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Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin?
Accurate evaluation of disease activity is essential for choosing an appropriate treatment and follow-up plan for patients with inflammatory bowel disease (IBD). Endoscopy is required for accurately evaluating disease activity, but the procedures are sometimes invasive and burdensome to patients. Th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for the Study of Intestinal Diseases
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754522/ https://www.ncbi.nlm.nih.gov/pubmed/26884729 http://dx.doi.org/10.5217/ir.2016.14.1.5 |
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author | Kato, Jun Hiraoka, Sakiko Nakarai, Asuka Takashima, Shiho Inokuchi, Toshihiro Ichinose, Masao |
author_facet | Kato, Jun Hiraoka, Sakiko Nakarai, Asuka Takashima, Shiho Inokuchi, Toshihiro Ichinose, Masao |
author_sort | Kato, Jun |
collection | PubMed |
description | Accurate evaluation of disease activity is essential for choosing an appropriate treatment and follow-up plan for patients with inflammatory bowel disease (IBD). Endoscopy is required for accurately evaluating disease activity, but the procedures are sometimes invasive and burdensome to patients. Therefore, alternative non-invasive methods for evaluating or predicting disease activity including mucosal status are desirable. Fecal calprotectin (Fcal) is the most widely used fecal marker for IBD, and many articles have described the performance of the marker in predicting disease activity, mucosal healing (MH), treatment efficacy, and risk of relapse. Fecal immunochemical test (FIT) can quantify the concentration of hemoglobin in stool and was originally used for the screening of colorectal cancer. We recently reported that FIT is also a useful biomarker for IBD. A direct comparison between the use of Fcal and FIT showed that both methods predicted MH in ulcerative colitis equally well. However, in the case of Crohn's disease, FIT was less sensitive to lesions in the small intestine, compared to Fcal. FIT holds several advantages over Fcal in regards to user-friendliness, including a lower cost, easy and clean handling, and the ability to make rapid measurements by using an automated measurement system. However, there is insufficient data to support the application of FIT in IBD. Further studies into the use of FIT for evaluating the inflammatory status of IBD are warranted. |
format | Online Article Text |
id | pubmed-4754522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Association for the Study of Intestinal Diseases |
record_format | MEDLINE/PubMed |
spelling | pubmed-47545222016-02-16 Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? Kato, Jun Hiraoka, Sakiko Nakarai, Asuka Takashima, Shiho Inokuchi, Toshihiro Ichinose, Masao Intest Res Review Accurate evaluation of disease activity is essential for choosing an appropriate treatment and follow-up plan for patients with inflammatory bowel disease (IBD). Endoscopy is required for accurately evaluating disease activity, but the procedures are sometimes invasive and burdensome to patients. Therefore, alternative non-invasive methods for evaluating or predicting disease activity including mucosal status are desirable. Fecal calprotectin (Fcal) is the most widely used fecal marker for IBD, and many articles have described the performance of the marker in predicting disease activity, mucosal healing (MH), treatment efficacy, and risk of relapse. Fecal immunochemical test (FIT) can quantify the concentration of hemoglobin in stool and was originally used for the screening of colorectal cancer. We recently reported that FIT is also a useful biomarker for IBD. A direct comparison between the use of Fcal and FIT showed that both methods predicted MH in ulcerative colitis equally well. However, in the case of Crohn's disease, FIT was less sensitive to lesions in the small intestine, compared to Fcal. FIT holds several advantages over Fcal in regards to user-friendliness, including a lower cost, easy and clean handling, and the ability to make rapid measurements by using an automated measurement system. However, there is insufficient data to support the application of FIT in IBD. Further studies into the use of FIT for evaluating the inflammatory status of IBD are warranted. Korean Association for the Study of Intestinal Diseases 2016-01 2016-01-25 /pmc/articles/PMC4754522/ /pubmed/26884729 http://dx.doi.org/10.5217/ir.2016.14.1.5 Text en © Copyright 2016. Korean Association for the Study of Intestinal Diseases. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Kato, Jun Hiraoka, Sakiko Nakarai, Asuka Takashima, Shiho Inokuchi, Toshihiro Ichinose, Masao Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title | Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title_full | Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title_fullStr | Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title_full_unstemmed | Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title_short | Fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
title_sort | fecal immunochemical test as a biomarker for inflammatory bowel diseases: can it rival fecal calprotectin? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754522/ https://www.ncbi.nlm.nih.gov/pubmed/26884729 http://dx.doi.org/10.5217/ir.2016.14.1.5 |
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