Randomised clinical trial: efficacy and safety of H. pylori eradication treatment with and without Saccharomyces boulardii supplementation.


Journal

European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)
ISSN: 1473-5709
Titre abrégé: Eur J Cancer Prev
Pays: England
ID NLM: 9300837

Informations de publication

Date de publication:
06 Nov 2023
Historique:
medline: 9 11 2023
pubmed: 9 11 2023
entrez: 9 11 2023
Statut: aheadofprint

Résumé

Standard triple therapy is commonly prescribed Helicobacter pylori eradication regimen in Europe. However, the world is witnessing declines in eradication success. It is crucial to find better treatment options. To evaluate efficacy, compliance and side effects of H. pylori eradication treatment by adding Saccharomyces boulardii. We conducted a randomized clinical trial within the GISTAR cohort, consisting of healthy individuals aged 40-64 years. Participants were administered clarithromycin-containing triple therapy (clarithromycin 500 mg, amoxicillin 1000 mg, esomeprazole 40 mg) twice daily. Randomization was applied based on two factors: 1)addition of Saccharomyces boulardii CNCM I-745 500 mg BID or not; 2)treatment duration of 10 or 14 days. Treatment completion and adverse events were assessed via telephone interview 21-28 days after medication delivery. The efficacy was evaluated using a 13C-urea breath test (UBT) six months after treatment. Altogether 404 participants were enrolled; data on adverse events were available from 391. Overall, 286 participants received follow-up UBT. Intention-to-treat analysis revealed higher eradication rates for 10-day probiotic treatment (70.8% vs. 54.6%, P = 0.022), but not for 14-day. Probiotic subgroups combined showed non-significantly higher efficacy in per-protocol analysis (90.6% vs. 85.0%, P = 0.183). S. boulardii reduced the frequency of adverse events (P = 0.033) in 14-day regimen, particularly treatment-associated diarrhea (P = 0.032). However, after the adjustment to control Type I error, results lost their significance. Addition of S. boulardii to 14-day clarithromycin-containing triple regimen non-significantly lowers the likelihood of diarrhea and does not increase the eradication rate.

Sections du résumé

BACKGROUND BACKGROUND
Standard triple therapy is commonly prescribed Helicobacter pylori eradication regimen in Europe. However, the world is witnessing declines in eradication success. It is crucial to find better treatment options.
AIMS OBJECTIVE
To evaluate efficacy, compliance and side effects of H. pylori eradication treatment by adding Saccharomyces boulardii.
METHODS METHODS
We conducted a randomized clinical trial within the GISTAR cohort, consisting of healthy individuals aged 40-64 years. Participants were administered clarithromycin-containing triple therapy (clarithromycin 500 mg, amoxicillin 1000 mg, esomeprazole 40 mg) twice daily. Randomization was applied based on two factors: 1)addition of Saccharomyces boulardii CNCM I-745 500 mg BID or not; 2)treatment duration of 10 or 14 days. Treatment completion and adverse events were assessed via telephone interview 21-28 days after medication delivery. The efficacy was evaluated using a 13C-urea breath test (UBT) six months after treatment.
RESULTS RESULTS
Altogether 404 participants were enrolled; data on adverse events were available from 391. Overall, 286 participants received follow-up UBT. Intention-to-treat analysis revealed higher eradication rates for 10-day probiotic treatment (70.8% vs. 54.6%, P = 0.022), but not for 14-day. Probiotic subgroups combined showed non-significantly higher efficacy in per-protocol analysis (90.6% vs. 85.0%, P = 0.183). S. boulardii reduced the frequency of adverse events (P = 0.033) in 14-day regimen, particularly treatment-associated diarrhea (P = 0.032). However, after the adjustment to control Type I error, results lost their significance.
CONCLUSION CONCLUSIONS
Addition of S. boulardii to 14-day clarithromycin-containing triple regimen non-significantly lowers the likelihood of diarrhea and does not increase the eradication rate.

Identifiants

pubmed: 37942999
doi: 10.1097/CEJ.0000000000000858
pii: 00008469-990000000-00108
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Références

Cindoruk M, Erkan G, Karakan T, Dursun A, Unal S (2007). Efficacy and safety of Saccharomyces boulardii in the 14-day triple anti-Helicobacter pylori therapy: a prospective randomized placebo-controlled double-blind study. Helicobacter 12:309–316.
Czerucka D, Piche T, Rampal P (2007). Review article: yeast as probiotics -- Saccharomyces boulardii. Aliment Pharmacol Ther 26:767–778.
Duman DG, Bor S, Ozutemiz O, Sahin T, Oguz D, Istan F, et al. (2005). Efficacy and safety of Saccharomyces boulardii in prevention of antibiotic-associated diarrhoea due to Helicobacter pylori eradication. Eur J Gastroenterol Hepatol 17:1357–1361.
Freisberg S, Schulz C, Bornschein J (2022). Review: pathogenesis of Helicobacter pylori infection. Microb Health Dis 4:e171.
Gotteland M, Poliak L, Cruchet S, Brunser O (2005). Effect of regular ingestion of Saccharomyces boulardii plus inulin or Lactobacillus acidophilus LB in children colonized by Helicobacter pylori. Acta Paediatr 94:1747–1751.
Graham DY, Fischbach L (2010). Helicobacter pylori treatment in the era of increasing antibiotic resistance. Gut 59:1143–1153.
Heianza Y, Ma W, Li X, Cao Y, Chan AT, Rimm EB, et al. (2020). Duration and life-stage of antibiotic use and risks of all-cause and cause-specific mortality: prospective cohort study. Circ Res 126:364–373.
Homan M, Orel R (2015). Are probiotics useful in Helicobacter pylori eradication? World J Gastroenterol 21:10644–10653.
Hooi JKY, Lai WY, Ng WK, Suen MMY, Underwood FE, Tanyingoh D, et al. (2017). Global prevalence of Helicobacter pylori infection: systematic review and meta-analysis. Gastroenterology 153:420–429.
Kelesidis T, Pothoulakis C (2012). Efficacy and safety of the probiotic Saccharomyces boulardii for the prevention and therapy of gastrointestinal disorders. Therap Adv Gastroenterol 5:111–125.
Leja M, Dumpis U (2020). What would the screen-and-treat strategy for Helicobacter pylori mean in terms of antibiotic consumption? Dig Dis Sci 65:1632–1642.
Leja M, Park JY, Murillo R, Liepniece-Karele I, Isajevs S, Kikuste I, et al. (2017). Multicentric randomised study of Helicobacter pylori eradication and pepsinogen testing for prevention of gastric cancer mortality: the GISTAR study. BMJ Open 7:e016999.
Malfertheiner P, Megraud F, O’Morain CA, Gisbert JP, Kuipers EJ, Axon AT, et al.; European Helicobacter and Microbiota Study Group and Consensus panel (2017). Management of helicobacter pylori infection-the Maastricht v/florence consensus report. Gut 66:6–30.
Malfertheiner P, Megraud F, Rokkas T, Gisbert JP, Liou JM, Schulz C, et al. (2022). Management of Helicobacter pylori infection: the Maastricht VI/Florence consensus report. Gut 71: Advance online publication.
McFarland LV (2010). Systematic review and meta-analysis of Saccharomyces boulardii in adult patients. World J Gastroenterol 16:2202–2222.
Megraud F (2004). H pylori antibiotic resistance: prevalence, importance, and advances in testing. Gut 53:1374–1384.
Megraud F, Bruyndonckx R, Coenen S, Wittkop L, Huang TD, Hoebeke M, et al.; European Helicobacter pylori Antimicrobial Susceptibility Testing Working Group (2021). Helicobacter pylori resistance to antibiotics in Europe in 2018 and its relationship to antibiotic consumption in the community. Gut 70:1815–1822.
den Hoed CM, Vila AJ, Holster IL, Perez-Perez GI, Blaser MJ, Jongste JC de, et al. (2011). Helicobacter pylori and the birth cohort effect: evidence for stabilized colonization rates in childhood. Helicobacter 16:405–409.
Nyssen OP, Bordin D, Tepes B, Perez-Aisa A, Vaira D, Caldas M, et al.; Hp-EuReg Investigators (2021). European registry on Helicobacter pylori management (Hp-EuReg): patterns and trends in first-line empirical eradication prescription and outcomes of 5 years and 21 533 patients. Gut 70:40–54.
O’Connor A, Liou JML, Gisbert JP, O’Morain C (2020). The Effect of Helicobacter pylori antibiotic therapy on the microbiome. Microb Health Dis 2:e205.
Park JY, Polaka I, Parshutin S, Kikuste I, Isajevs S, Santare D, et al. (2019). Trial profile: pilot study of the multicentre randomised trial of H pylori eradication and pepsinogen testing for prevention of gastric cancer mortality (the GISTAR Pilot study). Microb Health Dis 1:e165.
Ruiter R, Wunderink HF, Veenendaal RA, Visser LG, de Boer MGJ (2017). Helicobacter pylori resistance in the Netherlands: a growing problem? Neth J Med 75:394–398.
Sakarya S, Gunay N (2014). Saccharomyces boulardii expresses neuraminidase activity selective for alpha2,3-linked sialic acid that decreases Helicobacter pylori adhesion to host cells. APMIS 122:941–950.
SERVICES, USDOHAH, NIo Health, and NC Institute (2022). Common Terminology Criteria for Adverse Events (CTCAE). [November 27, 2017]; Version 5.0:https://ctep.cancer.gov/protocoldevelopment/electronic_applications/docs/CTCAE_v5_Quick_Reference_8.5x11.pdf
Shi X, Zhang J, Mo L, Shi J, Qin M, Huang X (2019). Efficacy and safety of probiotics in eradicating helicobacter pylori: a network meta-analysis. Medicine (Baltim) 98:e15180.
Sjomina O, Lielause A, Rudule A, Vangravs R, Parsutins S, Polaka I, et al. (2022). Randomised clinical trial: comparison of efficacy and adverse effects of a standard triple clarithromycin-containing regimen with high-dose amoxicillin and bismuth therapy in Helicobacter pylori eradication. Eur J Cancer Prev 31:333–338.
Song MJ, Park DI, Park JH, Kim HJ, Cho YK, Sohn CI, et al. (2010). The effect of probiotics and mucoprotective agents on PPI-based triple therapy for eradication of Helicobacter pylori. Helicobacter 15:206–213.
Sugano K, Tack J, Kuipers EJ, Graham DY, El-Omar EM, Miura S, et al.; faculty members of Kyoto Global Consensus Conference (2015). Kyoto Global Consensus Report on Helicobacter pylori gastritis. Gut 64:1353–1367.
Szajewska H, Kolodziej M (2015). Systematic review with meta-analysis: Saccharomyces boulardii in the prevention of antibiotic-associated diarrhoea. Aliment Pharmacol Ther 42:793–801.
Szajewska H, Horvath A, Piwowarczyk A (2010). Meta-analysis: the effects of Saccharomyces boulardii supplementation on Helicobacter pylori eradication rates and side effects during treatment. Aliment Pharmacol Ther 32:1069–1079.
Yap TW, Gan HM, Lee YP, Leow AH, Azmi AN, Francois F, et al. (2016). Helicobacter pylori Eradication Causes Perturbation of the Human Gut Microbiome in Young Adults. PLoS One 11:e0151893.
Zamani M, Ebrahimtabar F, Zamani V, Miller WH, Alizadeh-Navaei R, Shokri-Shirvani J, et al. (2018). Systematic review with meta-analysis: the worldwide prevalence of Helicobacter pylori infection. Aliment Pharmacol Ther 47:868–876.
Zojaji H, Ghobakhlou M, Rajabalinia H, Ataei E, Jahani Sherafat S, Moghimi-Dehkordi B, et al. (2013). The efficacy and safety of adding the probiotic Saccharomyces boulardii to standard triple therapy for eradication of H pylori: a randomized controlled trial. Gastroenterol Hepatol Bed Bench 6(Suppl 1):S99–S104.

Auteurs

Olga Sjomina (O)

Institute of Clinical and Preventive Medicine.
Faculty of Medicine, University of Latvia, Riga, Latvia.

Inese Poļaka (I)

Institute of Clinical and Preventive Medicine.

Jekaterina Suhorukova (J)

Institute of Clinical and Preventive Medicine.

Reinis Vangravs (R)

Institute of Clinical and Preventive Medicine.

Sergejs Paršutins (S)

Institute of Clinical and Preventive Medicine.

Viktoria Knaze (V)

International Agency for Research on Cancer (IARC/WHO), Early Detection, Prevention and Infections Branch, Lyon, France.

Jin Young Park (JY)

International Agency for Research on Cancer (IARC/WHO), Early Detection, Prevention and Infections Branch, Lyon, France.

Rolando Herrero (R)

International Agency for Research on Cancer (IARC/WHO), Early Detection, Prevention and Infections Branch, Lyon, France.
Agencia Costarricense de Investigaciones Biomédicas, Fundación INCIENSA, Costa Rica.

Raul Murillo (R)

Hospital Universitario San Ignacio, Bogota, Columbia.

Mārcis Leja (M)

Institute of Clinical and Preventive Medicine.
Faculty of Medicine, University of Latvia, Riga, Latvia.

Classifications MeSH