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Article

Comparison of Amoxicillin Administered Twice versus Four Times a Day in First-Line Helicobacter pylori Eradication Using Tegoprazan, Clarithromycin, and Bismuth: A Propensity Score Matching Analysis

by
Jun-Hyung Cho
1,* and
So-Young Jin
2
1
Digestive Disease Center, Soonchunhyang University Hospital, Yongsan-gu, Seoul 04401, Republic of Korea
2
Department of Pathology, Soonchunhyang University Hospital, Yongsan-gu, Seoul 04401, Republic of Korea
*
Author to whom correspondence should be addressed.
Microorganisms 2024, 12(10), 1952; https://doi.org/10.3390/microorganisms12101952
Submission received: 2 September 2024 / Revised: 23 September 2024 / Accepted: 24 September 2024 / Published: 27 September 2024
(This article belongs to the Special Issue New Trends in Medical Bacteriology: Diagnosis, Treatment and Prevention)
Browse Figure
Review Reports Versions Notes

Abstract

:
This study aimed to investigate the effects of different amoxicillin (AMX) dosing schedules on bismuth quadruple therapy in Helicobacter pylori treatment-naïve patients. A total of 139 H. pylori-infected patients received a 2-week eradication regimen consisting of 50 mg tegoprazan, 500 mg clarithromycin, and 300 mg bismuth tripotassium dicitrate twice daily, 1000 mg AMX twice daily (BID group), or 500 mg AMX four times daily (QID group). We performed a urea breath test to evaluate H. pylori eradication eight weeks after treatment and compared the H. pylori eradication rate, patient compliance, and adverse drug events between the BID and QID groups. Based on propensity score matching, 114 and 100 patients were included in intention-to-treat (ITT) and per-protocol (PP) analyses, respectively. The H. pylori eradication rate did not differ significantly according to the ITT (82.5% vs. 87.7%, p = 0.429) and PP (95.9% vs. 98.0%, p = 0.536) analyses between the BID and QID groups. No significant differences were found in treatment compliance or adverse drug event rates between the two groups. In conclusion, the eradication rate of first-line H. pylori therapy containing tegoprazan, clarithromycin, and bismuth was not affected by AMX dosing schedules administered twice and four times daily.

1. Introduction

Helicobacter pylori infection is a major cause of peptic ulcers and gastric cancer [1]. H. pylori therapy can reduce the recurrence of peptic ulcers and prevent gastric cancer development. Traditionally, standard triple therapy consisting of a standard dose of a proton pump inhibitor (PPI), 1000 mg of amoxicillin (AMX), and 500 mg of clarithromycin twice daily has been used to eradicate H. pylori [2]. Standard triple therapy for 1–2 weeks has long been effective as a first-line H. pylori eradication method. However, eradication rates have decreased due to increased antibiotic resistance to clarithromycin [3]. Among the antimicrobial agents used for H. pylori treatment, the AMX resistance rate is relatively low at 5–10% in Asia, Europe, and America [4].
AMX, a beta-lactamase antibiotic, binds to and inactivates penicillin-binding proteins, weakening the bacterial cell wall and causing cell lysis [5]. It has a short plasma half-life at approximately 1–2 h and a time-dependent bactericidal effect. In microbiology, the minimum inhibitory concentration (MIC) is the lowest antibiotic concentration that prevents bacterial growth in vitro [6]. Frequent AMX dosing has the clinical advantage of maintaining plasma concentrations higher than the MIC; theoretically, AMX 500 mg administered four times daily can maximize the time above the MIC for up to 24 h [7]. Nevertheless, H. pylori-infected patients received AMX 1000 mg twice daily as standard triple therapy.
Potassium-competitive acid blockers (P-CABs) and bismuth may serve as alternatives to other antibiotics to overcome the unsatisfactory results of conventional triple therapy [8,9]. In a previous study, we evaluated the efficacy of a 2-week quadruple therapy (tegoprazan 50 mg + AMX 1000 mg + clarithromycin 500 mg + bismuth tripotassium dicitrate 300 mg twice daily) in H. pylori treatment-naïve patients [10]. The eradication success rates were 82.9% and 95.8% in intention-to-treat (ITT) and per-protocol (PP) analyses, respectively. This study design compared H. pylori eradication, patient compliance, and adverse drug events between AMX 1000 mg twice daily and 500 mg four times daily in tegoprazan-based bismuth quadruple therapy to determine whether the frequent dosing schedule of AMX affects H. pylori treatment.

2. Materials and Methods

2.1. Patients and Study Design

We retrospectively reviewed the medical records of H. pylori-infected patients treated with a 2-week tegoprazan-based quadruple regimen containing AMX, clarithromycin, and bismuth at a single center from March 2022 to May 2024. From March 2023, the AMX dosing schedule was changed from 1000 mg twice daily to 500 mg four times daily to increase the H. pylori eradication rate. The reasons for H. pylori eradication include peptic ulcers, endoscopic resection of gastric neoplasia, and chronic active gastritis. The exclusion criteria were an age < 20 or >80 years, history of gastric surgery, previous H. pylori eradication, severe systemic disease, or other known causes. The study protocol was approved by the Institutional Review Board of our hospital (SCHUH 2024-04-011).

2.2. Helicobacter pylori Eradication Therapy

All patients received a 2-week first-line H. pylori eradication regimen consisting of 50 mg tegoprazan, 500 mg clarithromycin, and 300 mg bismuth tripotassium dicitrate twice daily, 1000 mg AMX twice daily (BID group), or 500 mg AMX four times daily (QID group). Six weeks after completing eradication therapy, the patients were followed up to assess compliance and adverse drug events. The eradication result was confirmed using the urea breath test (UBT) with a cut-off value of 2.5‰, as recommended by the manufacturer. All patients were instructed to discontinue PPIs and P-CABs for at least 2 weeks, as well as antibiotics and bismuth for at least 1 month before undergoing UBT.

2.3. Study Outcomes

The primary outcome of this study was H. pylori eradication rates in the BID and QID groups. In the ITT analysis, patients who were noncompliant or lost to follow-up were considered to have failed the H. pylori treatment. We performed the PP analysis after excluding patients who did not complete the eradication regimen or did not follow up. Secondary endpoints were patient compliance and adverse drug events, including bitter taste, abdominal pain, nausea or vomiting, diarrhea, and bloating. A physician (J-H Cho) evaluated treatment compliance and adverse drug events when the patients returned to the outpatient clinic to assess eradication success. Compliance with the eradication regimen was defined as more than 90% consumption of the medication.

2.4. Statistical Analysis

The eradication rate of 2-week quadruple therapy was 83% based on our previous study [10]. We assumed a difference of 12% between eradication rates achieved by the two regimens. The minimum sample size was calculated using α- and β-error values of 0.05 and 0.2, respectively. The calculated sample size was 94 in each group, considering a drop-out rate of 10%.
Continuous variables are presented as mean ± standard deviation and were compared using Student’s t-test. Categorical variables are presented as numbers with percentages and were compared using Pearson’s chi-square test. The retrospective nature of this study incorporated potential confounding and treatment-related selection biases between the two groups. To balance the two treatment groups, propensity score matching at a ratio of 1:1 was performed using a logistic regression model for covariates such as age, sex, alcohol intake, smoking status, body mass index (BMI), cause of need for eradication, and comorbidities. All statistical analyses were conducted using SPSS software (version 27.0; IBM Corp., Armonk, NY, USA). A p-value < 0.05 was considered significant.

3. Results

3.1. Study Population

Figure 1 presents a flowchart of patient enrollment in this study. After excluding three patients with a history of gastric surgery (n = 1) and those who refused follow-up UBT (n = 2), 136 patients were assessed for eligibility. In terms of AMX dosage and frequency of administration, 63 and 73 patients received 1000 mg AMX twice daily (BID group) or 500 mg AMX four times daily (QID group), respectively. We included 114 patients (57 in each group) in the ITT analysis through propensity score matching. After excluding 2 noncompliant patients and 12 who did not follow up, 49 and 51 patients in the BID and QID groups, respectively, remained for the PP analysis.
The baseline patient characteristics are presented in Table 1. Before propensity score matching, a marginal difference was observed between the BID and QID groups regarding current smoking habits (p = 0.055). However, all baseline characteristics after propensity score matching were similar between the groups. The mean age was 53.4 ± 12.6 and 54.8 ± 11.9 years in the BID and QID groups, respectively (p = 0.538). The proportion of male patients was 54.4% in both groups (p = 1.000). No significant differences in alcohol intake, smoking status, BMI, cause of need for eradication, or comorbidities were observed between the groups.

3.2. Eradication Rate

Table 2 shows the first-line H. pylori eradication rates of the two groups. In the ITT analysis, the eradication rates of H. pylori were 82.5% (n = 47/57) and 87.7% (n = 50/57) in the BID and QID groups, respectively. In the PP analysis, the eradication rates were 95.9% (n = 47/49) in the BID group and 98.0% (n = 50/51) in the QID group. The eradication rates did not differ between the two groups in the ITT (p = 0.429) and PP analyses (p = 0.536).

3.3. Compliance and Adverse Events

Patient compliance and adverse drug events are summarized in Table 3. In total, 98.0% of patients in the BID group and 98.1% in the QID group adhered to the eradication regimen. Treatment compliance between the groups did not differ significantly (p = 1.000). Adverse events associated with H. pylori eradication therapy were observed in 20 (40.0%) and 12 (23.1%) patients in the BID and QID groups, respectively (p = 0.066). The perception of bitter taste was the most common, accounting for 26.0% of the BID group and 17.3% of the QID group (p = 0.286). The incidence of nausea and/or vomiting was higher in the BID group (14.0%) than in the QID group (3.8%); however, this difference was marginally insignificant (p = 0.089). No significant differences were found in the frequencies of abdominal pain, diarrhea, bloating, or others between the two groups. No serious adverse events were observed in either group.

3.4. Analysis of Clinical Factors Affecting H. pylori Eradication

We investigated the various clinical factors that affect H. pylori eradication (Table 4). In relation to H. pylori eradication rate, no significant difference was found in terms of sex, age, BMI, smoking status, cause of need for eradication, presence of comorbidity, or occurrence of adverse drug events. The H. pylori eradication rate in alcohol drinkers was lower than in non-drinkers; however, this difference was not statistically significant (93.0% vs. 100%, p = 0.076).

4. Discussion

In an era of increasing antibiotic resistance, H. pylori eradication rates of conventional treatments have reached unacceptable levels. At 30–40%, the clarithromycin resistance rate of H. pylori shows unsatisfactory results with standard triple therapy in some countries [11]. The Maastricht VI consensus report recommends tailored H. pylori therapy or empirical regimens (classic bismuth quadruple and concomitant therapies) in areas of clarithromycin-resistant H. pylori rates greater than 15% [12]. Tailored therapy requires expertise in antimicrobial susceptibility testing before selecting the H. pylori eradication regimen [13]. In particular, culture-based H. pylori eradication is time consuming and challenging in clinical settings. Classic quadruple therapies, including tetracycline and metronidazole, are reportedly associated with a high incidence of adverse drug events [14]. Treatment compliance may decrease because of the high pill burden in patients receiving concomitant therapy with the three antibiotics, and if eradication is not achieved, secondary antibiotic resistance may develop in H. pylori [15].
In the latest South Korean guidelines for H. pylori treatment, empirical H. pylori treatment comprises three first-line regimens: standard triple therapy for 2 weeks, concomitant or sequential therapy for 10 days, and bismuth quadruple therapy for 10–14 days [16]. However, the pooled eradication rate of the 2-week standard triple therapy was 78.1%, which did not meet the international standards for first-line H. pylori treatment success rates. Classic quadruple and concomitant therapies are not the preferred first-line therapies, resulting in incredibly low prescription rates of 2.6% and 3.1%, respectively [17].
AMX is one of the most frequently used antibiotics for H. pylori eradication owing to its low resistance level. Since AMX is a time-dependent antibiotic, its antibacterial effect depends on whether its plasma concentration is maintained above the MIC. The standard administration schedule of AMX for other infectious diseases is three to four times a day [18]. An MIC of 1 μg/mL was reached 83.3% of the time with four-times-daily doses of AMX compared to 45.8% with the same total amount given twice daily [19]. Two previous studies evaluated the therapeutic efficacy of different AMX dosing schedules in PPI-based standard triple therapy. In a South Korean study, Kim et al. compared H. pylori eradication between AMX 1000 mg twice daily and AMX 500 mg four times daily for 2 weeks [20]. Regarding eradication rates, AMX 500 mg four times daily was not superior to AMX 1000 mg twice daily (ITT, 89.2% vs. 91.4%, p = 0.620; PP, 90.8% vs. 92.1%, p = 0.752). In a Japanese study, patients infected with clarithromycin-susceptible H. pylori strains were treated with a 1-week standard triple therapy containing three AMX dosing schedules (750 mg twice daily, 500 mg three times daily, and 500 mg four times daily) [21]. When AMX 500 mg was administered three or four times daily, the H. pylori eradication rate was higher than when AMX 750 mg was administered twice daily (ITT, 91.9–93.5% vs. 77.8%, p < 0.05; PP, 95.0–96.7% vs. 80.3%, p < 0.05, respectively). These inconsistent results may have been influenced by patient characteristics and antibiotic resistance rates in different regions. However, these studies were conducted before P-CAB development.
P-CABs have a faster onset of action and a stronger effect on suppressing gastric acid secretion than conventional PPIs [22]. When P-CAB increases the intragastric pH to >6 within four hours, H. pylori may be in the replication phase and thus more susceptible to antibiotics [23]. Owing to the acid lability of AMX, P-CAB may improve its stability and bioavailability in the stomach. Bismuth is a semi-metal that inhibits protein and cell wall synthesis in H. pylori [24]. In human studies, bismuth addition increased the eradication rate of resistant H. pylori strains by 30–40% [25]. A real-world evidence study showed that the bismuth addition improved H. pylori eradication compared to no bismuth addition in a 2-week P-CAB-based triple therapy (ITT, 82.9% vs. 71.8%, p = 0.029; PP, 95.8% vs. 87.5%, p = 0.227) [10].
The dose and administration schedule of antibiotics should be determined based on their pharmacological properties to optimize bacterial infection treatment [26]. Nevertheless, most H. pylori treatments containing AMX are prescribed twice daily. To our knowledge, no previous study has evaluated H. pylori eradication using tegoprazan, clarithromycin, and bismuth according to AMX dosing schedules. This study compared the treatment efficacy of AMX 1000 mg twice daily (BID group) and AMX 500 mg four times daily (QID group). The overall eradication rates between the two groups were similar (82.5–95.9% in the BID group and 87.7–98.0% in the QID group).
Recently, AMX-based dual therapy has emerged as an H. pylori eradication strategy [27]. Potent gastric acid blockers such as P-CAB enable AMX to treat H. pylori infection. In AMX-based dual therapy, AMX should be administered at divided doses of 2–3 g/day, preferably three or four times daily rather than twice daily [28]. A 14-day AMX dual therapy is recommended, rather than a 7- or 10-day treatment period [29]. In this study, we hypothesized that a low dose of AMX 2 g/day administered four times might provide an additive effect to dual therapy. However, no benefit was found in the QID group compared with the BID group. Hence, we suggest that AMX 1000 mg twice daily is sufficient when prescribing H. pylori eradication therapy consisting of tegoprazan, clarithromycin, and bismuth.
This study had several limitations. First, we did not evaluate the resistance of H. pylori to antimicrobial agents. The eradication rates were not assessed based on the presence of clarithromycin susceptibility in H. pylori. Second, the intragastric pH and plasma AMX concentration were not measured. Therefore, we could not investigate the correlation between the AMX dosing schedule and the pharmacokinetics of AMX. Third, this was a retrospective study based on data collected at our hospital. Although propensity score matching ensured that the baseline patient characteristics were similar between the groups, a randomized controlled trial (RCT) is needed to confirm our results. Finally, this study included a small number of patients and was conducted at a single center. Thus, the number of patients obtained through sample size calculation was not reached. The eradication outcomes may vary depending on the antibiotic resistance of H. pylori in each region of South Korea. Multicenter RCTs with larger sample sizes are required.

5. Conclusions

AMX dosing schedules of twice and four times daily did not affect the H. pylori eradication outcomes in the 2-week quadruple regimen containing tegoprazan, AMX, clarithromycin, and bismuth for treating H. pylori-infected patients.

Author Contributions

Conceptualization, J.-H.C.; methodology, J.-H.C. and S.-Y.J.; software, J.-H.C.; validation, J.-H.C.; formal analysis, J.-H.C.; investigation, J.-H.C.; resources, J.-H.C. and S.-Y.J.; data curation, J.-H.C.; writing—original draft preparation, J.-H.C.; writing—review and editing, J.-H.C.; visualization, J.-H.C.; supervision, J.-H.C. and S.-Y.J.; project administration, J.-H.C.; funding acquisition, J.-H.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Soonchunhyang University Research Fund (grant number: 2024-0028).

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.

Conflicts of Interest

The authors declare no conflicts of interest.

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Microorganisms 12 01952 g001
Figure 1. Flowchart for patient enrollment. BMI, body mass index.
Figure 1. Flowchart for patient enrollment. BMI, body mass index.
Microorganisms 12 01952 g001
Table 1. Baseline characteristics of patients before and after propensity score matching.
Table 1. Baseline characteristics of patients before and after propensity score matching.
VariableBefore MatchingAfter Matching
BID Group
(n = 63)		QID Group
(n = 73)		p-ValueBID Group
(n = 57)		QID Group
(n = 57)		p-Value
Age (years)53.3 ± 12.255.5 ± 11.50.28653.4 ± 12.654.8 ± 11.90.538
Male (%)35 (55.6)35 (47.9)0.37631 (54.4)31 (54.4)1.000
Alcohol drinking (%)28 (44.4)32 (43.8)0.94326 (45.6)23 (40.4)0.570
Current smoker (%)18 (28.6)11 (15.1)0.05513 (22.8)11 (19.3)0.646
Body mass index (kg/m2)24.2 ± 3.724.0 ± 3.30.71224.4 ± 3.724.1 ± 3.40.611
Cause of need for eradication (%) 0.344 0.404
Chronic active gastritis41 (65.1)53 (72.6) 39 (68.4)43 (75.4)
Peptic ulcer/neoplasia22 (34.9)20 (27.4) 18 (31.6)14 (24.6)
Laboratory finding, mean (SD)
Hemoglobin (g/dL)13.9 ± 1.813.7 ± 1.30.52914.0 ± 1.813.9 ± 1.40.814
AST (U/L)23.1 ± 8.723.8 ± 7.30.60023.5 ± 9.023.7 ± 7.20.887
ALT (U/L)24.4 ± 16.322.9 ± 9.80.53924.6 ± 16.922.8 ± 9.30.495
Creatinine (mg/dL)0.83 ± 0.170.83 ± 0.160.9440.84 ± 0.170.85 ± 0.170.682
Underlying disease (%)
Cardiovascular disease20 (31.7)24 (32.9)0.88818 (31.6)20 (35.1)0.691
Respiratory disease0 (0)0 (0)1.0000 (0)0 (0)1.000
Liver dysfunction0 (0)2 (2.7)0.4990 (0)2 (3.5)0.496
Renal dysfunction1 (1.6)0 (0)0.4631 (1.8)0 (0)1.000
Diabetes7 (11.1)5 (6.8)0.3825 (8.8)3 (5.3)0.716
SD, standard deviation; AST, aspartate aminotransferase; ALT, alanine aminotransferase.
Table 2. Comparison of eradication rates between two- and four-times-daily amoxicillin dosing.
Table 2. Comparison of eradication rates between two- and four-times-daily amoxicillin dosing.
BID GroupQID GroupAdjusted 95% CI
for Difference		p-Value
Intention-to-treat analysis
Eradication rate82.5% (47/57)87.7% (50/57)5.2% (−7.8 to 18.3%)0.429
Per-protocol analysis
Eradication rate95.9% (47/49)98.0% (50/51)2.1% (−4.6 to 8.8%)0.536
CI, confidence interval.
Table 3. Compliance and adverse events associated with two- and four-times-daily amoxicillin dosing.
Table 3. Compliance and adverse events associated with two- and four-times-daily amoxicillin dosing.
BID Group (n = 50)QID Group (n = 52)p-Value
Compliance49 (98.0%)51 (98.1%)1.000
Patients with adverse events20 (40.0%)12 (23.1%)0.066
Bitter taste13 (26.0%)9 (17.3%)0.286
Abdominal pain1 (2%)0 (0%)0.490
Nausea or vomiting7 (14.0%)2 (3.8%)0.089
Diarrhea3 (6.0%)0 (0%)0.114
Bloating1 (2.0%)1 (1.9%)1.000
Others3 (6.0%)0 (0%)0.114
Table 4. Association between clinical factors and Helicobacter pylori eradication.
Table 4. Association between clinical factors and Helicobacter pylori eradication.
VariableEradication Ratep-Value
Sex 0.245
 Male (n = 53)50 (94.3%)
 Female (n = 47)47 (100%)
Age, years 0.294
 <50 (n = 36)34 (94.4%)
 ≥50 (n = 64)63 (98.4%)
Body mass index, kg/m2 0.559
 <25 (n = 61)60 (98.4%)
 ≥25 (n = 39)37 (94.9%)
Alcohol drinking 0.076
 No (n = 57)57 (100%)
 Yes (n = 43)40 (93.0%)
Current smoker 1.000
 No (n = 81)78 (96.3%)
 Yes (n = 19)19 (100%)
Cause of need for eradication 1.000
 Chronic active gastritis (n = 73)71 (97.3%)
 Peptic ulcer/neoplasia (n = 27)26 (96.3%)
Comorbidity 0.562
 Absent (n = 60)59 (98.3%)
 Present (n = 40)38 (95.0%)
Adverse drug event 0.550
 Absent (n = 69)66 (95.7%)
 Present (n = 31)31 (100%)
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MDPI and ACS Style

Cho, J.-H.; Jin, S.-Y. Comparison of Amoxicillin Administered Twice versus Four Times a Day in First-Line Helicobacter pylori Eradication Using Tegoprazan, Clarithromycin, and Bismuth: A Propensity Score Matching Analysis. Microorganisms 2024, 12, 1952. https://doi.org/10.3390/microorganisms12101952

AMA Style

Cho J-H, Jin S-Y. Comparison of Amoxicillin Administered Twice versus Four Times a Day in First-Line Helicobacter pylori Eradication Using Tegoprazan, Clarithromycin, and Bismuth: A Propensity Score Matching Analysis. Microorganisms. 2024; 12(10):1952. https://doi.org/10.3390/microorganisms12101952

Chicago/Turabian Style

Cho, Jun-Hyung, and So-Young Jin. 2024. "Comparison of Amoxicillin Administered Twice versus Four Times a Day in First-Line Helicobacter pylori Eradication Using Tegoprazan, Clarithromycin, and Bismuth: A Propensity Score Matching Analysis" Microorganisms 12, no. 10: 1952. https://doi.org/10.3390/microorganisms12101952

APA Style

Cho, J. -H., & Jin, S. -Y. (2024). Comparison of Amoxicillin Administered Twice versus Four Times a Day in First-Line Helicobacter pylori Eradication Using Tegoprazan, Clarithromycin, and Bismuth: A Propensity Score Matching Analysis. Microorganisms, 12(10), 1952. https://doi.org/10.3390/microorganisms12101952

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