Mayo Clinic Laboratories > Inflammatory bowel disease testing

IBD: Testing for diagnosis and treatment monitoring

Improving lives through personalized testing  

From potentially lengthy diagnostic odysseys to repeated and ongoing monitoring to gauge treatment response, laboratory testing is an important aspect of a patient’s journey with inflammatory bowel disease (IBD). With varying causes and a growing slate of biologic medications to manage symptoms, choosing the best test for your patients can be complicated.

Helping patients move forward

When used appropriately, laboratory test results can be a powerful tool to improve the lives of patients affected by IBD. Implementing therapeutic drug monitoring to assess effectivity of tailored treatments provides a deep understanding into a patient’s therapeutic response and personalized insights to optimize medication selection.

End-to-end IBD testing translates into streamlined care that helps patients live symptom-free and move on with their lives.

Our testing use case scenario guide provides a detailed look at how targeted analysis can equip physicians and healthcare professionals with insights to diagnose patients and make treatment decisions.

Cases include:

  • Diagnostic testing
    • IBD diagnosis
    • Monogenic IBD testing
  • Therapeutic drug monitoring
    • Proactive testing: adalimumab
    • Reactive testing: infliximab
    • Proactive testing: infliximab
    • Reactive testing: risankizumab

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Inflammatory bowel disease: Diagnostic testing and therapeutic drug monitoring

“Therapeutic drug monitoring is routinely used to assess loss of response to therapy and proactively manage patients taking biologics. It has become standard of care in the gastroenterology practice, especially for inflammatory bowel disease, Crohn's disease, and ulcerative colitis.

Maria Alice Willrich, Ph.D., Mayo Clinic

Biologics treatment evolution

Biologic medications: an evolving landscape of treatment options

Heightened understanding of the complex pathophysiology of IBD has led to a boom in development of targeted therapies that focus on different aspects of the inflammatory process. In the last 10 years alone, eight new drugs, as well as biosimilar medications and subcutaneous versions of several drugs, have received approval from the U.S. Food and Drug Administration.

  • Anti-tumor necrosis factor agents block tumor necrosis factor (TNF)-mediated activation of proinflammatory pathways by using monoclonal antibody targeting to induce remission.
    • Infliximab and biosimilars
    • Adalimumab and biosimilars
    • Certolizumab (Crohn’s disease only)
    • Golimumab (ulcerative colitis only)
  • Anti-integrins block the movement of leukocytes to the site of inflammation within the intestinal vasculature.
    • Vedolizumab
    • Natalizumab
  • Interleukin 12/23 inhibitor uses monoclonal antibodies that block interleukin-12 and -23, which are key cytokines in IBD pathogenesis.
    • Ustekinumab
  • Interleukin 23 inhibitors use monoclonal antibodies that block interleukin-23, which is a key cytokine in IBD pathogenesis. 
    • Risankizumab-rzaa
    • Mirikizumab-mrkz (ulcerative colitis only)

Real-world impact of personalized medicine

For most of his adult life, Billy Dowell Jr. has lived with a serious immune-mediated disease process that causes multiple conditions, including ulcerative colitis. As a result of consistent follow-up care, biologic therapy, and laboratory testing to monitor his treatment, Billy’s symptoms have been well controlled for more than a decade.

“Laboratory test results are a great affirmation,” says Billy. “It takes a lot for me to want to slow down, but if I do experience that, or I think my disease is flaring, then I have the confidence that the laboratory is getting that information. With the test confirmation we know where to go with me.”

Read Billy’s story

Highlights


Resources
References
  1. Alatab S, Sepanlou S, Ikuta K, et al. The global, regional, and national burden of inflammatory bowel disease in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5(1):17-30. https://doi.org/10.1016/S2468-1253(19)30333-4.
  2. Genaro LM, Gomes LEM, Franceschini APMF, et al. Anti-TNF therapy and immunogenicity in inflammatory bowel diseases: a translational approach. Am J Transl Res. 2021 Dec 15;13(12):13916-13930. PMID: 35035733; PMCID: PMC8748125.
  3. Kennedy NA, Heap GA, Green HD, et al. Predictors of anti-TNF treatment failure in anti-TNF-naive patients with active luminal Crohn’s disease: a prospective, multicentre, cohort study. Lancet Gastroenterol Hepatol. 2019;4(5):341-353.
  4. Willrich MAV, Murray DL, Snyder MR. Tumor necrosis factor inhibitors: clinical utility in autoimmune diseases. Transl Res. 2015;165(2):270-282.
  5. Li X, Zhong Y, Yuan C, et al. Identifying patients with Crohn's disease at high risk of primary nonresponse to infliximab using a radiomic-clinical model. Int J Intell Syst. 2022 Sept;37(12): 11853-11870. https://doi.org/10.1002/int.23066.
  6. Cheifetz AS, Abreu MT, Afif W, et al. A comprehensive literature review and expert consensus statement on therapeutic drug monitoring of biologics in inflammatory bowel disease. Am J Gastroenterol. 2021 Oct 1;116(10):2014-2025. doi:10.14309/ajg.0000000000001396. PMID: 34388143; PMCID: PMC9674375.

Learn more about how testing can support evidence-based diagnosis and treatment strategies.