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The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis
BACKGROUND: The incidence of microscopic colitis has increased over time. To date, there is no specific biomarker for microscopic colitis, and the diagnosis relies on histopathological tissue obtained during colonoscopy which is an invasive and costly procedure. Unlike Crohn’s disease and ulcerative...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Greater Baltimore Medical Center
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589029/ https://www.ncbi.nlm.nih.gov/pubmed/37868242 http://dx.doi.org/10.55729/2000-9666.1215 |
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author | Songtanin, Busara Evans, Abbie Nugent, Kenneth Costilla, Vanessa |
author_facet | Songtanin, Busara Evans, Abbie Nugent, Kenneth Costilla, Vanessa |
author_sort | Songtanin, Busara |
collection | PubMed |
description | BACKGROUND: The incidence of microscopic colitis has increased over time. To date, there is no specific biomarker for microscopic colitis, and the diagnosis relies on histopathological tissue obtained during colonoscopy which is an invasive and costly procedure. Unlike Crohn’s disease and ulcerative colitis, the utility of fecal calprotectin in diagnosing or monitoring microscopic colitis has not been established, and studies on the role of fecal calprotectin in microscopic colitis are limited. In this retrospective study, we analyzed the utility of this biomarker in the diagnosis of microscopic colitis. METHODS: The medical records of patients who have been diagnosed with collagenous colitis and lymphocytic colitis aged 18–89 years old were retrospectively reviewed. Patient characteristics were recorded in those who had fecal calprotectin measured. RESULTS: There were 198 patients who were diagnosed with collagenous colitis and lymphocytic between October 1, 2015, and July 31, 2022. Twenty-three patients had fecal calprotectin levels measured and were included in this study. The mean age was 51.7 ± 7.8 years in all groups. Thirteen patients were female. Six patients (26.1%) were diagnosed with collagenous colitis, and 17 patients (73.9%) were diagnosed with lymphocytic colitis. The fecal calprotectin cut-off in this lab is 50 μg/g stool. Median fecal calprotectin levels were 30.1 μg/g (15.6, 122.5), 19.5 μg/g (16.5, 64.6), and 33.2 μg/g (15.6, 134.9) in all groups, collagenous colitis, and lymphocytic colitis, respectively. CONCLUSION: The utility of fecal calprotectin in diagnosing microscopic colitis is limited. Our study suggests the diagnosis should be based on histopathology tissue obtained during colonoscopy. |
format | Online Article Text |
id | pubmed-10589029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Greater Baltimore Medical Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-105890292023-10-21 The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis Songtanin, Busara Evans, Abbie Nugent, Kenneth Costilla, Vanessa J Community Hosp Intern Med Perspect Research Article BACKGROUND: The incidence of microscopic colitis has increased over time. To date, there is no specific biomarker for microscopic colitis, and the diagnosis relies on histopathological tissue obtained during colonoscopy which is an invasive and costly procedure. Unlike Crohn’s disease and ulcerative colitis, the utility of fecal calprotectin in diagnosing or monitoring microscopic colitis has not been established, and studies on the role of fecal calprotectin in microscopic colitis are limited. In this retrospective study, we analyzed the utility of this biomarker in the diagnosis of microscopic colitis. METHODS: The medical records of patients who have been diagnosed with collagenous colitis and lymphocytic colitis aged 18–89 years old were retrospectively reviewed. Patient characteristics were recorded in those who had fecal calprotectin measured. RESULTS: There were 198 patients who were diagnosed with collagenous colitis and lymphocytic between October 1, 2015, and July 31, 2022. Twenty-three patients had fecal calprotectin levels measured and were included in this study. The mean age was 51.7 ± 7.8 years in all groups. Thirteen patients were female. Six patients (26.1%) were diagnosed with collagenous colitis, and 17 patients (73.9%) were diagnosed with lymphocytic colitis. The fecal calprotectin cut-off in this lab is 50 μg/g stool. Median fecal calprotectin levels were 30.1 μg/g (15.6, 122.5), 19.5 μg/g (16.5, 64.6), and 33.2 μg/g (15.6, 134.9) in all groups, collagenous colitis, and lymphocytic colitis, respectively. CONCLUSION: The utility of fecal calprotectin in diagnosing microscopic colitis is limited. Our study suggests the diagnosis should be based on histopathology tissue obtained during colonoscopy. Greater Baltimore Medical Center 2023-06-29 /pmc/articles/PMC10589029/ /pubmed/37868242 http://dx.doi.org/10.55729/2000-9666.1215 Text en © 2023 Greater Baltimore Medical Center https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ). |
spellingShingle | Research Article Songtanin, Busara Evans, Abbie Nugent, Kenneth Costilla, Vanessa The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title | The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title_full | The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title_fullStr | The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title_full_unstemmed | The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title_short | The Utility of Fecal Calprotectin in the Diagnosis and Management of Microscopic Colitis |
title_sort | utility of fecal calprotectin in the diagnosis and management of microscopic colitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589029/ https://www.ncbi.nlm.nih.gov/pubmed/37868242 http://dx.doi.org/10.55729/2000-9666.1215 |
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