Abstract

Background—Tumour necrosis factor alpha (TNFα) plays an important role in the pathogenesis of inflammatory bowel disease (IBD) and in immunity to Mycobacterium tuberculosis. Patients should be tested for latent tuberculosis infection using interferon-gamma release assays (IGRA/QF) prior to anti-TNFα therapy. Indeterminate QF results can delay anti-TNFα therapy. We sought to investigate factors associated with indeterminate QF results. Method—Retrospective study of all IGRA tests requested for gastroenterology patients in 2017. We compared inpatients and outpatients and investigated factors potentially associated with QF usefulness (steroid exposure, C-reactive protein (CRP), hypoalbuminaemia, thrombophilia). Results—We included 286 outpatients and 74 inpatients with IBD. Significantly more inpatients had an indeterminate IGRA (52.7% vs. 3.14% in outpatients; p < 0.0001). Laboratory parameters reflecting inflammation (high CRP, low albumin, low haemoglobin and high platelets) were also associated with an indeterminate QF (p < 0.0001). Exposure to steroids was more common in patients with an indeterminate QF (p < 0.0001). A binary logistic regression analysis revealed inpatient status and steroid exposure to be independently predictive of an indeterminate QF (p < 0.0001). Conclusion—There is a high chance of indeterminate QF results in inpatients. QF testing should ideally be performed in the outpatient setting at diagnosis.

Highlights

  • Inflammatory bowel disease (IBD), which incorporates both Crohn’s disease and ulcerative colitis, is a chronic, relapsing and remitting inflammatory condition affecting the gastrointestinal tract [1]

  • We identified 91 inpatients who had a QuantiFERON® TB Gold In-Tube test sent as part of their inpatient stay under gastroenterology in 2017

  • 39 (53%) patients who were tested for latent TB during their inpatient stay returned an indeterminate QuantiFERON® TB Gold In-Tube

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Summary

Introduction

Inflammatory bowel disease (IBD), which incorporates both Crohn’s disease and ulcerative colitis, is a chronic, relapsing and remitting inflammatory condition affecting the gastrointestinal tract [1]. The role of tumour necrosis factor alpha (TNFα), a pro-inflammatory cytokine, is well recognised in the pathogenesis of IBD [2]. TNFα is produced by monocytes, macrophages and T lymphocytes, and several other cell types, and can be released in response to multiple stimuli, including bacteria, viruses, immune complexes and stress [3]. It is a highly pro-inflammatory cytokine which is involved in the activation of granulocytes and T cells and the induction of fever, amongst. Tumour necrosis factor alpha (TNFα) plays an important role in the pathogenesis of inflammatory bowel disease (IBD) and in immunity to Mycobacterium tuberculosis. Laboratory parameters reflecting inflammation (high CRP, low albumin, low haemoglobin and high platelets) were associated with an indeterminate QF (p < 0.0001)

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