Publication of the article:
«Bulletin of problems biology and medicine», 2014 Issue 3 part 1, 110,
Diagnostics of Dysplastic Changes in Gastric Mucosa Epithelium Made by Histological and Immuno- histochemical Methods in Patients with Chronic Gastric Ulcer
About the author:
Kharchenko A. V.
Heading:
CONTENTS
Type of article:
Scentific article
Annotation:
The highest rate of mitotic index (22,31,7%) has been detected in patients with chronic gastric ulcer in the area around the ulcer (AU). In the pyloric (P) part (20,02,8%) and the lesser curvature (LC) (19,82,3%) this rate was lower, but no significant difference has been detected. The lowest rate of mitotic index has been detected in the body (B) of stomach (14,34,5%), which is significantly lower р<0,01 than in other parts of the stomach. As regards the number of mitosis at metaphase, the index around the ulcer (37,3 ± 7,8%) was lower than in the pyloric part (46,9 ± 2,8%) and in lesser curvature (44,9 ± 2,8%). Number of mitosis at metaphase was significantly lower (р<0,01) in the body of stomach (20,68,3%) than around the ulcer, in pyloric part and lesser curvature, i. e., 37,37,8%, 46,92,8% and 44,92,8%, respectively. Similarly, the rate of pathological mitoses tended to be reduced, which was significantly lower (р<0,01) in the body of stomach (3,82,5%) as compared with the area around the ulcer (10,61,3%), in pyloric part (15,61,9%) and lesser curvature (13,71,9%). High proliferative activity is confirmed by the Кі-67 marker; marker index is > 30,0%. Diagnostics, made by the histological method, specifying the mitotic regimen, and by immunohistochemical Кі-67 marker (МІВ-1clone) showed changes in gastric mucosa epithelium, specific to gastric mucosa epithelium dysplasia of various severity in patients, suffering from chronic gastric ulcer. In cases of indicated dysplasia the Кі-67 marker expression is the evidence of high proliferative activity in the areas of recesses epithelium dysplasia and proliferation of infiltrate cells in stroma, which is specific to each group of dysplasia. Findings of correlation analysis between the degree of mucosa epithelium dysplasia, made by the histological method and Кі-67 marker indices of gastric mucosa samples showed that the Pearson’s correlation coefficient, rxy, constituted 0,931, which makes it possible to conclude about the existence of very strong relationship. Coefficient of determination, D=rxy^2, constituted 0,866. Critical value of correlation coefficient with probability of 0, 95 corre- sponded to 0, 2732. Critical value of correlation coefficient with probability of 0, 99 corresponded to 0, 3511. The comparison of correlation coefficient, rxy, with critical (tabulated) value, rcr, worth of 0, 95, corre- sponded to rxy>rcr. The comparison of correlation coefficient, rxy, with critical (tabulated) value, rcr, worth of 0, 99, corresponded to rxy>rcr. Covariation coefficient constituted 522,914, which makes it possible to conclude about sta- tistically significant dependence between the indices with probability of 0, 99. Between the indices of mitotic regimen of gastric mucosa, i. e., mitotic index, number of mitoses at metaphase, number of pathological mitoses, and degree of dysplasia of gastric mucosa epithelium in patients with chronic gas- tric ulcer, the Pearson’s correlation coefficient, rxy, constituted 0,197, 0,607 and 0,881, respectively, corresponding to weak, moderate and strong relationship. Coefficient of determination, D=rxy^2, constituted 0,039, 0,369 and 0,776, respectively. Critical value of correlation coefficient with probability of 0,95 constituted 0, 2732. Critical value of correlation coefficient with probability of 0,99 constituted 0,3511. The comparison of correlation coefficient, rxy, with critical (tabulated) value, rcr, worth of 0, 95, corresponded to rxyrcr, respectively. Critical value of correlation coefficient with probability of 0,99 corresponded to rxyrcr, respectively. Covariation coefficient constituted 0,389, 3,442 and 0,859, respec- tively, which concluded that no correlation has been detected between the mitotic index and degree of dysplasia of gastric mucosa epithelium; however, statistically significant dependence with probability of 0,99 has been detected between the rates of mitoses at metaphase, pathological mitoses and index of gastric mucosa epithelium dysplasia. Indices of mitotic regimen tend to be increased in the following direction: B→ AU →LC→P. Between the indices of mitotic regimen of gastric mucosa and degree of manifestation of dysplasia of gastric mucosa epithelium in patients with chronic gastric ulcer, the Pearson’s correlation coefficient, rxy, constituted 0,197, 0,607 and 0,881, respectively, corresponded to weak, moderate and strong relationship. Between the degree of dysplasia, judging by the indices, obtained by the histological method and Кі-67 marker indices of gastric mucosa samples, the Pearson’s correlation coefficient, rxy, constituted 0,931, identifying the ex- istence of very strong relationship. The Кі-67 marker expression correlates with indices of dysplasia, obtained by the histological method, showing that it is informative in detecting proliferative activity of gastric mucosa. The abovementioned concludes that there is very strong correlation between the degree of dysplasia, detected by the histological method and Кі-67 marker. The Pearson’s correlation coefficient, rxy, constituted 0,931. The over- all result shows statistically significant dependence with probability of 0, 99.
Tags:
mitotic regimen, Кі-67 marker, Pearson’s correlation coefficient
Bibliography:
- Алов И. А. Определение митотического режима ткани в патогистологической диагностике предраковых процессов и рака (методические указания) / И. А. Алов, М. Е. Аспиз., И. А. Казанцева. – М.: 1973. – 143 с.
- Аруин Л. И. Морфологическая диагностика болезней желудка и кишечника / Л. И. Аруин, Л. Л. Капуллер, В. А. Исаков. – М.: Триада – Х, 1998. – 483 с.
- Аруин Л. И. Международная классификация хронического гастрита: что следует принять и что вызывает сомнения / / Л. И. Аруин, А. В. Кононов, С. И. Мозговой // Арх. пат. – 2009. – Вып. 4. – С. 11–18.
- Карселадзе А. И. Некоторые основополагающие понятия онкоморфологии в свете достижений современной молеку- лярной биологии / А. И. Карселадзе // Арх. пат. – 2009. – Вып. 5. – С. 17–21.
- Кононов А. В. Морфогенез атрофии слизистой оболочки желудка как основа фенотипа хронического гастрита / А. В. Кононов, С. И. Мозговой, М. В. Маркелова, А. Г. Шиманская // Арх. пат. – 2011. – Вып. 3. – С. 26 – 31.
- Меркулов А. Т. Курс патологoгистологической техники / А. Т. Меркулов. – Л.: Медицина, 1969. – 243 с.
- Садчиков В. Д. Рак из язвы или изъязвлённый рак желудка? / В. Д. Садчиков, К. А. Галахин // Врач. дело. – 1997. – № 2. – С. 137–141.
- Садчиков В. Д. Хроническая язва и рак желудка / В. Д. Садчиков, А. С. Дудниченко, М. В. Садчикова // Проблеми медичної науки та освіти. – 2000. – № 3. – С. 17–20.
- Farinati F. Early and advanced gastric cancer during Follow-up of apparently benign gastric ulcer: Significance of the presence of epithelial dysplasia / F. Farinati, F. Cardin, F. Di Mario // J. Surg. Oncol. – 1987. – Vol. 36, № 4. – P. 263–267.
- Figus I. A. A gyomornyal kahartya dysplasia janak clinical jelentosege / I. A. Figus, I. Papp, A. Vitez // Orv. hetilap. – 1986. –Vol. 127, №47. – P. 2875 – 2880.
- Nagayo T. Histogenesis and precursors of human gastric cancer. Research and practice / T. Nagayo. – Berlin : Springer- Verlag. – 1988. – 190 p.
Publication of the article:
«Bulletin of problems biology and medicine» Issue 3 part 1 (110), 2014 year, 366-370 pages, index UDK 616. 33 – 008. 3 : 6 : [616 – 07]