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Past
Long-term survivors of distal gastric cancer who underwent subtotal gastrectomy with Billroth II reconstruction (SGB2) are likely to experience gastrointestinal symptoms even years after surgery, which impacts negatively on their quality of life.1,2 The anatomical and physiological changes introduced by SGB2 suppress the gastric acid production and lead to a subsequent increase in gastric pH. This weakens the gastric barrier against food-borne and oral bacteria.3
Studies of long-term proton pump inhibitor (PPI) use (i.e. pharmacological suppression of gastric acid) have shown that a breach in gastric barrier is accompanied by very distinct changes of the microbiome that are associated with intestinal inflammation and even mortality.4 If similar changes are present after SGB2, this could be relevant for host health and long-term outcome after surgery. Therefore, we investigated if these specific changes are present in the microbiome of patients after SGB2.
Present
This cross-sectional proof-of-concept study included patients after SGB2 for early gastric cancer, and their non-gastrectomized in-house relatives as controls. Patients showed significant changes in their microbiomes compared with their relatives. These changes bore an obvious resemblance to changes observed in long-term PPI users, including an overrepresentation of Escherichia-Shigella, Enterococcus, and typical oral bacteria, such as Streptococcus, Veillonella, Oribacterium, and Mogibacterium (i.e. oralization). Furthermore, SGB2 was associated with intestinal inflammation showing an approximately 3.9-fold higher level of fecal calprotectin than their non-gastrectomized relatives. The most commonly documented gastrointestinal symptoms in gastrectomized patients were abdominal discomfort, diarrhea, and bloating, which were associated with distinct taxonomic changes of the gut microbiome.5
Future
This proof-of-concept study provided evidence for gut microbiome oralization and intestinal inflammation after SGB2. Similar to the situation in long-term PPI users, changes in the microbiome of SGB2 patients are associated with gastrointestinal symptoms, such as bloating, diarrhea, or discomfort. If longitudinal studies can confirm the causal link between SGB2 surgery and the here-described novel findings, it could introduce the gut microbiome as a new therapeutic target to improve general host health and quality of life in long-term survivors after SGB2. Microbiome-targeting therapies, such as pro- or prebiotics, fecal microbiota transplant, or even phage therapy, could be trialed to improve patients’ gastrointestinal health and reduce the severe impact of SGB2 on patients’ everyday life and well-being.
References
1. Yu W, Park KB, Chung HY, Kwon OK, Lee SS. Chronological changes of quality of life in long-term survivors after gastrectomy for gastric cancer. Cancer Res Treat. 2016;48(3):1030–6.
2. Brenkman HJF, Tegels JJW, Ruurda JP, Luyer MDP, Kouwenhoven EA, Draaisma WA, et al. Factors influencing health-related quality of life after gastrectomy for cancer. Gastric Cancer. 2018;21(3):524–32.
3. Carboni M, Guadagni S, Pistoia MA, Amicucci G, Tuscano D, Negro P, et al. The microflora of the gastric juice after billroth I and billroth II partial gastrectomy. Scand J Gastroenterol. 1986;21(4):461–70.
4. Horvath A, Rainer F, Bashir M, Leber B, Schmerboeck B, Klymiuk I, et al. Biomarkers for oralization during long-term proton pump inhibitor therapy predict survival in cirrhosis. Sci Rep. 2019;9(1):12000
Horvath A, Bausys A, Sabaliauskaite R, Stratilatovas E, Jarmalaite S, Shuetz B, et al. Distal gastrectomy with Billroth II reconstruction is associated with oralization of gut microbiome and intestinal inflammation: a proof-of-concept study. Ann Surg Oncol. 2020. https://doi.org/10.1245/s10434-020-08678-1.
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Augustinas Bausys and Angela Horvath declares no conflict of interest.
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Bausys, A., Horvath, A. ASO Author Reflections: Gut Microbiome Oralization and Intestinal Inflammation After Distal Gastrectomy with Billroth II Reconstruction is Linked to Gastrointestinal Symptoms. Ann Surg Oncol 27 (Suppl 3), 775–776 (2020). https://doi.org/10.1245/s10434-020-08703-3
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DOI: https://doi.org/10.1245/s10434-020-08703-3