Trial Title:
Epidemiology of Helicobacter Pylori Infection in Moscow
NCT ID:
NCT05775120
Condition:
Gastric Atrophy
Gastric Cancer
Helicobacter Pylori Infection
Conditions: Official terms:
Infections
Communicable Diseases
Helicobacter Infections
Gastritis, Atrophic
Study type:
Observational
Overall status:
Recruiting
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Diagnostic Test
Intervention name:
OLGA and H.pylori culture
Description:
Upper endoscopy will be performed by endoscopists using modern endoscopes (Fujinon
EG-590WR, Olimpus GIF-H190 and others) while patient is sedated. Using sterile biopsy
forceps, biopsy specimens will be taken from five areas of the stomach (two biopsy
specimens - greater and lesser curvature of the antrum of the stomach; two biopsy
specimens - lesser and greater curvature (or anterior and posterior wall) of the body of
the stomach and one from the corner of the stomach) for pathology assessment. Pathology
assessment of the gastritis stage and degree will be conducted according to the OLGA
system developed by the international group of gastroenterologists and pathologists
(Atrophy Club).
Arm group label:
Cohort 2
Summary:
H. pylori is transmitted from individual to individual and causes chronic active
gastritis in all infected people. H. pylori infection can result in gastroduodenal
ulcers, atrophic gastritis (AG), gastric carcinoma, and gastric MALT lymphoma.
More than 90% of gastric carcinomas are linked to H. pylori infection that causes chronic
AG. A long course of the disease leads to the loss of gastric glands (chronic AG)
followed by gastric intestinal metaplasia (GIM), dysplasia, and cancer. This defines two
cancer prevention strategies: primary that consists of detection and eradication of H.
pylori and secondary that focuses on endoscopic screening for pre-neoplastic lesions and
follow-up.
Primary prevention planning requires reliable information on the H. pylori prevalence in
the population. To design secondary prevention measures, an understanding of the age-sex
structure of precancerous changes in the gastric mucosa (the prevalence of atrophic
gastritis) is necessary.
H. pylori eradication is the basis of primary prevention of gastric cancer (GC).
Approximately 36,000 new cases of GC are registered in the Russian Federation each year,
and more than 34,000 patients die from the disease. Men get sick 1.3 times more often
than women, the peak incidence occurs at the age of over 50 years. The poor outcomes
reflect the late stage of diagnosis of this potentially preventable and treatable cancer.
The lack of up-to-date data on the H. pylori prevalence in Moscow hinders developing of
measures for the detection and timely treatment of this infection as well as the
reduction of GC morbidity and mortality.
Detailed description:
Aim: to analyze the prevalence of H. pylori infection and pre-neoplastic lesions in the
gastric mucosa in the Moscow population to develop a strategy for gastric cancer and
early detection.
Main goals:
1. To determine the prevalence of H. pylori in the Moscow population according to the
non-invasive diagnostic method - 13C-urea breath test.
2. To determine the prevalence of H. pylori in the Moscow population according to the
serological method - level of IgG antibodies to H.pylori.
3. To assess the prevalence of the gastric mucosa atrophy using serological markers
(pepsinogen-I, pepsinogen-II and Gastrin-17) in the different age groups of the
Moscow population.
4. To assess the state of the gastric mucosa according to endoscopic and morphological
studies using the OLGA system, and their correlation with serological markers of
atrophy (pepsinogen I level less than 30 µg/l and/or pepsinogen I/pepsinogen II
ratio less than 3).
5. Develop recommendations for GC prevention and early detection strategy.
The planned study will contain two sample cohorts:
Cohort 1 Screening for H. pylori infection is planned in 5121 citizens living in
different administrative districts of Moscow. The cohort will be formed based on age and
sex structure of the Moscow population. The presence of H. pylori will be analyzed using
2 non-invasive methods - 13C-urease breath test and serological test (detection of IgG
antibodies to H. pylori). An epidemiological questionnaire will be filled out for each
respondent which will display basic information on the patient (gender, age, eating
habits, bad habits, family history of cancer, etc.), as well as characterize the main
symptoms, if any.
Based on pepsinogen (PG) I levels and PG II (serological markers of atrophy of the
gastric mucosa), patients with a high risk of atrophic gastritis and precancerous lesions
in the gastric mucosa will be identified and the age and sex structure of atrophic
gastritis prevalence in Moscow will be constructed.
Cohort 2 From 5121 respondents, 500 patients with confirmed H. pylori infection and
serological markers of atrophic gastritis and a control group of infected with H. pylori
without serological markers of gastric mucosa atrophy will be selected. They will undergo
esophagogastroduodenoscopy with two gastric mucosa biopsies. The first will be conducted
according to the OLGA system with a pathology assessment of the stage and degree of
gastritis, while the second will be taken to determine the antimicrobial susceptibility
of H. (polymerase chain reaction and culture). Correlations between serological and
patholgy data on atrophy will be assessed in order to determine the reliability of
serological screening for atrophy in the Moscow population.
Research methods Diagnostics of H. pylori will be carried out using a modern,
non-invasive and accurate method - 13C-urea breath test (13C-UBT).
13C-UBT is recognized as the "gold standard" in the non-invasive diagnosis of H. pylori
infection, has a high sensitivity and specificity, above 95%. The test is easy to
perform, convenient for patients, and has no side effects.
The main reagent in this test is a solution of urea labeled with the carbon isotope C13.
The test is based on the hydrolysis of urea by urease produced by H. pylori that forms
ammonia and CO2. After an individual takes a test solution with 13C-labeled urea,
13C-labeled urea, and then 13C carbon dioxide, are absorbed into the bloodstream, enter
the lungs and are excreted with exhaled air. Initially, before taking the test solution,
the patient's exhaled air is collected in a special sealed bag No. 1. The patient then
drinks the test solution. After 30 minutes, a second air sample is exhaled into bag No. 2
that is also hermetically sealed. Then the air samples are analyzed on an infrared
spectrometer IR-force 200 that determines the isotope ratio 13С/12С. The increase in
labeled CO2 is expressed as delta over baseline (DOB). A DOB greater than 2.0‰ is used as
a diagnostic criterion for H. pylori infection.
The infrared (IR) spectrometers of IR-force generation consist of 13C and 12C isotope
high selectivity detectors. The specific absorption of CO2 in infrared light with a
wavelength of 2-8 microns is used. The spectrometer uses specific optical and
mathematical principles to reduce the mutual influence of 13CO2 and 12CO2, which
increases the accuracy of the instrument and guarantees the reliability of the entire
system. The IR analyzer determines the excess of the 13C/12C ratio over the baseline,
i.e. level before taking 13C-urea. In addition, a thermostat is used to maintain a
constant temperature and exclude the influence of the external environment.
This test will be conducted in Moscow Clinical Research Center named after A.S. Loginov
that is equipped with an IR-force infrared spectrometer and trained specialists.
The second diagnostic test for the presence of H. pylori infection is a serological
method - the detection of IgG antibodies to H. pylori. This method is recommended for
epidemiological studies but is inferior to the 13C-urease breath test in terms of
sensitivity, which is 76% to 84% while the specificity of the method is quite high - 90%.
The serological method is based on the detection of specific circulating antibodies to H.
pylori in the blood with enzyme immunoassay. The serological analysis will be carried out
in Moscow Clinical Research Center named after A.S. Loginov.
Pepsinogens analyses will allow identifying chronic atrophic gastritis and can be used in
large-cohorts screening to identify groups of individuals with a high risk of GC, which
would require further follow-up with basic endoscopy and pathology investigations. The
analysis of PG I provides information on the state of the glands in gastric fundus, PG II
- of all parts of the stomach, and their ratio (PG I / PG II) reflects the functional
status of the gastric mucosa and closely correlates with the progression of atrophic
changes in the gastric mucosa. Normal test results indicate a good condition of the
mucous membrane; PG I - 30-165 µg/l, Pepsinogen II - 4 to 22 µg/l, PG I / PG II ratio >
3. Patients with a low concentration of pepsinogen I (<30 ng/ml) and a low PG I / PG II
ratio (<3) are likely to have atrophic gastritis of the body of the stomach, precancerous
lesions (metaplasia, diplasia), as well as adenocarcinoma that will have to be confirmed
by endoscopic and pathology examination. One of the diagnostic sets that assess the serum
levels of PG I, PG II, and their ratio (PG I / PG II), as well as determine the
concentration of gastrin-17 and the presence of IgG antibodies to H. pylori, is
"GastroPanel". The analysis will be carried out in one of the labs of Moscow Clinical
Research Center named after A.S. Loginov using enzyme immunoassay.
Upper endoscopy will be performed by endoscopists using modern endoscopes (Fujinon
EG-590WR, Olimpus GIF-H190 and others) while patient is sedated. Using sterile biopsy
forceps, biopsy specimens will be taken from five areas of the stomach (two biopsy
specimens - greater and lesser curvature of the antrum of the stomach; two biopsy
specimens - lesser and greater curvature (or anterior and posterior wall) of the body of
the stomach and one from the corner of the stomach) for pathology assessment. Pathology
assessment of the gastritis stage and degree will be conducted according to the OLGA
system developed by the international group of gastroenterologists and pathologists
(Atrophy Club).
The stage of atrophy will be assessed on a 4-point scale from 0 to 3, depending on the
percentage of atrophied glands. No atrophy (0%) - 0 points, mild atrophy (1-30%) - 1
point, moderate atrophy (31-60%) - 2 points and 3 points - severe atrophy (more than
60%). The obtained data in points will be compared with the developed tables and
determine the stage of gastritis from 0 to IV. The degree of gastritis reflects the
severity of inflammation, is assessed in the same biopsy specimens by the
lymphoplasmacytic and leukocytic infiltration dense in accordance with the visual analog
scale, and is expressed in accordance with its assessment table in gradations from 0 to
IV.
Number of respondents: 5121 citizens.
Inclusion Criteria:
- Age 18 to 80 years;
- Signed informed consent form.
Criteria for non-inclusion:
- history of taking antibiotics, bismuth-containing drugs within 30 days before the
visit and proton pump inhibitors within 14 days before the visit;
- The presence of clinically significant neurological, cardiovascular,
gastrointestinal (total of partial gastrectomy), hepatic, renal, immune and other
diseases in medical history;
- Patients with diagnosed cancers of any kind who require specialized treatment and/or
are currently undergoing anticancer treatment;
- Psychiatric illnesses, including in the past, which, in the opinion of the
investigator, make the patient's participation in the study unacceptable;
- Pregnancy;
- Patients who tend to refuse to participate in the study and comply with doctor's
recommendations;
- Inability or unwillingness to give informed consent to participate in the study or
to fulfill the requirements of the study;
Criteria for exclusion of patients from the study
1. Refusal of further use of the drug;
2. Deterioration of objective indicators of the patient's condition;
Study design The total duration of participation of each patient in the study will be
about 2-6 weeks.
Visit 1 (5121 respondents) - day 0: inclusion in the study, informed consent signing,
filling out the questionnaire, conducting a 13C-urease breath test, taking a blood test
for Gastropanel.
Visit 2 - 500 respondents with serological signs of atrophy (pepsinogen I < 30 ng/ml
and/or PGI/PGII < 3 µg/l) and from the control group (14±7 days): EGDS + biopsy according
to OLGA.
Expected results
- Large-scale screening of persons for H. pylori infection will allow estimating the
actual prevalence of infection among residents of Moscow, which is necessary for
planning measures for the primary prevention of gastric cancer.
- Determination of serological markers of atrophy and their correlation with the data
of morphological studies will allow assessing the sex and age structure of
pre-neoplastic changes in the gastric mucosa, which is necessary to develop an
algorithm for secondary prevention of gastric cancer.
- The results of the study will allow developing a comprehensive program for the
prevention and early detection of gastric cancer based on an evidence-based
combination of primary and secondary prevention strategies.
Criteria for eligibility:
Study pop:
Screening for H. pylori infection is planned in 5121 citizens living in different
administrative districts of Moscow.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- • Age 18 to 80 years;
- Signed informed consent form.
Exclusion Criteria:
- Criteria for non-inclusion:
- history of taking antibiotics, bismuth-containing drugs within 30 days before
the visit and proton pump inhibitors within 14 days before the visit;
- The presence of clinically significant neurological, cardiovascular,
gastrointestinal (total of partial gastrectomy), hepatic, renal, immune and
other diseases in medical history;
- Patients with diagnosed cancers of any kind who require specialized treatment
and/or are currently undergoing anticancer treatment;
- Psychiatric illnesses, including in the past, which, in the opinion of the
investigator, make the patient's participation in the study unacceptable;
- Pregnancy;
- Patients who tend to refuse to participate in the study and comply with
doctor's recommendations;
- Inability or unwillingness to give informed consent to participate in the study
or to fulfill the requirements of the study;
Criteria for exclusion of patients from the study
1. Refusal of further use of the drug;
2. Deterioration of objective indicators of the patient's condition;
Gender:
All
Minimum age:
18 Years
Maximum age:
99 Years
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
A.S. Loginov Moscow Clinical Scientific Center
Address:
City:
Moscow
Country:
Russian Federation
Status:
Recruiting
Contact:
Last name:
Mariia Kiriukova, MD
Phone:
+7 495 303 15 57
Email:
d.bordin@mknc.ru
Investigator:
Last name:
Dmitry Bordin, MD,PHD
Email:
Principal Investigator
Start date:
July 1, 2022
Completion date:
January 15, 2025
Lead sponsor:
Agency:
Moscow Clinical Scientific Center
Agency class:
Other
Source:
Moscow Clinical Scientific Center
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05775120
