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Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series
BACKGROUND AND AIMS: Adrenomedullin (AM) is a multifunctional biologically active peptide that has an ameliorative effect against inflammatory bowel disease in several experimental models. We reported the first case where AM infusion dramatically improved symptoms and colonoscopy findings in patient...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761007/ https://www.ncbi.nlm.nih.gov/pubmed/26470867 http://dx.doi.org/10.1007/s10620-015-3917-0 |
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author | Ashizuka, Shinya Inatsu, Haruhiko Kita, Toshihiro Kitamura, Kazuo |
author_facet | Ashizuka, Shinya Inatsu, Haruhiko Kita, Toshihiro Kitamura, Kazuo |
author_sort | Ashizuka, Shinya |
collection | PubMed |
description | BACKGROUND AND AIMS: Adrenomedullin (AM) is a multifunctional biologically active peptide that has an ameliorative effect against inflammatory bowel disease in several experimental models. We reported the first case where AM infusion dramatically improved symptoms and colonoscopy findings in patients with refractory ulcerative colitis (UC). To confirm the reproducibility of the efficacy and safety of AM infusion, this pilot study evaluated the clinical feasibility of intravenous administration of AM in patients with refractory UC. METHODS: Seven patients with active refractory UC participated and received intravenous infusion of AM (1.5 pmol/kg/min) for 8 h daily for 14 days, and their Disease Activity Index (DAI) were evaluated before and 2 and 12 weeks after beginning AM administration. RESULTS: DAI were improved in all patients after AM administration. Within 2 weeks, marked declines in DAI (≥3 points and ≥30 %) were observed in six patients (85.7 %), while a more modest decline was observed in one patient (14.3 %). Overall mean DAI improved from 9.3 ± 0.6 at baseline to 4.6 ± 0.8 at 2 weeks, and then to 1.2 ± 0.5 at 12 weeks. Endoscopic examination revealed substantial amelioration of ulcers, with mucosal healing and scarring. Four patients remained in clinical remission 12 months after AM treatment. AM administration produced significant increases in plasma AM concentrations (approximately 2.5-fold) that had a mild effect on blood pressure and heart rate, but with no serious adverse effects. CONCLUSION: AM is a potentially useful agent that acts via a novel mechanism to safely induce mucosal healing and clinical remission in patients with refractory UC. |
format | Online Article Text |
id | pubmed-4761007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-47610072016-03-01 Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series Ashizuka, Shinya Inatsu, Haruhiko Kita, Toshihiro Kitamura, Kazuo Dig Dis Sci Original Article BACKGROUND AND AIMS: Adrenomedullin (AM) is a multifunctional biologically active peptide that has an ameliorative effect against inflammatory bowel disease in several experimental models. We reported the first case where AM infusion dramatically improved symptoms and colonoscopy findings in patients with refractory ulcerative colitis (UC). To confirm the reproducibility of the efficacy and safety of AM infusion, this pilot study evaluated the clinical feasibility of intravenous administration of AM in patients with refractory UC. METHODS: Seven patients with active refractory UC participated and received intravenous infusion of AM (1.5 pmol/kg/min) for 8 h daily for 14 days, and their Disease Activity Index (DAI) were evaluated before and 2 and 12 weeks after beginning AM administration. RESULTS: DAI were improved in all patients after AM administration. Within 2 weeks, marked declines in DAI (≥3 points and ≥30 %) were observed in six patients (85.7 %), while a more modest decline was observed in one patient (14.3 %). Overall mean DAI improved from 9.3 ± 0.6 at baseline to 4.6 ± 0.8 at 2 weeks, and then to 1.2 ± 0.5 at 12 weeks. Endoscopic examination revealed substantial amelioration of ulcers, with mucosal healing and scarring. Four patients remained in clinical remission 12 months after AM treatment. AM administration produced significant increases in plasma AM concentrations (approximately 2.5-fold) that had a mild effect on blood pressure and heart rate, but with no serious adverse effects. CONCLUSION: AM is a potentially useful agent that acts via a novel mechanism to safely induce mucosal healing and clinical remission in patients with refractory UC. Springer US 2015-10-15 2016 /pmc/articles/PMC4761007/ /pubmed/26470867 http://dx.doi.org/10.1007/s10620-015-3917-0 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Ashizuka, Shinya Inatsu, Haruhiko Kita, Toshihiro Kitamura, Kazuo Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title | Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title_full | Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title_fullStr | Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title_full_unstemmed | Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title_short | Adrenomedullin Therapy in Patients with Refractory Ulcerative Colitis: A Case Series |
title_sort | adrenomedullin therapy in patients with refractory ulcerative colitis: a case series |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761007/ https://www.ncbi.nlm.nih.gov/pubmed/26470867 http://dx.doi.org/10.1007/s10620-015-3917-0 |
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