Combined endocytoscopy with pit pattern diagnosis in ulcerative colitis‐associated neoplasia: a pilot study

2021 ◽  
Author(s):  
Shin‐ei Kudo ◽  
Yasuharu Maeda ◽  
Noriyuki Ogata ◽  
Masashi Misawa ◽  
Yushi Ogawa ◽  
...  
2007 ◽  
Vol 65 (5) ◽  
pp. AB254
Author(s):  
Kazuo Ohtsuka ◽  
Ken-Ichi Mizuno ◽  
Hiroshi Kashida ◽  
Ryo Chinzei ◽  
Jun-Ichi Ukegawa ◽  
...  

2006 ◽  
Vol 63 (5) ◽  
pp. AB214
Author(s):  
Nobuyuki Hida ◽  
Kenji Watanabe ◽  
Kazutoshi Hori ◽  
Hiroki Ikeuchi ◽  
Yoshio Ohda ◽  
...  

2004 ◽  
Vol 126 (1) ◽  
pp. 374-376 ◽  
Author(s):  
Keisuke Hata ◽  
Toshiaki Watanabe ◽  
Toru Motoi ◽  
Hirokazu Nagawa

2008 ◽  
Vol 134 (4) ◽  
pp. A-205
Author(s):  
Ken-ichi Mizuno ◽  
Kazuo Ohtsuka ◽  
Kenta Kodama ◽  
Shigeharu Hamatani ◽  
Shin-ei Kudo

2021 ◽  
Vol 27 (Supplement_1) ◽  
pp. S38-S38
Author(s):  
Chen Sarbagili-Shabat ◽  
Lindsey Albenberg ◽  
Johan Van Limbergen ◽  
Dror Weiner ◽  
Michal Yaakov ◽  
...  

Abstract Background Newer strategies that target the microbiome may offer an alternative therapeutic approach for Ulcerative Colitis (UC). We developed a novel diet that targets changes in the microbiome and barrier function that have been reported in UC. The goal of the current study was to evaluate the efficacy of two sequential induction of remission strategies that target the microbiota: the novel diet termed the ulcerative colitis diet (UCD) and an antibiotics cocktail combination in dietary non responders. Methods This was a prospective, single arm, open label, pilot study in patients aged 8–19, with a pediatric UC activity index (PUCAI) scores >10 and ≤45 on stable maintenance therapy (5ASA or thiopurines). PUCAI score was assessed at week 3 and 6. Patients failing to enter remission or intolerant to dietary therapy could receive an open label 14-day course of Amoxycillin, Metronidazole and Doxycycline (AMD), and had PUCAI scored at day 21. Response was defined a decline in PUCAI ≥ 10 points, remission as PUCAI< 10. The primary endpoint was intention to treat (ITT) remission at week 6 with diet as the sole intervention. Results Twenty-three children mean age of 15.1±2.9 years were enrolled. Two patients (1 responder, 1 remission) withdrew by 3 weeks, four required additional therapy by week 3, all were considered failures by ITT. Mean PUCAI decreased at week 3 and 6 from 34.5±9.8 to 21.7±14.9 and 17.6±17.2 respectively (P=0.005, P=0.001) at ITT analysis including all patients. Sixteen out of twenty-three patients (69.6%) responded by week 6. Ten of twenty-three (43.5%) achieved remission by week 6, and nine (39.1%) had clinical remission at week 6. The median fecal calprotectin (FC) level decreased in patients (n=5) who achieved remission from 630 (IQR, 332–1586) μg/g at week 0 to 230 (75–1298) μg/g at week 6. Eight patients received treatment with antibiotics after failing diet, 4/8 (50.0%) subsequently entered remission. Conclusion A dietary intervention called the UC Diet appears to be effective for induction of remission in children with mild to moderate UC. Sequential use of diet, followed by antibiotic therapy in dietary non responders, needs further evaluation as a microbiome directed steroid sparing therapy in patient’s refractory to 5ASA and thiopurines.


Nutrients ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 1429
Author(s):  
Theo Wallimann ◽  
Caroline H. T. Hall ◽  
Sean P. Colgan ◽  
Louise E. Glover

Based on theoretical considerations, experimental data with cells in vitro, animal studies in vivo, as well as a single case pilot study with one colitis patient, a consolidated hypothesis can be put forward, stating that “oral supplementation with creatine monohydrate (Cr), a pleiotropic cellular energy precursor, is likely to be effective in inducing a favorable response and/or remission in patients with inflammatory bowel diseases (IBD), like ulcerative colitis and/or Crohn’s disease”. A current pilot clinical trial that incorporates the use of oral Cr at a dose of 2 × 7 g per day, over an initial period of 2 months in conjunction with ongoing therapies (NCT02463305) will be informative for the proposed larger, more long-term Cr supplementation study of 2 × 3–5 g of Cr per day for a time of 3–6 months. This strategy should be insightful to the potential for Cr in reducing or alleviating the symptoms of IBD. Supplementation with chemically pure Cr, a natural nutritional supplement, is well tolerated not only by healthy subjects, but also by patients with diverse neuromuscular diseases. If the outcome of such a clinical pilot study with Cr as monotherapy or in conjunction with metformin were positive, oral Cr supplementation could then be used in the future as potentially useful adjuvant therapeutic intervention for patients with IBD, preferably together with standard medication used for treating patients with chronic ulcerative colitis and/or Crohn’s disease.


2020 ◽  
Vol 158 (6) ◽  
pp. S-964-S-965
Author(s):  
Srishti Saha ◽  
Prabhjot Grace Dosanjh ◽  
Edward V. Loftus ◽  
Sahil Khanna ◽  
Darrell S. Pardi

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