Comparison of clinical-metabolic efficacy of pre- and probiotics in the conducted optimized protocols of eradication therapy of Helicobacter pylori infection

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Abstract

Low patient compliance due to the development of adverse events in the form of antibiotic-associated diarrhea (AAD) is considered as the main reason for the failure of the eradication of optimized anti-Helicobacter therapy regimens. A key mechanism for the development of AAD is to reduce the number and species diversity of bacteria that form butyric acid.

Aim. The purpose of this study was to study the comparative effect on the clinical effectiveness of eradication therapy (ET) of Helicobacter pylori infection and metabolic changes in the colon microbiota of additional inclusion in the optimized treatment regimen of the combined prebiotic Zakofalk® (inulin + butyrate) with probiotics (lacto- and bifidobacteria in an amount of at least 1017 СFU).

Materials and methods. 120 patients with chronic gastroduodenal diseases and infected H. pylori were еxamined. A comparative analysis of the effect of a combined prebiotic and lacto-bifid-containing probiotics on improving the effectiveness of the optimized ET scheme and improving its tolerability, as well as on the quantitative and qualitative content of short-chain fatty acids (SFA) in feces. The success of eradication was controlled by a 13C urease breath test.

Results. According to the results of the study in randomized groups of patients, an excellent percentage of eradication (95%) was achieved in patients who performed ET with the addition of the prebiotic Zakofalk®. In the same group of patients, there was an increase in the absolute content of SFA and a significant increase in the concentration of butyric acid. In the group of patients who received ET with the addition of probiotics, an acceptable level of eradication was achieved (85.7%), but no changes in SFA were found indicating an increase in the number or activity of the butyrate-producing flora. Patients who performed ET without the addition of pre-probiotics did not achieve the «target» percentage of successful eradication (83.3%), and a significant quantitative decrease in SFA was found with a significant decrease in the proportion of butyric acid.

Conclusion. The inclusion of Zakofalk® in the ET scheme, in comparison with probiotics, significantly increases the probability of successful eradication, more effectively restores the metabolic potential of the microbiota, and prevents the development of AAD.

About the authors

L. I. Butorova

Sechenov First Moscow State Medical University (Sechenov University)

Author for correspondence.
Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0003-4689-2844

к.м.н., доц. каф. поликлинической терапии Института клинической медицины им. Н.В. Склифосовского

Russian Federation, Moscow

M. D. Ardatskaya

Central State Medical Academy of the President of the Russian Federation

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0001-8150-307X

д.м.н., проф. каф. гастроэнтерологии

Russian Federation, Moscow

M. A. Osadchuk

Sechenov First Moscow State Medical University (Sechenov University)

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0003-0485-6802

д.м.н., проф., зав. каф. поликлинической терапии Института клинической медицины им. Н.В. Склифосовского

Russian Federation, Moscow

N. G. Kadnikova

Central Clinical Hospital for Rehabilitation Treatment

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0002-8228-0522

зав. отд-нием, врач-гастроэнтеролог

Russian Federation, Moscow

E. I. Lukianova

City Polyclinic №201

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0002-4989-9964

врач-гастроэнтеролог высшей квалификационной категории, внештат. специалист, гастроэнтеролог Зеленоградского округа Москвы

Russian Federation, Zelenograd

R. G. Plavnik

ISOCARB LLC

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0001-5448-8812
SPIN-code: 9614-1127

к.м.н., зам. ген. дир. по науке и внедрению

Russian Federation, Moscow

E. V. Sayutina

Sechenov First Moscow State Medical University (Sechenov University)

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0001-9611-5096

к.м.н., ассистент каф. поликлинической терапии Института клинической медицины им. Н.В. Склифософского

Russian Federation, Moscow

T. B. Topchiy

Central State Medical Academy of the President of the Russian Federation

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0003-4491-881X

к.м.н., доц. каф. гастроэнтерологии

Russian Federation, Moscow

E. M. Tuayeva

Sechenov First Moscow State Medical University (Sechenov University)

Email: ludmilabutorova@mail.ru
ORCID iD: 0000-0002-6542-2277

к.м.н., ассистент каф. поликлинической терапии Института клинической медицины им. Н.В. Склифософского

Russian Federation, Moscow

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