研究者業績
基本情報
経歴
3-
2021年4月 - 現在
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2020年4月 - 2021年3月
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- 2019年3月
学歴
1-
1986年4月 - 現在
委員歴
6受賞
13-
2017年5月
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2016年5月
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2015年4月
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2014年5月
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2013年5月
論文
1243-
Digestion 2025年4月9日INTRODUCTION: Gastrectomy considerably affects the gut microbiome; however, the association between dysbiosis and post-gastrectomy syndrome remains to be explored. This study prospectively explored fecal gut microbiota alterations before and 3 months after gastrectomy, investigating their potential association with weight loss. METHODS: The gut microbiome of 21 patients with gastric cancer scheduled for gastrectomy in April-October 2022 was analyzed using 16S rRNA gene Next-Generation Sequencing. Their microbiome profiles were compared to those of healthy controls. Bacterial taxa demonstrating significant changes were determined using the Linear Discriminant Analysis Effect Size algorithm and further analyzed for their relationship with weight loss in the gastrectomy cohort. RESULTS: Postoperative complications (≥grade 2) were observed in 14.3% of patients. Postoperative weight loss was -10.9%, with the following breakdown: distal (-7.0%), total (-13.5%), and proximal (-14.0%) gastrectomy (P = 0.003). Microbiota analysis demonstrated a significant incline in the abundance of the Streptococcus salivarius group and a decline in Bacteroides uniformis in patients with gastric cancer compared to healthy controls. The S. salivarius group exhibited a further increase, while B. uniformis showed signs of recovery after gastrectomy. Additionally, 5α-reductase gene levels, reported to decrease as several cancers progress, were found to elevate post-surgery. Furthermore, patients experiencing greater weight loss showed a significant reduction in Faecalibacterium prausnitzii levels, while lower serum prealbumin and zinc levels were associated with the abundance of Escherichia coli. CONCLUSION: Gastrectomy significantly alters the gut microbiome. Supporting microbiome health with prebiotics may help alleviate postoperative issues and improve patients' quality of life.
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DEN open 5(1) e413 2025年4月The new Kyoto guidelines for the management of intraductal papillary mucinous neoplasm (IPMN) provide evidence-based recommendations for the diagnosis and treatment of IPMN. Endoscopic ultrasonography (EUS) is a diagnostic modality with a high spatial resolution that allows detailed observation and obtaining cyst fluid or tissue samples via EUS-guided fine needle aspiration (EUS-FNA). Currently, EUS is an indispensable examination method for the diagnosis of pancreatic diseases. On the other hand, there have been concerns that EUS imaging tends to be highly operator-dependent, and may lack objectivity. Previous guidelines have assigned EUS as an option for patients with worrisome features. However, recent reports indicate that the sensitivity of EUS for the diagnosis of mural nodules (MNs) is more than 90%, comparable or superior to that of contrast-enhanced computed tomography or magnetic resonance cholangiopancreatography. The specific advantages of EUS in the diagnosis of IPMN are: (1) high spatial resolution imaging for the diagnosis of MNs, (2) contrast-enhanced EUS for differentiation of intra-cystic MNs from mucous clots, and (3) pathological diagnosis using EUS-FNA and differential diagnosis of a pancreatic cystic tumor by cystic fluid analysis. In order to utilize EUS in the diagnosis of IPMN, endoscopists are required to have the skills to provide sufficiently objective imaging findings.
MISC
440-
GASTROINTESTINAL ENDOSCOPY 65(5) AB207-AB207 2007年4月
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Endoscopy 39(Suppl 1) E7-E8 2007年2月 査読有り
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J Biomed Mater Res A 79(4) 771-778 2006年12月15日 査読有りRecently, decellularized tissue has been reported to have the potential to regenerate a variety of tissues. However, the optimal protocol for a decellularized esophagus has not been studied. Here, we investigated the effect of different decellularization protocols on the histology and biocompatibility of decellularized esophagi in view of future applications to tissue engineering. The esophageal mucosal epithelium (EP) from 4-week-old Wistar rats was enzymatically dissociated and cultured with growth-arrested feeder cells. Two methods for decellularization using deoxycholic acid (DEOX) or Triton X-100 (TRITON) were compared on esophagi from adult Wistar rats. Those treated with DEOX showed superior mechanical properties, maintenance of extracellular matrix, and lower DNA content than those treated with TRITON. To evaluate the biocompatibility of the scaffold, cultured (passage 3) esophageal epithelial cells were seeded inside the decellularized esophagus and cultured for 7 days. The cells seeded onto the decellularized esophagus were examined histologically and immunocytochemically. Esophageal epithelial cells were stratified into three to four cellular layers in vitro inside the decellularized esophagus, to show polarity. The results from immunocytochemistry indicated that the seeded epithelial cells expressed characteristic marker proteins for native esophageal EP. Decellularized esophagus showed suitable compatibility as a scaffold material for esophageal tissue engineering.
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PLASMA PHYSICS AND CONTROLLED FUSION 48(12B) B383-B390 2006年12月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB167-AB167 2006年4月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB175-AB175 2006年4月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB307-AB307 2006年4月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB179-AB179 2006年4月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB258-AB258 2006年4月
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GASTROINTESTINAL ENDOSCOPY 63(5) AB167-AB167 2006年4月
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GASTROENTEROLOGY 130(4) A642-A643 2006年4月
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GASTROENTEROLOGY 130(4) A421-A422 2006年4月
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GASTROENTEROLOGY 130(4) A637-A637 2006年4月
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J Gastroenterol Hepatol 21(3) 545-551 2006年3月 査読有りBACKGROUND AND AIMS: Infection with Helicobacter pylori (Hp) has been linked to atrophic gastritis, an inflammatory precursor of non-cardia gastric carcinoma. Mutations in the p53 gene are one of the most frequent genetic alterations in gastric carcinoma. In a subgroup of atrophic gastritis, antiparietal cell antibody (APCA) has been detected. This study was aimed to clarify the role of APCA in the progression of atrophic gastritis and gastric carcinogenesis, and to determine the relationship of the severity of atrophic gastritis to gastric carcinoma and to p53 mutations. METHODS: In 494 control subjects and 284 gastric carcinoma patients, serum APCA was evaluated and all subjects and patients were classified into four groups using serologic markers (anti-Hp IgG antibody and pepsinogen (PG) test: positive; PG I < 70 microg/L and PG I/II ratio < 3.0) as follows: A, HP- PG-; B, HP+ PG-; C, HP+ PG+ and D, HP- PG+. p53 mutations were analyzed in 174 of 284 patients. RESULTS: Antiparietal cell antibody seropositivity increased from group B to D, however, no difference in its positivity was found between controls and patients. The incidence of gastric carcinoma increased from A to D, especially the intestinal subtype. The frequency of p53 gene mutations was higher in PG+ than in PG- gastric carcinoma. CONCLUSIONS: Antiparietal cell antibody seropositivity is involved in the progression of a subgroup of atrophic gastritis, but not associated with gastric carcinogenesis. Severe atrophic gastritis is associated with susceptibility to gastric carcinoma, especially the intestinal subtype, and p53 mutations.
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Nippon rinsho. Japanese journal of clinical medicine 64 107-113 2006年
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Endoscopy 38(1) 59-66 2006年1月 査読有り
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Endoscopy 37(12) 1215-1219 2005年12月 査読有り
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Cancer Epidemiol Biomarkers Prev 14(11 Pt 1) 2487-2493 2005年11月 査読有りHost genetic susceptibility may influence gastric carcinogenesis caused by Helicobacter pylori infection. We aimed to clarify the relationship of interleukin (IL)-8 polymorphism with the risk of atrophic gastritis and gastric cancer. We examined IL-8 -251 T > A, IL-1B -511 C > T, and IL-1RN intron 2 polymorphisms in 252 healthy controls, 215 individuals with atrophic gastritis, and 396 patients with gastric cancer. We also investigated the effect of the IL-8 polymorphism on IL-8 production and histologic degree of gastritis in noncancerous gastric mucosa. Although no correlation was found in the analysis of the IL-1B and IL-1RN polymorphisms, IL-8 -251 A/A genotype held a higher risk of atrophic gastritis [odds ratio (OR), 2.35; 95% confidence interval (CI), 1.12-4.94] and gastric cancer (OR, 2.22; 95% CI, 1.08-4.56) compared with the T/T genotype. We also found that the A/A genotype increased the risk of upper-third location (OR, 3.66; 95% CI, 1.46-9.17), diffuse (OR, 2.79; 95% CI, 1.21-6.39), poorly differentiated (OR, 2.70; 95% CI, 1.14-6.38), lymph node (OR, 2.50; 95% CI, 1.01-6.20), and liver metastasis (OR, 5.63; 95% CI, 1.06-30.04), and p53-mutated (OR, 1.91; 95% CI, 1.13-3.26) subtypes of gastric cancer. The A/A and A/T genotypes were significantly associated with higher levels of IL-8 protein compared with the T/T genotype. Neutrophil infiltration score was significantly higher in the A/A genotype than in the T/T genotype. In conclusion, we showed that the IL-8 -251 T > A polymorphism is associated with higher expression of IL-8 protein, more severe neutrophil infiltration, and increased risk of atrophic gastritis and gastric cancer.
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Japanese journal of medical ultrasonics = 超音波医学 32 S105 2005年4月15日
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GASTROENTEROLOGY 128(4) A401-A401 2005年4月
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胆道 = Journal of Japan Biliary Association 18(5) 614-619 2004年12月28日
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GASTROENTEROLOGY 126(4) A455-A456 2004年4月
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GASTROENTEROLOGY 126(4) A455-A455 2004年4月
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消化器外科 27(3) 347-352 2004年著者等が行った超音波大腸内視鏡下穿刺について概説した.具体的な対象は粘膜下腫瘍(GIST,腸管子宮内膜症など),粘膜下を中心に発育した癌(カルチノイド腫瘍や4型の大腸癌など),直腸癌や結腸癌術後の再発,他の悪性腫瘍による消化管近傍の腫瘤,直腸或いは下部消化管周囲の膿瘍であった.スライディングチューブやガイドワイヤーを用いることにより,深部結腸への挿入も可能であった.EUS-FNABを行った大腸疾患22例中,95.5%で組織診断が可能であった.EUS-FNAB施行後に治療方針が変更となった症例も多く認めた.以上,本法の開発で悪性腫瘍との鑑別が必要な消化管及びその周囲の腫瘤に対して下部消化管からもアプローチが可能となった
所属学協会
15共同研究・競争的資金等の研究課題
11-
日本学術振興会 科学研究費助成事業 2024年4月 - 2029年3月
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日本学術振興会 科学研究費助成事業 2024年4月 - 2027年3月
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日本学術振興会 科学研究費助成事業 2023年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 2019年4月 - 2022年3月
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日本学術振興会 科学研究費助成事業 2018年4月 - 2022年3月