Профилактика рака желудка, как первичная, так и вторичная, является крайне важным компонентом ведения пациентов гастроэнтерологического профиля. Весьма актуальны правильный сбор анамнеза с оценкой вероятности развития наследственного (семейного) рака, устранение факторов риска (нарушенное питание, привычные/хронические интоксикации, ожирение, инфекция Helicobacter pylori и другие), а также применение гастропротекторов (в частности, препарата Регастим Гастро), особенно у лиц с потенциально предраковым состоянием – хроническим атрофическим гастритом. По данным двойного слепого плацебо-контролируемого рандомизированного исследования препарата Регастим Гастро (действующее вещество – альфа-глутамил триптофан) в терапии хронического атрофического гастрита установлено, что этот препарат обладает мощным противовоспалительным действием и регенераторной активностью. Прием препарата Регастим Гастро по сравнению с плацебо статистически значимо способствовал снижению количества клеток воспалительной инфильтрации на 1 мм2 слизистой оболочки желудка. В большей степени Регастим Гастро способствовал уменьшению эозинофильной (в 3 раза) и нейтрофильной (в 4 раза) инфильтрации слизистой оболочки желудка. Он также снижал количество макрофагов, лимфоцитов и плазмоцитов. Помимо противовоспалительных свойств препарат оказывал выраженный регенераторный эффект. На фоне приема Регастим Гастро имело место статистически значимое (р=0,028) увеличение количества желез на 1 мм2 слизистой оболочки желудка – на 26,1% в сравнении с исходными показателями скрининга. В группе пациентов, принимавших плацебо, напротив, отмечалось прогрессирование патологического процесса, сопровождавшееся снижением количества желез на 1 мм2 слизистой оболочки желудка после окончания лечения в сравнении с исходными показателями. После курса терапии у пациентов, принимавших препарат Регастим Гастро количество желез на 1 мм2 слизистой оболочки желудка было статистически значимо больше в сравнении с результатами в группе принимавших плацебо (р=0,013). Вследствие комплексного воздействия препарата отмечалось улучшение функциональных параметров слизистой оболочки желудка. После курса Регастим Гастро отмечалось улучшение кислотопродукции: смещение в кислую сторону среднего значения рН (в 1,6 раза) и повышение значения индекса кислотности как при сравнении с исходными значениями (в 5,4 раза), так и в сравнении с группой принимавших плацебо (в 2,9 раза). Назначение Регастим Гастро пациентам с гастритом, как H. pylori (+), так и H. pylori (-), еще до развития атрофии слизистой оболочки желудка с целью уменьшения фактора воспаления и предупреждения возникновения атрофии может иметь максимальную антиканцерогенную активность.
Prevention of gastric cancer, both primary and secondary, is an extremely important component of the management of gastroenterological patients. The correct collection of anamnesis with an assessment of the hereditary (family) cancer risk, the action of risk factors (eating disorders, habitual/chronic intoxication, obesity, Helicobacter pylori infection, etc.), as well as the use of gastroprotectors (in particular, the drug Regastim Gastro), especially in persons with potentially precancerous the condition is chronic atrophic gastritis. According to the data of a double-blind placebo-controlled randomized study Regastim Gastro (active ingredient – alpha-glutamyl tryptophan) in the treatment of chronic atrophic gastritis, it was found that this drug has a powerful anti-inflammatory effect and regenerative activity. Taking the drug Regastim Gastro, compared with placebo, statistically significantly contributed to a decrease in the number of inflammatory infiltration cells per 1 mm2 of the gastric mucosa. Regastim Gastro decreases in eosinophilic (3 times) and neutrophilic (4 times) infiltration of the gastric mucosa and also reduced the number of macrophages, lymphocytes and plasmocytes. In addition to anti-inflammatory properties, the drug also had a pronounced regenerative effect. Taking of Regastim Gastro statistically significant (p=0.028) increases in the number of glands per 1 mm2 of the gastric mucosa – by 26.1% compared with the initial screening indicators. In the group of patients taking placebo, on the contrary, there was a further progression of the pathological process, accompanied by a decrease in the number of glands per 1 mm2 of the gastric mucosa after the end of treatment in comparison with the initial indicators. After the course of therapy, the number of glands per 1 mm2 of the gastric mucosa in patients taking the drug Regastim Gastro was statistically significantly higher in comparison with the results in the placebo group (p=0.013). After the course of Regastim Gastro, there was an improvement in acid production: a shift in the acidic side of the average pH value (1.6 times) and an increase in the value of the acidity index, both when compared with the initial values (5.4 times) and in comparison with the placebo group (2.9 times). The intake of Regastim Gastro to patients with gastritis, both H. pylori (+) and H. pylori (-) before the development of atrophy of the gastric mucosa can reduce the inflammatory factor, prevent the occurrence of atrophy and may have maximum anti-carcinogenic action.
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1 ФГБОУ ВО «Санкт-Петербургский государственный педиатрический медицинский университет» Минздрава России, Санкт-Петербург, Россия;
2 ФГБОУ ВО «Первый Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова» Минздрава России, Санкт-Петербург, Россия;
3 ФГБНУ «Институт экспериментальной медицины», Санкт-Петербург, Россия;
4 ФГБОУ ВО «Российский государственный педагогический университет им. А.И. Герцена», Санкт-Петербург, Россия;
5 ФГБУ «Научно-клинический центр токсикологии им. акад. С.Н. Голикова» ФМБА России, Санкт-Петербург, Россия;
6 АННО ВО «Научно-исследовательский центр “Санкт-Петербургский институт биорегуляции и геронтологии”», Санкт-Петербург, Россия
*baryshnikova_nv@mail.ru
________________________________________________
Yury P. Uspenskiy1,2, Natalia V. Baryshnikova*1,2,3, Alexey A. Krasnov4, Sergey V. Petlenko5, Vera A. Apryatina6
1 Saint Petersburg State Pediatric Medical University, Saint Petersburg, Russia;
2 Pavlov First Saint Petersburg State Medical University, Saint Petersburg, Russia;
3 Institute of Experimental Medicine, Saint Petersburg, Russia;
4 Herzen Russian State Pedagogical University, Saint Petersburg, Russia;
5 Golikov Research Clinical Center of Toxicology, Saint Petersburg, Russia;
6 Saint Petersburg Institute of Bioregulation and Gerontology, Saint Petersburg, Russia
*baryshnikova_nv@mail.ru