Vegetable Extracts and Nutrients Useful in the Recovery from Helicobacter pylori Infection: A Systematic Review on Clinical Trials
Abstract
:1. Introduction
2. Methodology
3. Preclinical Studies on H. pylori Infections
4. Vegetable Extracts and H. pylori Infections: Clinical Studies
5. Micronutrients and H. pylori Infections: Clinical Studies
6. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Study Design | Study Sample | Experimental Intervention | Control Intervention | Main Outcomes | References |
---|---|---|---|---|---|
RCT | 32 patients underwent gastroscopy (23 patients completed trial) | Cinnamon extract (40 mg twice daily) for 4 weeks | Placebo | Slight and non-significant improvement in urea breath counts. | [62] |
RCT | 86 diabetic patients with positive H. pylori stool antigen test (77 patients completed trial) | Broccoli sprouts powder (6 g/day) alone or in combination with standard triple therapy for 4 weeks | Standard triple therapy (omeprazole 20 mg, clarithromycin 500 mg, amoxicillin 1000 mg) | H. pylori eradication rates with Broccoli sprouts powder, standard triple therapy, and combination of both were 56%, 89.3% and 91.7%, respectively. | [63] |
RCT | 89 volunteer subjects randomized in group A (H. pylori positive, broccoli sprout extract containing sulforaphane), group B (placebo) and group C (H. pylori negative, broccoli sprout extract containing sulforaphane). | One capsule containing 250 mg broccoli sprout extract yielding 1000 μg sulforaphane. | Placebo | No significant effect was found in treatment group regards to H. pylori infection density. MDA concentration was significantly reduced in groups A and C with broccoli sprout treatment. | [64] |
Controlled clinical trial | 25 H. pylori positive patients (mean age: 50 ± 12 years) with functional dyspepsia | Curcumin 30 mg, bovine lactoferrin 100 mg, N-acetylcysteine 600 mg, and pantoprazole 20 mg twice daily for 7 days | - | Significant improvement of the severity of symptoms and serologic signs of gastric inflammation. 12% H. pylori eradication rate. | [65] |
RCT | 68 H. pylori positive patients aged 20–50 years with peptic ulcer (60 patients, 30 in each group completed study) | Curcumin 500 mg/day, as adjunct to standard triple therapy (clarithromycin 500 mg, amoxicillin 1000 mg, and pantoprazole 40 mg twice daily) | Placebo | Improvement of dyspepsia in curcumin group was significantly higher (27.6%) vs. placebo (6.7%). H. pylori eradication rate was 73.3% in both groups. | [66] |
RCT | H. pylori patients were randomized in two groups, 50 patients each, with mean age of 54.65 ± 16.54 in triple therapy group, and 53.65 ± 15.65 in triple therapy + curcumin group. | Triple therapy twice a day for one week + turmeric tablets (700 mg) thrice a day for 28 days. | Triple therapy (omeprazole, amoxicillin, and metronidazole) twice a day for one week. | Significantly decrease in MDA levels and increase in TAC of the gastric mucosa in triple therapy + curcumin treated patients. | [67] |
RCT | 36 patients (47% males and 53% females) with mean age of 40.87 ± 16.45 years in the treatment group and 35.40 ± 11.26 years in the control group | 2 tablets of garlic powder daily (2 g each) for 8 weeks. | Placebo | 87% H. pylori negative cases in Garlic treated group and 73% H. pylori negative cases in placebo group, as confirmed by UBT. | [68] |
Pilot study | 20 dyspeptic patients aged 18–75 years with positive H. pylori (5 patients completed study) | Garlic oil capsule (4 mg) four times daily for 14 days | - | No improvement in H. pylori symptoms or eradication | [69] |
Single-center, prospective crossover study | 12 healthy H. pylori infected adults (average age: 41.4 years) |
| Bismuth subsalicylate (2 tablets) with 3 meals per test day | No beneficial effects by garlic or capsaicin on H. pylori. Median urease activity before and after therapy for garlic was 28.5 vs. 39.8, for capsaicin was 43.7 vs. 46.6, and for bismuth was 55.8 vs. 14.3. | [70] |
RCT | 40 volunteers with H. pylori infection | Burdock complex (Arctium lappa, Angelica sinensis, Lithospermum erythrorhizon, and Sesamum indicum oil) 2 bottles (2 × 10 mL) every day after breakfast and dinner, for 8 weeks. | Placebo | A significant decrease in urea breath counts and inflammatory markers (TNF-α and IL-8), and improved antioxidant capacity, with Burdock complex | [71] |
RCT | 107 participants with H. pylori infection, aged 18–45 years | GutGard (Root extract of Glycyrrhiza glabra) 150 mg for 60 days | Placebo | H. pylori stool antigen (HpSA) was negative in 56% and 4% of patients treated with GutGard or placebo, respectively | [72] |
RCT | 88 H. pylori patients, with non-ulcer dyspepsia (age range of 18–65 years) | 1-, 2- or 3-g Nigella sativa + 40 mg omeprazole | Standard triple therapy (clarithromycin, amoxicillin, and omeprazole) | No significant difference in H. pylori eradication rate between triple therapy (82.6%) and 2-g N. sativa (66.7%). Effect on dyspeptic symptoms was similar in all groups. | [73] |
RCT | 142 patients aged 19–70 years were enrolled in the trial. | Fermented milk containing 1.0 × 106 CFU/mL L. paracasei HP7 and 100 mg G. glabra. | Placebo | Significant improvement in GI symptoms, 13C-UBT scores, and chronic inflammation was observed in treatment group. | [74] |
RCT | 120 patients suffering from non-ulcer dyspepsia or peptic ulcer disease randomized into treatment group (mean age: 38.8 years) or control group (mean age: 40.1 years). | Clarithromycin based triple regimen + G. glabra 380 mg twice daily, for 2 weeks. | Clarithromycin based triple regimen (clarithromycin twice daily, amoxicillin once daily, omeprazole twice daily), for 2 weeks. | H. pylori eradication rate for treatment and control groups was found as 83.3% and 62.5%, respectively. | [75] |
RCT | 70 patients were randomized in treatment (mean age: 42.31713.85) and control (mean age: 36.31713.64) groups. | Anti-secretory agent 1 + honey-based formulation of N. sativa (5 mL N. sativa) once daily, for 8 weeks. | Placebo | The mean Hong Kong index of dyspepsia scores and H. pylori infection rates were significantly lower in treatment group. | [76] |
RCT | 52 H. pylori positive patients were randomized in group A (low dose mastic gum), group B (high dose mastic gum), group C (pantoprazole), and group D (standard therapy). | Pure mastic gum [350 mg (group A) or 1 g (group B) thrice daily] or combination of pure mastic gum (350 mg thrice daily) and pantoprazole (20 mg twice daily) (group C). | Standard therapy (pantoprazole 20 mg, amoxicillin 1 g and clarithromycin 500 mg) for 10 days (group D). | H. pylori eradication was observed in 4/13 patients in group A, 5/13 patients in group B, none of the patients in group C, and 10/13 patients in group D. No significant differences were found in mean UBT values in groups A, B and C. | [77] |
Study Design | Study Samples | Experimental Intervention | Control Intervention | Main Outcomes | References |
---|---|---|---|---|---|
RCT | 312 patients, with an indication for endoscopy of dyspeptic symptoms were randomized in group A (n = 162; mean age: 45 years) and group B (n = 150; mean age: 43 years). | Standard therapy (amoxicillin 1 g, metronidazole 500 mg, bismuth 240 mg and omeprazole 40 mg) plus Vitamin C 500 mg/day (Group B). | Standard therapy (amoxicillin 1 g, metronidazole 500 mg, bismuth 240 mg and omeprazole 40 mg) (Group A). | H. pylori eradication rates in group B was significantly higher (78%) than group A (48.8%). | [78] |
RCT | 200 patients were randomized in group A (mean age: 39.7 ± 10) and group B (mean age: 42.7 ± 10.8). | Standard triple therapy (lansoprazole, amoxicillin, and clarithromycin) for 14 days plus vitamins C (500 mg) and E (200 mg) for 30 days (Group A). | Standard triple therapy alone for 14 days (Group B). | H. pylori eradication rates in group A was significantly higher as compared to group B. | [79] |
RCT | 160 patients were randomized in group A (mean age: 44 ± 10) and group B (mean age: 43 ± 11) | Conventional therapy for 2 weeks plus vitamins C (1000 mg/day) and E (400 IU/day) for 1 month (Group B). | Conventional anti-H. pylori therapy (lansoprazole, amoxicillin, clarithromycin, and bismuth subcitrate) for 2 weeks (Group A). | H. pylori eradication rates were significantly higher in group B. No difference was found in TAC among both groups. | [80] |
RCT | 117 patients were randomized into 4 groups: conventional therapy, vitamins (C and E), combination of both or placebo. | Triple therapy alone ( Bismuth chelate, tetracycline, and metronidazole for 2 weeks ), vitamins C (200 mg) and E (50 mg) twice a day for 4 weeks, or combination of both treatments. | Placebo | No significant effect was found on MDA levels and ROS with vitamins supplementation. | [81] |
RCT | 171 H. pylori infected patients. | One-week triple therapies of omeprazole and amoxicillin, plus on the following twice daily: (1) clarithromycin 250 mg; (2) clarithromycin 250 mg and vitamin C 500 mg; (3) clarithromycin 500 mg | Clarithromycin 250 and 500 mg. | Combination of clarithromycin 250 and vitamin C showed higher eradication rates than clarithromycin 250 mg, and equivalent eradication rates to clarithromycin 500 mg. | [82] |
RCT | 400 patients, with non-ulcer dyspepsia. The patients were randomized in 4 groups, 100 patients each: Group A aged 26–66 years), Group B (aged 21–65 years), Group C (aged 24–66 years) and Group D (aged 22–65 years). | Triple therapy for 2 weeks plus vitamins C (500 mg/day) and E (100 U/day) for 1 month (Group B).Quadruple therapy for 2 weeks plus vitamins C (500 mg/day) and E (100 U/day) for 1 month (Group D). | Standard triple therapy (amoxicillin, clarithromycin, and lansoprazole) for 2 weeks (Group A). Standard quadruple therapy (amoxicillin, clarithromycin, lansoprazole, and bismuth subcitrate) for 2 weeks (Group C). | No difference was found in H. pylori eradication rates among Groups A and B, and similarly Group C and D. | [83] |
RCT | 332 patients with H. pylori associated gastritis, aged 18–70 years infection. |
| Triple therapy (omeprazole, amoxicillin, and clarithromycin) for 14 days. | Triple therapy in combination with Polaprezinc 75/150 mg showed higher efficacy in eradication of infection, with no significant difference between both groups. | [84] |
RCT | 66 patients (mean age: 48.5 years) suffering from dyspeptic symptoms with H. pylori infection. | Triple therapy plus polaprezinc 150 mg twice daily. | Triple therapy (lansoprazole, amoxycillin and clarithromycin) twice daily. | Triple therapy in combination with polaprezinc showed in improvement of infection eradication rates. | [85] |
RCT | 90 patients with peptic ulcer disease and with mean age 47.5 ± 17.2 years in intervention group, and 52.6 ± 18.4 years in placebo group. | Standard triple therapy plus zinc 220 mg/day for 2 weeks. | Placebo | No significant difference was found between both groups in infection eradication, and improvement of peptic ulcer disease. | [86] |
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Ullah, H.; Di Minno, A.; Santarcangelo, C.; Khan, H.; Xiao, J.; Arciola, C.R.; Daglia, M. Vegetable Extracts and Nutrients Useful in the Recovery from Helicobacter pylori Infection: A Systematic Review on Clinical Trials. Molecules 2021, 26, 2272. https://doi.org/10.3390/molecules26082272
Ullah H, Di Minno A, Santarcangelo C, Khan H, Xiao J, Arciola CR, Daglia M. Vegetable Extracts and Nutrients Useful in the Recovery from Helicobacter pylori Infection: A Systematic Review on Clinical Trials. Molecules. 2021; 26(8):2272. https://doi.org/10.3390/molecules26082272
Chicago/Turabian StyleUllah, Hammad, Alessandro Di Minno, Cristina Santarcangelo, Haroon Khan, Jianbo Xiao, Carla Renata Arciola, and Maria Daglia. 2021. "Vegetable Extracts and Nutrients Useful in the Recovery from Helicobacter pylori Infection: A Systematic Review on Clinical Trials" Molecules 26, no. 8: 2272. https://doi.org/10.3390/molecules26082272
APA StyleUllah, H., Di Minno, A., Santarcangelo, C., Khan, H., Xiao, J., Arciola, C. R., & Daglia, M. (2021). Vegetable Extracts and Nutrients Useful in the Recovery from Helicobacter pylori Infection: A Systematic Review on Clinical Trials. Molecules, 26(8), 2272. https://doi.org/10.3390/molecules26082272