Biomarkers in inflammatory bowel disease: current practices and recent advances.
Open accessAbstract
Crohn's disease and ulcerative colitis represent the two main forms of the idiopathic chronic inflammatory bowel diseases (IBD). Currently available blood and stool based biomarkers provide reproducible, quantitative tools that can complement clinical assessment to aid clinicians in IBD diagnosis and management. C-reactive protein and fecal based leukocyte markers can help the clinician distinguish IBD from noninflammatory diarrhea and assess disease activity. The ability to differentiate between forms of IBD and predict risk for disease complications is specific to serologic tests including antibodies against Saccharomyces cerevisiae and perinuclear antineutrophil cytoplasmic proteins. Advances in genomic, proteomic, and metabolomic array based technologies are facilitating the development of new biomarkers for IBD. The discovery of novel biomarkers, which can correlate with mucosal healing or predict long-term disease course has the potential to significantly improve patient care. This article reviews the uses and limitations of currently available biomarkers and highlights recent advances in IBD biomarker discovery.
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Tricyclic antidepressants at doses below the usual antidepressant range have been used to control symptoms in irritable bowel syndrome.
“Tricyclic antidepressants (TCAs), at doses below the traditional antidepressant range, have been used for symptom control in IBS.6,7”
From Tricyclic Antidepressants for Management of Residual Symptoms in Inflammatory Bowel Disease (2014) · cites this paper as [7]
Tricyclic antidepressants are effective for treating irritable bowel syndrome.
“Tricyclic antidepressants (TCAs) have efficacy in treating irritable bowel syndrome (IBS).”
From Tricyclic Antidepressants for Management of Residual Symptoms in Inflammatory Bowel Disease (2014) · cites this paper as [7]
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- Authors
- Iskandar, H. N., & Ciorba, M. A.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Ciorba, Matthew A.
- ORCID
- Ciorba, Matthew A.
- Venue
- Translational Research
- Publisher
- Elsevier BV
- Published
- 2012-04
- Volume
- 159
- Issue
- 4
- Pages
- 313-325
- ISSN
- 1878-1810 (ISSN-L)
- 1931-5244
- PMC
- PMC3308116
- OpenAlex
- W2100688872
- Cited by
- 210
- References
- 140
- Citations by year
- 2026: 8 · 2025: 15 · 2024: 13 · 2023: 14 · 2022: 10 · 2021: 11 · 2020: 13 · 2019: 15 · 2018: 12 · 2017: 16 · 2016: 22 · 2015: 19 · 2014: 21 · 2013: 15 · 2012: 6
- FWCI
- 2.39
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Translational research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (UL1TR000448)
- National Institute of Diabetes and Digestive and Kidney Diseases (K08DK089016, T32DK007130)
- National Center for Research Resources (L30-RR030244)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Health Sciences › Medicine › Ophthalmology › Ocular Diseases and Behçet’s Syndrome
- Health Sciences › Medicine › Rheumatology › Spondyloarthritis Studies and Treatments
- Keywords
- inflammatory bowel disease, biomarkers, Crohn's disease, ulcerative colitis, C-reactive protein, fecal calprotectin, ASCA, mucosal healing, disease activity assessment, biomarker discovery, proteomics, metabolomics, genomics
- MeSH terms
- Humans, Predictive Value of Tests, Inflammatory Bowel Diseases, Biomarkers
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