal endoscopy is recommended.
Thus, the joint European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN)/North American Society of Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) guidelines recommend the use of H. pylori-positive culture or a combination of histology and one another biopsy-based test such as RUT or polymerase chain reaction (PCR) [4].
The isolation of H. pylori via culture is deemed the gold standard technique, given its attainment of 100% specificity [4]. Nonetheless, it is characterized by its demanding nature, influenced by factors such as meticulous pre-analytical conditions and the necessity for a well-equipped microbiology laboratory, which ultimately curtails its widespread applicability. As an alternative, molecular-based methods might be favored for identifying the infection and generating antimicrobial susceptibility profiles. Moreover, all the invasive methods require discontinuing proton pump inhibitors (PPIs) for at least 2 weeks and antibiotics for at least 4 weeks preceding endoscopy [4,71].
The diagnostic accuracy of histology varies with bacterial load and the examiner’s experience. Fortunately, the incorporation of immunohistochemistry, which is progressively becoming more accessible in laboratories, substantially bolsters the sensitivity and specificity of histological assessments [72]. Alongside its capacity to detect the bacteria, histology furnishes invaluable insights into the condition of the gastric mucosa, a conclusion supported by recent findings from a meta-analysis conducted in a pediatric population [48].
Molecular methods are less often used to diagnose H. pylori infection in pediatrics. However, a Turkish study found 94% concordance between PCR and histology for H. pylori diagnosis in children [73]. In a more recent study, Bogiel et al. demonstrated the robust accuracy of the PCR-based approach compared to histology in a group of 104 children [74]. RUT is strongly recommended in Japanese guidelines to diagnose active H. pylori infection in children [75]. However, the utility of RUT remains constrained in various regions owing to the unavailability of commercial assays [76].
In addition to the classical methods, endoscopic findings could be helpful in the diagnosis strategy. An analysis of 13 studies comparing endoscopic methods to standard diagnostic approaches (culture, RUT, UBT, SAT, and serology) for H. pylori infection found that the presence of Regular Arrangement of Collecting venules (RACs) was a highly significant predictor of H. pylori absence (OR: 55, sensitivity 78.3%, and specificity 93.8%) [77], and a subsequent systematic review with 4070 patients confirmed this exclusion criterion with even higher specificity (97%) [78], suggesting its potential utility in combination with traditional diagnostic methods, particularly when RAC results are negative. This could be helpful in combination with classical diagnostic tools, especially in cases where RAC is negative.
As in adults, it is recommended to monitor the success of eradication in children at least 4 weeks after the end of the treatment. For this purpose, non-invasive tests are indicated, particularly UBT or SAT. PPIs should be discontinued for at least 2 weeks (and antimicrobial agents for 4 weeks) as they interfere with the sensitivity of UBT and SAT [4,75]. A historical pan-European consensus including 18 countries has resulted in a practical guideline for an optimal and harmonized use of UBT from the prescription to the interpretation of the results [79]. SAT is less sensitive than UBT; nevertheless, it is the easiest method for children regarding sample collection and the most accessible for countries with reduced incomes. Many recent studies have confirmed the reliability of various SATs for H. pylori diagnosis [80,81].
Serology is not recommended for diagnosing H. pylori infection in children, neither for initial diagnosis nor eradication control due to a lower sensitivity. Its use is, therefore, limited to epidemiological studies [4,75].

7. Antimicrobial Susceptibility Testing

Culture-based methods and molecular tests provide both diagnosis and susceptibility testing. Unlike culture-based methods, molecular methods are often limited to one (clarithromycin) or two antibiotics (clarithromycin and levofloxacin). Nevertheless, molecular techniques are increasingly used due to the culture’s time-consuming and fastidious nature [82]. Feng et al. found that the success of tailored therapy based on clarithromycin susceptibility is significantly higher when employing the molecular detection of point mutations (92%) in comparison to the phenotypic method (70.4%) [83].
The most promising advances in recent years for the child population involve the combination of diagnosis and susceptibility testing in stool samples, saliva, and gastric juice using various molecular methods [1,70,80,84].

8. Antibiotic Resistance

The widespread use of antibiotics provides H. pylori with the opportunity to develop various resistance mechanisms, with point mutations being the predominant occurrences [82,85]. Table 1 below summarizes some recent data on primary resistance to antibiotics obtained worldwide in pediatrics during the last years [73,86,87,88,89,90,91,92]. Amoxicillin resistance is rare (0–1%) in most of the studies, except in Germany (20%) and Vietnam (50%), but these last data are questionable and need additional confirmation. Except for the Belgian series, clarithromycin primary resistance is dramatically high (more than 20%), with a maximum of resistance observed respectively in China (45%), Poland (54%), and Vietnam (92%). Quinolones are not generally recommended for children. However, we observe a very high rate (31%) of resistance in some studies, notably in Germany and Vietnam. Primary metronidazole resistance rates are highest in Asian countries, probably related to the most frequent use of this drug to cure parasitic infections. Tetracycline resistance is rare (null in most of the studies), except in the German (12%) and Poland (4.5%) series.
Borka Balas et al. [93] and Boyanova et al. [94] recently reviewed the evolution of H. pylori resistance to antibiotics in different countries and regions worldwide, including pediatric population and mixed adults and children, respectively. The general trend in children is stability for amoxicillin and tetracycline and increasing resistance rates for clarithromycin, metronidazole, and fluoroquinolones. Nevertheless, an increase in resistance to tetracycline in Iran (3% [1999–2000], 12% [2011–2016] and 18% [2017–2019]), to amoxicillin in Iran (9% [1999–2000], 14% [2011–2016 and 36% [2017–2019]), and in Bulgaria (4.2% [2007–2014] and 8.2% [2015–2021]) can be noted. We are also surprised by the decreased resistance rates to metronidazole found in Chile.
Secondary resistance: Previous attempts at eradication is a well-known risk factor to the development of antibiotic resistance. This phenomenon is underscored by data from the EuroPedHp registry, revealing substantially higher resistance rates—51.4% for clarithromycin, 40% for metronidazole, and 25.5% for the combination of clarithromycin and metronidazole—when compared to the relatively lower rates of 25%, 17.7%, and 3.8% observed for primary resistance to the same antibiotics [87].
These observations are consistent with similar trends observed in other independent studies [78,93,94], reinforcing the significance of prior eradication attempts in driving increased antibiotic resistance rates. Addressing this challenge is crucial for informing antimicrobial stewardship strategies and public health interventions aimed at curbing the emergence and dissemination of antibiotic-resistant pathogens.
Multidrug resistance: In line with the dramatic increase in H. pylori resistance to the major antibiotics used for eradication, multidrug resistance in children is also a topic of increasing concern. A systematic review and meta-analysis published in 2022 further underscored this concern, revealing an aggregated prevalence of primary multidrug-resistant H. pylori strains isolated in children at 6.0% (95% CI, 3.1–11.6%) [95]. This finding emphasizes the urgency of robust surveillance and strategic intervention to manage and mitigate the spread of multidrug resistance, thereby protecting the efficacy of treatment regimens for pediatric H. pylori infections.
Heteroresistance: Heteroresistance is characterized by the simultaneous presence of both resistant and susceptible pathogens within the same patient, and it can possibly lead to underestimating antimicrobial resistance. In their comprehensive meta-analysis of 22 studies, Lopo et al. reported a documented prevalence of 6.8% (95% CI, 5.1–8.6%) for clarithromycin heteroresistance and 13.8% (95% CI, 8.9–18.6%) for metronidazole heteroresistance [96]. Furthermore, research conducted on children by Gosciniak et al. indicated notable discrepancies of 20% for clarithromycin and 13.3% for metronidazole. The findings from the Belgian study conducted in 2021 revealed heteroresistance rates of 1.8% for clarithromycin, 3.5% for levofloxacin, and 10.5% for metronidazole among pediatric patients [86]. These results collectively emphasize the importance of adopting more sensitive diagnostic techniques to accurately detect and quantify heteroresistance, ensuring effective antimicrobial stewardship and better-informed clinical decision-making to address the challenges posed by diverse resistance profiles within individual patients.
Comparison to adults: In general, when compared to the adult population, H. pylori resistance rates in infected children tend to be lower. A meta-analysis including 178 studies across 65 countries worldwide confirmed this trend with only a few notable exceptions. These exceptions include higher metronidazole resistance rates in children compared to adults in the Eastern Mediterranean region (81% versus 61%) and in America (40% versus 22%), elevated clarithromycin resistance in children compared to adults in the Western Pacific region (85% versus 32%), and surprisingly, increased levofloxacin resistance among children in the Eastern Mediterranean region compared to adults (29% versus 18%) [97].

9. Treatment

In contrast to the adult guidelines, which recommended the eradication of H. pylori in all patients with an infection (regardless of the presence of peptic ulcer disease or background risk of gastric cancer), the pediatric guidelines take a different approach. The accepted indications for eradication treatment in children are gastro–duodenal ulcer disease, infection if a first-degree relative has gastric cancer, and refractory IDA. However, the definition of refractory IDA is imprecise and subject to various interpretations. The ‘test and treat’ strategy have not been recommended in pediatrics. However, if an infection by H. pylori is found during an upper GI endoscopy performed for suspicion of an organic disease but no ulcer (or erosion) is visualized, treatment can be offered after adequate discussion with the child and their family. In such cases, it is essential to address the possible side effects linked to treatment and the absence of proven benefits [4].
The goal of treatment is to achieve at least 90% eradication on a per-protocol basis on the first attempt [98]. A high eradication rate prevents the development of antibiotic resistance, the spread of resistant strains of H. pylori in the population, and reduces the number of re-treatments and eradication controls. The standard of care since the late 1990s, in children, is the combination of two antibiotics (mostly amoxicillin combined with either clarithromycin or metronidazole) and a proton pump inhibitor [99,100]. This treatment should be given for 14 days, as clearly emphasized in the adult consensus guidelines [71] and the latest pediatric consensus guidelines [4]. Since the frequency of resistance is increasing worldwide as shown in the section ‘Antibiotic resistance’ of this manuscript, determination of antimicrobial susceptibility is requested to tailor the eradication scheme. Indeed, recent studies showed that empirical triple therapy, especially when containing clarithromycin, performs poorly [91,101,102,103,104,105]. The meta-analysis of Wen et al. also showed an eradication rate of 71% with empirical triple therapy containing either clarithromycin or metronidazole [106]. On the contrary, using a tailored triple therapy containing clarithromycin or metronidazole for 14 days, the eradication rate obtained in the most recent multicenter registry reach the target of 90% (95% CI, 87–93%) [87]. These studies suggest that empirical treatment should no longer be used.
In the absence of available antimicrobial susceptibility testing, or in case of resistance to both clarithromycin and metronidazole, the recommendation in pediatrics suggests using an empirical triple therapy for 14 days combining a proton pump inhibitor with amoxicillin and metronidazole. Studies published during the last 5 years with this treatment have shown, however, substantial variability in the eradication rate but all remain substantially below the target of 90% [101,102,103,107,108]. With a duration of 14 days and a treatment tailored to antimicrobial susceptibility, the eradication rate obtained in the most recently published registry reached 92% [87].
Other regimens have been proposed such as sequential treatment consisting of two successive treatment periods of 5 days: amoxicillin and a proton pump inhibitor in two doses per day then a combination of metronidazole and clarithromycin with a proton pump inhibitor [109]. The rationale for using this sequential treatment is that amoxicillin would reduce the bacterial load (thus the risk of mutations) and destroy the bacterial cell wall during the first 5 days. Subsequently, the intracellular diffusion of clarithromycin may be increased. However, this treatment has not been proven to be more effective than a triple therapy for 14 days [87,110] and it exposes the child to three different antimicrobial agents, plus a proton pump inhibitor, which may induce more adverse events and more antimicrobial resistance in the case of treatment failure. The same is true for concomitant quadruple therapy without bismuth, which has not been adequately studied in children.
Bismuth-based therapies were frequently used in the 80s and the 90s before being abandoned for more than a decade. However, such combinations have been re-introduced after 2011 [71] and are even recommended as a first-line therapy in adults when available. Bismuth-based quadruple therapies containing tetracycline have not been properly studied in children and, due to the possible side effects, are not indicated before adulthood. Recent data in children exist with quadruple therapies containing bismuth sub-citrate, a proton pump inhibitor, amoxicillin, and metronidazole, and seem to be very efficient. The more recent prospective open cross-sectional study of 288 Chinese children comparing four different regiments showed that this treatment given for 14 days allowed the reaching of 90%, superior to 74% with standard triple therapy [111]. In a prospective single-arm trial in Belgium in 36 children, the same treatment given for only 10 days also showed a very high eradication rate (97%) [112]. Another recently published study proposes a sequential 7-day proton pump inhibitor with amoxicillin followed by a 7-day proton pump inhibitor, tetracycline, metronidazole, and bismuth subsalicylate in Turkish adolescents (mean age 15.1 ± 2.4 years) with a high eradication rate (92%) [113]. Finally, in Vietnam, in a prospective trial involving 237 children treated with different tailored regimens, 43 children infected with multidrug-resistant H. pylori strains received 14 days of bismuth-based quadruple therapy and the eradication rate of the bismuth quadruple scheme was 88% [114].

10. Rescue Treatment

Providing there is an adequate indication for treatment, a rescue treatment should be proposed in case of eradication failure. Compliance to the previous treatment must be assessed since this is a major cause of failure [108]. Previously used antibiotics, especially clarithromycin and metronidazole, should be avoided from the rescue regimen given the high likelihood of resistance. Nevertheless, the success of rescue treatment seems to be lower, as shown by a multicenter registry performed in Europe where success of a rescue treatment was only 59% [87]. Tetracycline or fluoroquinolones should be avoided in children and certainly used with extreme precautions. Tetracycline can cause yellow discoloration, hypoplasia of the enamel, and bone deposits. Fluroquinolones are associated with disabling side effects involving tendons, muscles, joints, nerves, and the central nervous system. These side effects can occur hours to weeks after exposure and may potentially be permanent.

11. Conclusions

In recent years, a growing interest has emerged in understanding H. pylori infection among children. Despite indications of a declining trend, the prevalence of H. pylori infection remains markedly high among both children and adolescents globally, with variations based on location and sanitation standards. Addressing this challenge requires concerted efforts to enhance hygiene, sanitary conditions, and access to clean water sources, thereby reducing the burden of H pylori infection on a global level.
New insights have been uncovered regarding lower mucosal immune responses and the possible role of H. pylori in preventing immune disorders such as allergies. Further research is needed to explore immune responses and clinical manifestations in children and to develop targeted interventions to reduce the burden of H. pylori-related diseases in pediatric populations.
Clinical investigation should prioritize identifying the cause of abdominal symptoms instead of solely focusing on detecting H. pylori infection. Unfortunately, in practical situations, it is not always possible to adhere to the guidelines. Failing to eradicate the infection during the first-line treatment not only reduces the chance of success with rescue therapy but also leads to secondary antimicrobial resistance and increase healthcare costs. To avoid these challenges, consensus guidelines advocate for an upper gastrointestinal endoscopic examination with at least six gastric biopsy samples for histology and culture, or PCR.
Over the last years, many studies have highlighted a concerning surge in antimicrobial resistance rates in children across various countries, especially the frequency of multidrug resistance. Considering this, we recommend standard antibiotic susceptibility testing of H. pylori in pediatric patients prior to initiating antibiotic therapy. All pediatric guidelines emphasize genotypic methods (PCR-based) over relying solely on phenotypic (culture-based) approaches for tailored eradication therapy due to their higher analytic performance and resilience to gastric biopsy conditions. However, their cost remains a limiting factor, and their availability for a broader spectrum of antibiotics remains limited.
In conclusion, considering all the aspects discussed above, we anticipate that this review will contribute to a reduction in the use of inappropriate tests (non-invasive tests such as H. pylori serology or breath tests) as diagnostic methods and while eradication treatment is necessary for children with peptic ulcer disease, it may not be warranted for all detected cases. As antibiotic resistance rates rise and treatment options in the pediatric population remain limited, persistent research is imperative to understand disease pathogenesis and develop effective prevention and treatment strategies for children affected by the infection. Additionally, when devising national preventive strategies, factors such as socioeconomic status, living conditions, local population eradication rates, and antimicrobial susceptibility profiles should all be considered.

Author Contributions

J.N. wrote, structured the manuscript, and reviewed the manuscript. K.K. wrote and critically reviewed the manuscript. V.Y.M.D. conceptualized the work and reviewed the manuscript. P.B. supervised the project, structured, and critically reviewed the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The authors received no financial support for this review.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Aguilera Matos, I.; Diaz Oliva, S.E.; Escobedo, A.A.; Villa Jiménez, O.M.; Velazco Villaurrutia, Y.D.C. Helicobacter Pylori Infection in Children. BMJ Paediatr. Open 2020, 4, 1–7. [Google Scholar] [CrossRef] [PubMed]
  2. Kotilea, K.; Kalach, N.; Homan, M.; Bontems, P. Helicobacter Pylori Infection in Pediatric Patients: Update on Diagnosis and Eradication Strategies. Pediatr. Drugs 2018, 20, 337–351. [Google Scholar] [CrossRef]
  3. Ravikumara, M. Helicobacter Pylori in Children: Think before You Kill the Bug! Therap. Adv. Gastroenterol. 2023, 16, 17562848231177610. [Google Scholar] [CrossRef] [PubMed]
  4. Jones, N.L.; Koletzko, S.; Goodman, K.; Bontems, P.; Cadranel, S.; Casswall, T.; Czinn, S.; Gold, B.D.; Guarner, J.; Elitsur, Y.; et al. Joint ESPGHAN/NASPGHAN Guidelines for the Management of Helicobacter Pylori in Children and Adolescents (Update 2016). J. Pediatr. Gastroenterol. Nutr. 2017, 64, 991–1003. [Google Scholar] [CrossRef] [PubMed]
  5. Maixner, F.; Thorell, K.; Granehäll, L.; Linz, B.; Moodley, Y.; Rattei, T.; Engstrand, L.; Zink, A. Helicobacter Pylori in Ancient Human Remains. World J. Gastroenterol. 2019, 25, 6289–6298. [Google Scholar] [CrossRef]
  6. Falush, D.; Wirth, T.; Linz, B.; Pritchard, J.K.; Stephens, M.; Kidd, M.; Blaser, M.J.; Graham, D.Y.; Vacher, S.; Perez-Perez, G.I.; et al. Traces of Human Migrations in Helicobacter Pylori Populations. Science 2003, 299, 1582–1585. [Google Scholar] [CrossRef]
  7. Hooi, J.K.Y.; Lai, W.Y.; Ng, W.K.; Suen, M.M.Y.; Underwood, F.E.; Tanyingoh, D.; Malfertheiner, P.; Graham, D.Y.; Wong, V.W.S.; Wu, J.C.Y.; et al. Global Prevalence of Helicobacter Pylori Infection: Systematic Review and Meta-Analysis. Gastroenterology 2017, 153, 420–429. [Google Scholar] [CrossRef]
  8. Yuan, C.; Adeloye, D.; Luk, T.T.; Huang, L.; He, Y.; Xu, Y.; Ye, X.; Yi, Q.; Song, P.; Rudan, I. The Global Prevalence of and Factors Associated with Helicobacter Pylori Infection in Children: A Systematic Review and Meta-Analysis. Lancet Child Adolesc. Health 2022, 6, 185–194. [Google Scholar] [CrossRef]
  9. Alfaray, R.I.; Saruuljavkhlan, B.; Ansari, S.; Fauzia, K.A.; Yamaoka, Y. REVIEW: EPIDEMIOLOGY OF HELICOBACTER PYLORI INFECTION. Microb. Health Dis. 2022, 4, e543. [Google Scholar]
  10. Park, J.S.; Jun, J.S.; Seo, J.H.; Youn, H.S.; Rhee, K.H. Changing Prevalence of Helicobacter Pylori Infection in Children and Adolescents. Clin. Exp. Pediatr. 2021, 64, 21–25. [Google Scholar] [CrossRef]
  11. Seo, J.H.; Bortolin, K.; Jones, N.L. Review: Helicobacter Pylori Infection in Children. Helicobacter 2020, 25, 3–7. [Google Scholar] [CrossRef]
  12. Antunes, R.; Oleastro, M.; Nogueira, J.P.; Lopes, A.I. Time Trend Prevalence of Helicobacter Pylori Infection and Endoscopic Findings in Symptomatic Children in Portugal: A Retrospective Study Based on Three Time Points in 2009, 2014, and 2019. Helicobacter 2023, 28, e12963. [Google Scholar] [CrossRef]
  13. Ren, S.; Cai, P.; Liu, Y.; Wang, T.; Zhang, Y.; Li, Q.; Gu, Y.; Wei, L.; Yan, C.; Jin, G. Prevalence of Helicobacter Pylori Infection in China: A Systematic Review and Meta-Analysis. J. Gastroenterol. Hepatol. 2022, 37, 464–470. [Google Scholar] [CrossRef]
  14. Wang, C.; Nishiyama, T.; Kikuchi, S.; Inoue, M.; Sawada, N.; Tsugane, S.; Lin, Y. Changing Trends in the Prevalence of H. Pylori Infection in Japan (1908–2003): A Systematic Review and Meta-Regression Analysis of 170,752 Individuals. Sci. Rep. 2017, 7, 15491. [Google Scholar] [CrossRef] [PubMed]
  15. Chen, M.-J.; Bair, M.-J.; Chen, P.-Y.; Lee, J.-Y.; Yang, T.-H.; Fang, Y.-J.; Chen, C.-C.; Chang, A.-T.; Hsiao, W.-D.; Yu, J.-J.; et al. Declining Trends of Prevalence of Helicobacter Pylori Infection and Incidence of Gastric Cancer in Taiwan: An Updated Cross-Sectional Survey and Meta-Analysis. Helicobacter 2022, 27, e12914. [Google Scholar] [CrossRef] [PubMed]
  16. Malfertheiner, P.; Camargo, M.; El-Omar, E.M.; Liou, J.-M.; Peek, R.M.; Schulz, C.; Smith, S.; Suerbaum, S. Helicobacter Pylori Infection. Nat. Rev. Dis. Prim. 2023, 9, 19. [Google Scholar] [CrossRef]
  17. Torrres, B.Z.; Lucero, Y.; Lagomarcino, A.J.; George, A.O.S.; Torres, J.P.; Ryan, M.O. Review: Prevalence and Dynamics of Helicobacter Pylori Infection during Childhood. Helicobacter 2017, 22, e12399. [Google Scholar] [CrossRef]
  18. O’Ryan, M.L.; Lucero, Y.; Rabello, M.; Mamani, N.; Salinas, A.M.; Peña, A.; Torres-Torreti, J.P.; Mejías, A.; Ramilo, O.; Suarez, N.; et al. Persistent and Transient Helicobacter Pylori Infections in Early Childhood. Clin. Infect. Dis. 2015, 61, 211–218. [Google Scholar] [CrossRef] [PubMed]
  19. El-Omar, E.M.; Penman, I.D.; Ardill, J.E.S.; Chittajallu, R.S.; Howie, C.; McColl, K.E.L. Helicobacter Pylori Infection and Abnormalities of Acid Secretion in Patients with Duodenal Ulcer Disease. Gastroenterology 1995, 109, 681–691. [Google Scholar] [CrossRef]
  20. Atherton, J.C. The Pathogenesis of Helicobacter Pylori-Induced Gastro-Duodenal Diseases. Annu. Rev. Pathol. 2006, 1, 63–96. [Google Scholar]
  21. Parsonnet, J.; Hansen, S.; Rodriguez, L.; Gelb, A.B.; Warnke, R.A.; Jellum, E.; Orentreich, N.; Vogelman, J.H.; Friedman, G.D. Helicobacter Pylori Infection and Gastric Lymphoma. N. Engl. J. Med. 1994, 330, 1267–1271. [Google Scholar] [CrossRef] [PubMed]
  22. Wotherspoon, A.C. Helicobacter Pylori Infection and Gastric Lymphoma. Br. Med. Bull. 1998, 54, 79–85. [Google Scholar] [CrossRef] [PubMed]
  23. Stolte, M.; Bayerdörffer, E.; Morgner, A.; Alpen, B.; Wündisch, T.; Thiede, C.; Neubauer, A. Helicobacter and Gastric MALT Lymphoma. Gut 2002, 50 (Suppl. 3), iii19–iii24. [Google Scholar] [CrossRef] [PubMed]
  24. Alexander, S.M.; Retnakumar, R.J.; Chouhan, D.; Devi, T.N.B.; Dharmaseelan, S.; Devadas, K.; Thapa, N.; Tamang, J.P.; Lamtha, S.C.; Chattopadhyay, S. Helicobacter Pylori in Human Stomach: The Inconsistencies in Clinical Outcomes and the Probable Causes. Front. Microbiol. 2021, 12, 713955. [Google Scholar]
  25. Serrano, C.; Wright, S.W.; Bimczok, D.; Shaffer, C.L.; Cover, T.L.; Venegas, A.; Salazar, M.G.; Smythies, L.E.; Harris, P.R.; Smith, P.D. Downregulated Th17 Responses Are Associated with Reduced Gastritis in Helicobacter Pylori-Infected Children. Mucosal Immunol. 2013, 6, 950–959. [Google Scholar] [CrossRef]
  26. Arnold, I.C.; Lee, J.Y.; Amieva, M.R.; Roers, A.; Flavell, R.A.; Sparwasser, T.; Müller, A. Tolerance Rather than Immunity Protects from Helicobacter Pylori-Induced Gastric Preneoplasia. Gastroenterology 2011, 140, 199–209. [Google Scholar] [CrossRef]
  27. Harris, P.R.; Wright, S.W.; Serrano, C.; Riera, F.; Duarte, I.; Torres, J.; Peña, A.; Rollán, A.; Viviani, P.; Guiraldes, E.; et al. Helicobacter Pylori Gastritis in Children Is Associated With a Regulatory T-Cell Response. Gastroenterology 2008, 134, 491–499. [Google Scholar] [CrossRef]
  28. Bontems, P.; Aksoy, E.; Burette, A.; Segers, V.; Deprez, C.; Mascart, F.; Cadranel, S. NF-ΚB Activation and Severity of Gastritis in Helicobacter Pylori-Infected Children and Adults. Helicobacter 2014, 19, 157–167. [Google Scholar] [CrossRef]
  29. Harris, P.R.; Smythies, L.E.; Smith, P.D.; Perez-Perez, G.I. Role of Childhood Infection in the Sequelae of H. Pylori Disease. Gut Microbes 2013, 4, 426–438. [Google Scholar] [CrossRef]
  30. Bontems, P.; Robert, F.; Van Gossum, A.; Cadranel, S.; Mascart, F. Helicobacter Pylori Modulation of Gastric and Duodenal Mucosal T Cell Cytokine Secretions in Children Compared with Adults. Helicobacter 2003, 8, 216–226. [Google Scholar] [CrossRef]
  31. D’Elios, M.M.; Manghetti, M.; De Carli, M.; Costa, F.; Baldari, C.T.; Burroni, D.; Telford, J.L.; Romagnani, S.; Del Prete, G. T Helper 1 Effector Cells Specific for Helicobacter Pylori in the Gastric Antrum of Patients with Peptic Ulcer Disease. J. Immunol. 1997, 158, 962–967. [Google Scholar] [CrossRef] [PubMed]
  32. Razavi, A.; Bagheri, N.; Azadegan-Dehkordi, F.; Shirzad, M.; Rahimian, G.; Rafieian-Kopaei, M.; Shirzad, H. Comparative Immune Response in Children and Adults with H. Pylori Infection. J. Immunol. Res. 2015, 2015, 315957. [Google Scholar] [CrossRef] [PubMed]
  33. Michalkiewicz, J.; Helmin-Basa, A.; Grzywa, R.; Czerwionka-Szaflarska, M.; Szaflarska-Poplawska, A.; Mierzwa, G.; Marszalek, A.; Bodnar, M.; Nowak, M.; Dzierzanowska-Fangrat, K. Innate Immunity Components and Cytokines in Gastric Mucosa in Children with Helicobacter Pylori Infection. Mediators Inflamm. 2015, 2015, 176726. [Google Scholar] [CrossRef]
  34. Yörgüç, E.; Gülerman, H.F.; Kalkan, İ.H.; Güven, B.; Balcı, M.; Yörgüç, M.Ç. Comparison of Clinical Outcomes and FOXP3, IL-17A Responses in Helicobacter Pylori Infection in Children versus Adults. Helicobacter 2021, 26, e12795. [Google Scholar] [CrossRef] [PubMed]
  35. Conteduca, V.; Sansonno, D.; Lauletta, G.; Russi, S.; Ingravallo, G.; Dammacco, F. H. Pylori Infection and Gastric Cancer: State of the Art (Review). Int. J. Oncol. 2013, 42, 5–18. [Google Scholar] [CrossRef]
  36. GBD 2016 Causes of Death Collaborators. Erratum: Global, Regional, and National Age-Sex Specific Mortality for 264 Causes of Death, 1980–2016: A Systematic Analysis for the Global Burden of Disease Study 2016. Lancet 2017, 390, 1151–1210. [Google Scholar] [CrossRef]
  37. Bray, F.; Ferlay, J.; Soerjomataram, I.; Siegel, R.L.; Torre, L.A.; Jemal, A. Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2018, 68, 394–424. [Google Scholar] [CrossRef]
  38. International Agency for Research on Cancer; World Health Organization. Schistosomes, Liver Flukes and Helicobacter Pylori. IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. In Proceedings of the IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, Lyon, France, 7–14 June 1994; Volume 61. [Google Scholar]
  39. Sugano, K.; Tack, J.; Kuipers, E.J.; Graham, D.Y.; El-Omar, E.M.; Miura, S.; Haruma, K.; Asaka, M.; Uemura, N.; Malfertheiner, P.; et al. Kyoto Global Consensus Report on Helicobacter Pylori Gastritis. Gut 2015, 64, 1353–1367. [Google Scholar] [CrossRef]
  40. World Health Organization. International Classification of Diseases (ICD-11); Elsevier: Geneva, Switzerland, 2022. [Google Scholar]
  41. Huang, J.Q.; Sridhar, S.; Hunt, R.H. Role of Helicobacter Pylori Infection and Non-Steroidal Anti-Inflammatory Drugs in Peptic-Ulcer Disease: A Meta-Analysis. Lancet 2002, 359, 14–22. [Google Scholar] [CrossRef]
  42. Talamini, G.; Zamboni, G.; Cavallini, G. Antral Mucosal helicobacter Pylori Infection Density as a Risk Factor of Duodenal Ulcer. Digestion 1997, 58, 211–217. [Google Scholar] [CrossRef]
  43. Fallone, C.A.; Barkun, A.N.; Friedman, G.; Mayrand, S.; Loo, V.; Beech, R.; Best, L.; Joseph, L. Is Helicobacter Pylori Eradication Associated with Gastroesophageal Reflux Disease? Am. J. Gastroenterol. 2000, 95, 914–920. [Google Scholar] [CrossRef] [PubMed]
  44. Wang, Q.; Yu, C.; Sun, Y. The Association between Asthma and Helicobacter Pylori: A Meta-Analysis. Helicobacter 2013, 18, 41–53. [Google Scholar] [CrossRef] [PubMed]
  45. Rubenstein, J.H.; Inadomi, J.M.; Scheiman, J.; Schoenfeld, P.; Appelman, H.; Zhang, M.; Metko, V.; Kao, J.Y. Association between Helicobacter Pylori and Barrett’s Esophagus, Erosive Esophagitis, and Gastroesophageal Reflux Symptoms. Clin. Gastroenterol. Hepatol. 2014, 12, 239–245. [Google Scholar] [CrossRef] [PubMed]
  46. Hojo, M.; Ueda, K.; Takeda, T.; Akazawa, Y.; Ueyama, H.; Shimada, Y.; Asaoka, D.; Nagahara, A. The Relationship between Helicobacter Pylori Infection and Reflux Esophagitis and the Long-Term Effects of Eradication of Helicobacter Pylori on Reflux Esophagitis. Therap. Adv. Gastroenterol. 2021, 14. [Google Scholar] [CrossRef] [PubMed]
  47. Miftahussurur, M.; Nusi, I.A.; Graham, D.Y.; Yamaoka, Y. Helicobacter, Hygiene, Atopy, and Asthma. Front. Microbiol. 2017, 8, 1034. [Google Scholar] [CrossRef] [PubMed]
  48. Kalach, N.; Zrinjka, M.; Bontems, P.; Kori, M.; Homan, M.; Cabral, J.; Casswall, T.; Chong, S.; Cilleruelo, M.L.; Faraci, S.; et al. Systematic Review and Meta-Analysis of Histological Gastric Biopsy Aspects According to the Updated Sydney System in Children. J. Pediatr. Gastroenterol. Nutr. 2022, 74, 13–19. [Google Scholar] [CrossRef] [PubMed]
  49. Kako, S.; Iwaya, Y.; Nagaya, T.; Hara, D.; Okamura, T.; Iwaya, M.; Kurasawa, S.; Kato, S.; Nakayama, Y.; Akamatsu, T.; et al. Clinicopathological Features of Nodular Gastritis in Three Classes of Age. Helicobacter 2021, 26, e12845. [Google Scholar] [CrossRef]
  50. Frank, F.; Stricker, T.; Stallmach, T.; Braegger, C.P. Helicobacter Pylori Infection in Recurrent Abdominal Pain. J. Pediatr. Gastroenterol. Nutr. 2000, 31, 424–427. [Google Scholar] [CrossRef]
  51. Shashidhar, H.; Peters, J.; Lin, C.H.; Rabah, R.; Thomas, R.; Tolia, V. A Prospective Trial of Lansoprazole Triple Therapy for Pediatric Helicobacter Pylori Infection. J. Pediatr. Gastroenterol. Nutr. 2000, 30, 276–282. [Google Scholar] [CrossRef]
  52. Özen, H.; Dinler, G.; Akyön, Y.; Koçak, N.; Yüce, A.; Gürakan, F. Helicobacter Pylori Infection and Recurrent Abdominal Pain in Turkish Children. Helicobacter 2001, 6, 234–238. [Google Scholar] [CrossRef]
  53. Uc, A.; Chong, S.K.F. Treatment of Helicobacter Pylori Gastritis Improves Dyspeptic Symptoms in Children. J. Pediatr. Gastroenterol. Nutr. 2002, 34, 281–285. [Google Scholar] [CrossRef] [PubMed]
  54. Farrell, S.; Milliken, I.; Murphy, J.L.; Wootton, S.A.; McCallion, W.A. Nonulcer Dyspepsia and Helicobacter Pylori Eradication in Children. J. Pediatr. Surg. 2005, 40, 1547–1550. [Google Scholar] [CrossRef] [PubMed]
  55. Ashorn, M.; Rägö, T.; Kokkonen, J.; Ruuska, T.; Rautelin, H.; Karikoski, R. Symptomatic Response to Helicobacter Pylori Eradication in Children with Recurrent Abdominal Pain: Double Blind Randomized Placebo-Controlled Trial. J. Clin. Gastroenterol. 2004, 38, 646–650. [Google Scholar] [CrossRef]
  56. Spee, L.A.A.; Madderom, M.B.; Pijpers, M.; Van Leeuwen, Y.; Berger, M.Y. Association between Helicobacter Pylori and Gastrointestinal Symptoms in Children. Pediatrics 2010, 125, e651–e669. [Google Scholar] [CrossRef]
  57. Correa Silva, R.; MacHado, N.; Carvalho, M.; Rodrigues, M. Helicobacter Pylori Infection Is High in Paediatric Nonulcer Dyspepsia but Not Associated with Specific Gastrointestinal Symptoms. Acta Paediatr. Int. J. Paediatr. 2016, 105, e228–e231. [Google Scholar] [CrossRef]
  58. Alimohammadi, H.; Fouladi, N.; Salehzadeh, F.; Alipour, S.; Javadi, M. Childhood Recurrent Abdominal Pain and Helicobacter Pylori Infection, Islamic Republic of Iran. East. Mediterr. Health J. 2016, 22, 860–864. [Google Scholar] [CrossRef]
  59. Castanõ-Rodríguez, N.; Kaakoush, N.O.; Lee, W.S.; Mitchell, H.M. Dual Role of Helicobacter and Campylobacter Species in IBD: A Systematic Review and Meta-Analysis. Gut 2017, 66, 235–249. [Google Scholar] [CrossRef]
  60. Wang, W.L.; Xu, X.J. Correlation between Helicobacter Pylori Infection and Crohn’s Disease: A Meta-Analysis. Eur. Rev. Med. Pharmacol. Sci. 2019, 23, 10509–10516. [Google Scholar] [CrossRef]
  61. Chen, C.; Xun, P.; Tsinovoi, C.; He, K. Accumulated Evidence on Helicobacter Pylori Infection and the Risk of Asthma: A Meta-Analysis. Ann. Allergy Asthma Immunol. 2017, 119, 137–145.e2. [Google Scholar] [CrossRef]
  62. Kato, S.; Gold, B.D.; Kato, A. Helicobacter Pylori-Associated Iron Deficiency Anemia in Childhood and Adolescence-Pathogenesis and Clinical Management Strategy. J. Clin. Med. 2022, 11, 7351. [Google Scholar] [CrossRef]
  63. Pacifico, L.; Osborn, J.F.; Tromba, V.; Romaggioli, S.; Bascetta, S.; Chiesa, C. Helicobacter Pylori Infection and Extragastric Disorders in Children: A Critical Update. World J. Gastroenterol. 2014, 20, 1379–1401. [Google Scholar] [CrossRef] [PubMed]
  64. Muhsen, K.; Cohen, D. Helicobacter Pylori Infection and Iron Stores: A Systematic Review and Meta-Analysis. Helicobacter 2008, 13, 323–340. [Google Scholar] [CrossRef] [PubMed]
  65. Qu, X.H.; Huang, X.L.; Xiong, P.; Zhu, C.Y.; Huang, Y.L.; Lu, N.G.; Sun, X.; Rong, L.; Zhong, L.; Sun, D.Y.; et al. Does Helicobacter Pylori Infection Play a Role in Iron Deficiency Anemia? A Meta-Analysis. World J. Gastroenterol. 2010, 16, 886–896. [Google Scholar] [CrossRef] [PubMed]
  66. Huang, X.; Qu, X.; Yan, W.; Huang, Y.; Cai, M.; Hu, B.; Wu, L.; Lin, H.; Chen, Z.; Zhu, C.; et al. Iron Deficiency Anaemia Can Be Improved after Eradication of Helicobacter Pylori. Postgrad. Med. J. 2010, 86, 272–278. [Google Scholar] [CrossRef]
  67. Wenzhen, Y.; Yumin, L.; Kehu, Y.; Bin, M.; Quanlin, G.; Donghai, W.; Lijuan, Y. Iron Deficiency Anemia in Helicobacter Pylori Infection: Meta-Analysis of Randomized Controlled Trials. Scand. J. Gastroenterol. 2010, 45, 665–676. [Google Scholar] [CrossRef]
  68. Kim, B.J.; Kim, H.S.; Jang, H.J.; Kim, J.H. Helicobacter Pylori Eradication in Idiopathic Thrombocytopenic Purpura: A Meta-Analysis of Randomized Trials. Gastroenterol. Res. Pract. 2018, 2018, 6090878. [Google Scholar] [CrossRef]
  69. Xu, C.; Wu, Y.; Xu, S. Association between Helicobacter Pylori Infection and Growth Outcomes in Children: A Meta-Analysis. Helicobacter 2022, 27, e12861. [Google Scholar] [CrossRef]
  70. Marginean, C.D.; MArginean, C.O.; Melit, L.E. Helicobacter Related Extraintestinal Manifestations—Myth or Reality. Children 2022, 9, 1352. [Google Scholar]
  71. Malfertheiner, P.; Megraud, F.; Rokkas, T.; Gisbert, J.P.; Liou, J.-M.; Schulz, C.; Gasbarrini, A.; Hunt, R.H.; Leja, M.; O’Morain, C.; et al. Management of Helicobacter Pylori Infection: The Maastricht VI/Florence Consensus Report. Gut 2022, 71, 1724–1762. [Google Scholar] [CrossRef]
  72. Lash, R.H.; Genta, R.M. Routine Anti-Helicobacter Immunohistochemical Staining Is Significantly Superior to Reflex Staining Protocols for the Detection of Helicobacter in Gastric Biopsy Specimens. Helicobacter 2016, 21, 581–585. [Google Scholar] [CrossRef]
  73. Güven, B.; Gülerman, F.; Kaçmaz, B. Helicobacter Pylori Resistance to Clarithromycin and Fluoroquinolones in a Pediatric Population in Turkey: A Cross-Sectional Study. Helicobacter 2019, 24, e12581. [Google Scholar] [CrossRef]
  74. Bogiel, T.; Mikucka, A.; Szaflarska-Popławska, A.; Grzanka, D. Usefulness of Molecular Methods for Helicobacter Pylori Detection in Pediatric Patients and Their Correlation with Histopathological Sydney Classification. Int. J. Mol. Sci. 2022, 24, 179. [Google Scholar] [CrossRef] [PubMed]
  75. Kato, S.; Shimizu, T.; Toyoda, S.; Gold, B.D.; Ida, S.; Ishige, T.; Fujimura, S.; Kamiya, S.; Konno, M.; Kuwabara, K.; et al. The Updated JSPGHAN Guidelines for the Management of Helicobacter Pylori Infection in Childhood. Pediatr. Int. 2020, 62, 1315–1331. [Google Scholar] [CrossRef] [PubMed]
  76. Garcés-Duran, R.; Kindt, S.; Kotilea, K.; François, S.; Rasschaert, G.; Smet, A.; Hauser, B.; Driessen, A.; Nkuize, M.; Burette, A.; et al. Belgian Consensus for Helicobacter Pylori Management 2023. Acta Gastroenterol. Belg. 2023, 86, 74–91. [Google Scholar] [PubMed]
  77. Glover, B.; Teare, J.; Ashrafian, H.; Patel, N. The Endoscopic Predictors of Helicobacter Pylori Status: A Meta-Analysis of Diagnostic Performance. Ther. Adv. Gastrointest. Endosc. 2020, 13, 2631774520950840. [Google Scholar] [CrossRef]
  78. Li, L.; Jing, J.; Gao, H.; Zhang, C.; Lou, H.; Pan, W. Regular Arrangement of Collecting Venules under Endoscopy for Predicting a Helicobacter Pylori-Negative Stomach: A Systematic Review and Meta-Analysis. Gastroenterol. Hepatol. 2021, 44, 286–292. [Google Scholar] [CrossRef]
  79. Keller, J.; Hammer, H.F.; Afolabi, P.R.; Benninga, M.; Borrelli, O.; Dominguez-Munoz, E.; Dumitrascu, D.; Goetze, O.; Haas, S.L.; Hauser, B.; et al. European Guideline on Indications, Performance and Clinical Impact of (13) C-Breath Tests in Adult and Pediatric Patients: An EAGEN, ESNM, and ESPGHAN Consensus, Supported by EPC. United Eur. Gastroenterol. J. 2021, 9, 598–625. [Google Scholar] [CrossRef]
  80. Qiu, E.; Li, Z.; Han, S. Methods for Detection of Helicobacter Pylori from Stool Sample: Current Options and Developments. Brazilian J. Microbiol. 2021, 52, 2057–2062. [Google Scholar] [CrossRef]
  81. Mărginean, C.O.; Meliț, L.E.; Săsăran, M.O. Traditional and Modern Diagnostic Approaches in Diagnosing Pediatric Helicobacter Pylori Infection. Children 2022, 9, 994. [Google Scholar] [CrossRef]
  82. Brennan, D.; O’Morain, C.; McNamara, D.; Smith, S.M. Molecular Detection of Antibiotic-Resistant Helicobacter Pylori. Methods Mol. Biol. 2021, 2283, 29–36. [Google Scholar] [CrossRef]
  83. Feng, Y.; Hu, W.; Wang, Y.; Lu, J.; Zhang, Y.; Tang, Z.; Miao, S.; Zhou, Y.; Huang, Y. Efficacy of Phenotype-vs. Genotype-Guided Therapy Based on Clarithromycin Resistance for Helicobacter Pylori Infection in Children. Front. Pediatr. 2022, 10, 854519. [Google Scholar] [CrossRef] [PubMed]
  84. Yin, G.; Bie, S.; Gu, H.; Shu, X.; Zheng, W.; Peng, K.; Zhao, H.; Li, F.; Chen, B.; Botchway, B.O.A.; et al. Application of Gene Chip Technology in the Diagnostic and Drug Resistance Detection of Helicobacter Pylori in Children. J. Gastroenterol. Hepatol. 2020, 35, 1331–1339. [Google Scholar] [CrossRef] [PubMed]
  85. Lin, Y.; Shao, Y.; Yan, J.; Ye, G. Antibiotic Resistance in Helicobacter Pylori: From Potential Biomolecular Mechanisms to Clinical Practice. J. Clin. Lab. Anal. 2023, 37, e24885. [Google Scholar] [CrossRef] [PubMed]
  86. Miendje Deyi, V.Y.; Ntounda, R.; Louis, H.; Kahegeshe, N.L.; Nkuize, M.; Burette, A.; Kotilea, K.; Van Gossum, M.; Delhaye, M.; Bontems, P. Primary Helicobacter Pylori Resistance to Antimicrobials in the Brussels Area in 2021. Diagn. Microbiol. Infect. Dis. 2023, 105, 115855. [Google Scholar] [CrossRef]
  87. Le Thi, T.G.; Werkstetter, K.; Kotilea, K.; Bontems, P.; Cabral, J.; Cilleruelo Pascual, M.L.; Kori, M.; Barrio, J.; Homan, M.; Kalach, N.; et al. Management of Helicobacter Pylori Infection in Paediatric Patients in Europe: Results from the EuroPedHp Registry. Infection 2022, 51, 921–934. [Google Scholar] [CrossRef]
  88. Geng, T.; Yu, Z.-S.; Zhou, X.-X.; Liu, B.; Zhang, H.-H.; Li, Z.-Y. Antibiotic Resistance of Helicobacter Pylori Isolated from Children in Chongqing, China. Eur. J. Pediatr. 2022, 181, 2715–2722. [Google Scholar] [CrossRef]
  89. Shu, X.; Ye, D.; Hu, C.; Peng, K.; Zhao, H.; Li, H.; Jiang, M. Alarming Antibiotics Resistance of Helicobacter Pylori from Children in Southeast China over 6 Years. Sci. Rep. 2022, 12, 17754. [Google Scholar] [CrossRef]
  90. Helmbold, L.; Ghebremedhin, B.; Bellm, A.; Hopkins, M.A.; Wirth, S.; Aydin, M. Increased Antibiotic Resistance in Children with Helicobacter Pylori Infection: A Retrospective Study. Pathogens 2022, 11, 178. [Google Scholar] [CrossRef]
  91. Van Thieu, H.; Duc, N.M.; Nghi, B.T.D.; Van Bach, N.; Khoi, H.H.; Tien, V.N.T.; Bang, M.T.L.; Ngoc, T.L.C. Antimicrobial Resistance and the Successful Eradication of Helicobacter Pylori-Induced Gastroduodenal Ulcers in Vietnamese Children. Med. Arch. 2021, 75, 112–115. [Google Scholar] [CrossRef]
  92. Krzyżek, P.; Pawełka, D.; Iwańczak, B.; Kempiński, R.; Leśniakowski, K.; Mégraud, F.; Łaczmański, Ł.; Biernat, M.; Gościniak, G. High Primary Antibiotic Resistance of Helicobacter Pylori Strains Isolated from Pediatric and Adult Patients in Poland during 2016–2018. Antibiotics 2020, 9, 228. [Google Scholar] [CrossRef]
  93. Borka Balas, R.; Meliț, L.E.; Mărginean, C.O. Current Worldwide Trends in Pediatric Helicobacter Pylori Antimicrobial Resistance. Children 2023, 10, 403. [Google Scholar] [CrossRef]
  94. Boyanova, L.; Hadzhiyski, P.; Gergova, R.; Markovska, R. Evolution of Helicobacter Pylori Resistance to Antibiotics: A Topic of Increasing Concern. Antibiotics 2023, 12, 332. [Google Scholar] [CrossRef] [PubMed]
  95. Kouhsari, E.; Sadeghifard, N.; Khadiv, A.; Sayadi, H.; Amiriani, T.; Ghafourian, S.; Valadbeigi, H.; Krutova, M. Heteroresistance to Clarithromycin and Metronidazole in Patients with a Helicobacter Pylori Infection: A Systematic Review and Meta-Analysis. Ann. Clin. Microbiol. Antimicrob. 2022, 21, 19. [Google Scholar] [CrossRef] [PubMed]
  96. Lopo, I.; Libânio, D.; Pita, I.; Dinis-Ribeiro, M.; Pimentel-Nunes, P. Helicobacter Pylori Antibiotic Resistance in Portugal: Systematic Review and Meta-Analysis. Helicobacter 2018, 23, e12493. [Google Scholar] [CrossRef] [PubMed]
  97. Savoldi, A.; Carrara, E.; Graham, D.Y.; Conti, M.; Tacconelli, E. Prevalence of Antibiotic Resistance in Helicobacter Pylori: A Systematic Review and Meta-Analysis in World Health Organization Regions. Gastroenterology 2018, 155, 1372–1382.e17. [Google Scholar] [CrossRef]
  98. Graham, D.Y.; Lee, Y.-C.; Wu, M.-S. Rational Helicobacter Pylori Therapy: Evidence-Based Medicine Rather than Medicine-Based Evidence. Clin. Gastroenterol. Hepatol. Off. Clin. Pract. J. Am. Gastroenterol. Assoc. 2014, 12, 173–177. [Google Scholar] [CrossRef]
  99. Oderda, G.; Shcherbakov, P.; Bontems, P.; Urruzuno, P.; Romano, C.; Gottrand, F.; Gómez, M.J.M.; Ravelli, A.; Gandullia, P.; Roma, E.; et al. Results from the Pediatric European Register for Treatment of Helicobacter Pylori (PERTH). Helicobacter 2007, 12, 150–156. [Google Scholar] [CrossRef]
  100. Cadranel, S.; Bontemps, P.; Van Biervliet, S.; Alliet, P.; Lauvau, D.; Vandenhoven, G.; Vandenplas, Y. Improvement of the Eradication Rate of Helicobacter Pylori Gastritis in Children Is by Adjunction of Omeprazole to a Dual Antibiotherapy. Acta Paediatr. 2007, 96, 82–86. [Google Scholar] [CrossRef]
  101. Moubri, M.; Kalach, N.; Larras, R.; Berrah, H.; Mouffok, F.; Guechi, Z.; Cadranel, S. Adapted First-Line Treatment of Helicobacter Pylori Infection in Algerian Children. Ann. Gastroenterol. 2019, 32, 60–66. [Google Scholar] [CrossRef]
  102. Iwańczak, B.M.; Borys-Iwanicka, A.; Biernat, M.; Gościniak, G. Assessment of Sequential and Standard Triple Therapy in Treatment of Helicobacter Pylori Infection in Children Dependent on Bacteria Sensitivity to Antibiotics. Adv. Clin. Exp. Med. Off. Organ Wroclaw Med. Univ. 2016, 25, 701–708. [Google Scholar] [CrossRef]
  103. Argueta, E.A.; Alsamman, M.A.; Moss, S.F.; D’Agata, E.M.C. Impact of Antimicrobial Resistance Rates on Eradication of Helicobacter Pylori in a US Population. Gastroenterology 2021, 160, 2181–2183.e1. [Google Scholar] [CrossRef] [PubMed]
  104. Serrano, C.A.; Leon, M.A.; Palma, C.; Vera, M.; Hernandez, C.; Harris, P.R. Helicobacter Pylori-Clarithromycin Resistance in Symptomatic Pediatric Patients in a High Prevalence Country. J. Pediatr. Gastroenterol. Nutr. 2017, 64, e56–e60. [Google Scholar] [CrossRef] [PubMed]
  105. Ustundag, G.H.; Altuntas, H.; Soysal, Y.D.; Kokturk, F. The Effects of Synbiotic “Bifidobacterium Lactis B94 plus Inulin” Addition on Standard Triple Therapy of Helicobacter Pylori Eradication in Children. Can. J. Gastroenterol. Hepatol. 2017, 2017, 8130596. [Google Scholar] [CrossRef] [PubMed]
  106. Wen, J.; Peng, P.; Chen, P.; Zeng, L.; Pan, Q.; Wei, W.; He, J. Probiotics in 14-Day Triple Therapy for Asian Pediatric Patients with Helicobacter Pylori Infection: A Network Meta-Analysis. Oncotarget 2017, 8, 96409–96418. [Google Scholar] [CrossRef]
  107. Su, D.-J.; Chang, M.-H.; Yang, J.-C.; Ni, Y.-H.; Hsu, H.-Y.; Wu, J.-F. Fourteen-Day Sequential Therapy Is Superior to 7-Day Triple Therapy as First-Line Regimen for Helicobacter Pylori Infected Children. J. Formos. Med. Assoc. 2022, 121, 202–209. [Google Scholar] [CrossRef] [PubMed]
  108. Kotilea, K.; Mekhael, J.; Salame, A.; Mahler, T.; Miendje-Deyi, V.Y.; Cadranel, S.; Bontems, P. Eradication Rate of Helicobacter Pylori Infection Is Directly Influenced by Adherence to Therapy in Children. Helicobacter 2017, 22, e12383. [Google Scholar] [CrossRef]
  109. Francavilla, R.; Lionetti, E.; Castellaneta, S.P.; Magistà, A.M.; Boscarelli, G.; Piscitelli, D.; Amoruso, A.; Di Leo, A.; Miniello, V.L.; Francavilla, A.; et al. Improved Efficacy of 10-Day Sequential Treatment for Helicobacter Pylori Eradication in Children: A Randomized Trial. Gastroenterology 2005, 129, 1414–1419. [Google Scholar] [CrossRef]
  110. Huang, Y.; Zhan, X. Sequential Therapy Is Superior to Triple Therapy for Helicobacter Pylori Infection in Children: A Meta-Analysis. Indian J. Pediatr. 2016, 83, 307–315. [Google Scholar] [CrossRef]
  111. Zhou, Y.; Ye, Z.; Wang, Y.; Zhang, Y.; Tang, Z.; Yan, W.; Jiang, Y.; Huang, Y. Comparison of Four Different Regimens against Helicobacter Pylori as a First-Line Treatment: A Prospective, Cross-Sectional, Comparative, Open Trial in Chinese Children. Helicobacter 2020, 25, e12679. [Google Scholar] [CrossRef]
  112. Kotilea, K.; Cadranel, S.; Salame, A.; Nguyen, J.; Mahler, T.; Miendje Deyi, V.Y.; Verset, L.; Bontems, P. Efficacy and Safety of Bismuth-Based Quadruple Therapy for Helicobacter Pylori Eradication in Children. Helicobacter 2021, 26, e12825. [Google Scholar] [CrossRef]
  113. Arslan, M.; Balamtekin, N.; Günal, A. Efficacy of a Novel Sequential Treatment Regimen Containing Bismuth for Helicobacter Pylori Eradication in Turkish Children. Helicobacter 2020, 25, e12757. [Google Scholar] [CrossRef] [PubMed]
  114. Le, L.T.T.; Nguyen, T.A.; Nguyen, N.A.; Nguyen, Y.T.H.; Nguyen, H.T.B.; Nguyen, L.T.; Vi, M.T.; Nguyen, T. Helicobacter Pylori Eradication Efficacy of Therapy Based on the Antimicrobial Susceptibility in Children with Gastritis and Peptic Ulcer in Mekong Delta, Vietnam. Children 2022, 9, 1019. [Google Scholar] [CrossRef] [PubMed]
Table 1. Recent worldwide data on primary antibiotic resistance of Helicobacter pylori in pediatric populations over the past few years.
Table 1. Recent worldwide data on primary antibiotic resistance of Helicobacter pylori in pediatric populations over the past few years.
First Author, YearRegionPeriodNAMO (%)CLA (%) LEV (%)MET (%)TET (%)RIF
(%)		CLA-MET (%)CLA-LEV (%)CLA-MET-LEV (%)Comments
Miendje Deyi et al., 2023BelgiumJanuary–December 202172013.913.943.10-8.31.41.4*1
Le Thi et al., 2022Europe2017–20206511255.417.7 8.53.8
Geng et al., 2022China (Chongqing)March–July 2020112047.3 18.888.40-30.41.810.7
Shu et al., 2022China (Southeast)March 2015–December 20201638032.822.881.70-16.41.89%*2
Helmbold et al., 2022GermanyOctober 2015–July 20195120453159122222.4--
Su et al., 2022TaiwanJanuary 2009–August 201970223.18.220 ----
Li et al., 2021China (Southwest)201953045.3 15.173.6060.428.3 (including CLA-MET RIF)-9.4 (+Rif)*3
Van Thieu et al., 2021VietnamNovember 2019–June 2020765092.131.614.50-13.2 *4
Krzyzek et al., 2020Poland2016–201822054.59.131.84.5-27.34.54.5*5
Guven et al., 2019TurkeyDecember 2016–April 201893-2715--- *6
AMO: amoxicillin; CLA: clarithromycin; LEV: levofloxacin; MET: metronidazole; TET: tetracycline; RIF: rifampicin; *1: lower overall resistance compared to adults; *2: MET-LEV:10.8%; *3: MET-LEV:10.8%; *4: AST method not detailed, and the authors fail to explain the remarkably high AMO resistance rate; *5: higher CLA resistance compared to adults; *6: concordance histology and PCR 94%.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Nguyen, J.; Kotilea, K.; Bontems, P.; Miendje Deyi, V.Y. Helicobacter pylori Infections in Children. Antibiotics 2023, 12, 1440. https://doi.org/10.3390/antibiotics12091440

AMA Style

Nguyen J, Kotilea K, Bontems P, Miendje Deyi VY. Helicobacter pylori Infections in Children. Antibiotics. 2023; 12(9):1440. https://doi.org/10.3390/antibiotics12091440

Chicago/Turabian Style

Nguyen, Julie, Kallirroi Kotilea, Patrick Bontems, and Veronique Yvette Miendje Deyi. 2023. "Helicobacter pylori Infections in Children" Antibiotics 12, no. 9: 1440. https://doi.org/10.3390/antibiotics12091440

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop