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Article

The Association between ABCB1 C1236T/C3435T SNPs and H. pylori Infection among Jordanians

by
Mohammed N. BaniHani
1,*,
Omar F. Khabour
2,
Karem H. Alzoubi
3,
Nabil A. Bashir
4,
Muhamad Ali K. Shakhatreh
2,
Salsabeel H. Sabi
2 and
Nasr Alrabadi
5
1
Department of General Surgery and Urology, Jordan University of Science and Technology, Irbid 22110, Jordan
2
Department of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan
3
Department of Clinical Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan
4
Department of Physiology and Biochemistry, Jordan University of Science and Technology, Irbid 22110, Jordan
5
Department of Pharmacology, Faculty of Medicine, Jordan University of Science and Technology, Irbid 22110, Jordan
*
Author to whom correspondence should be addressed.
Genes 2020, 11(1), 63; https://doi.org/10.3390/genes11010063
Submission received: 29 November 2019 / Revised: 27 December 2019 / Accepted: 3 January 2020 / Published: 5 January 2020
(This article belongs to the Special Issue Selected Papers From the Advanced Genetics Conference 2019)
Versions Notes

Abstract

:
Infection with Helicobacter pylori (H. pylori) is very common and affecting about 50% of the worldwide population. Several genetic variations have been implicated in determining the clinical susceptibility to this infection. In the current study, we examined the association between C1236T (rs1045642) and C3435T (rs1045642) single nucleotide polymorphisms (SNPs) in the ABCB1 gene and the prevalence of H. pylori infection among Jordanians. A total of 412 subjects (257 H. pylori-positive cases and 155 H. pylori-negative controls) were recruited and participated in the study, and the genotyping of the ABCB1 gene was performed using RFLP-PCR techniques. A significant association was detected between C1236T and H. pylori infection (p < 0.01). The frequency of CT genotype was significantly higher in the positive cases (40.1%) compared to the controls (21.3%). In addition, the C3435T SNP was weakly associated with H. pylori infection (p = 0.077). Haplotype analysis of C1236T and C3435T SNPs showed that the TT haplotype was present in 22.7% of the positive cases compared to 30.7% of the negative controls (p < 0.05, odds ratio = 0.663, 95% CI: (0.483–0.911)). Consequently, the TT haplotype seems to decrease the risk of H. pylori infection. In conclusion, the current results suggest an association between ABCB1 SNPs and H. pylori infection in the Jordanian population.

1. Introduction

H. pylori infection is one of the most common bacterial infections, affecting approximately half of the world population [1,2]. It can cause chronic gastritis, which in turn may be complicated with peptic ulcer disease, lymphoma, and gastric adenocarcinoma [3,4]. The major factor that affects the rates of cure from H. pylori infection is the sufficient inhibition of acid secretion using the anti-secretory agents such as proton pump inhibitors (PPIs) [5,6]. However, the incidence of H. pylori infection and its sufficient eradication using pharmacological therapies are also affected by genetic factors, such as those affecting inflammatory cytokines and variants of the genes encoding drug-metabolizing enzymes and drug transporters [1,7,8].
The multi-drug resistance gene (ABCB1) is a gene that maps to chromosome 7 and encodes for P-glycoprotein (P-gp), which is a large transmembrane protein of 170 Kd and functions as an ATP-dependent efflux pump [9]. The gene is also highly expressed in normal tissues such as brain, liver, kidney, lymphocytes, placenta, gut, and testes [10]. P-gp plays an important role in regulating absorption, distribution, and the elimination of drugs [11]. ABCB1 has also been found to mediate the energy-dependent efflux of xenobiotics in epithelial tissues throughout the human body [12]. On the other hand, the expression of the ABCB1 gene is highly variable among subjects of the same and different races, and many variants have been identified in its genetic sequence [9].
Several studies have investigated the relationship between ABCB1 polymorphisms and H. pylori infection [13,14,15]. For instance, two Australian studies showed a strong association between them [16,17]. In other studies from Japan, the methylation status of the ABCB1 gene was found to be strongly associated with H. pylori infection and gastric cancer [18,19]. In addition, ABCB1 polymorphisms were found to be associated with gastric cancer and were identified as one of the determinants for the successful eradication of H. pylori using triple therapy with lansoprazole, amoxicillin, and clarithromycin [20]. Similar findings were reported in a study that was conducted on Polish patients [21]. However, reports on the association between ABCB1 polymorphisms and H. pylori infection from Arabic populations are still lacking. Therefore, in the current investigation, the association between ABCB1 polymorphisms (C1236T: rs1045642 and C3435T: rs1045642) and H. pylori infection was examined.

2. Materials and Methods

The study was first approved by the Institutional Review Board of Jordan University of Science and Technology (approval number: 16/6/4/3141, date: 18-10-2017). Patients (>18 years old) who were scheduled to undergo a gastroscopic examination at King Abdullah University Hospital (KAUH) were invited to participate in the study. Recruitments were from September 2017 to July 2019. All participants gave informed consent after a full explanation of the study objectives and procedures. Patients diagnosed with non-ulcer dyspepsia as established during gastroscopy with normal findings or mild gastritis were included in the study. On the other hand, patients with a history of gastric surgery or those who were taking medications in the preceding four weeks (such as anticoagulants, antibiotics, and proton pump inhibitors) were excluded from the study [22,23]. Participants’ demographics such as age, gender, height, and weight were collected using a structured questionnaire, and their clinical history was obtained from their medical files and records.

2.1. Diagnosis of H. pylori Infection

The diagnosis of H. pylori infection was performed using biopsy samples from gastric antrum. Biopsy sampling is a routine part of the standard diagnostic procedure for those patients who undergo gastroscopic examination at KAUH. Those samples from the gastric antrum were subjected to further laboratory testing (see below) for the diagnosis of H. pylori infection [24]. Those patients with positive tests were considered the positive cases, and those with negative tests were considered the negative controls.

2.2. Isolation of Genomic DNA

Blood samples for genomic DNA isolation were obtained in EDTA tubes. The DNA was extracted using a Promega blood kit (Madison, WI, USA) according to the manufacturer’s instructions [25,26]. Concentration of the extracted DNA was measured using a Bio-Rad SmartSpect_3000 device (Hertfordshire, UK), and the isolated DNA was stored at room temperature (20 °C) until used.

2.3. Genotyping of ABCB1 Polymorphisms

Two common polymorphisms in the ABCB1 gene—C1236T and C3435T—were genotyped. The polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) assay was used for genotyping. PCR conditions, primer sequences, and restriction assays were conducted similar to what has been described in our previous work [27]. Restricted fragments were visualized using 2% agarose gel for both polymorphisms. All gels were documented using a Bio-Rad gel documentation system (Gel Doc 2000, Hercules, CA, USA).

2.4. Statistical Analysis

Data were analyzed using the SPSS package version for windows. Data were expressed as continuous variables (mean ± standard deviation) and discrete variables (counts and frequencies), and were compared using the chi square test. Association between examined SNPs and H. pylori infection was calculated using the SNPStats website (https://www.snpstats.net/start.htm). Three-locus haplotype frequencies were calculated using the SHEsis program. Power analysis was carried out using G*Power version 3.0.10 (Franz Faul, Universität Kiel, Kiel, Germany). Genotype distributions were analyzed for Hardy–Weinberg equilibrium. A p-value <0.05 was considered significant.

3. Results

A total of 412 subjects who agreed to participate in the study and who were referred for a gastroscopic examination as part of the diagnosis for H. pylori infection were included. After complete diagnosis of the patients using a rapid urease test and a histological examination, 257 subjects were confirmed to be H. pylori-positive (cases), whereas 155 subjects were confirmed to be H. pylori-negative (controls). Table 1 shows the demographics and clinical characteristics for those participants. The mean age of controls and cases were 42.6 ± 14.7 years and 40.8 ± 15.2 years, respectively (p > 0.05). Female subjects represent 48.7% of controls and 51% of cases. Body mass indices (BMIs) were not different between the two groups. In addition, no differences with respect to the frequencies of hypertension, diabetes, cardiovascular disease, thyroid dysfunction, and kidney/liver diseases were observed (Table 1).
The association between the SNPs of the ABCB1 gene (C1236T and C3435T) and H. pylori infection is shown in Table 2. A significant association between C1236T and H. pylori infection was detected (p < 0.01). The frequency of the CT genotype was significantly higher in cases (40.1%) compared to controls (21.3%). Thus, the heterozygotes state was associated with a higher risk for H. pylori infection compared to the other genotypes.
With respect to C3435T SNP, a weak association was detected between this SNP and H. pylori infection. The TT genotype was lower, whereas TT was higher among H. pylori-positive patients when compared to H. pylori-negative ones (p = 0.07). When alleles were considered, the frequency of the C allele was significantly higher among H. pylori-positive subjects (p < 0.05).
Haplotype analysis of C1236T and C3435T SNPs is shown in Table 3. Among all examined haplotypes, the TT haplotype was present in 22.7% of cases compared to 30.7% of controls (p < 0.05, odds ratio = 0.663, 95% CI: (0.483–0.911)). Thus, the TT haplotype seems to decrease the risk of H. pylori infection. No significant association between the rest of the haplotypes and H. pylori infection was observed (p > 0.05, Table 3).

4. Discussion

In the current study, the association between H. pylori infection and the ABCB1 gene polymorphisms were examined. The results showed a strong association between C1236T, G2677T/A, and H. pylori infection. In addition, a weak effect for C3435T on H. pylori infection was also observed.
ABCB1 encodes for P-glycoprotein (P-gp), which functions as an ATP-dependent efflux pump and plays a role in the absorption, distribution, and elimination of drugs [28]. In addition, ABCB1 has been found to mediate the efflux of xenobiotics in epithelial tissues throughout the human body including the gut [10]. However, the level of expression of ABCB1 varies between subjects depending on certain polymorphisms that are present in the gene [9].
The results of the current study showed an association between C1236T and C3435T SNPs and H. pylori infection. This finding is in agreement with previous literature that examined the relationship between the ABCB1 gene and H. pylori infection and the response to eradication therapies. For example, a positive relationship between C3435T SNP and H. pylori infection was detected among Australians, with the TT genotype being associated with a significantly lower P-gp expression compared with the CC genotype [16]. In addition, differential modulation of P-gp expression was observed in the TT genotype carriers between H. pylori-negative and H. pylori-positive patients [16]. Thus, a low expression of P-gp in the stomach epithelium might be associated with an increased risk of H. pylori infection. In agreement with those findings, the methylation status of the ABCB1 gene was found to be strongly associated with H. pylori infection [18,19]. Furthermore, the C3435T polymorphism of MDR1 has been shown to influence H. pylori-related inflammatory conditions in the stomach [17] and to increase the risk of gastric cancer among Iranian and Japanese subjects [20,29,30]. Finally, the C3435T SNP has been shown to be associated with clinical outcomes in gastric cancer patients treated with postoperative adjuvant chemotherapy [31] and H. pylori eradication therapy [32]. Therefore, it can be postulated that the C1236T and G2677T/A SNPs could be influencing the course of H. pylori infection via modulating the expression of P-gp and/or the methylation status of corresponding genes leading to changes in inflammatory processes in the stomach.
With respect to C1236T SNP, the current report is pioneering in that the association of these variants with H. pylori infection is defined. However, the clinical significance of C1236T in gastric diseases is not yet well studied. In a previous study, ABCB1 C1236T has been shown to be correlated with gastric cancer progression [33]. Thus, more studies are needed to confirm the present findings.
Other SNPs in the ABCB1 gene has been shown to be associated with gastric diseases. For example, a study that was conducted in China showed that G2677T/A SNP was a beneficial predictor of clinical treatment outcomes in gastric cancer [34]. Similarly, a G2677T/A SNP was shown to be associated with the chemosensitivity of paclitaxel in gastric cancer [35]. The G159T, A3073C, and A1564T SNPs were found to be associated with gastric cancer risk [36,37]. Thus, ABCB1 genetic variations seem to play a role in the susceptibility to H. pylori infection and the subsequent development of gastric cancer.
The findings that ABCB1 SNPs are associated with H. pylori infection are important, as this infection is found in approximately 60% of the world population [38]. Globally, gastric cancer is still one of the leading causes of cancer-related deaths worldwide [39,40]. In most of the cases, gastric cancer is often asymptomatic in its early stages and by the time symptoms starts, the cancer has often reached an advanced stage and metastasized to other parts of the body [41]. Understanding the risk factors of H. pylori infection will help in the management of the disease and the subsequent prevention of gastric cancer.
In the current study, we attempted also to examine the role of the ABCB1 SNPs in the eradication of H. pylori using the triple therapy regimen. However, most of the recruited patients (>90%) showed complete eradications, so such analysis was not feasible. Increasing the sample size in future studies might allow for such an analysis. In addition, we did not examine the relationships between SNPs and the pathogenesis of chronic stomach issues or the methylation status of ABCB1 DNA or how such methylation might affect the expression of the ABCB1 gene. Moreover, for diagnosis of H. pylori infection, we sampled antrum only and used it, in addition to immunoglobulin testing, as a base for H. pylori diagnosis. Previous studies have shown that, in some cases, H. pylori may migrate towards the corpus [42]. Therefore, the presence of some false negatives among H. pylori-negative patients cannot be excluded. Overcoming such limitations in future studies is strongly recommended.
In conclusion, ABCB1 SNPs seem to be associated with H. pylori infection in the Jordanian population. A strong association between C1236T and H. pylori infection was detected, whereas C3435T SNP showed a weak effect.

Author Contributions

Conceptualization: M.N.B., O.F.K., K.H.A., N.A.B., M.A.K.S., S.H.S., and N.A.; data curation: O.F.K., K.H.A., and N.A.; formal analysis: O.F.K. and K.H.A.; funding acquisition: K.H.A. and N.A.B.; investigation: M.N.B., K.H.A., and S.H.S.; methodology: M.N.B., M.A.K.S., S.H.S., and N.A.; project administration: M.N.B., O.F.K., K.H.A., and N.A.B.; resources: M.N.B., K.H.A., and M.A.K.S.; software: K.H.A. and N.A.; supervision: M.N.B., O.F.K., and K.H.A.; validation: M.N.B. and N.A.; visualization: M.N.B.; writing—original draft: M.N.B., O.F.K., K.H.A., and S.H.S.; writing—review & editing: M.N.B., O.F.K., K.H.A., N.A.B., M.A.K.S., and N.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Scientific Research Funds (SRF), Ministry of Higher Education and Scientific Research, Amman, Jordan: MPH/2/19/2016.

Acknowledgments

The authors would like to thank Jordan SRF for funding the study (MPH/2/19/2016). In addition, the authors thank Jordan University of Science and Technology for its support.

Conflicts of Interest

The authors declare that there is no conflict of interest.

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Table
Table 1. Demographics and clinical characteristics of participants.
Table 1. Demographics and clinical characteristics of participants.
VariableControlsCasesp Value
Age42.6 ± 14.740.8 ± 15.20.239
Gender
male64 (41.3)126 (49.0)
Female91 (48.7)131 (51.0)0.153
BMI28.1 ± 4.528.5 ± 5.20.503
Hypertension25 (16.1)57 (22.2)0.161
Diabetes14 (9.0%)35 (13.6)0.209
Cardiovascular Diseases4 (2.6)10 (3.9)0.582
Thyroid Disease87 (5.1)8 (3.5)0.588
Kidney Diseases2 (1.3)3 (1.2)0.912
Liver Diseases1 (0.6)5 (1.9)0.286
Table
Table 2. Association between SNPs and H. pylori infection as calculated using SNPStats.
Table 2. Association between SNPs and H. pylori infection as calculated using SNPStats.
MDR1 SNPCasesControlsOdds Ratio (95% CI)p-Value
C1236T
CC81 (31.5%)56 (36.1%)1.00
CT103 (40.1%)33 (21.3%)0.35 (0.21–0.59)
TT73 (28.4%)66 (42.6%)0.76 (0.47–1.23)<0.001
Allele C265 (52%)145 (47%)
Allele T249 (48%)165 (53%)1.21 (0.91–1.61)<0.001
C3435T
CC70 (27.3%)59 (38.1%)1.00
TC134 (52.1%)70 (45.2%)0.62 (0.39–0.97)
TT53 (20.6%)26 (16.8%)0.59 (0.33–1.06)0.070
C274 (53.3%)188 (0.61%)
T240 (46.7%)122 (39%)0.74 (0.55–0.98)0.039
Table
Table 3. Haplotype analysis.
Table 3. Haplotype analysis.
Haplotype C1236T/C3435TCase (Frequency)Control (Frequency)Pearson’s pOdds Ratio (95%CI)
CC157.24 (0.306)92.79 (0.299)0.841.032 (0.759–1.403)
TC107.76 (0.210)52.21 (0.168)0.141.310 (0.909–1.888)
TT116.76 (0.227)95.21 (0.307)0.010.663 (0.483–0.911)
CT132.24 (0.257)69.79 (0.225)0.291.192 (0.856–1.662)

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BaniHani, M.N.; Khabour, O.F.; Alzoubi, K.H.; Bashir, N.A.; Shakhatreh, M.A.K.; Sabi, S.H.; Alrabadi, N. The Association between ABCB1 C1236T/C3435T SNPs and H. pylori Infection among Jordanians. Genes 2020, 11, 63. https://doi.org/10.3390/genes11010063

AMA Style

BaniHani MN, Khabour OF, Alzoubi KH, Bashir NA, Shakhatreh MAK, Sabi SH, Alrabadi N. The Association between ABCB1 C1236T/C3435T SNPs and H. pylori Infection among Jordanians. Genes. 2020; 11(1):63. https://doi.org/10.3390/genes11010063

Chicago/Turabian Style

BaniHani, Mohammed N., Omar F. Khabour, Karem H. Alzoubi, Nabil A. Bashir, Muhamad Ali K. Shakhatreh, Salsabeel H. Sabi, and Nasr Alrabadi. 2020. "The Association between ABCB1 C1236T/C3435T SNPs and H. pylori Infection among Jordanians" Genes 11, no. 1: 63. https://doi.org/10.3390/genes11010063

APA Style

BaniHani, M. N., Khabour, O. F., Alzoubi, K. H., Bashir, N. A., Shakhatreh, M. A. K., Sabi, S. H., & Alrabadi, N. (2020). The Association between ABCB1 C1236T/C3435T SNPs and H. pylori Infection among Jordanians. Genes, 11(1), 63. https://doi.org/10.3390/genes11010063

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