Yuko Morino1
Mitsushige Sugimoto2*
Naoyoshi Nagata2Ryota Niikiura2Eri Iwata2Mariko Hamada2Yusuke Kawai2
Tatsuhiro Fujimiya3Hironori Takeuchi4
Sakae Unezaki3
Takashi Kawai2- 1Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
- 2Department of Gastroenterological Endoscopy, Tokyo Medical University Hospital, Tokyo, Japan
- 3Department of Practical Pharmacy, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
- 4Department of Pharmacy, Tokyo Medical University Hospital, Tokyo, Japan
Background: Proton pump inhibitors (PPIs) are the first-line treatment for acid-related diseases. The pharmacokinetics and therapeutic efficacy of PPIs, however, are influenced by genetic factors such as variants in genes encoding drug-metabolizing enzymes (e.g., cytochrome P450 2C19 [CYP2C19]) and drug transporters. We performed a meta-analysis to evaluate the influence of CYP2C19 genotype and PPI class, PPI dose, treatment duration and clarithromycin dose on the cure rate of PPI-containing Helicobacter pylori eradication therapy.
Methods: Randomized control trials (RCTs) investigating cure rates using a PPI-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes through May 2021 were included.
Results: A total of 25 studies (5,318 patients) were included. The overall eradication rate in the intention-to-treat analysis was 79.0% (3,689/4,669, 95% confidence interval [CI]: 77.8–80.2%), and that in CYP2C19 extensive metabolizers (EMs), intermediate metabolizer (IMs) and poor metabolizers (PMs) was 77.7% (1,137/1,464, 95% CI: 75.3–79.6%), 81.2% (1,498/1,844, 95% CI: 79.3–83.0%) and 86.8% (644/742, 95% CI: 83.9–88.9%), respectively. Meta-analysis showed that the relaTakashitive risk of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.21 (95% CI: 1.06–1.39, P = 0.006) and 1.57 (95% CI: 1.27–1.94, P < 0.001), respectively, in the fixed-effects model. The cure rate of omeprazole and lansoprazole-containing eradication regimens differed among CYP2C19 genotypes (P < 0.05), while that of rabeprazole and esomeprazole-containing regimens was similar.
Conclusion: The cure rates of PPI-amoxicillin-clarithromycin H. pylori eradication regimen, especially those containing omeprazole and lansoprazole, differ among CYP2C19 genotypes. Therefore, selection of a second-generation PPI or tailored treatment may achieve higher eradication rates than first-generation PPI-amoxicillin-clarithromycin triple regimen.
Introduction
The Maastricht V/Florence Consensus Report issued by the European Helicobacter Study Group in 2017 provides a guideline on how to manage Helicobacter pylori (H. pylori) infection (Malfertheiner et al., 2017). This guideline indicates that, despite increasing H. pylori resistance rates to antibiotics such as clarithromycin (CAM), metronidazole (MNZ) and levofloxacin (LVFX) in most parts of the world, clinicians worldwide continue to use general first-line H. pylori triple eradication therapy consisting of a proton pump inhibitor (PPI) and two kinds of antimicrobial agents [i.e., CAM, amoxicillin (AMPC), MNZ, or LVFX], especially in areas with lower rates of the clarithromycin-resistant strain (Malfertheiner et al., 2017). In Japan, H. pylori eradication therapy is limited to regimens comprising an acid-inhibitory drug such as a PPI (e.g., esomeprazole, rabeprazole, lansoprazole and omeprazole) or vonoprazan at a standard dose at twice-daily dosing (bid), AMPC 750 mg bid, and CAM 200 mg or 400 mg bid for 7 days as a first-line regimen (Kato et al., 2019). This is despite the fact that eradication therapy for all H. pylori-positive patients with gastritis confirmed by endoscopy is currently covered by the Japanese National Health Insurance system. From 1990 to 2000, eradication rates achieved in Japan using PPI-AMPC-CAM triple therapy ranged from approximately 85–91% (Asaka et al., 2001). However, because this rate has subsequently decreased to 60–75%, the factors affecting cure rates of PPI-AMPC-CAM therapy need to be identified.
The cure rate for H. pylori infection may be affected by several factors, including antibiotic susceptibility (e.g., CAM, AMPC, MNZ and LVFX) (Asaka et al., 2001; Furuta et al., 2001b; Murakami et al., 2002), insufficient acid inhibition during eradication therapy (e.g., CYP2C19 and CYP3A4/5 genotype, PPI dose, treatment schedule and type of acid-inhibitory drug) (Furuta et al., 2001b; Sugimoto et al., 2007; Sugimoto and Yamaoka, 2009), poor adherence to medication, the environment (e.g., smoking), and the presence of an H. pylori strain with low virulence activity (e.g., cagA-negative strains, vacA s2 genotype and dupA-negative strains) (Sugimoto and Yamaoka, 2009; Shiota et al., 2012). Of these, acid inhibition for 24 h has re-emerged as an important factor for successful eradication therapy (Furuta et al., 2001b; Sugimoto et al., 2007; Sugimoto and Yamaoka, 2009). In fact, the European guideline states that “the use of high dose PPI bid increases the efficacy of triple therapy” (Malfertheiner et al., 2017).
PPIs are currently used as the first-line treatment for acid-related diseases. However, because PPIs undergo extensive hepatic metabolism by the cytochrome P450 (CYP) system, which includes CYP2C19 and CYP3A4 (Ishizaki and Horai, 1999), CYP2C19 genetic polymorphisms influence both the pharmacokinetics and pharmacodynamics (i.e., intragastric pH) of PPIs (Chang et al., 1995a; Chang et al., 1995b; Kubota et al., 1996; Ishizaki and Horai, 1999). At least 20 CYP2C19 variants have been identified, with the majority of patients with these variants being classified into three genotypes: extensive metabolizers (EMs), intermediate metabolizers (IMs), and poor metabolizers (PMs). The acid inhibition achieved using PPIs is greater in PMs than IMs or EMs because of the different pharmacokinetics among the three genotypes. Therefore, CYP2C19 polymorphisms are expected to influence the eradication rates of PPI-based eradication therapy. Many randomized control trials (RCTs) have investigated the efficacy of PPI-AMPC-CAM regimen among CYP2C19 genotypes (Dojo et al., 2001; Inaba et al., 2002; Isomoto et al., 2003; Kawabata et al., 2003; Miki et al., 2003; Take et al., 2003; Kuwayama et al., 2005; Okudaira et al., 2005; Sheu et al., 2005; Higuchi et al., 2006; Furuta et al., 2007; Hagiwara et al., 2007; Kuwayama et al., 2007; Lee et al., 2010; Zhang et al., 2010; Prasertpetmanee et al., 2013; Yang et al., 2015; Liou et al., 2016; Phiphatpatthamaamphan et al., 2016; Chunlertlith et al., 2017; Shimoyama et al., 2017; Ozaki et al., 2018; Arevalo Galvis et al., 2019; Chen et al., 2020; Lee et al., 2020). A meta-analysis conducted in 2013 to examine the effects in CYP2C19 PMs revealed significant differences in eradication rates between EMs and IMs (odds ratio (OR) 0.72; 95% confidence interval (CI): 0.59–0.88), between EMs and PMs (0.51; 0.38–0.68), and between IMs and PMs (0.69; 0.52–0.92) (Tang et al., 2013). However, this meta-analysis examined a small number studies (n = 16) that were written in English and Chinese and evaluated eradication by both PPI-AMPC-CAM and non-PPI-AMPC-CAM regimen (Tang et al., 2013). In addition, the year-by-year changes in the incidence rates of antimicrobial resistance mandate that the efficacy of these regimens be periodically re-evaluated.
Here, we performed a meta-analysis to re-evaluate the efficacy and safety of PPI-AMPC-CAM therapy alone among different CYP2C19 genotypes in RCTs written in English.
Material Methods
Search Strategy and Inclusion Criteria
This meta-analysis was conducted using data from RCTs identified by searching the medical literature on PubMed and Cochrane Library databases. We compared H. pylori eradication rates of PPI-AMPC-CAM triple therapy (each given over 7–14 days) as first-line therapy among different CYP2C19 genotypes (EMs, IMs and PMs). Two researchers (YM and MS) independently searched both the PubMed and Cochrane Library databases using the terms “Helicobacter pylori,” “eradication,” and “CYP2C19” and reviewed the titles and abstracts of all potential studies (Supplementary Figure S1). The inclusion criteria were 1) RCTs published through June 2021; 2) studies that used PPI-AMPC-CAM as first-line treatment; 3) studies comparing cure rates of PPI-AMPC-CAM regimen for H. pylori infection; and 4) studies written in English. Exclusion criteria were 1) non-RCT studies, 2) studies performed on non-PPI-AMPC-CAM regimen, 3) studies written in non-English languages, and 4) studies with abstracts alone. The author’s names, year of publication, country where the study was conducted, number of patients, eradication rate of each regimen, patient characteristics (sex and age), CYP2C19 genotype, susceptibility to antimicrobial agents, and incidence of adverse events were extracted from each study.
Statistical Analysis
All meta-analyses were conducted using open-source statistical software (Review Manager Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014). First, a meta-analysis of RCTs comparing the cure rates of PPI-AMPC-CAM therapy in all patients and among CYP2C19 genotypes was performed. For each comparison, intention-to-treat (ITT) and per-protocol (PP) analyses of cure rates were conducted. Relative risk (RR) and the corresponding 95% CI were used to summarize the effect of each comparison in fixed-effects models and random-effects models (46–48). Potential bias in each study was evaluated using funnel plots. Heterogeneity was evaluated using the I2 value and Cochran’s Q. The I2 values used to define heterogeneity were as follows: 0–39%, low heterogeneity; and 40–74%, moderate heterogeneity. All p values were two-sided, and p < 0.05 was considered statistically significant. Calculations were performed using commercial software (SPSS version 27, IBM Inc.; Armonk NY, United States).
Results
Literature Search and Data Extraction
The search strategy yielded 222 potentially eligible studies from PubMed and Cochrane Library databases and 15 studies from handsearching through other sources and papers (Supplementary Figure S1). A total of 120 were selected from the extracted studies. Of these, 44 studies involved non-PPI-AMPC-CAM regimen, seven investigated its use as second-line treatment, 22 studies were non-RCTs, 11 were reviews or meta-analyses, and 11 were written in a non-English language and were excluded. Ultimately, a total of 25 full articles were assessed for eligibility (Supplementary Figure S1) (Dojo et al., 2001; Inaba et al., 2002; Isomoto et al., 2003; Kawabata et al., 2003; Miki et al., 2003; Take et al., 2003; Kuwayama et al., 2005; Okudaira et al., 2005; Sheu et al., 2005; Higuchi et al., 2006; Furuta et al., 2007; Hagiwara et al., 2007; Kuwayama et al., 2007; Lee et al., 2010; Zhang et al., 2010; Prasertpetmanee et al., 2013; Yang et al., 2015; Liou et al., 2016; Phiphatpatthamaamphan et al., 2016; Chunlertlith et al., 2017; Shimoyama et al., 2017; Ozaki et al., 2018; Arevalo Galvis et al., 2019; Chen et al., 2020; Lee et al., 2020) and a total of 5,318 patients treated with a PPI-AMPC-CAM regimen for H. pylori infection were included in the analysis. Most of the studies (96%, 24/25) were performed in East and South-East Asian countries.
The characteristics of the trials investigating cure rates among CYP2C19 genotypes are shown in Table 1. Eradication therapy comprised a regimen of a PPI (omeprazole (20 mg, bid), lansoprazole (30 or 60 mg, bid), rabeprazole (10 or 20 mg, bid), esomeprazole (20 or 40 mg, bid), ilaprazole (10 mg, bid) or dexlansoprazole (60 mg, once-daily dosing (oid), AMPC (750 or 1,000 mg, bid, or 500 mg, three-times-daily dosing (tid) or four-times-daily dosing (qid) and CAM (200, 400, or 500 mg, bid, 200 mg, tid or 1,000 mg, oid). Although most of the studies used an administration period of 7 days, one used 10 days (Arevalo Galvis et al., 2019), three used 14 days (Liou et al., 2016; Phiphatpatthamaamphan et al., 2016; Chen et al., 2020), one used 7–10 days (Lee et al., 2020) and one used 7–14 days (Prasertpetmanee et al., 2013) (Table 1).
TABLE 1. Characteristics of studies that investigated the H. pylori eradication outcome among CYP2C19 genotypes.
All studies genotyped patients for CYP2C19 variants. Two studies combined the number of CYP2C19 EMs and IMs (Liou et al., 2016; Chen et al., 2020) and one combined the number of IMs and PMs (Shimoyama et al., 2017). The prevalence of CYP2C19 EMs, IMs and PMs was 35.4% (1,357/3,834), 48.0% (1,844/3,838), and 16.6% (633/3,834), respectively.
Meta-Analysis of Eradication Rate of PPI-AMPC-CAM Therapy
All 25 trials were analyzed for the efficacy of the eradication therapy used. The ITT and PP cure rates of the PPI-AMPC-CAM therapy were 79.0% (3,689/4,669, 95% CI 77.8–80.2%) and 84.0% (4,232/5,039, 95% CI 82.9–85.0%), respectively (Table 2). When we divided H. pylori-positive patients by CYP2C19 genotype, the cure rate was 77.7% (1,137/1,464, 95% CI: 75.3–79.6%) in CYP2C19 EMs, 81.2% (1,498/1,844, 95% CI: 79.3–83.0%) in IMs and 86.8% (644/742, 95% CI: 83.9–88.9%) in PMs (Table 2).
TABLE 2. Eradication rates of PPI-amoxicillin-clarithromycin triple therapy among CYP2C19 genotypes.
Meta-analysis showed that the RR of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.21 (95% CI: 1.06–1.39, p = 0.006) and 1.57 (95% CI: 1.27–1.94, p < 0.001) in the fixed-effects model (Figures 1A,B (95% CI: 1.05–1.43, p = 0.010) and 1.44 (95% CI: 1.14–1.81, p = 0.002) in the random-effects model (Supplementary Figure S2A and Supplementary S2B), respectively. The fixed-effects model also showed that there was a significant increase in RR in CYP2C19 IMs compared with PMs (1.27, 95% CI: 1.02–1.56, p = 0.030) (Figure 1C). There was low heterogeneity among the studies (CYP2C19 EMs vs IMs: Chi2 = 24.65, p = 0.26, I2 = 15%; EMs vs PMs: Chi2 = 21.78, p = 0.35, I2 = 8%; and IMs vs PMs: Chi2 = 16.88, p = 0.60, I2 = 0%) (Figure 1). The funnel plots of all included studies showed symmetry between different genotypes (Supplementary Figure S3).
FIGURE 1. Forest plots of H. pylori cure rates of PPI-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes in the fixed-effects model. (A) CYP2C19 EMs vs IMs, (B) EMs vs PMs and (C) IMs and PMs.
Subgroup Analysis of Eradication Rate by Class of PPI
We divided patients based on their use of four PPIs: omeprazole (Dojo et al., 2001; Inaba et al., 2002; Kuwayama et al., 2005; Sheu et al., 2005; Higuchi et al., 2006; Zhang et al., 2010; Chunlertlith et al., 2017; Arevalo Galvis et al., 2019), lansoprazole (Inaba et al., 2002; Isomoto et al., 2003; Kawabata et al., 2003; Miki et al., 2003; Okudaira et al., 2005; Furuta et al., 2007; Hagiwara et al., 2007; Lee et al., 2010; Prasertpetmanee et al., 2013; Liou et al., 2016), rabeprazole (Dojo et al., 2001; Inaba et al., 2002; Kawabata et al., 2003; Miki et al., 2003; Kuwayama et al., 2007; Lee et al., 2010; Zhang et al., 2010; Yang et al., 2015; Phiphatpatthamaamphan et al., 2016; Ozaki et al., 2018; Lee et al., 2020) and esomeprazole (Sheu et al., 2005; Shimoyama et al., 2017; Ozaki et al., 2018) (Table 3). The ITT and PP cure rates of omeprazole-AMPC-CAM therapy were 81.3% (891/1,095, 95% CI: 78.9–83.6%) and 86.1% (961/1,116, 95% CI: 83.9–88.1%), respectively (Table 3). The ITT cure rates of lansoprazole, rabeprazole and esomeprazole were 80.9% (1,235/1,515, 95% CI: 79.5–83.4%), 81.1% (1,485/1,831, 95% CI: 79.2–82.9%) and 80.0% (216/270, 95% CI: 74.7–84.6%), respectively, which were similar among different PPI-containing treatment regimens (p = 0.998) (Table 3).
TABLE 3. Studies that investigated H. pylori eradication outcome among CYP2C19 genotypes.
The cure rates of omeprazole-, lansoprazole-, rabeprazole- and esomeprazole-AMPC-CAM therapy in CYP2C19 EMs were 79.4% (374/469), 73.6% (220/299), 83.4% (547/656) and 77.5% (69/89), respectively (p = 0.696). Those in CYP2C19 PMs were 85.7% (168/196), 91.6% (196/203), 87.0% (215/247) and 88.5% (23/26), respectively (p = 0.972).
Meta-analysis of studies that used omeprazole and lansoprazole as the first-generation PPI showed that the RR of failed eradication in CYP2C19 EMs compared with PMs was 1.66 (95% CI: 1.12–2.46, p = 0.01) and 2.47 (95% CI: 1.44–4.23, p = 0.001), respectively, in the fixed-effects model (Figure 2B, Figure 3B). In contrast, studies that used rabeprazole and esomeprazole showed no significant differences in the RR of failed eradication among the three genotypes (Figures 4, Figure 5). There was low to moderate heterogeneity among these studies (Figures 2–5).
FIGURE 2. Forest plots of H. pylori cure rates of OPZ-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes in the fixed-effects model. (A) CYP2C19 EMs vs IMs, (B) EMs vs PMs and (C) IMs and PMs.; Abbreviations: CI, confidence interval; EM, extensive metabolizer of CYP2C19; IM, intermediate metabolizer of CYP2C19; OPZ, omeprazole; PPI, proton pump inhibitor; PM, poor metabolizer of CYP2C19; PPI, proton pump inhibitor.
FIGURE 3. Forest plots of H. pylori cure rates of LPZ-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes in the fixed-effects model. (A) CYP2C19 EMs vs IMs, (B) EMs vs PMs and (C) IMs and PMs.; Abbreviations: CI, confidence interval; EM, extensive metabolizer of CYP2C19; IM, intermediate metabolizer of CYP2C19; LPZ, lansoprazole; PPI, proton pump inhibitor; PM, poor metabolizer of CYP2C19; PPI, proton pump inhibitor.
FIGURE 4. Forest plots of H. pylori cure rates of RPZ-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes in the fixed-effects model. (A) CYP2C19 EMs vs IMs, (B) EMs vs PMs and (C) IMs and PMs.; Abbreviations: CI, confidence interval; EM, extensive metabolizer of CYP2C19; IM, intermediate metabolizer of CYP2C19; PPI, proton pump inhibitor; PM, poor metabolizer of CYP2C19; PPI, proton pump inhibitor; RPZ, rabeprazole.
FIGURE 5. Forest plots of H. pylori cure rates of EPZ-amoxicillin-clarithromycin regimen among different CYP2C19 genotypes in the fixed-effects model. (A) CYP2C19 EMs vs IMs, (B) EMs vs PMs and (C) IMs and PMs.; Abbreviations: CI, confidence interval; EM, extensive metabolizer of CYP2C19; EPZ, esomeprazole; IM, intermediate metabolizer of CYP2C19; PPI, proton pump inhibitor; PM, poor metabolizer of CYP2C19; PPI, proton pump inhibitor.
Subgroup Analysis of Eradication Rates Between CAM-Sensitive and CAM-Resistant Cases
Sixteen studies (68%, 17/25) reported data on susceptibility to clarithromycin (Inaba et al., 2002; Kawabata et al., 2003; Miki et al., 2003; Take et al., 2003; Kuwayama et al., 2005; Sheu et al., 2005; Higuchi et al., 2006; Furuta et al., 2007; Hagiwara et al., 2007; Kuwayama et al., 2007; Yang et al., 2015; Liou et al., 2016; Phiphatpatthamaamphan et al., 2016; Chunlertlith et al., 2017; Ozaki et al., 2018; Chen et al., 2020) (Supplementary Table S1). Resistance rates to CAM, AMPC and MNZ were 13.1% (372/2,840), 8.9% (109/1,227), and 29.9% (165/552), respectively. Cure rates in patients infected with CAM-sensitive and resistant strains were 89.7% (1787/1992, 95% CI: 88.3–91.0%) and 42.1% (142/337, 95% CI: 36.8–47.6%), respectively.
Subgroup Analysis of Eradication Rates Among Different PPI Dose, Among Different Treatment Duration and Among Different CAM Dose
We divided studies based on their dose of PPIs: standard-dose (omeprazole: 20 mg, lansoprazole: 30 mg, rabeprazole: 10 mg and esomeprazole 20 mg) and double dose (omeprazole: 20 mg, lansoprazole: 60mg, rabeprazole: 20 mg and esomeprazole 40 mg). The cure rates of standard-dose-PPI therapy and double-dose-PPI therapy were 80.6% (1,847/2,292) and 85.2% (901/1,057), respectively (Table 4). Meta-analysis of studies that standard-dose-PPI therapy showed that the RR of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.28 (95% CI: 1.07–1.53) and 1.72 (95% CI: 1.30–2.29), respectively. In contrast, studies that used double-dose-PPI therapy showed no significant differences in the RR of eradication among the three CYP2C19 genotypes (Table 4).
TABLE 4. Effect of CYP2C19 genotypes on the eradication rate of PPI-based triple therapies among different dose of PPI, among different duration of eradication and different dose of CAM.
We divided studies based on their treatment duration: 7 days and 10–14 days. The cure rates of 7-days therapy and 10–14 days therapy were 80.3% (2,902/3,615) and 81.5% (349/428), respectively (Table 4). Meta-analysis of studies that 7-days therapy showed that the RR of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.22 (95% CI: 1.06–1.41) and 1.72 (95% CI: 1.29–1.98), respectively. In contrast, studies that used 10–14 days therapy showed no significant differences in the RR of failed eradication among CYP2C19 genotypes.
The cure rates of CAM 400 mg/day therapy and 800–1,000 mg/day therapy were similar [83.1% (654/787) and 80.1% (2,479/3,093), respectively] (Table 4). Meta-analysis of studies that CAM 400 mg/day and 800–1,000 mg/day therapies showed that the RR of failed eradication in CYP2C19 EMs compared with PMs were 2.15 (95% CI: 1.25–3.69) and 1.46 (95% CI: 1.16–1.84), respectively.
Incidence of Adverse Events due to PPI-AMPC-CAM Therapy
All studies reported data on adverse events, namely diarrhea, loose stools, dysgeusia, and abdominal pain (Supplementary Table S2). The incidence of adverse events due to PPI-AMPC-CAM therapy was 38.1% (1,175/3,084, 95% CI: 36.4–39.8%) (Supplementary Table S2).
Discussion
This meta-analysis included 25 RCTs from 24 Asian and 1 South American country to re-evaluate the association between the cure rate of first-line PPI-AMPC-CAM triple H. pylori eradication therapy and CYP2C19 genotype. Of a total of 5,318 patients with resistance rates of 13.1% for CAM and 8.9% for AMPC, the overall cure rate in ITT analysis was 79.0% (95% CI: 77.8–80.2%). Meta-analysis indicated that cure rates significantly differed among CYP2C19 genotypes, and the RR of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.21 (95% CI: 1.06–1.39) and 1.57 (95% CI: 1.27–1.94), respectively, in the fixed-effects model. In addition, although sub-analysis of studies that used omeprazole and lansoprazole showed that the RR in CYP2C19 EMs compared with PMs was 1.66 (95% CI: 1.12–2.46) and 2.47 (95% CI: 1.44–4.23), there were no significant differences in RR in studies that used rabeprazole and esomeprazole among genotypes. These results suggest that when PPI-containing triple regimen is selected at the eradication therapy for H. pylori infection, second-generation PPI or high-dose of first-generation PPI should be used with triple therapy, especially in Asian populations.
Acid Inhibition and H. pylori Eradication Therapy
An optimal intragastric pH during prolonged potent acid inhibition in the stomach increases the stability and bioavailability of acid-sensitive antibacterial agents (e.g., CAM and AMPC) (Grayson et al., 1989; Hunt, 1993). This in turn leads to an increase in the gastric mucosal concentration of antimicrobial agents and exhibits antibacterial effects (Grayson et al., 1989; Goddard et al., 1996; Scott et al., 1998). In addition, acid inhibition increases the susceptibility of H. pylori to antimicrobial agents (Scott et al., 1998). Therefore, rapid, potent and prolonged neutralization of pH after optimal PPI treatment is required to cure H. pylori infection and increases eradication rate. We previously showed, using a PPI/AMPC/CAM regimen, that the median 24-h pH during eradication therapy was higher (6.4) and the median pH < 4 holding time ratio (HTR) (0.5%) was shorter in patients who experienced successful eradication than those who experienced failed eradication (pH 5.2 and pH < 4 HTR 26.7%) (Sugimoto et al., 2007). Because the degree and duration of acid inhibition correlates with the cure rate, pH > 4 should be maintained for 24 h, and a target pH higher than 6.0 is needed for acid inhibition to cure patients using PPI/AMPC/CAM therapy, irrespective with infection of CAM-resistant strain.
A critical subsequent question then becomes: how do we plan treatment using acid inhibitory drugs to achieve this target pH for acid inhibition? Controlling pH with PPIs depends on the dosing schedule, dose, and a combination of acid inhibitors (Shirai et al., 2001; Shirai et al., 2002; Sugimoto et al., 2004; Sugimoto et al., 2005; Sugimoto et al., 2012). Further, polymorphisms in genes encoding drug-metabolizing enzymes and drug transporters such as CYP2C19 and multidrug resistance protein-1 (ABCB1) affect pH during treatment (Furuta et al., 1999; Shirai et al., 2001; Shirai et al., 2002; Sugimoto et al., 2004; Sugimoto et al., 2005; Kodaira et al., 2009; Sugimoto et al., 2012). In general, the pharmacokinetics and pharmacodynamics of PPIs significantly differ among CYP2C19 genotypes. A previous meta-analysis reported significantly different cure rates of PPI therapy in patients with gastroesophageal reflux disease, a major acid-related disease, with different CYP2C19 genotypes (ITT analysis: EMs, 52.2%; IMs, 56.7%; PMs, 61.3%; p = 0.047), and that CYP2C19 EMs had an increased risk of being refractory to PPI therapy compared to PMs (OR: 1.661, 95% CI 1.023–2.659, p = 0.040) (Ichikawa et al., 2016). Therefore, it is necessary to note that some patients who become resistant to PPI treatment may be CYP2C19 EMs. It may be possible to overcome this disadvantage of genetic variations affecting response to PPIs by using frequent dosing of PPIs, which has been shown to be more efficacious for acid inhibition through 24 h than a one-time increase in dose (Furuta et al., 2001c; Sugimoto et al., 2004; Lou et al., 2009). This phenomenon is due to the fact that frequent dosing sustains plasma levels of PPIs through a 24-h period and continues to inactivate H+, K+-ATPase consistently for 24 h (Furuta et al., 2001c; Sugimoto et al., 2004; Lou et al., 2009). However, because acid inhibition by omeprazole, lansoprazole, rabeprazole and esomeprazole bid in CYP2C19 EMs is 5.0 (2.4–5.9), 4.7 (3.7–5.5), 4.8 (2.5–6.4) and 5.4 (3.5–6.8) (Sahara et al., 2013), respectively, maintaining acid secretion for 24 h in all patients may be difficult. In fact, a previous meta-analysis conducted in 2013 showed that CYP2C19 EM is a risk factor for eradication (Tang et al., 2013). In the present study, we re-evaluated the effect of CYP2C19 genotype on the cure rate of first-line PPI-AMPC-CAM eradication therapy by analyzing RCTs written in English and demonstrated that the cure rate was 77.7% in CYP2C19 EMs, 81.2% in IMs and 86.8% in PMs, and that the RR of failed eradication in CYP2C19 EMs compared with IMs and PMs was 1.21 and 1.57, respectively. Because the incidence rates of antimicrobial resistance change year-by-year, determining the antibiotic susceptibility of H. pylori using either culture or genetic testing or both is of great importance, particularly in populations with a high rate of drug-resistant strains. Therefore, we think our finding that CYP2C19 genotype has a major effect on patients’ response to first-line PPI-AMPC-CAM therapy has great clinical relevance.
In 2015, the potassium-competitive acid blocker, vonoprazan, became clinically available in Japan. Vonoprazan competitively inhibits H+/K+-ATPase activity more firstly and potently than PPIs (Kagami et al., 2016). Therefore, a vonoprazan-containing eradication regimen is expected to increase the eradication rate compared with PPI-containing conventional regimens. In fact, a recent meta-analysis that investigated the efficacy of first-line eradication therapy showed that a vonoprazan-containing regimen achieved a higher eradication rate than a PPI-containing regimen (88.1% (95%CI: 86.1–89.9%) in the vonoprazan therapy and 72.8% (95%CI: 71.0–75.4%) in PPI therapy) (Jung et al., 2017; Sugimoto and Yamaoka, 2018). Because eradication rate for patients infected with CAM-sensitive strain is similar between vonoprazan and PPI, a benefit by vonoprazan-induced potent acid inhibition may play in patients infected with CAM-resistance strain. Therefore, as the first-line standard treatment for H. pylori eradication in Japan, a vonoprazan-containing regimen is selected. However, there is no study to investigate the efficacy and safety of vonoprazan-AMPC-CAM therapy among CYP2C19 genotypes by the RCT. Further trials should be planned to clarify association with vonoprazan and CYP2C19 genotypes and association with PPI/vonoprazan and other genetic variation including CYP3A4 (Sugimoto et al., 2020).
Class of PPI and H. pylori Eradication Therapy
PPIs can be divided into first generation (e.g., omeprazole and lansoprazole) and second generation (e.g., rabeprazole and esomeprazole), which differ in the degree to which they are metabolized by CYP2C19. Rabeprazole is metabolized to thioether-rabeprazole mainly via a non-enzymatic pathway, with minor contribution from CYP2C19 (Yasuda et al., 1995). Esomeprazole is a pure S-isomer of omeprazole and interindividual variations in plasma concentrations of the S-isomer are lower than those in the R-isomer. In this meta-analysis, we found that the cure rates of omeprazole-, lansoprazole-, rabeprazole- and esomeprazole-AMPC-CAM therapy were similar. However, for first-generation PPIs, the RR of failed eradication in CYP2C19 EMs compared with PMs was 1.66 (95% CI 1.12–2.46) for omeprazole and 2.47 (1.44–4.23) for lansoprazole. In contrast, there were no significant differences in cure rates of regimen using second-generation PPIs among genotypes. In addition, because second generation PPIs are more effective for eradication therapy than first generation PPIs, second-generation PPIs or vonoprazan should be selected to ensure high efficacy in all patients, irrespective of CYP2C19 genotype.
CAM Resistance and H. pylori Eradication Therapy
There is growing evidence that the cure rate of PPI-AMPC-CAM regimen decreases with an increase in CAM-resistant strains, and recent rates of CAM-resistant strains in Japan and Europe have exceeded 35 and 20%, respectively (Furuta et al., 2001a; Asaka et al., 2001; Murakami et al., 2002; Megraud, 2007). Although previous studies have reported that cure rates in patients infected with CAM-resistant strains have markedly decreased to 20–40% (Fischbach and Evans, 2007; Megraud, 2007), this meta-analysis obtained cure rates of 89.7% (95% CI 88.3–91.0%) and 42.1% (95% CI 36.8–47.6%) in patients infected with CAM-sensitive and resistant strains, respectively. The Maastricht V/Florence Consensus Report recommends first-line therapy using a CAM-containing regimen with PPI/AMPC or PPI/MNZ and an alternative treatment using bismuth-containing quadruple treatment in areas with low prevalence of CAM-resistant strains or bismuth or non-bismuth quadruple treatment and concomitant therapies in areas with high (>15%) CAM resistance (Malfertheiner et al., 2017). This indicates the need to carefully select antimicrobial agents and/or regimens based on individual’s antibiotic resistance to H. pylori and/or known regional characteristics.
Recent studies have demonstrated the efficacy of tailored treatment based on sensitivity to CAM, with eradication rates exceeding 90% (Furuta et al., 2007; Kawai et al., 2008; Sugimoto et al., 2014). Although it is unfeasible to provide tailored treatment based on sensitivity to CAM to all patients with H. pylori infection or all areas/populations around the world due to limitations in culture testing and PCR in clinical practice, tailored treatment based on sensitivity to CAM should be considered in areas with a high incidence rate of CAM-resistant H. pylori.
Because eradication rate for patients infected with CAM-sensitive strain is similar between vonoprazan and PPI (Jung et al., 2017; Sugimoto and Yamaoka, 2018), insufficient acid inhibition by PPI in CYP2C19 EMs may reduce eradication rate for CAM-resistance H. pylori strain. Therefore, different efficacy among CYP2C19 genotypes shown by our meta-analysis may depends on rate of CAM-resistance strain in each study. This observation will support hypothesis that potent acid inhibition (e.g., PPI high-dose, PPI qid with high adherence, vonoprazan and tailored PPI therapy based on CYP2C19 genotype) is important to be high eradication rate in patients infected with CAM-resistant strain (Furuta et al., 2007; Sugimoto et al., 2014). In fact, despite the dual therapy of vonoprazan/AMPC, it was reported to show a high eradication rate in patients infected with CAM-resistant strain (Suzuki et al., 2020). Although this observation suggests that when vonoprazan and AMPC are selected for eradication therapy, CAM may be unnecessary. Therefore, we think that culture test and susceptibility-based treatment provides best outcome for H. pylori eradication therapy. Although potency of PPI differs among kind of PPIs and resistant rate to CYP2C19 differs among kind of PPIs, acid inhibition by PPI also depends on the dosing schedule (oid, bid and qid) and dose. Therefore, I should be evaluated to determine optimal eradication regimen by combined analysis with various factors (dosing schedule, dose, genetic factor, potency, and generation) that affect intragastric pH at the time of PPI administration, as further study.
Limitations
This meta-analysis has a few limitations. First, there is a possibility of selection bias due to the exclusion of studies published in languages other than English, those with abstracts alone and studies that used non-RCT designs. Second, only one RCT has examined the association of CYP2C19 genotype with cure rate outside of East Asia. Third, the small sample size may have affected the statistical power of sub-group analyses. Because background (e.g., race and sex), treatment (e.g., class of PPI, regimen, dose of PPI, kinds of antimicrobial agents) and bacterial factors (e.g., resistance to antimicrobial agents and virulence factors) are associated with the outcome of eradication therapy, future meta-analyses of a larger number of RCTs should account for these factors to gain a clearer understanding of the association of cure rate with CYP2C19 genotype. Forth, because there were a few reports investigating effect of CYP2C19 genotype between clarithromycin-sensitive and resistant strain, we cannot meta-analyze associations in this time.
Conclusion
Cure rates of first-line PPI-AMPC-CAM eradication therapy differ among CYP2C19 genotypes, especially in Asian populations. This meta-analysis suggest that PPI-AMPC-CAM therapy has the potential to eradicate H. pylori infection in >85% of CYP2C19 PMs, but a low proportion of CYP2C19 EMs. Thus, the cure rate of this regimen in CYP2C19 EMs may be insufficient to eradicate H. pylori infection. Therefore, genotyping patients for CYP2C19 variants before eradication therapy may help to achieve higher eradication rates. To receive eradication rate >90% is important in clinical practice (Graham et al., 2007). However, most of regimen cannot reach to this goal, due to insufficient acid inhibition during treatment and susceptibility to antimicrobial agents. Therefore, second generation PPI-high-dose, high-frequent (qid) or vonoprazan-containing tailored treatment based on susceptibility to antimicrobial agents may optimal to ignore CYP2C19 genotype status and to receive high eradication rate.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Author Contributions
Conception and design: MS; acquisition of data: MS and YM; analysis and interpretation of data: MS and YM; drafting of the manuscript: MS and YM; critical revision of the manuscript: YM, MS, NN, RN, EI, MH, YK, HT and TK; statistical analysis: MS and YM; and study supervision: HT, TK. All authors listed have contributed substantially to the design, data collection and analysis, and editing of the manuscript.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
We thank HT and Guy Harris DO from DMC Corp. (www.dmed.co.jp <http://www.dmed.co.jp/>) for editing drafts of this manuscript.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2021.759249/full#supplementary-material
Abbreviations
CI, confidence interval; EM, extensive metabolizer of CYP2C19; IM, intermediate metabolizer of CYP2C19; PPI, proton pump inhibitor; PM, poor metabolizer of CYP2C19; PPI, proton pump inhibitor.
References
Arévalo Galvis, A., Trespalacios Rangel, A. A., and Otero Regino, W. (2019). Personalized Therapy for Helicobacter pylori: CYP2C19 Genotype Effect on First-Line Triple Therapy. Helicobacter 24 (3), e12574. doi:10.1111/hel.12574
Asaka, M., Sugiyama, T., Kato, M., Satoh, K., Kuwayama, H., Fukuda, Y., et al. (2001). A Multicenter, Double-Blind Study on Triple Therapy with Lansoprazole, Amoxicillin and Clarithromycin for Eradication of Helicobacter pylori in Japanese Peptic Ulcer Patients. Helicobacter 6 (3), 254–261. doi:10.1046/j.1523-5378.2001.00037.x
Chang, M., Dahl, M. L., Tybring, G., Götharson, E., and Bertilsson, L. (1995a). Use of Omeprazole as a Probe Drug for CYP2C19 Phenotype in Swedish Caucasians: Comparison with S-Mephenytoin Hydroxylation Phenotype and CYP2C19 Genotype. Pharmacogenetics 5 (6), 358–363. doi:10.1097/00008571-199512000-00004
Chang, M., Tybring, G., Dahl, M. L., Götharson, E., Sagar, M., Seensalu, R., et al. (1995b). Interphenotype Differences in Disposition and Effect on Gastrin Levels of Omeprazole-Ssuitability of Omeprazole as a Probe for CYP2C19. Br. J. Clin. Pharmacol. 39 (5), 511–518. doi:10.1111/j.1365-2125.1995.tb04488.x
Chen, C. C., Luo, J. C., Fang, Y. J., Lee, J. Y., Kuo, C. C., Yang, T. H., et al. (2020). Comparison of the Effect of Clarithromycin Triple Therapy with or without N-Acetylcysteine in the Eradication of Helicobacter pylori: a Randomized Controlled Trial. Therap Adv. Gastroenterol. 13, 1756284820927306. doi:10.1177/1756284820927306
Chunlertlith, K., Limpapanasit, U., Mairiang, P., Vannaprasaht, S., Tassaneeyakul, W., Sangchan, A., et al. (2017). Outcomes of a Randomized Controlled Trial Comparing Modified High Dose Omeprazole and Amoxicillin Triple Therapy with Standard Triple Therapy for Helicobacter Pylori Eradication. Asian Pac. J. Cancer Prev. 18 (4), 927–932. doi:10.22034/APJCP.2017.18.4.927
Dojo, M., Azuma, T., Saito, T., Ohtani, M., Muramatsu, A., and Kuriyama, M. (2001). Effects of CYP2C19 Gene Polymorphism on Cure Rates for Helicobacter pylori Infection by Triple Therapy with Proton Pump Inhibitor (Omeprazole or Rabeprazole), Amoxycillin and Clarithromycin in Japan. Dig. Liver Dis. 33 (8), 671–675. doi:10.1016/s1590-8658(01)80043-8
Fischbach, L., and Evans, E. L. (2007). Meta-analysis: the Effect of Antibiotic Resistance Status on the Efficacy of Triple and Quadruple First-Line Therapies for Helicobacter pylori. Aliment. Pharmacol. Ther. 26 (3), 343–357. doi:10.1111/j.1365-2036.2007.03386.x
Furuta, T., Ohashi, K., Kosuge, K., Zhao, X. J., Takashima, M., Kimura, M., et al. (1999). CYP2C19 Genotype Status and Effect of Omeprazole on Intragastric pH in Humans. Clin. Pharmacol. Ther. 65 (5), 552–561. doi:10.1016/S0009-9236(99)70075-5
Furuta, T., Shirai, N., Kodaira, M., Sugimoto, M., Nogaki, A., Kuriyama, S., et al. (2007). Pharmacogenomics-based Tailored versus Standard Therapeutic Regimen for Eradication of H. pylori. Clin. Pharmacol. Ther. 81 (4), 521–528. doi:10.1038/sj.clpt.6100043
Furuta, T., Shirai, N., Takashima, M., Xiao, F., Hanai, H., Nakagawa, K., et al. (2001a). Effects of Genotypic Differences in CYP2C19 Status on Cure Rates for Helicobacter pylori Infection by Dual Therapy with Rabeprazole Plus Amoxicillin. Pharmacogenetics 11 (4), 341–348. doi:10.1097/00008571-200106000-00009
Furuta, T., Shirai, N., Takashima, M., Xiao, F., Hanai, H., Sugimura, H., et al. (2001b). Effect of Genotypic Differences in CYP2C19 on Cure Rates for Helicobacter pylori Infection by Triple Therapy with a Proton Pump Inhibitor, Amoxicillin, and Clarithromycin. Clin. Pharmacol. Ther. 69 (3), 158–168. doi:10.1067/mcp.2001.113959
Furuta, T., Shirai, N., Xiao, F., Ohashi, K., and Ishizaki, T. (2001c). Effect of High-Dose Lansoprazole on Intragastic pH in Subjects Who Are Homozygous Extensive Metabolizers of Cytochrome P4502C19. Clin. Pharmacol. Ther. 70 (5), 484–492. doi:10.1067/mcp.2001.119721
Goddard, A. F., Jessa, M. J., Barrett, D. A., Shaw, P. N., Idström, J. P., Cederberg, C., et al. (1996). Effect of Omeprazole on the Distribution of Metronidazole, Amoxicillin, and Clarithromycin in Human Gastric Juice. Gastroenterology 111 (2), 358–367. doi:10.1053/gast.1996.v111.pm8690200
Graham, D. Y., Lu, H., and Yamaoka, Y. (2007). A Report Card to Grade Helicobacter pylori Therapy. Helicobacter 12 (4), 275–278. doi:10.1111/j.1523-5378.2007.00518.x
Grayson, M. L., Eliopoulos, G. M., Ferraro, M. J., and Moellering, R. C. (1989). Effect of Varying pH on the Susceptibility of Campylobacter pylori to Antimicrobial Agents. Eur. J. Clin. Microbiol. Infect. Dis. 8 (10), 888–889. doi:10.1007/BF01963775
Hagiwara, T., Kato, M., Anbo, T., Imamura, A., Suga, T., Uchida, T., et al. (2007). Improvement in Symptoms after H2-Receptor Antagonist-Based Therapy for Eradication of H Pylori Infection. World J. Gastroenterol. 13 (28), 3836–3840. doi:10.3748/wjg.v13.i28.3836
Higuchi, K., Maekawa, T., Nakagawa, K., Chouno, S., Hayakumo, T., Tomono, N., et al. (2006). Efficacy and Safety of Helicobacter pylori Eradication Therapy with Omeprazole, Amoxicillin and High- and Low-Dose Clarithromycin in Japanese Patients: a Randomised, Double-Blind, Multicentre Study. Clin. Drug Investig. 26 (7), 403–414. doi:10.2165/00044011-200626070-00002
Hunt, R. H. (1993). pH and Hp-Ggastric Acid Secretion and Helicobacter pylori: Implications for Ulcer Healing and Eradication of the Organism. Am. J. Gastroenterol. 88 (4), 481–483.
Ichikawa, H., Sugimoto, M., Sugimoto, K., Andoh, A., and Furuta, T. (2016). Rapid Metabolizer Genotype of CYP2C19 Is a Risk Factor of Being Refractory to Proton Pump Inhibitor Therapy for Reflux Esophagitis. J. Gastroenterol. Hepatol. 31 (4), 716–726. doi:10.1111/jgh.13233
Inaba, T., Mizuno, M., Kawai, K., Yokota, K., Oguma, K., Miyoshi, M., et al. (2002). Randomized Open Trial for Comparison of Proton Pump Inhibitors in Triple Therapy for Helicobacter pylori Infection in Relation to CYP2C19 Genotype. J. Gastroenterol. Hepatol. 17 (7), 748–753. doi:10.1046/j.1440-1746.2002.02790.x
Ishizaki, T., and Horai, Y. (1999). Review Article: Cytochrome P450 and the Metabolism of Proton Pump Inhibitors-Eemphasis on Rabeprazole. Aliment. Pharmacol. Ther. 13 (Suppl. 3), 27–36. doi:10.1046/j.1365-2036.1999.00022.x
Isomoto, H., Inoue, K., Furusu, H., Enjoji, A., Fujimoto, C., Yamakawa, M., et al. (2003). High-dose Rabeprazole-Amoxicillin versus Rabeprazole-Amoxicillin-Metronidazole as Second-Line Treatment after Failure of the Japanese Standard Regimen for Helicobacter pylori Infection. Aliment. Pharmacol. Ther. 18 (1), 101–107. doi:10.1046/j.1365-2036.2003.01659.x
Jung, Y. S., Kim, E. H., and Park, C. H. (2017). Systematic Review with Meta-Analysis: the Efficacy of Vonoprazan-Based Triple Therapy on Helicobacter pylori Eradication. Aliment. Pharmacol. Ther. 46 (2), 106–114. doi:10.1111/apt.14130
Kagami, T., Sahara, S., Ichikawa, H., Uotani, T., Yamade, M., Sugimoto, M., et al. (2016). Potent Acid Inhibition by Vonoprazan in Comparison with Esomeprazole, with Reference to CYP2C19 Genotype. Aliment. Pharmacol. Ther. 43 (10), 1048–1059. doi:10.1111/apt.13588
Kato, M., Ota, H., Okuda, M., Kikuchi, S., Satoh, K., Shimoyama, T., et al. (2019). Guidelines for the Management of Helicobacter pylori Infection in Japan: 2016 Revised Edition. Helicobacter 24 (4), e12597. doi:10.1111/hel.12597
Kawabata, H., Habu, Y., Tomioka, H., Kutsumi, H., Kobayashi, M., Oyasu, K., et al. (2003). Effect of Different Proton Pump Inhibitors, Differences in CYP2C19 Genotype and Antibiotic Resistance on the Eradication Rate of Helicobacter pylori Infection by a 1-week Regimen of Proton Pump Inhibitor, Amoxicillin and Clarithromycin. Aliment. Pharmacol. Ther. 17 (2), 259–264. doi:10.1046/j.1365-2036.2003.01406.x
Kawai, T., Yamagishi, T., Yagi, K., Kataoka, M., Kawakami, K., Sofuni, A., et al. (2008). Tailored Eradication Therapy Based on Fecal Helicobacter pylori Clarithromycin Sensitivities. J. Gastroenterol. Hepatol. 23 (Suppl. 2), S171–S174. doi:10.1111/j.1440-1746.2008.05408.x
Kodaira, C., Sugimoto, M., Nishino, M., Yamade, M., Shirai, N., Uchida, S., et al. (2009). Effect of MDR1 C3435T Polymorphism on Lansoprazole in Healthy Japanese Subjects. Eur. J. Clin. Pharmacol. 65 (6), 593–600. doi:10.1007/s00228-009-0625-8
Kubota, T., Chiba, K., and Ishizaki, T. (1996). Genotyping of S-Mephenytoin 4'-hydroxylation in an Extended Japanese Population. Clin. Pharmacol. Ther. 60 (6), 661–666. doi:10.1016/S0009-9236(96)90214-3
Kuwayama, H., Asaka, M., Sugiyama, T., Fukuda, Y., Aoyama, N., Hirai, Y., et al. (2007). Rabeprazole-based Eradication Therapy for Helicobacter pylori: a Large-Scale Study in Japan. Aliment. Pharmacol. Ther. 25 (9), 1105–1113. doi:10.1111/j.1365-2036.2007.03298.x
Kuwayama, H., Luk, G., Yoshida, S., Nakamura, T., Kubo, M., Uemura, N., et al. (2005). Efficacy of a Low-Dose Omeprazole-Based Triple-Therapy Regimen for Helicobacter pylori Eradication Independent of Cytochrome P450 Genotype : The Japanese MACH Study. Clin. Drug Investig. 25 (5), 293–305. doi:10.2165/00044011-200525050-00002
Lee, J. H., Jung, H. Y., Choi, K. D., Song, H. J., Lee, G. H., and Kim, J. H. (2010). The Influence of CYP2C19 Polymorphism on Eradication of Helicobacter pylori: A Prospective Randomized Study of Lansoprazole and Rabeprazole. Gut Liver 4 (2), 201–206. doi:10.5009/gnl.2010.4.2.201
Lee, S. W., Moon, S. J., Kim, S. H., Jung, S. H., Song, K. H., Kim, S. M., et al. (2020). The Prolongation Effect of Ilaprazole-Based Standard Triple Therapy for Helicobacter pylori. Medicine (Baltimore) 99 (38), e22137. doi:10.1097/MD.0000000000022137
Liou, J. M., Chen, C. C., Chang, C. Y., Chen, M. J., Chen, C. C., Fang, Y. J., et al. (2016). Sequential Therapy for 10 Days versus Triple Therapy for 14 Days in the Eradication of Helicobacter pylori in the Community and Hospital Populations: a Randomised Trial. Gut 65 (11), 1784–1792. doi:10.1136/gutjnl-2015-310142
Lou, H. Y., Chang, C. C., Sheu, M. T., Chen, Y. C., and Ho, H. O. (2009). Optimal Dose Regimens of Esomeprazole for Gastric Acid Suppression with Minimal Influence of the CYP2C19 Polymorphism. Eur. J. Clin. Pharmacol. 65 (1), 55–64. doi:10.1007/s00228-008-0552-0
Malfertheiner, P., Megraud, F., O'Morain, C. A., Gisbert, J. P., Kuipers, E. J., Axon, A. T., et al. (2017). Management of Helicobacter pylori Infection-The Maastricht V/Florence Consensus Report. Gut 66 (1), 6–30. doi:10.1136/gutjnl-2016-312288
Megraud, F. (2007). Helicobacter pylori and Antibiotic Resistance. Gut 56 (11), 1502. doi:10.1136/gut.2007.132514
Miki, I., Aoyama, N., Sakai, T., Shirasaka, D., Wambura, C. M., Maekawa, S., et al. (2003). Impact of Clarithromycin Resistance and CYP2C19 Genetic Polymorphism on Treatment Efficacy of Helicobacter pylori Infection with Lansoprazole- or Rabeprazole-Based Triple Therapy in Japan. Eur. J. Gastroenterol. Hepatol. 15 (1), 27–33. doi:10.1097/00042737-200301000-00006
Murakami, K., Sato, R., Okimoto, T., Nasu, M., Fujioka, T., Kodama, M., et al. (2002). Eradication Rates of Clarithromycin-Resistant Helicobacter pylori Using Either Rabeprazole or Lansoprazole Plus Amoxicillin and Clarithromycin. Aliment. Pharmacol. Ther. 16 (11), 1933–1938. doi:10.1046/j.1365-2036.2002.01368.x
Okudaira, K., Furuta, T., Shirai, N., Sugimoto, M., and Miura, S. (2005). Concomitant Dosing of Famotidine with a Triple Therapy Increases the Cure Rates of Helicobacter pylori Infections in Patients with the Homozygous Extensive Metabolizer Genotype of CYP2C19. Aliment. Pharmacol. Ther. 21 (4), 491–497. doi:10.1111/j.1365-2036.2005.02353.x
Ozaki, H., Harada, S., Takeuchi, T., Kawaguchi, S., Takahashi, Y., Kojima, Y., et al. (2018). Vonoprazan, a Novel Potassium-Competitive Acid Blocker, Should Be Used for the Helicobacter pylori Eradication Therapy as First Choice: A Large Sample Study of Vonoprazan in Real World Compared with Our Randomized Control Trial Using Second-Generation Proton Pump Inhibitors for Helicobacter pylori Eradication Therapy. Digestion 97 (3), 212–218. doi:10.1159/000485097
Phiphatpatthamaamphan, K., Vilaichone, R. K., Siramolpiwat, S., Tangaroonsanti, A., Chonprasertsuk, S., Bhanthumkomol, P., et al. (2016). Effect of IL-1 Polymorphisms, CYP2C19 Genotype and Antibiotic Resistance on Helicobacter pylori Eradication Comparing between 10-day Sequential Therapy and 14-day Standard Triple Therapy with Four-Times-Daily-Dosing of Amoxicillin in Thailand: a Prospective Randomized Study. Asian Pac. J. Cancer Prev. 17 (4), 1903–1907. doi:10.7314/apjcp.2016.17.4.1903
Prasertpetmanee, S., Mahachai, V., and Vilaichone, R. K. (2013). Improved Efficacy of Proton Pump Inhibitor - Amoxicillin - Clarithromycin Triple Therapy for Helicobacter pylori Eradication in Low Clarithromycin Resistance Areas or for Tailored Therapy. Helicobacter 18 (4), 270–273. doi:10.1111/hel.12041
Sahara, S., Sugimoto, M., Uotani, T., Ichikawa, H., Yamade, M., Iwaizumi, M., et al. (2013). Twice-daily Dosing of Esomeprazole Effectively Inhibits Acid Secretion in CYP2C19 Rapid Metabolisers Compared with Twice-Daily Omeprazole, Rabeprazole or Lansoprazole. Aliment. Pharmacol. Ther. 38 (9), 1129–1137. doi:10.1111/apt.12492
Scott, D., Weeks, D., Melchers, K., and Sachs, G. (1998). The Life and Death of Helicobacter pylori. Gut 43 Suppl 1 (Suppl. 1), S56–S60. doi:10.1136/gut.43.2008.s56
Sheu, B. S., Kao, A. W., Cheng, H. C., Hunag, S. F., Chen, T. W., Lu, C. C., et al. (2005). Esomeprazole 40 Mg Twice Daily in Triple Therapy and the Efficacy of Helicobacter pylori Eradication Related to CYP2C19 Metabolism. Aliment. Pharmacol. Ther. 21 (3), 283–288. doi:10.1111/j.1365-2036.2005.02281.x
Shimoyama, T., Chinda, D., Sawada, Y., Komai, K., Chiba, H., Saito, Y., et al. (2017). Randomized Trial Comparing Esomeprazole and Rabeprazole in First-Line Eradication Therapy for Helicobacter pylori Infection Based on the Serum Levels of Pepsinogens. Intern. Med. 56 (13), 1621–1627. doi:10.2169/internalmedicine.56.7823
Shiota, S., Nguyen, L. T., Murakami, K., Kuroda, A., Mizukami, K., Okimoto, T., et al. (2012). Association of helicobacter Pylori dupA with the Failure of Primary Eradication. J. Clin. Gastroenterol. 46 (4), 297–301. doi:10.1097/MCG.0b013e318243201c
Shirai, N., Furuta, T., Moriyama, Y., Okochi, H., Kobayashi, K., Takashima, M., et al. (2001). Effects of CYP2C19 Genotypic Differences in the Metabolism of Omeprazole and Rabeprazole on Intragastric pH. Aliment. Pharmacol. Ther. 15 (12), 1929–1937. doi:10.1046/j.1365-2036.2001.01108.x
Shirai, N., Furuta, T., Xiao, F., Kajimura, M., Hanai, H., Ohashi, K., et al. (2002). Comparison of Lansoprazole and Famotidine for Gastric Acid Inhibition during the Daytime and Night-Time in Different CYP2C19 Genotype Groups. Aliment. Pharmacol. Ther. 16 (4), 837–846. doi:10.1046/j.1365-2036.2002.01229.x
Sugimoto, M., Furuta, T., Shirai, N., Kajimura, M., Hishida, A., Sakurai, M., et al. (2004). Different Dosage Regimens of Rabeprazole for Nocturnal Gastric Acid Inhibition in Relation to Cytochrome P450 2C19 Genotype Status. Clin. Pharmacol. Ther. 76 (4), 290–301. doi:10.1016/j.clpt.2004.06.008
Sugimoto, M., Furuta, T., Shirai, N., Kodaira, C., Nishino, M., Ikuma, M., et al. (2007). Evidence that the Degree and Duration of Acid Suppression Are Related to Helicobacter pylori Eradication by Triple Therapy. Helicobacter 12 (4), 317–323. doi:10.1111/j.1523-5378.2007.00508.x
Sugimoto, M., Furuta, T., Shirai, N., Nakamura, A., Kajimura, M., Hishida, A., et al. (2005). Comparison of an Increased Dosage Regimen of Rabeprazole versus a Concomitant Dosage Regimen of Famotidine with Rabeprazole for Nocturnal Gastric Acid Inhibition in Relation to Cytochrome P450 2C19 Genotypes. Clin. Pharmacol. Ther. 77 (4), 302–311. doi:10.1016/j.clpt.2004.10.010
Sugimoto, M., Hira, D., Murata, M., Kawai, T., and Terada, T. (2020). Effect of Antibiotic Susceptibility and CYP3A4/5 and CYP2C19 Genotype on the Outcome of Vonoprazan-Containing Helicobacter pylori Eradication Therapy. Antibiotics (Basel) 9 (10). doi:10.3390/antibiotics9100645
Sugimoto, M., Shirai, N., Nishino, M., Kodaira, C., Uotani, T., Yamade, M., et al. (2012). Rabeprazole 10 Mg q.d.S. Decreases 24-h Intragastric Acidity Significantly More Than Rabeprazole 20 Mg b.D. Or 40 Mg o.m., Overcoming CYP2C19 Genotype. Aliment. Pharmacol. Ther. 36 (7), 627–634. doi:10.1111/apt.12014
Sugimoto, M., Uotani, T., Sahara, S., Ichikawa, H., Yamade, M., Sugimoto, K., et al. (2014). Efficacy of Tailored Helicobacter pylori Eradication Treatment Based on Clarithromycin Susceptibility and Maintenance of Acid Secretion. Helicobacter 19 (4), 312–318. doi:10.1111/hel.12128
Sugimoto, M., and Yamaoka, Y. (2018). Role of Vonoprazan in Helicobacter pylori Eradication Therapy in Japan. Front. Pharmacol. 9, 1560. doi:10.3389/fphar.2018.01560
Sugimoto, M., and Yamaoka, Y. (2009). Virulence Factor Genotypes of Helicobacter pylori Affect Cure Rates of Eradication Therapy. Arch. Immunol. Ther. Exp. (Warsz) 57 (1), 45–56. doi:10.1007/s00005-009-0007-z
Suzuki, S., Gotoda, T., Kusano, C., Ikehara, H., Ichijima, R., Ohyauchi, M., et al. (2020). Seven-day Vonoprazan and Low-Dose Amoxicillin Dual Therapy as First-Line Helicobacter pylori Treatment: a Multicentre Randomised Trial in Japan. Gut 69 (6), 1019–1026. doi:10.1136/gutjnl-2019-319954
Take, S., Mizuno, M., Ishiki, K., Nagahara, Y., Yoshida, T., Inaba, T., et al. (2003). Interleukin-1beta Genetic Polymorphism Influences the Effect of Cytochrome P 2C19 Genotype on the Cure Rate of 1-week Triple Therapy for Helicobacter pylori Infection. Am. J. Gastroenterol. 98 (11), 2403–2408. doi:10.1111/j.1572-0241.2003.07707.x
Tang, H. L., Li, Y., Hu, Y. F., Xie, H. G., and Zhai, S. D. (2013). Effects of CYP2C19 Loss-Of-Function Variants on the Eradication of H. pylori Infection in Patients Treated with Proton Pump Inhibitor-Based Triple Therapy Regimens: a Meta-Analysis of Randomized Clinical Trials. PloS one 8 (4), e62162. doi:10.1371/journal.pone.0062162
Yang, J. C., Lin, C. J., Wang, H. L., Chen, J. D., Kao, J. Y., Shun, C. T., et al. (2015). High-dose Dual Therapy Is superior to Standard First-Line or rescue Therapy for Helicobacter pylori Infection. Clin. Gastroenterol. Hepatol. 13 (5), 895–e5. doi:10.1016/j.cgh.2014.10.036
Yasuda, S., Horai, Y., Tomono, Y., Nakai, H., Yamato, C., Manabe, K., et al. (1995). Comparison of the Kinetic Disposition and Metabolism of E3810, a New Proton Pump Inhibitor, and Omeprazole in Relation to S-Mephenytoin 4'-hydroxylation Status. Clin. Pharmacol. Ther. 58 (2), 143–154. doi:10.1016/0009-9236(95)90192-2
Zhang, L., Mei, Q., Li, Q. S., Hu, Y. M., and Xu, J. M. (2010). The Effect of Cytochrome P2C19 and Interleukin-1 Polymorphisms on H. pylori Eradication Rate of 1-week Triple Therapy with Omeprazole or Rabeprazole, Amoxycillin and Clarithromycin in Chinese People. J. Clin. Pharm. Ther. 35 (6), 713–722. doi:10.1111/j.1365-2710.2009.01140.x
Keywords: H. pylori, eradication, CYP2C19, tailored treatment, esomeprazole, rebaprezole
Citation: Morino Y, Sugimoto M, Nagata N, Niikiura R, Iwata E, Hamada M, Kawai Y, Fujimiya T, Takeuchi H, Unezaki S and Kawai T (2021) Influence of Cytochrome P450 2C19 Genotype on Helicobacter pylori Proton Pump Inhibitor-Amoxicillin-Clarithromycin Eradication Therapy: A Meta-Analysis. Front. Pharmacol. 12:759249. doi: 10.3389/fphar.2021.759249
Received: 16 August 2021; Accepted: 16 September 2021;
Published: 15 October 2021.
Edited by:
Ralf Weiskirchen, RWTH Aachen University, GermanyReviewed by:
Yuji Naito, Kyoto Prefectural University of Medicine, JapanDavid Yates Graham, Michael E. DeBakey VA Medical Center, United States
Satoshi Osawa, Hamamatsu University School of Medicine, Japan
Copyright © 2021 Morino, Sugimoto, Nagata, Niikiura, Iwata, Hamada, Kawai, Fujimiya, Takeuchi, Unezaki and Kawai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Mitsushige Sugimoto, c3VnaW1vQHRva3lvLW1lZC5hYy5qcA==