Abstract
The article provides a characterization of functional gastrointestinal disorders and highlights their prevalence. The prevalence of dyspepsia varies significantly across populations, which is attributed to differences in symptom interpretation and severity, diagnostic criteria, environmental factors, and the local prevalence of organic diseases such as ulcers or stomach cancer. Attention is drawn to the classification of these disorders, including functional gastrointestinal disorders (dyspepsia, chronic nausea and vomiting, bloating, rumination); functional esophageal disorders (functional chest pain, functional heartburn, reflux esophagitis, hypersensitivity, globus, functional dysphagia); functional bowel disorders (irritable bowel disease, functional bloating, functional constipation, functional diarrhea); and functional anorectal disorders (anorectal pain, functional defecation disorders).
Given that functional dyspepsia (FD) is one of the most common gastrointestinal conditions, the authors focus on the definitions and diagnosis of FD in accordance with the Rome IV criteria. It is emphasized that the Rome Committee proposed refining the definition of FD through more detailed symptom characterization. The diagnosis of "FD" is recommended for conditions of non-organic origin accompanied by a typical syndrome of dyspeptic complaints (epigastric pain, early satiety, postprandial fullness, epigastric burning) persisting for at least 12 weeks (not necessarily consecutive) over the last six months and not caused by an organic pathology that could explain these symptoms.
Attention is drawn to the classification of patients based on the presence of postprandial distress syndrome (PDS), epigastric pain syndrome (EPS), and the overlap of PDS and EPS symptoms, which is crucial for determining pharmacological treatment. The role of risk factors in tailoring individual treatments is also emphasized, particularly in cases of small intestinal bacterial overgrowth syndrome, which can persist in FD patients and contribute to pharmacotherapy resistance due to disruptions in the gut microbiome, necessitating changes in treatment algorithms.
The article underscores that H. pylori infection is considered a possible causative factor of FD only if eradication therapy is successful. Environmental influences, psychosocial factors, and gut-brain axis dysregulation are also discussed as contributing to the development and persistence of symptoms. The authors elaborate on pathophysiological mechanisms such as gastric emptying, impaired gastric accommodation, hypersensitivity (gastric and duodenal, triggered by distention, acid, etc.), persistent low-grade duodenal inflammation, increased mucosal permeability, and the role of dietary antigens.
References
2. Гріднєв О. Є. Сучасні можливості замісної терапії за допомогою травних ферментів мікробного походження. Здоров’я України. 2022; 1: 12–16.
3. Губергріц Н. Б. Диспепсія при функціональних та органічних захворюваннях органів травлення: між Сціллою і Харібдою. Вісник клубу панкреатологів. 2022; 2–3(55–56): 6–15.
4. Губергріц Н. Б., Бєляєва Н. В., Супрун О. О. Купірування проявів шлункової та кишкової диспепсії при хронічному панкреатиті. Вісник клубу панкреатологів. 2023; 3(60): 45–50.
5. Губергріц Н. Б., Бєляєва Н. В. Обміркований вибір ферментного препарату: як зробити? Вісник Клубу панкреатологів. 2023; 4: 39–48.
6. Губергриц Н. Б. «Їв би очима, та живіт не приймає!» — Панжест допоможе». Вісник клубу панкреатологів. 2024; 4(65): 4–7.
7. Ткач С. М., Харченко Н. В., Дорофєєв А. Е. Ерадикація надмірного бактеріального росту як метод лікування функціональної диспепсії. Сучасна гастроентерологія. 2021; 5–6(121–122): 12–20.
8. Ткач С. М. Сучасні підходи до ведення хворих із синдромом надмірного бактеріального росту. Здоров’я України. 2021; 1(59): 8–9.
9. Хайтович М. В. Екзокринна недостатність підшлункової залози: сучасні можливості замісної терапії. Здоров’я України. 2021; 22: 68–69.
10. Beger H. G., Buchler M., Hruban R. H. et al. The pancreas: an integrated textbook of basic science, medicine, and surgery. Oxford: Willey-Blackwell. 2023. 1360 p.
11. Crean G. P., Holden R. J., Knill-Jones R. P. et al. A database on dyspepsia. Gut. 1994; 35: 191–202.
12. Darwin E., Murni A. W., Nurdin A. E. The Effect of psychological stress on mucosal IL-6 and Helicobacter pylori activity in functional dyspepsia. Acta Med. Indones. 2017; 49(2): 99–104.
13. De Bortoli N., Tolone S., Frazzoni M. et al. Gastroesophageal reflux disease, functional dyspepsia and irritable bowel syndrome: common overlapping gastrointestinal disorders. Ann. Gastroenterol. 2018; 31(6): 639–648.
14. Drossman D. A. Functional gastrointestinal disorde history, pathophysiology, clinical features and Rome I. Gastroenterology. 2016; 150: 1262–1279.
15. Du L., Shen J., Kim J. J. et al. Impact of gluten consumption in patients with functional dyspepsia: A case-control study. J. Gastroenterol. Hepatol. 2018; 33(1): 128–133. http://doi.org/10.1111/jgh.13813.
16. Emara M. H., Salama R. I., Salem A. A. Demographic, endoscopic and histopathologic features among stool H. pylori positive and stool H. pylori negative patients with dyspepsia. Gastroenterology Res. 2017; 10(5): 305–310.
17. Hortmann G., Shah A., Morrison M. Pathophysiology of functional gastrointestinal disorders: a holistic overview. Dig. Dis. 2017; 35: 5–13.
18. Ford A. C., Marwaha A., Sood R. et al. Global prevalence of, and risk factors for, uninvestigated dyspepsia: a meta-analysis. Gut. 2015; 64(7): 1049–1057.
19. Gurusamy S. R., Shah A., Talley N. J. et al. Small sitestinal bacterial overgrowth in functional dyspepsia: A systematic review and meta-analysis. Am. J. Gastroenterol. 2021; 116: 935–942.
20. Losurdo G., Salvatore D’Abramo F. et al. The influence of small intestinal bacterial overgrowth in digestsve and extra-intestinal disoders. Int. J. Mol. Sci. 2020; 21(10): 3531. http://doi.org/10.3390/ijms21103531.
21. Mahadeva S., Goh K. L. Epidemiology of functional dyspepsia: a global perspective. World J. Gastroenterol. 2006; 12(17): 2661–2666. http://doi.org/10.3748/wjg.v12.i17.2661.
22. Mahadeva S., Ford A. C. Clinical and epidemiological differences in functional dyspepsia between the East and the West. Neurogastroenterol. Motil. 2016; 28(2): 167–174.
23. on Wulffen M., Talley N. J., Hammer J. et al. Overlap of irritable bowel syndrome and functional dyspepsia in the clinical setting: prevalence and risk factors. Dig. Dis. Sci. 2019; 64(2): 480–486.
24. Shanahan F., Quigley E. M. James Joyce and gastroenterology. Clin. Med. (Lond) 2008; 8: 632–633.
25. Shimura S., Ishimura N., Mikami H. et al. Small intestinal bacterial overgrowth in patients with refractory functional gastrointestinal disorders. J. Neurogastroenterol. Motil. 2016; 22(1): 60–68. http://doi.org/10.5056/jnm15116.
26. Whitcomb D. C., Lowe M. E. Human Pancreatic Digestive Enzymes. Dig. Sci. 2007; 52: 1–17.
27. Wang X., Li X., Ge W. et al. Quantitative evaluation of duodenal eosinophils and mast cells in adult patients with functional dyspepsia. Ann. Diagn. Pathol. 2015; 19(2): 50–56.