HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Abstract Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Sheu, B.-S. Articles by Wu, J.-J. Search for Related Content PubMed PubMed Citation Articles by Sheu, B.-S. Articles by Wu, J.-J. Agricola Articles by Sheu, B.-S. Articles by Wu, J.-J.

Pretreatment with Lactobacillus- and Bifidobacterium-containing yogurt can improve the efficacy of quadruple therapy in eradicating residual Helicobacter pylori infection after failed triple therapy ^1,2,3

¹ From the Departments of Internal Medicine (B-SS, H-CC, and A-WK), Pathology (H-BY), and Medical Technology (J-JW), the Institute of Public Health (S-TW), and the Institute of Clinical Medicine (B-SS, H-CC, and Y-JY), Medical College, National Cheng Kung University, Tainan, Taiwan

² Supported by research grant 93-2314-B-006-089 and 93-2314-B-006-011 from the National Science Council, Taiwan.

³ Address reprint requests to B-S Sheu, Department of Internal Medicine, National Cheng Kung University Hospital, 138 Sheng Li Road, Tainan 70428, Taiwan. E-mail: sheubs{at}mail.ncku.edu.tw.

	ABSTRACT

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Background: Lactobacillus- and Bifidobacterium-containing yogurt (AB-yogurt) can suppress Helicobacter pylori. Improvement of the eradication rate by quadruple therapy of residual H. pylori after failed triple therapy is needed.

Objective: We tested whether prior treatment with AB-yogurt improved the efficacy of quadruple therapy in eradicating residual H. pylori after failed triple therapy.

Design: One hundred thirty-eight patients in whom triple therapy failed were enrolled for a culture study of H. pylori to assess antimicrobial resistance. These patients were then randomly assigned in equal numbers to either a yogurt-plus-quadruple therapy group or a quadruple therapy-only group. The patients received 1 wk of quadruple therapy with or without a 4-wk pretreatment with AB-yogurt (400 mL/d). In the yogurt-plus-quadruple group, excessive ¹³CO₂/mL values of the ¹³C-urea breath test were collected before and every 2 wk during the 4-wk ingestion of yogurt. For both groups, a ¹³C-urea breath test was conducted 6 wk after the quadruple therapy to assess the outcome of residual H. pylori eradication.

Results: For the patients in the yogurt-plus-quadruple therapy group infected with either antibiotic-sensitive or -resistant H. pylori, the excessive ¹³CO₂/mL values of the ¹³C-urea breath test were significantly decreased after the 4-wk ingestion of AB-yogurt (P < 0.0001). The yogurt-plus-quadruple therapy group had a higher H. pylori eradication rate than did the quadruple therapy-only group (intention-to-treat analysis: 85% compared with 71.1%, P < 0.05; per-protocol analysis: 90.8% compared with 76.6%, P < 0.05).

Conclusion: A 4-wk pretreatment with AB-yogurt can decrease H. pylori loads despite antimicrobial resistance, thus improving the efficacy of quadruple therapy in eradicating residual H. pylori.

Key Words: Helicobacter pylori • triple therapy • quadruple therapy • Lactobacillus • Bifidobacterium • yogurt

	INTRODUCTION

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Triple therapy, which combines a proton pump inhibitor with 2 antibiotics, is the current standard of therapy for eradicating Helicobacter pylori (1-5). Amoxicillin and clarithromycin plus a proton pump inhibitor is the first-line triple therapy choice recommended by the Maastricht-2 Consensus Group (1). However, this first-line regimen still has a 10–23% failure rate (2-8) and needs an effective rescue regimen, such as quadruple therapy (1, 9, 10). Many clinical studies have applied versatile regimens of quadruple therapy to eradicate primary H. pylori infection; these regimens have eradication rates from 70% to 90% (9-12). Moreover, applying quadruple therapy as a second-line therapy to rescue the failure of amoxicillin-omeprazole-clarithromycin triple therapy may achieve only 75–85% eradication rate (12, 13). Therefore, the application of new approaches to improve the efficacy of quadruple therapy as either the first line or, especially, the second line regimen is clinically important.

Increasing evidence has shown the direct suppression of H. pylori urease or growth in vitro by Lactobacillus acidophilus–and Bifidobacterium-containing yogurt (AB-yogurt) (14-16). Moreover, such yogurt can also exert therapeutic properties and improve the eradication rate of primary therapy against H. pylori in infected clinical patients (7, 15). In the present study, we investigated whether pretreatment with AB-yogurt improved the efficacy of quadruple therapy in the eradication of residual H. pylori after failed triple therapy.

Furthermore, the influence of antimicrobial-resistant H. pylori on the efficacy of quadruple therapy needs additional validation (9, 17), especially in areas of high endemic metronidazole-resistant H. pylori. Thus, the present study also tested whether the eradication efficacy of quadruple therapy against residual metronidazole-resistant H. pylori could be improved by pretreatment with AB-yogurt.

	SUBJECTS AND METHODS

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Patients and study design
One hundred thirty-eight dyspeptic patients with an initial diagnosis of duodenal ulcers or gastritis were consecutively enrolled after 1-wk of triple therapy (1 g amoxicillin, 500 mg clarithromycin, and 20 mg omeprazole twice daily) failed to eradicate H. pylori infection. The present study fulfilled the Consolidated Standards of Reporting Trials guidelines and was approved by the human ethics and research committee of our institute in Taiwan. The patients who were enrolled into the present study had good compliance (5 d) during the 1-wk triple therapy. Failure of triple therapy was defined as a positive ¹³C-urea breath test (UBT), with an excessive ¹³CO₂/mL (ECR) value >2.5 (18). The same breath test was performed for each patient during the fifth week, after cessation of triple therapy. Medications, including proton pump inhibitors, bismuth salt, and antimicrobial agents, were withheld for 4 wk before each UBT, to reduce the possibility of interference with the results. Patients with evident milk intolerance were not included in the present study.

After obtaining informed consent, each of the 138 patients in whom triple-therapy failed underwent an endoscopy to obtain H. pylori cultures, as previously described (9, 13, 19). The successfully collected H. pylori isolates were then checked for the presence of antimicrobial resistance, which was defined by the minimal inhibitory concentration of an E-test (9, 13). Each patient underwent a gastric biopsy procedure to reconfirm H. pylori status by histology, regardless of a positive UBT. Patients with negative results for both histology and cultures obtained during the follow-up endoscopy, those known to be allergic to bismuth or metronidazole, or those having gastric malignancy were excluded. None of the 138 patients were excluded due to the above-mentioned conditions.

Helicobacter pylori
The infected patients were randomly assigned to 1of 2 groups and received either 1-wk quadruple therapy with (yogurt-plus-quadruple therapy group) or without (quadruple therapy-only group) a 4-wk pretreatment supplement of L. acidobacillus–and Bifidobacterium-containing yogurt (AB-yogurt; President Enterprise Corporation, Tainan, Taiwan) for the eradication of H. pylori. The randomization was based on a prescheduled serial number. The AB-yogurt used in the present study was made with fermented milk with sugar, high-fructose corn syrup, pectin, galactooligosaccharide, and an approximately equal mixture of L. acidophilus La5, Bifidobacterium lactis Bb12, Lactobacillus bulgaricus, and Streptococcus thermophilus at a concentration of 10⁹ bacteria/mL. The yogurt product containing the 2 specific isolates (L. acidophilus La5 and Bifidobacterium lactis Bb12) was previously validated to have a positive effect on H. pylori suppression (7, 15). In both groups, the regimen of 1-wk quadruple therapy, which included 1 g amoxicillin twice daily, 500 mg metronidazole twice daily, 20 mg omeprazole twice daily, and 120 mg bismuth subcitrate three times daily, was adminstered. In the yogurt-plus-quadruple therapy group, AB-yogurt was prescribed for each patient in dosages of 200 mL AB-yogurt twice daily for 4 wk (7). In contrast, the patients of the quadruple therapy-only group were prohibited to consume yogurt, although regular milk consumption was not prohibited during the study period. Moreover, all patients were instructed to maintain a regular dietary pattern and to avoid dairy products, honey, spicy foods, Chinese herbs, cranberries, and products with live lactic acid bacteria as much as possible during the study period (15).

In the yogurt-plus-quadruple therapy group, the ECR values of the UBT, which indirectly represented intragastric H. pylori loads, were serially collected before and every 2 wk during the 4-wk ingestion of yogurt. Drug compliance and side effects of the rescue therapy were recorded at the clinics. The degree of drug compliance was categorized as "good" (7-d quadruple therapy completely ingested), "modest" (therapy ingested 5 d), and "poor" (therapy ingested <5 d), as previously described (9).

At least 6 wk after the rescue regimen, the UBT was repeated to check for H. pylori eradication. The staff that processed the UBTs was blinded to the patient's grouping. For those with a negative result for the UBT after quadruple therapy, a repeat UBT was performed 3 mo after the rescue regimen ended to prevent a false negative result. Thus, both negative results on the UBT during the sixth week and third month were needed to define successful H. pylori eradication by the quadruple rescue therapy. Proton pump inhibitors and antibiotic medications were withheld from the subjects before the 6-wk test and for subjects who tested negative for H. pylori at 6 wk until the 3-mo follow-up test. To attain a statistical power of 0.8 and to achieve a 15% difference in the eradication rate between the 2 groups, the number of patients included had to be 100 and, thus, 50 patients per group.

Gastric biopsy samples for Helicobacter pylori culture and histology
For each patient, 2 pairs of gastric biopsy samples (each pair included one from the antrum and one from the lower body) were obtained during an endoscopy. Each pair of biopsy samples was sent for a culture and histologic staining (with haematoxylin and eosin) of H. pylori (13). Patients in whom gastric ulceration was found during the follow-up endoscopy were excluded. These 2 gastric biopsy samples were taken for H. pylori culture, as done in our previous studies (9, 13, 19). For each H. pylori isolate, the presence of clarithromycin, metronidazole, and amoxicillin resistance was defined by an E-test with a minimal inhibitory concentration of >1, >1, and >8 µg/mL, respectively (9, 13).

Statistics
Student's t test, one-way analysis of variance (ANOVA) with Bonferroni correction, Bonferroni t test, chi-square test, and Fisher's exact test were used, as appropriate, to determine parametric differences and nonparametric proportions. Pearson's correlation coefficients were applied to test the correlation between the pretreatment ECR value and the difference between the 2 ECR values to check on 2 different time intervals. In addition, a 2-factor repeated-measures ANOVA was used for analysis of serial ECR measurements after AB-yogurt ingestion according to the clarithromycin resistance and metronidazole resistance status of the residual H. pylori. All tests of significance were two-tailed with a P value < 0.05, and tests were conducted with SAS version 8.0 (SAS Institute Inc, Cary, NC) and SPSS version 8.0 (SPSS Inc, Chicago, IL) software programs. Data from all enrolled patients for rescue therapy were analyzed with an intention-to-treat analysis. The patients who stopped medication, had poor drug compliance, or who were lost to follow-up were excluded from the per-protocol (PP) analysis.

	RESULTS

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 
Demographic background and compliance with quadruple therapy of the study groups
All 138 enrolled patients had a positive histology of H. pylori infection and were randomly assigned in equal numbers to 1 of the 2 study groups. No significant differences in demographic features, endoscopic diagnoses, and compliance with rescue therapy were observed between the 2 study groups (P > 0.05); side effects were more frequent in the quadruple therapy-only group than in the yogurt-plus-quadruple therapy group (Table 1).

Rescue efficacy of the quadruple therapy with and without AB-yogurt pretreatment
All 138 patients had histologies that were positive for residual H. pylori infection and received 1 wk of quadruple therapy. Excluded from the PP analysis were 4 patients in the yogurt-plus-quadruple therapy group (3 dropped out during follow-up and 1 showed poor drug compliance) and 5 patients in the quadruple therapy-only group (3 dropped out during follow-up and 2 showed poor drug compliance). Accordingly, 129 patients (65 patients in the yogurt-plus-quadruple therapy group and 64 patients in the quadruple therapy-only group) completed the rescue therapy protocol. The eradication rate for residual H. pylori was higher in the yogurt-plus-quadruple therapy group than in the quadruple therapy-only group (intention-to-treat analysis: 85.5% compared with 71.1%, P < 0.05; PP analysis: 90.8% compared with 76.6%, P < 0.05; Table 2).

AB-yogurt decreased the ECR of UBT indicating the suppression of H. pylori loads
No significant difference in the mean pretreatment ECR value of UBT was observed between the yogurt-plus-quadruple therapy group and the quadruple therapy-only group (16.9 ± 7.8 compared with 0.17.8 ± 7.9, P > 0.05). Of the 65 patients who completed the study design in the yogurt-plus-quadruple group, the ECR of wk 4, but not that of wk 2, was significantly lower than that of wk 0 [11.8 ± 6.2 for week 4 compared with 16.9 ± 6.9 for week 0, P < 0.001; week 2 compared with week 0: 16.2 ± 7.6 compared with 16.9 ± 6.9, P > 0.5 (Bonferroni t test)]. The ECR of week 4 was also lower than that of week 2 [11.8 ± 6.2 for week 4 compared with 16.2 ± 7.6 for week 2, P < 0.001(Bonferroni t test)].

The pretreatment ECR value did not show a significant correlation with the difference in the ECR value between week 0 and week 2 (P = 0.960, r = –0.006; Figure 1). In contrast, after the 4-wk ingestion of AB-yogurt, a significant negative correlation was observed between the baseline ECR value and the difference in the ECR value from week 0 to week 4 (P < 0.001, r = –0.401; Figure 1).

View larger version (12K): [in this window] [in a new window]   FIGURE 1.. Correlation between urea breath test (UBT) values at week 0 (UBT0) and the difference between UBT0 values and values at week 2 (UBT0-2) or week 4 (UBT0-4) in the yogurt-plus-quadruple therapy group. n = 65 (). The correlation between UBT0 and UBT02 was not significant (Pearson's correlation coefficient: r = –0.006; P = 0.960). The correlation between UBT0 and UBT04 was significant (r = –0.401, P < 0.001).

Figure 2

View larger version (25K): [in this window] [in a new window]   FIGURE 2.. Serial mean (±SD) excess 13CO2/mL (ECR) values of the urea breath test performed at enrollment into the study (week 0), week 2 (2 wk after yogurt ingestion), and week 4 (4 wk after yogurt ingestion) are listed for the patients infected by Helicobacter pylori isolates with different antimicrobial resistant status, including clarithromycin- and metronidazole-sensitive H. pylori infection (C–M–; n = 7), clarithromycin-resistant and metronidazole-sensitive H. pylori infection (C+M–; n = 20), clarithromycin-sensitive and metronidazole-resistant H. pylori infection (C–M+; n = 10), and clarithromycin- and metronidazole-resistant H. pylori infection (C+M+; n = 10). *The ECR of the C+M+ subgroup was significantly higher than the ECRs of the other 3 subgroups at week 0, P < 0.001 (one-way ANOVA with Bonferroni correction). **The ECR of the C–M– subgroup was significantly lower than that of the C+M– subgroup at week 0, P = 0.004 (one-way ANOVA with Bonferroni correction). A 2-factor repeated-measures ANOVA uncovered a significant main effect of time (P < 0.001) but no significant main effect of resistance status on the ECR values after AB-yogurt ingestion; the status-by-time interaction was not significant for the ECR values after AB-yogurt ingestion.

	DISCUSSION

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

Several studies have confirmed that supernatant fluids and food products that contain certain Lactobacillus species can reduce H. pylori densities in humans (20, 21). Wang et al (15) showed that the UBT values of primary H. pylori-infected humans could be significantly decreased after 4 wks of AB-yogurt ingestion. However, in the present study, we found that the suppression effect of AB-yogurt remained significant for residual H. pylori loads after failed triple therapy. These data suggest an important clinical application of AB-yogurt in improving the efficacy of rescue therapy against residual H. pylori, which is usually unmanageable during rescue treatment due to a high prevalence of antimicrobial resistance.

At least 6 possible mechanisms can explain how H. pylori loads are decreased by the AB-yogurt. First, on the basis of the findings by Wang et al (15), there may be a direct competition between H. pylori and the Lactobacillus and Bifidobacteria in AB-yogurt for nutrients, thus resulting in a reciprocal inhibition between the different bacterial species. Second, Lactobacillus may directly inhibit H. pylori attachment to the gastric epithelium (22). Third, attachment of Lactobacillus and Bifidobacterium in AB-yogurt to the gastric epithelium may produce a barrier effect and thereby decrease H. pylori attachment. Fourth, Lactobacillus and Bifidobacterium have been found to exert a positive immunomodulatory effect in the gut (23-25) and thus could suppress gastric H. pylori loads. Fifth, ingestion of Bifidobacterium-containing yogurt counteracts the hydrogen-producing action of coliform bacteria in the bowels, which mediate increased colonization of H. pylori loads in the stomach (26). Accordingly, a decrease of hydrogen production by coliform bacteria in the bowel may have decreased H. pylori loads. Finally, the direct inhibition of urease, which is an important colonization factor for H. pylori, by Lactobacillus and Bifidobacterium may have played some role.

In the present study, we excluded patients with milk intolerance before randomization. Only 4 patients in the yogurt-plus-quadruple therapy group did not complete the study design. However, only 1 of the 4 patients had poor tolerance of the 4-wk ingestion of AB-yogurt. This indicates that pretreatment with AB-yogurt can be well tolerated in milk-tolerant patients who have residual H. pylori after failed triple therapy. Moreover, the adverse effects of quadruple therapy were evidently lower in the yogurt-plus-quadruple therapy group than in the quadruple therapy-only group (Table 1). These data provide additional support for the finding that pretreatment with AB-yogurt may diminish the side effects of quadruple therapy while serving as a rescue regimen for failed triple therapy.

High prevalence rates of antimicrobial resistance were observed in the H. pylori isolates of patients with failed triple therapy (Table 1). In both study groups, the patients who were infected with metronidazole-resistant H. pylori had a lower PP eradication rate with quadruple therapy than those who were infected with metronidazole-sensitive H. pylori (P < 0.05). This finding indicates that metronidazole resistance is still a major factor in determining the outcome of quadruple therapy as a rescue regimen. Therefore, it would be interesting to investigate whether ingestion of AB-yogurt can decrease bacterial loads of metronidazole-resistant H. pylori isolates.

A 2-factor repeated-measures ANOVA showed a significant main effect of time (P < 0.001), but no significant main effect of resistance status or status-by-time interaction, on the ECR value after AB-yogurt ingestion. These data indicate that the H. pylori loads could be significantly decreased in patients infected by metronidazole resistant isolates as well as other isolates. After the 4-wk ingestion of AB-yogurt, a significant negative correlation was found between the baseline ECR value and the difference in ECRs between week 0 and week 4 (P < 0.001, r = –0.401; Figure 1). These data suggest that more reduction in the ECR value after a 4-wk ingestion of AB-yogurt occurs in the patients with a higher initial ECR value at baseline than in those with a lower ECR value at baseline. Therefore, combining 4-wk AB-yogurt can decrease the bacterial loads of residual H. pylori despite their antimicrobial resistance. The clinical administration of such pretreatment is widely helpful for those with high residual bacterial loads or with any antimicrobial-resistant H. pylori isolates.

Because the present study included patients with refractory H. pylori after failure of a standard first line therapy, we measured the efficacy of a fortified yogurt (yogurt plus probiotic isolates together) instead of simply an unfortified yogurt. Nevertheless, it is of scientific interest to know whether the yogurt or the probiotic was more effective in increasing the success rate. Because yogurt is part of daily food consumption, it would be interesting to know whether yogurt types with or without different probiotic isolates exert different effects. Moreover, because different quadruple therapies may yield different rescue rates for failed triple therapy (9, 13, 17), it is prudent to determine whether supplementation of such yogurt to different quadruple therapy regimens results in the same positive rescue effect. In conclusion, 4-wk, but not 2-wk, pretreatment with AB-yogurt can decrease bacterial loads of H. pylori despite their antimicrobial resistance and can thus improve the efficacy of quadruple therapy in the eradication of residual H. pylori after failed triple therapy.

	ACKNOWLEDGMENTS

 
B-SS was responsible for obtaining grant funding and for conducting the entire study. H-CC and A-WK collected cases for clinical therapy. Y-JY was responsible for the urea breath test analyses. S-TW served as a statistical consultant for the analyses of the study results. J-JW and H-BY reviewed the histology results. J-JW was responsible for checking the status of H. pylori antimicrobial resistance. None of the researchers had any conflicts of interest.

	REFERENCES

TOP ABSTRACT INTRODUCTION SUBJECTS AND METHODS RESULTS DISCUSSION REFERENCES

 

1. Malfertheiner P, Megraud F, O'Morain C, et al. Current concepts in the management of Helicobacter pylori infection–the Maastricht 2–2000 Consensus report. Aliment Pharmacol Ther 2002; 16: 167-80.[Medline]
2. Peterson WL, Fendrick AM, Cave DR, et al. Helicobacter pylori-related disease: guidelines for testing and treatment. Arch Intern Med 2000; 160: 1285-91.[Abstract/Free Full Text]
3. Huang AH, Sheu BS, Yang HB, et al Antimicrobial resistance of H. pylori to the outcome of one-week lansoprazole-based triple therapy. J Formosan Med Assoc 2000; 90: 704-9.
4. Lind T, Megraud F, Unge P, et al. The MACH2 study: role of omeprazole in eradication of Helicobacter pylori with one-week triple therapies. Gastroenterology 1999; 116: 248-53.[Medline]
5. Sheu BS, Yang HB, Sheu SM, Huang AH, Wu JJ. Higher gastric cyclooxygenase-2 expression and precancerous change in Helicobacter pylori-infected relatives of gastric cancer patients. Clin Cancer Res 2003; 9: 5245-51.[Abstract/Free Full Text]
6. Bazzoli F, Pozzato P, Rokkas T. Helicobacter pylori: the challenge in therapy. Helicobacter 2002; 7(suppl): 43-9.[Medline]
7. Sheu BS, Wu JJ, Lo CY, et al. Lactobacillus and Bifidobacteria containing yogurt can improve the drug compliance of triple therapy for Helicobacter pylori eradication. Aliment Pharmacol Ther 2002; 16: 1669-75.[Medline]
8. O'Morain C, Borody T, Farley A, et al. Efficacy and safety of single-triple capsules of bismuth biskalcitrate, metronidazole and tetracycline, given with omeprazole, for the eradication of Helicobacter pylori: an international multi-center study. Aliment Pharmacol Ther 2003; 17: 415-20.[Medline]
9. Chi CH. Lin CY, Sheu BS, Yang HB, Huang AH, Wu JJ. Quadruple therapy containing amoxicillin and tetracycline is an effective regimen to rescue failed triple therapy by overcoming the antimicrobial resistance of Helicobacter pylori. Aliment Pharmacol Ther 2003; 18: 347-53.[Medline]
10. Katelaris PH, Forbes GM, Talley NJ, Crotty B. A randomized comparison of quadruple and triple therapies for Helicobacter pylori eradication: the QUADRATE study. Gastroenterology 2002; 123: 1763-9.[Medline]
11. Mascitelli L, Pezzetta F. Quadruple treatments for Helicobacter pylori. Lancet 2003; 361: 86.[Medline]
12. Kao AW, Cheng HC, Sheu BS, et al. Post-treatment 13C-urea breath test is predictive of antimicrobial resistance to H. pylori after failed therapy. J Gen Intern Med 2005; 20: 139-42.[Medline]
13. Georgopoulos SD, Ladas SD, Laratapanis S, et al. Effectiveness of two quadruple, tetracycline- or clarithromycin containing, second line, Helicobacter pylori eradication therapies. Aliment Pharmacol Ther 2002; 16: 569-75.[Medline]
14. Coconnier MH, Lievin V, Hemery E, et al. Antagonistic activity against Helicobacter infection in vitro and in vivo by the human Lactobacillus acidophilus strain LB. Appl Environ Microbiol 1998; 64: 4573-80.[Abstract/Free Full Text]
15. Wang KY, Li SN, Liu CS, et al. Effects of ingesting Lactobacillus- and Bifidobacterium-containing yogurt in subjects with colonized Helicobacter pylori. Am J Clin Nutr 2004; 80: 737-41.[Abstract/Free Full Text]
16. Midolo PD, Lambert JR, Hull R, et al. In vitro inhibition of Helicobacter pylori NCTC 11637 by organic acids and lactic acid bacteria. J Appl Bacteriol 1995; 79: 475-9.[Medline]
17. Peitz U, Sulliga M, Wolle K, et al. High rate of post-therapeutic resistance of failure of macrolide-nitromidazole triple therapy to cure Helicobacter pylori infection: impact of two second-line therapies in a randomized study. Aliment Pharmacol Ther 2002; 16: 315-24.[Medline]
18. Sheu BS, Lee SC, Yang HB, et al. Selection a lower cut-off value of ¹³C-urea breath test is mandatory to detect H. pylori infection of patients after proton pump inhibitor-based triple therapy. Dig Dis Sci 2000; 45: 1330-6.[Medline]
19. Sheu BS, Sheu SM, Yang HB, Huang AH, Wu JJ. Host gastric Lewis expressions determine the bacterial density of Helicobacter pylori in babA2-genopositive infection. Gut 2003; 52: 927-32.[Abstract/Free Full Text]
20. Felley CP, Corthésy-Theulaz I, Rivero JL, et al. Favourable effect of an acidified milk (LC-1) on Helicobacter pylori gastritis in man. Eur J Gastroenterol Hepatol 2001; 13: 25-9.[Medline]
21. Michetti P, Dorta G, Wiesel PH, et al. Effect of whey-based culture supernatant of Lactobacillus acidophilus (Johnsonian) La1 on Helicobacter pylori infection in humans. Digestion 1999; 60: 203-9.[Medline]
22. Kabir AMA, Aiba Y, Takagi S, et al. Prevention of Helicobacter pylori infection by lactobacilli in a gnotobiotic murine model. Gut 1997; 41: 49-5.[Abstract/Free Full Text]
23. Perdigon G, Nader de Macias ME, Alvarez S, et al. Systemic augmentation of the immune response in mice by feeding fermented milk with Lactobacillus casei and Lactobacillus acidophilus. Immunology 1988; 63: 17-23.[Medline]
24. De Simone C, Salvadori BB, Negri R, et al. The adjuvant effect of yogurt on production of gamma-interferon by con A-stimulated human peripheral blood lymphocytes. Nutr Rep Int 1986; 33: 419-33.
25. Bartram H-P, Scheppach W, Gerlach S, Ruckdeschel G, Kelber E, Kasper H. Does yogurt enriched with Bifidobacterium longum affect colonic microbiology and fecal metabolites in healthy subjects? Am J Clin Nutr 1994; 59: 428-32.[Abstract/Free Full Text]
26. Olson JW, Maier RJ. Molecular hydrogen as an energy source for Helicobacter pylori. Science 2002; 298: 1788-90.[Abstract/Free Full Text]

This Article Abstract Full Text (PDF) Purchase Article View Shopping Cart Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Sheu, B.-S. Articles by Wu, J.-J. Search for Related Content PubMed PubMed Citation Articles by Sheu, B.-S. Articles by Wu, J.-J. Agricola Articles by Sheu, B.-S. Articles by Wu, J.-J.