IDDF2024-ABS-0052 Changes in gastric mucosa-associated microbiota associated with the development of neuroendocrine tumor in autoimmune gastritis

<h3>Background</h3> Autoimmune gastritis is accompanied by severe gastric corpus atrophy and hypergastrinemia, and neuroendocrine tumor (NET) sometimes develops. We aimed to investigate changes in gastric mucosa-associated microbiota associated with the development of gastric NET in autoimmune gastritis. <h3>Methods</h3> In a total of 19 patients diagnosed with autoimmune gastritis based on achlorhydria by 24 h impedance-pH monitoring examination, anti-gastric parietal cell antibody/anti-intrinsic factor antibody, and severe gastric corpus atrophy in upper gastrointestinal endoscopy at Osaka Metropolitan University Hospital, NET (+) group included patients who have developed NET (n=7) and NET (-) group included patients who have never developed NET (n=12). The control group included 11 patients diagnosed as <i>H. pylori</i>-uninfected. Bacterial DNA was enzymatically extracted from biopsy specimens of gastric mucosa, amplified by polymerase chain reaction using primers specific to the V3–V4 region of 16S rRNA, and analyzed using QIIME2<sup>™</sup>. <h3>Results</h3> The median tumor size of NETs was 5.5 mm (interquartile range, 4.5–6.0), 50.0% of lesions were located at the upper gastric body, and all lesions were NETG1 in WHO classification. In changes of microbial species in Fusobacteriota phylum, <i>Fusobacterium nucleatum</i> (<i>p</i> = 0.012) and<i> Fusobacterium periodonticum</i> (<i>p</i> &lt; 0.001) were significantly increased in NET (+) group. In changes of microbial species in Proteobacteria phylum, <i>Haemophilus parainfluenzae</i> (<i>p</i> &lt; 0.001),<i> Haemophilus parahaemolyticus</i> (<i>p</i> = 0.001), and <i>Haemophilus haemolyticus</i> (<i>p</i> &lt; 0.001) were significantly increased in NET (+) group. In contrast, in changes of microbial species in Firmicutes phylum, <i>Streptococcus salivarius</i> (<i>p</i> &lt; 0.001) and <i>Veillonella atypica</i> (<i>p</i> = 0.004) were significantly decreased in NET (+) group. Number of operational taxonomic unit was not significantly different between 3 groups. Alpha diversity (Faith’s phylogenetic diversity) was significantly higher in NET (+) group than in NET (-) group (<i>p</i> = 0.043). Beta diversity (weighted and unweighted UniFrac) was significantly different between NET (-) group and NET (+) group (<i>p</i> = 0.001). <h3>Conclusions</h3> It was suggested that gastric mucosa-associated microbiota in patients with autoimmune gastritis who had developed gastric NETs may have changed compared to those who had not.

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Journal
Clinical Gastroenterology
Published
2024-08-01
DOI
https://doi.org/10.1136/gutjnl-2024-iddf.236
Primary Topic
Helicobacter pylori-related gastroenterology studies
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article

IDDF2024-ABS-0052 Changes in gastric mucosa-associated microbiota associated with the development of neuroendocrine tumor in autoimmune gastritis

Koji Otani, Shuhei Hosomi, Fumio Tanaka, Yasuhiro Fujiwara et al.
Clinical Gastroenterology
Helicobacter pylori-related gastroenterology studies
article

IDDF2024-ABS-0052 Changes in gastric mucosa-associated microbiota associated with the development of neuroendocrine tumor in autoimmune gastritis

Koji Otani, Shuhei Hosomi, Fumio Tanaka, Yasuhiro Fujiwara, Akira Higashimori
article en

Abstract

<h3>Background</h3> Autoimmune gastritis is accompanied by severe gastric corpus atrophy and hypergastrinemia, and neuroendocrine tumor (NET) sometimes develops. We aimed to investigate changes in gastric mucosa-associated microbiota associated with the development of gastric NET in autoimmune gastritis. <h3>Methods</h3> In a total of 19 patients diagnosed with autoimmune gastritis based on achlorhydria by 24 h impedance-pH monitoring examination, anti-gastric parietal cell antibody/anti-intrinsic factor antibody, and severe gastric corpus atrophy in upper gastrointestinal endoscopy at Osaka Metropolitan University Hospital, NET (+) group included patients who have developed NET (n=7) and NET (-) group included patients who have never developed NET (n=12). The control group included 11 patients diagnosed as <i>H. pylori</i>-uninfected. Bacterial DNA was enzymatically extracted from biopsy specimens of gastric mucosa, amplified by polymerase chain reaction using primers specific to the V3–V4 region of 16S rRNA, and analyzed using QIIME2<sup>™</sup>. <h3>Results</h3> The median tumor size of NETs was 5.5 mm (interquartile range, 4.5–6.0), 50.0% of lesions were located at the upper gastric body, and all lesions were NETG1 in WHO classification. In changes of microbial species in Fusobacteriota phylum, <i>Fusobacterium nucleatum</i> (<i>p</i> = 0.012) and<i> Fusobacterium periodonticum</i> (<i>p</i> &lt; 0.001) were significantly increased in NET (+) group. In changes of microbial species in Proteobacteria phylum, <i>Haemophilus parainfluenzae</i> (<i>p</i> &lt; 0.001),<i> Haemophilus parahaemolyticus</i> (<i>p</i> = 0.001), and <i>Haemophilus haemolyticus</i> (<i>p</i> &lt; 0.001) were significantly increased in NET (+) group. In contrast, in changes of microbial species in Firmicutes phylum, <i>Streptococcus salivarius</i> (<i>p</i> &lt; 0.001) and <i>Veillonella atypica</i> (<i>p</i> = 0.004) were significantly decreased in NET (+) group. Number of operational taxonomic unit was not significantly different between 3 groups. Alpha diversity (Faith’s phylogenetic diversity) was significantly higher in NET (+) group than in NET (-) group (<i>p</i> = 0.043). Beta diversity (weighted and unweighted UniFrac) was significantly different between NET (-) group and NET (+) group (<i>p</i> = 0.001). <h3>Conclusions</h3> It was suggested that gastric mucosa-associated microbiota in patients with autoimmune gastritis who had developed gastric NETs may have changed compared to those who had not.

Clinical Gastroenterology
Osaka Metropolitan University (JP), Tokyo Metropolitan University (JP)
Good health and well-being
Openalex Percentile: Top 62%
Helicobacter pylori-related gastroenterology studies
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